加藤 規弘 - 研究業績

I. 英文原著論文（*corresponding author）

  1. Sung YJ, de Las Fuentes L, Winkler TW, Chasman DI, Bentley AR, Kraja AT, Ntalla I, Warren HR, Guo X, Schwander K, Manning AK, Brown MR, Aschard H, Feitosa MF, Franceschini N, Lu Y, Cheng CY, Sim X, Vojinovic D, Marten J, Musani SK, Kilpeläinen TO, Richard MA, Aslibekyan S, Bartz TM,Dorajoo R, Li C, Liu Y, Rankinen T, Smith AV, Tajuddin SM, Tayo BO, Zhao W, Zhou Y, Matoba N, Sofer T, Alver M, Amini M, Boissel M, Chai JF, Chen X, Divers J, Gandin I, Gao C, Giulianini F, Goel A,Harris SE, Hartwig FP, He M, Horimoto ARVR, Hsu FC, Jackson AU, Kammerer CM, Kasturiratne A, Komulainen P, Kühnel B, Leander K, Lee WJ, Lin KH, Luan J, Lyytikäinen LP, McKenzie CA, Nelson CP, Noordam R, Scott RA, Sheu WHH, Stančáková A, Takeuchi F, van der Most PJ, Varga TV, Waken RJ, Wang H, Wang Y, Ware EB, Weiss S, Wen W, Yanek LR, Zhang W, Zhao JH, Afaq S, Alfred T, Amin N, Arking DE, Aung T, Barr RG, Bielak LF, Boerwinkle E, Bottinger EP, Braund PS, Brody JA, Broeckel U, Cade B, Campbell A, Canouil M, Chakravarti A, Cocca M, Collins FS, Connell JM, de Mutsert R, de Silva HJ, Dörr M, Duan Q, Eaton CB, Ehret G, Evangelou E, Faul JD, Forouhi NG, Franco OH, Friedlander Y, Gao H, Gigante B, Gu CC, Gupta P, Hagenaars SP, Harris TB, He J, Heikkinen S, Heng CK, Hofman A, Howard BV, Hunt SC, Irvin MR, Jia Y, Katsuya T, Kaufman J, Kerrison ND, Khor CC, Koh WP, Koistinen HA, Kooperberg CB, Krieger JE, Kubo M, Kutalik Z,Kuusisto J, Lakka TA, Langefeld CD, Langenberg C, Launer LJ, Lee JH, Lehne B, Levy D, Lewis CE, Li Y; Lifelines Cohort Study, Lim SH, Liu CT, Liu J, Liu J, Liu Y, Loh M, Lohman KK, Louie T, Mägi R, Matsuda K, Meitinger T, Metspalu A, Milani L, Momozawa Y, Mosley TH Jr, Nalls MA, Nasri U, O'Connell JR, Ogunniyi A, Palmas WR, Palmer ND, Pankow JS, Pedersen NL, Peters A, Peyser PA, Polasek O, Porteous D, Raitakari OT, Renström F, Rice TK, Ridker PM, Robino A, Robinson JG, Rose LM, Rudan I, Sabanayagam C, Salako BL, Sandow K, Schmidt CO, Schreiner PJ, Scott WR, Sever P, Sims M, Sitlani CM, Smith BH, Smith JA, Snieder H, Starr JM, Strauch K, Tang H, Taylor KD, Teo YY, Tham YC, Uitterlinden AG, Waldenberger M, Wang L, Wang YX, Wei WB, Wilson G,Wojczynski MK, Xiang YB, Yao J, Yuan JM, Zonderman AB, Becker DM, Boehnke M, Bowden DW, Chambers JC, Chen YI, Weir DR, de Faire U, Deary IJ, Esko T, Farrall M, Forrester T, Freedman BI,Froguel P, Gasparini P, Gieger C, Horta BL, Hung YJ, Jonas JB, Kato N, Kooner JS, Laakso M, Lehtimäki T, Liang KW, Magnusson PKE, Oldehinkel AJ, Pereira AC, Perls T, Rauramaa R, Redline S,Rettig R, Samani NJ, Scott J, Shu XO, van der Harst P, Wagenknecht LE, Wareham NJ, Watkins H, Wickremasinghe AR, Wu T, Kamatani Y, Laurie CC, Bouchard C, Cooper RS, Evans MK, Gudnason V, Hixson J, Kardia SLR, Kritchevsky SB, Psaty BM, van Dam RM, Arnett DK, Mook-Kanamori DO, Fornage M, Fox ER, Hayward C, van Duijn CM, Tai ES, Wong TY, Loos RJF, Reiner AP, Rotimi CN,Bierut LJ, Zhu X, Cupples LA, Province MA, Rotter JI, Franks PW, Rice K, Elliott P, Caulfield MJ, Gauderman WJ, Munroe PB, Rao DC, Morrison AC. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum Mol Genet.2019 Apr 10. [Epub ahead of print]. PMID: 31127295
  2. Nakatochi M, Kanai M, Nakayama A, Hishida A, Kawamura Y, Ichihara S, Akiyama M, Ikezaki H,Furusyo N, Shimizu S, Yamamoto K, Hirata M, Okada R, Kawai S, Kawaguchi M, Nishida Y, Shimanoe C, Ibusuki R, Takezaki T, Nakajima M, Takao M, Ozaki E, Matsui D, Nishiyama T, Suzuki S,Takashima N, Kita Y, Endoh K, Kuriki K, Uemura H, Arisawa K, Oze I, Matsuo K, Nakamura Y, Mikami H, Tamura T, Nakashima H, Nakamura T, Kato N, Matsuda K, Murakami Y, Matsubara T, Naito M,Kubo M, Kamatani Y, Shinomiya N, Yokota M, Wakai K, Okada Y, Matsuo H. Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals. Commun Biol. 2019 Apr 8;2:115 PMID: 30993211
  3. Bentley AR, Sung YJ, Brown MR, Winkler TW, Kraja AT, Ntalla I, Schwander K, Chasman DI, Lim E,Deng X, Guo X, Liu J, Lu Y, Cheng CY, Sim X, Vojinovic D, Huffman JE, Musani SK, Li C, Feitosa MF, Richard MA, Noordam R, Baker J, Chen G, Aschard H, Bartz TM, Ding J, Dorajoo R, Manning AK, Rankinen T, Smith AV, Tajuddin SM, Zhao W, Graff M, Alver M, Boissel M, Chai JF, Chen X, Divers J, Evangelou E, Gao C, Goel A, Hagemeijer Y, Harris SE, Hartwig FP, He M, Horimoto ARVR, Hsu FC,Hung YJ, Jackson AU, Kasturiratne A, Komulainen P, Kühnel B, Leander K, Lin KH, Luan J, Lyytikäinen LP, Matoba N, Nolte IM, Pietzner M, Prins B, Riaz M, Robino A, Said MA, Schupf N, Scott RA, Sofer T, Stancáková A, Takeuchi F, Tayo BO, van der Most PJ, Varga TV, Wang TD, Wang Y, Ware EB, Wen W, Xiang YB, Yanek LR, Zhang W, Zhao JH, Adeyemo A, Afaq S, Amin N, Amini M,Arking DE, Arzumanyan Z, Aung T, Ballantyne C, Barr RG, Bielak LF, Boerwinkle E, Bottinger EP, Broeckel U, Brown M, Cade BE, Campbell A, Canouil M, Charumathi S, Chen YI, Christensen K;COGENT-Kidney Consortium, Concas MP, Connell JM, de Las Fuentes L, de Silva HJ, de Vries PS, Doumatey A, Duan Q, Eaton CB, Eppinga RN, Faul JD, Floyd JS, Forouhi NG, Forrester T,Friedlander Y, Gandin I, Gao H, Ghanbari M, Gharib SA, Gigante B, Giulianini F, Grabe HJ, Gu CC, Harris TB, Heikkinen S, Heng CK, Hirata M, Hixson JE, Ikram MA; EPIC-InterAct Consortium, Jia Y,Joehanes R, Johnson C, Jonas JB, Justice AE, Katsuya T, Khor CC, Kilpeläinen TO, Koh WP, Kolcic I, Kooperberg C, Krieger JE, Kritchevsky SB, Kubo M, Kuusisto J, Lakka TA, Langefeld CD, Langenberg C, Launer LJ, Lehne B, Lewis CE, Li Y, Liang J, Lin S, Liu CT, Liu J, Liu K, Loh M, Lohman KK, Louie T, Luzzi A, Mägi R, Mahajan A, Manichaikul AW, McKenzie CA, Meitinger T,Metspalu A, Milaneschi Y, Milani L, Mohlke KL, Momozawa Y, Morris AP, Murray AD, Nalls MA, Nauck M, Nelson CP, North KE, O'Connell JR, Palmer ND, Papanicolau GJ, Pedersen NL, Peters A,Peyser PA, Polasek O, Poulter N, Raitakari OT, Reiner AP, Renström F, Rice TK, Rich SS, Robinson JG, Rose LM, Rosendaal FR, Rudan I, Schmidt CO, Schreiner PJ, Scott WR, Sever P, Shi Y, Sidney S, Sims M, Smith JA, Snieder H, Starr JM, Strauch K, Stringham HM, Tan NYQ, Tang H, Taylor KD, Teo YY, Tham YC, Tiemeier H, Turner ST, Uitterlinden AG; Understanding Society Scientific Group, van Heemst D, Waldenberger M, Wang H, Wang L, Wang L, Wei WB, Williams CA, Wilson G Sr, Wojczynski MK, Yao J, Young K, Yu C, Yuan JM, Zhou J, Zonderman AB, Becker DM, Boehnke M,Bowden DW, Chambers JC, Cooper RS, de Faire U, Deary IJ, Elliott P, Esko T, Farrall M, Franks PW, Freedman BI, Froguel P, Gasparini P, Gieger C, Horta BL, Juang JJ, Kamatani Y, Kammerer CM, Kato N, Kooner JS, Laakso M, Laurie CC, Lee IT, Lehtimäki T; Lifelines Cohort, Magnusson PKE, Oldehinkel AJ, Penninx BWJH, Pereira AC, Rauramaa R, Redline S, Samani NJ, Scott J, Shu XO,van der Harst P, Wagenknecht LE, Wang JS, Wang YX, Wareham NJ, Watkins H, Weir DR, Wickremasinghe AR, Wu T, Zeggini E, Zheng W, Bouchard C, Evans MK, Gudnason V, Kardia SLR,Liu Y, Psaty BM, Ridker PM, van Dam RM, Mook-Kanamori DO, Fornage M, Province MA, Kelly TN, Fox ER, Hayward C, van Duijn CM, Tai ES, Wong TY, Loos RJF, Franceschini N, Rotter JI, Zhu X,Bierut LJ, Gauderman WJ, Rice K, Munroe PB, Morrison AC, Rao DC, Rotimi CN, Cupples LA. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat Genet. 2019 Apr;51(4):636-648. PMID: 30926973
  4. de Vries PS, Brown MR, Bentley AR, Sung YJ, Winkler TW, Ntalla I, Schwander K, Kraja AT, Guo X,Franceschini N, Cheng CY, Sim X, Vojinovic D, Huffman JE, Musani SK, Li C, Feitosa MF, Richard MA, Noordam R, Aschard H, Bartz TM, Bielak LF, Deng X, Dorajoo R, Lohman KK, Manning AK,Rankinen T, Smith AV, Tajuddin SM, Evangelou E, Graff M, Alver M, Boissel M, Chai JF, Chen X, Divers J, Gandin I, Gao C, Goel A, Hagemeijer Y, Harris SE, Hartwig FP, He M, Horimoto ARVR, Hsu FC, Jackson AU, Kasturiratne A, Komulainen P, Kühnel B, Laguzzi F, Lee JH, Luan J, Lyytikäinen LP, Matoba N, Nolte IM, Pietzner M, Riaz M, Said MA, Scott RA, Sofer T, Stancáková A, Takeuchi F, Tayo BO, van der Most PJ, Varga TV, Wang Y, Ware EB, Wen W, Yanek LR, Zhang W, Zhao JH, Afaq S, Amin N, Amini M, Arking DE, Aung T, Ballantyne C, Boerwinkle E, Broeckel U, Campbell A, Canouil M,Charumathi S, Chen YI, Connell JM, de Faire U, de Las Fuentes L, de Mutsert R, de Silva HJ, Ding J, Dominiczak AF, Duan Q, Eaton CB, Eppinga RN, Faul JD, Fisher V, Forrester T, Franco OH, Friedlander Y, Ghanbari M, Giulianini F, Grabe HJ, Grove ML, Gu CC, Harris TB, Heikkinen S, Heng CK, Hirata M, Hixson JE, Howard BV, Ikram MA; InterAct Consortium, Jacobs DR Jr, Johnson C,Jonas JB, Kammerer CM, Katsuya T, Khor CC, Kilpeläinen TO, Koh WP, Koistinen HA, Kolcic I, Kooperberg C, Krieger JE, Kritchevsky SB, Kubo M, Kuusisto J, Lakka TA, Langefeld CD, Langenberg C, Launer LJ, Lehne B, Lemaitre RN, Li Y, Liang J, Liu J, Liu K, Loh M, Louie T, Mägi R, Manichaikul AW, McKenzie CA, Meitinger T, Metspalu A, Milaneschi Y, Milani L, Mohlke KL, Mosley TH Jr, Mukamal KJ, Nalls MA, Nauck M, Nelson CP, Sotoodehnia N, O'Connell JR, Palmer ND, Pazoki R, Pedersen NL, Peters A, Peyser PA, Polasek O, Poulter N, Raffel LJ, Raitakari OT, Reiner AP, Rice TK, Rich SS, Robino A, Robinson JG, Rose LM, Rudan I, Schmidt CO, Schreiner PJ, Scott WR, Sever P, Shi Y, Sidney S, Sims M, Smith BH, Smith JA, Snieder H, Starr JM, Strauch K, Tan N,Taylor KD, Teo YY, Tham YC, Uitterlinden AG, van Heemst D, Vuckovic D, Waldenberger M, Wang L, Wang Y, Wang Z, Wei WB, Williams C, Wilson G Sr, Wojczynski MK, Yao J, Yu B, Yu C, Yuan JM,Zhao W, Zonderman AB, Becker DM, Boehnke M, Bowden DW, Chambers JC, Deary IJ, Esko T, Farrall M, Franks PW, Freedman BI, Froguel P, Gasparini P, Gieger C, Horta BL, Kamatani Y, Kato N,Kooner JS, Laakso M, Leander K, Lehtimäki T; Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study), Magnusson PKE, Penninx B, Pereira AC, Rauramaa R, Samani NJ, Scott J,Shu XO, van der Harst P, Wagenknecht LE, Wang YX, Wareham NJ, Watkins H, Weir DR, Wickremasinghe AR, Zheng W, Elliott P, North KE, Bouchard C, Evans MK, Gudnason V, Liu CT, Liu Y, Psaty BM, Ridker PM, van Dam RM, Kardia SLR, Zhu X, Rotimi CN, Mook-Kanamori DO, Fornage M, Kelly TN, Fox ER, Hayward C, van Duijn CM, Tai ES, Wong TY, Liu J, Rotter JI, Gauderman WJ,Province MA, Munroe PB, Rice K, Chasman DI, Cupples LA, Rao DC, Morrison AC. Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Am J Epidemiol. 2019 Jun 1;188(6):1033-1054. PMID: 30698716
  5. Niriella MA, Kasturiratne A, Pathmeswaran A, De Silva ST, Perera KR, Subasinghe SKCE,Kodisinghe SK, Piyaratna TACL, Vithiya K, Dassanayaka AS, De Silva AP, Wickramasinghe AR, Takeuchi F, Kato N, de Silva HJ. Lean non-alcoholic fatty liver disease (lean NAFLD): characteristics, metabolic outcomes and risk factors from a 7-year prospective, community cohort study from Sri Lanka. Hepatol Int. 2019 May;13(3):314-322. PMID: 30539516
  6. Chauhan G, Adams HHH, Satizabal CL, Bis JC, Teumer A, Sargurupremraj M, Hofer E, Trompet S,Hilal S, Smith AV, Jian X, Malik R, Traylor M, Pulit SL, Amouyel P, Mazoyer B, Zhu YC, Kaffashian S, Schilling S, Beecham GW, Montine TJ, Schellenberg GD, Kjartansson O, Guðnason V, Knopman DS,Griswold ME, Windham BG, Gottesman RF, Mosley TH, Schmidt R, Saba Y, Schmidt H, Takeuchi F, Yamaguchi S, Nabika T, Kato N, Rajan KB, Aggarwal NT, De Jager PL, Evans DA, Psaty BM, Rotter JI, Rice K, Lopez OL, Liao J, Chen C, Cheng CY, Wong TY, Ikram MK, van der Lee SJ, Amin N, Chouraki V, DeStefano AL, Aparicio HJ, Romero JR, Maillard P, DeCarli C, Wardlaw JM, Hernández MDCV, Luciano M, Liewald D, Deary IJ, Starr JM, Bastin ME, Muñoz Maniega S, Slagboom PE, Beekman M, Deelen J, Uh HW, Lemmens R, Brodaty H, Wright MJ, Ames D, Boncoraglio GB,Hopewell JC, Beecham AH, Blanton SH, Wright CB, Sacco RL, Wen W, Thalamuthu A, Armstrong NJ, Chong E, Schofield PR, Kwok JB, van der Grond J, Stott DJ, Ford I, Jukema JW, Vernooij MW,Hofman A, Uitterlinden AG, van der Lugt A, Wittfeld K, Grabe HJ, Hosten N, von Sarnowski B, Völker U, Levi C, Jimenez-Conde J, Sharma P, Sudlow CLM, Rosand J, Woo D, Cole JW, Meschia JF,Slowik A, Thijs V, Lindgren A, Melander O, Grewal RP, Rundek T, Rexrode K, Rothwell PM, Arnett DK, Jern C, Johnson JA, Benavente OR, Wasssertheil-Smoller S, Lee JM, Wong Q, Mitchell BD, Rich SS,McArdle PF, Geerlings MI, van der Graaf Y, de Bakker PIW, Asselbergs FW, Srikanth V, Thomson R, McWhirter R, Moran C, Callisaya M, Phan T, Rutten-Jacobs LCA, Bevan S, Tzourio C, Mather KA, Sachdev PS, van Duijn CM, Worrall BB, Dichgans M, Kittner SJ, Markus HS, Ikram MA, Fornage M, Launer LJ, Seshadri S, Longstreth WT Jr, Debette S; Stroke Genetics Network (SiGN), the International Stroke Genetics Consortium (ISGC), METASTROKE, Alzheimer's Disease Genetics Consortium (ADGC), and the Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. Neurology. 2019 Jan 16. [Epub ahead of print] PMID: 30651383
  7. Kilpeläinen TO, Bentley AR, Noordam R, Sung YJ, Schwander K, Winkler TW, Jakupović H, Chasman DI, Manning A, Ntalla I, Aschard H, Brown MR, de Las Fuentes L, Franceschini N, Guo X, Vojinovic D, Aslibekyan S, Feitosa MF, Kho M, Musani SK, Richard M, Wang H, Wang Z, Bartz TM, Bielak LF,Campbell A, Dorajoo R, Fisher V, Hartwig FP, Horimoto ARVR, Li C, Lohman KK, Marten J, Sim X, Smith AV, Tajuddin SM, Alver M, Amini M, Boissel M, Chai JF, Chen X, Divers J, Evangelou E, Gao C, Graff M, Harris SE, He M, Hsu FC, Jackson AU, Zhao JH, Kraja AT, Kühnel B, Laguzzi F, Lyytikäinen LP, Nolte IM, Rauramaa R, Riaz M, Robino A, Rueedi R, Stringham HM, Takeuchi F, van der Most PJ,Varga TV, Verweij N, Ware EB, Wen W, Li X, Yanek LR, Amin N, Arnett DK, Boerwinkle E, Brumat M, Cade B, Canouil M, Chen YI, Concas MP, Connell J, de Mutsert R, de Silva HJ, de Vries PS,Demirkan A, Ding J, Eaton CB, Faul JD, Friedlander Y, Gabriel KP, Ghanbari M, Giulianini F, Gu CC, Gu D, Harris TB, He J, Heikkinen S, Heng CK, Hunt SC, Ikram MA, Jonas JB, Koh WP, Komulainen P,Krieger JE, Kritchevsky SB, Kutalik Z, Kuusisto J, Langefeld CD, Langenberg C, Launer LJ, Leander K, Lemaitre RN, Lewis CE, Liang J; Lifelines Cohort Study, Liu J, Mägi R, Manichaikul A, Meitinger T,Metspalu A, Milaneschi Y, Mohlke KL, Mosley TH Jr, Murray AD, Nalls MA, Nang EK, Nelson CP, Nona S, Norris JM, Nwuba CV, O'Connell J, Palmer ND, Papanicolau GJ, Pazoki R, Pedersen NL,Peters A, Peyser PA, Polasek O, Porteous DJ, Poveda A, Raitakari OT, Rich SS, Risch N, Robinson JG, Rose LM, Rudan I, Schreiner PJ, Scott RA, Sidney SS, Sims M, Smith JA, Snieder H, Sofer T, Starr JM, Sternfeld B, Strauch K, Tang H, Taylor KD, Tsai MY, Tuomilehto J, Uitterlinden AG, van der Ende MY, van Heemst D, Voortman T, Waldenberger M, Wennberg P, Wilson G, Xiang YB, Yao J, Yu C, Yuan JM, Zhao W, Zonderman AB, Becker DM, Boehnke M, Bowden DW, de Faire U, Deary IJ, Elliott P, Esko T, Freedman BI, Froguel P, Gasparini P, Gieger C, Kato N, Laakso M, Lakka TA, Lehtimäki T, Magnusson PKE, Oldehinkel AJ, Penninx BWJH, Samani NJ, Shu XO, van der Harst P, Van Vliet-Ostaptchouk JV, Vollenweider P, Wagenknecht LE, Wang YX, Wareham NJ, Weir DR, Wu T, Zheng W, Zhu X, Evans MK, Franks PW, Gudnason V, Hayward C, Horta BL, Kelly TN, Liu Y, North KE, Pereira AC, Ridker PM, Tai ES, van Dam RM, Fox ER, Kardia SLR, Liu CT, Mook-Kanamori DO,Province MA, Redline S, van Duijn CM, Rotter JI, Kooperberg CB, Gauderman WJ, Psaty BM, Rice K, Munroe PB, Fornage M, Cupples LA, Rotimi CN, Morrison AC, Rao DC, Loos RJF. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat Commun. 2019 Jan 22;10(1):376. PMID: 30670697
  8. Takeuchi F, Akiyama M, Matoba N, Katsuya T, Nakatochi M, Tabara Y, Narita A, Saw WY, Moon S, Spracklen CN, Chai JF, Kim YJ, Zhang L, Wang C, Li H, Li H, Wu JY, Dorajoo R, Nierenberg JL, Wang YX, He J, Bennett DA, Takahashi A, Momozawa Y, Hirata M, Matsuda K, Rakugi H, Nakashima E, Isono M, Shirota M, Hozawa A, Ichihara S, Matsubara T, Yamamoto K, Kohara K, Igase M, Han S, Gordon-Larsen P, Huang W, Lee NR, Adair LS, Hwang MY, Lee J, Chee ML, Sabanayagam C, Zhao W, Liu J, Reilly DF, Sun L, Huo S, Edwards TL, Long J, Chang LC, Chen CH, Yuan JM, Koh WP, Friedlander Y, Kelly TN, Bin Wei W, Xu L, Cai H, Xiang YB, Lin K, Clarke R, Walters RG, Millwood IY, Li L, Chambers JC, Kooner JS, Elliott P, van der Harst P; International Genomics of Blood Pressure (iGEN-BP) Consortium, Chen Z, Sasaki M, Shu XO, Jonas JB, He J, Heng CK, Chen YT, Zheng W, Lin X, Teo YY, Tai ES, Cheng CY, Wong TY, Sim X, Mohlke KL, Yamamoto M, Kim BJ, Miki T, Nabika T, Yokota M, Kamatani Y, Kubo M, Kato N*. Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Nat Commun. 2018 Nov 28;9(1):5052. PMID: 30487518
  9. Niiya K, Ohara H, Isono M, Sheikh AM, Matsuo H, Fujikawa K, Isomura M, Kato N, Nabika T. Further dissection of QTLs for salt-induced stroke and identification of candidate genes in the stroke-prone spontaneously hypertensive rat. Sci Rep. 2018 Jun 20;8(1):9403. PMID: 29925869
  10. Feitosa MF, Kraja AT, Chasman DI, Sung YJ, Winkler TW, Ntalla I, Guo X, Franceschini N, Cheng CY, Sim X, Vojinovic D, Marten J, Musani SK, Li C, Bentley AR, Brown MR, Schwander K, Richard MA, Noordam R, Aschard H, Bartz TM, Bielak LF, Dorajoo R, Fisher V, Hartwig FP, Horimoto ARVR, Lohman KK, Manning AK, Rankinen T, Smith AV, Tajuddin SM, Wojczynski MK, Alver M, Boissel M, Cai Q, Campbell A, Chai JF, Chen X, Divers J, Gao C, Goel A, Hagemeijer Y, Harris SE, He M, Hsu FC, Jackson AU, Kähönen M, Kasturiratne A, Komulainen P, Kühnel B, Laguzzi F, Luan J, Matoba N, Nolte IM, Padmanabhan S, Riaz M, Rueedi R, Robino A, Said MA, Scott RA, Sofer T, Stančáková A, Takeuchi F, Tayo BO, van der Most PJ, Varga TV, Vitart V, Wang Y, Ware EB, Warren HR, Weiss S, Wen W, Yanek LR, Zhang W, Zhao JH, Afaq S, Amin N, Amini M, Arking DE, Aung T, Boerwinkle E, Borecki I, Broeckel U, Brown M, Brumat M, Burke GL, Canouil M, Chakravarti A, Charumathi S, Ida Chen YD, Connell JM, Correa A, de Las Fuentes L, de Mutsert R, de Silva HJ, Deng X, Ding J, Duan Q, Eaton CB, Ehret G, Eppinga RN, Evangelou E, Faul JD, Felix SB, Forouhi NG, Forrester T, Franco OH, Friedlander Y, Gandin I, Gao H, Ghanbari M, Gigante B, Gu CC, Gu D, Hagenaars SP, Hallmans G, Harris TB, He J, Heikkinen S, Heng CK, Hirata M, Howard BV, Ikram MA; InterAct Consortium, John U, Katsuya T, Khor CC, Kilpeläinen TO, Koh WP, Krieger JE, Kritchevsky SB, Kubo M, Kuusisto J, Lakka TA, Langefeld CD, Langenberg C, Launer LJ, Lehne B, Lewis CE, Li Y, Lin S, Liu J, Liu J, Loh M, Louie T, Mägi R, McKenzie CA, Meitinger T, Metspalu A, Milaneschi Y, Milani L, Mohlke KL, Momozawa Y, Nalls MA, Nelson CP, Sotoodehnia N, Norris JM, O'Connell JR, Palmer ND, Perls T, Pedersen NL, Peters A, Peyser PA, Poulter N, Raffel LJ, Raitakari OT, Roll K, Rose LM, Rosendaal FR, Rotter JI, Schmidt CO, Schreiner PJ, Schupf N, Scott WR, Sever PS, Shi Y, Sidney S, Sims M, Sitlani CM, Smith JA, Snieder H, Starr JM, Strauch K, Stringham HM, Tan NYQ, Tang H, Taylor KD, Teo YY, Tham YC, Turner ST, Uitterlinden AG, Vollenweider P, Waldenberger M, Wang L, Wang YX, Wei WB, Williams C, Yao J, Yu C, Yuan JM, Zhao W, Zonderman AB, Becker DM, Boehnke M, Bowden DW, Chambers JC, Deary IJ, Esko T, Farrall M, Franks PW, Freedman BI, Froguel P, Gasparini P, Gieger C, Jonas JB, Kamatani Y, Kato N, Kooner JS, Kutalik Z, Laakso M, Laurie CC, Leander K, Lehtimäki T, Study LC, Magnusson PKE, Oldehinkel AJ, Penninx BWJH, Polasek O, Porteous DJ, Rauramaa R, Samani NJ, Scott J, Shu XO, van der Harst P, Wagenknecht LE, Wareham NJ, Watkins H, Weir DR, Wickremasinghe AR, Wu T, Zheng W, Bouchard C, Christensen K, Evans MK, Gudnason V, Horta BL, Kardia SLR, Liu Y, Pereira AC, Psaty BM, Ridker PM, van Dam RM, Gauderman WJ, Zhu X, Mook-Kanamori DO, Fornage M, Rotimi CN, Cupples LA, Kelly TN, Fox ER, Hayward C, van Duijn CM, Tai ES, Wong TY, Kooperberg C, Palmas W, Rice K, Morrison AC, Elliott P, Caulfield MJ, Munroe PB, Rao DC, Province MA, Levy D. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. PLoS One. 2018 Jun 18;13(6):e0198166. PMID: 29912962
  11. 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  58. Xi B, Takeuchi F, Chandak GR, Kato N, Pan HW; AGEN-T2D Consortium, Zhou DH, Pan HY, Mi J. Common polymorphism near the MC4R gene is associated with type 2 diabetes: data from a meta-analysis of 123,373 individuals. Diabetologia. 2012 Oct;55(10):2660-6. PMID: 22869321
  59. Takeuchi F, Yamamoto K, Katsuya T, Sugiyama T, Nabika T, Ohnaka K, Yamaguchi S, Takayanagi R, Ogihara T, Kato N*. Reevaluation of blood pressure and hypertension association with seven candidate genes by replication study and meta-analysis with larger sample size. Hypertens Res. 2012 Aug;35(8):825-31. PMID: 22456346
  60. Okada Y, Sim X, Go MJ, Wu JY, Gu D, Takeuchi F, Takahashi A, Maeda S, Tsunoda T, Chen P, Lim SC, Wong TY, Liu J, Young TL, Aung T, Seielstad M, Teo YY, Kim YJ, Lee JY, Han BG, Kang D, Chen CH, Tsai FJ, Chang LC, Fann SJ, Mei H, Rao DC, Hixson JE, Chen S, Katsuya T, Isono M, Ogihara T, Chambers JC, Zhang W, Kooner JS; The KidneyGen Consortium; The CKDGen Consortium, Albrecht E; The GUGC consortium, Yamamoto K, Kubo M, Nakamura Y, Kamatani N, Kato N, He J, Chen YT, Cho YS, Tai ES, Tanaka T. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Nature Genet. 2012 Jul 15;44(8):904-909. PMID: 22797727
  61. Kato N*. Ethnic diversity in type 2 diabetes genetics between East Asians and Europeans. J Diabetes Invest. 2012 Aug;3(4):349-351.
  62. Kato N*. Ethnic differences in genetic predisposition to hypertension. Hypertens Res. 2012 Jun;35(6):574-81. PMID: 22476227
  63. Nabika T*, Ohara H, Kato N, Isomura M. The stroke-prone spontaneously hypertensive rat: still a useful model for post-GWAS genetic studies? Hypertens Res. 2012 May;35(5):477-84. PMID: 22399095
  64. Li H, Kilpelainen T, Liu C, Zhu J, Liu Y, Hu C, Yang Z, Bao W, Cha S, Wu Y, Yang T-L, Sekine A, Choi BY, Yajnik CS, Zhou D, Takeuchi F, Yamamoto K, Chan JC, Mani KR, Been LF, Imamura M, Nakashima E, Lee N, Fujisawa T, Karasawa S, Wen W, Lu W, Chang Y-C, Xiang Y-B, Gao Y, Liu S, Song Y, Kwak SH, Shin HD, Park KS, Fall C, Kim JY, Sham PC, Lam KSL, Zheng W, Shu XO, Deng H-W, Ikegami H, Sanghera DK, Chuang L-M, Liegang Liu, Hu R, Kim Y-M, Daimon M, Hotta K, Jia W, Kooner JS, Chambers JC, Chandak GR, Ma RC, Maeda S, Dorajoo R, Yokota M, Takayanagi R, Kato N. Lin X, Loos RJF. Association of genetic variation in FTO with risk of obesity and type 2 diabetes in up to 96,551 East and South Asians. Diabetologia. 2012 Apr;55(4):981-95. PMID: 22109280
  65. Okada Y, Kubo M, Ohmiya H, Takahashi A, Kumasaka N, Hosono N, Maeda S, Wen W, Dorajoo R, Go MJ, Zheng W, Kato N, Wu J-Y, Lu Q, GIANT consortium, Tsunoda T, Yamamoto K, Nakamura Y, Kamatani N, Tanaka T. Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations. Nature Genet. 2012 Feb 19;44(3):302-6. PMID: 22344221
  66. Wen W, Cho Y-S, Zheng W, Dorajoo R, Kato N, Lu Q, Chen C-H, Delahanty RJ, Okada Y, Tabara Y, Gu D, Zhu D, Haiman CA, Mo Z, Gao Y-T, Saw S-M, Go M-J, Takeuchi F, Chang L-C, Kokubo Y, Liang J, Hao M, Marchand LL, Zhang Y, Hu Y, Wong T-Y, Long J, Han B-G, Kubo M, Yamamoto K, Su M-H, Miki T, Henderson BE, Song H, Tan A, He J, Ng DP-K, Cai Q, Tsunoda T, Tsai F-J, Iwai N, Chen GK, Shi J, Xu J, Sim X, Xiang Y-B, Maeda S, Ong RTH, Li C, Nakamura Y, Aung T, Kamatani N, Liu J-J, Lu W, Yokota M, Seielstad M, Fann CSJ, The Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Wu J-Y, Lee J-Y, Hu FB, Tanaka T, Tai ES, Shu X-O. Meta-analysis identifies common variants associated with body mass index in east Asians. Nature Genet. 2012 Feb 19;44(3):307-311. PMID: 22344219
  67. Cho YS, Chen C-H, Hu C, Long J, Ong RTH, Sim X, Takeuchi F, Wu Y, Go MJ, Yamauchi T, Chang Y-C, Kwak SH, Ma RCW, Yamamoto K, Adair LS, Aung T, Cai Q, Chang L-C, Chen Y-T, Gao Y, Hu FB, Kim H-L, Kim S, Kim YJ, Lee JJ-M, Lee NR, Li Y, Liu JJ, Lu W, Nakamura J, Nakashima E, NgDP-K, Tay WT, Tsai F-J, Wong TY, Yokota M, Zheng W, Zhang R, Wang C, So WY, Ohnaka K, Ikegami H, Hara K, Cho YM, Cho NH, Chang T-J, Bao Y, Hedman AK, P Morris AP, McCarthy MI, DIAGRAM consortium36, MuTHER consortium36, Takayanagi R, Park KS, Jia W, Chuang L-M, ChanJCN, Maeda S, Kadowaki T, Lee J-Y, Wu J-Y, TeoYY, Tai ES, Shu XO, Mohlke KL, Kato N, Han B-G, Seielstad M. Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nature Genet. 2011 Dec 11;44(1):67-72. PMID: 22158537
  68. Kato N*, Takeuchi F, Tabara Y, Kelly TN, Go MJ, Sim X, Tay WT, Chen CH, Zhang Y, Yamamoto K, Katsuya T, Yokota M, Kim YJ, Ong RT, Nabika T, Gu D, Chang LC, Kokubo Y, Huang W, Ohnaka K, Yamori Y, Nakashima E, Jaquish CE, Lee JY, Seielstad M, Isono M, Hixson JE, Chen YT, Miki T, Zhou X, Sugiyama T, Jeon JP, Liu JJ, Takayanagi R, Kim SS, Aung T, Sung YJ, Zhang X, Wong TY, Han BG, Kobayashi S, Ogihara T, Zhu D, Iwai N, Wu JY, Teo YY, Tai ES, Cho YS, He J. Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nature Genet. 2011, Jun;43(6):531-8. PMID: 21572416
  69. Kooner JS*, Saleheen D, Sim X, Sehmi J, Zhang W, Frossard P, Been LF, Chia K-S, Dimas AS, Hassanali N, Jafar T, Jowett JBM, Venkatesan R, Rees SD, Takeuchi F, Young R, Aung T, Basit A, Chidambaram M, Das D, Grunberg E, Hedman AK, Hydrie ZI, Islam M, Khor C-C, Kowlessur S, Kristensen MM, Liju S, Lim W-Y, Matthews DR, Liu J, Morris AP, Nica AC, Pinidiyapathirage JM, Prokopenko I, Rasheed A, Samuel M, Shah N, Shera AS, Small KS, Suo C, Wickremasinghe AR, Wong TY, Yang M, Zhang F, DIAGRAM, MuTHER, Abecasis GR, Barnett AH, Caulfield M, Deloukas P, Frayling T, Froguel P, Kato N, Katulanda P, Kelly MA, Liang J, Mohan V, Sanghera DK, Scott J, Seielstad M, Zimmet PZ, Elliott P, Teo YY, McCarthy MI, Danesh J, Tai ES, Chambers JC*. Genome-wide association study in people of South Asian ancestry identifies six novel susceptibility loci for Type 2 Diabetes. Nature Genet. 2011 Aug 28;43(10):984-9. PMID: 21874001
  70. Takeuchi F, Yokota M, Yamamoto K, Nakashima E, Katsuya T, Asano H, Isono M, Nabika T, Sugiyama T, Fujioka A, Awata N, Ohnaka K, Nakatochi M, Kitajima H, Rakugi H, Nakamura J, Ohkubo T, Imai Y, Shimamoto K, Yamori Y, Yamaguchi S, Kobayashi S, Takayanagi R, Ogihara T, Kato N*. Genome-wide association study of coronary artery disease in the Japanese. Eur J Hum Genet. 2012 Mar;20(3):333-40. PMID: 21971053
  71. Takeuchi F*, Kobayashi S, Ogihara T, Fujioka A, Kato N. Detection of common single nucleotide polymorphisms synthesizing quantitative trait association of rarer causal variants. Genome Res. 2011, Jul;21(7):1122-30. PMID: 21441355
  72. Pinidiyapathirage MJ, Dassanayake AS, Rajindrajith S, Kalubowila U, Kato N, Wickremasinghe AR, de Silva HJ. Non-alcoholic fatty liver disease in a rural, physically active, low income population in Sri Lanka. BMC Res Notes. 2011 Nov 24;4:513. PMID: 22115060
  73. Njelekela M, Muhihi A*, Mpembeni R, Masesa Z, Kitamori K, Mori-Yamori M, Kato N, Mtabaji J, Yamori Y. Prevalence of Cardiovascular Disease Risk Factors among Young and Middle-age Men in Urban Mwanza, Tanzania. J Public Health. 2011, 19(6):2011.19:553-61.
  74. Takeuchi F, Yamamoto K, Katsuya T, Nabika T, Sugiyama T, Fujioka A, Isono M, Ohnaka K, Fujisawa T, Nakashima E, Ikegami H, Nakamura J, Yamori Y, Yamaguchi S, Kobayashi S, Ogihara T, Takayanagi R, Kato N*. Association of obesity susceptibility genetic variants with type 2 diabetes in the Japanese. Diabetologia. 2011, 54(6):1350-9. PMID: 21369819
  75. Dassanayake AS, Kasturiratne A, Niriella MA, Kalubovila U, Rajindrajith S, De Silva AP, Kato N, Wickremasinghe R and de Silva J. Prevalence of acanthosis nigricans in an urban population in Sri Lanka and its utility to detect metabolic syndrome. BMC Research Notes.2011, 4(1):２5. PMID: 21276250
  76. Sasawatari S, Okamura T, Kasumi E, Tanaka-Furuyama K, Yanobu-Takanashi R, Shirasawa S, Kato N. Toyama-Sorimachi N. The solute carrier family15A4 regulates TLR9 and NOD1 functions in the innate immune system and promotes colitis in mice. Gastroenterology. 2011, 140(5):1513-２5. PMID:21277849
  77. Takeuchi F, Isono M, Nabika T, Katsuya T, Sugiyama T, Yamaguchi S, Kobayashi S, Ogihara T, Yamori Y, Fujioka A, Kato N*. Confirmation of ALDH2 as a major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in Japanese. Circ J. 2011, 75(4):911-8. PMID: 21372407
  78. Ohara-Imaizumi M, Yoshida M, Aoyagi K, Saito T, Okamura T, Takenaka H, Akimoto Y, Nakamichi Y, Takanashi-Yanobu R, Nishiwaki C, Kawakami H, Kato N, Hisanaga S, Kakei M, Nagamatsu S. Deletion of CDKAL1 affects mitochondrial ATP generation and first-phase insulin exocytosis. PLoS One. 2010 Dec 9;5(12):e15553. PMID: 21151568
  79. Takeuchi F, Isono M, Katsuya T, Yamamoto K, Yokota M, Sugiyama T, Nabika T, Fujioka A, Ohnaka K, Asano H, Yamori Y, Yamaguchi S, Kobayashi S, Takayanagi R, Ogihara T, A, Kato N*.Blood pressure and hypertension are associated with seven loci showing male-specific interaction with age among the Japanese. Circulation. 2010 ,121(21):2302-9. PMID: 20479155
  80. Takeuchi F, Kashida M, Okazaki O, Tanaka Y, Fukuda S, Kashima T, Hosaka S, Hiroe M, Kimura S, Kato N*. Evaluation of pharmacogenetic algorithm for warfarin dose requirements in Japanese patients. Circ J. 2010, 74:977-82. PMID: 20339191
  81. Taniguchi-Yanai K, Koike Y, Hasegawa T, Furuta Y, Serizawa M, Ohshima N, Kato N*, Yanai K*. Identification and characterization of glucocorticoid receptor-binding sites in the human genome. J Recept Signal Transduct Res. 2010, 30(2):88-105. PMID: 20163328
  82. Jesmin S*, Mowa CN, Sultana SN, Shimojo N, Togashi H, Iwashima Y, Kato N, Sato A, Sakuma I, Hiroe M, Hattori Y, Yamaguchi N, Kobayashi H. VEGF signaling is disrupted in the hearts of mice lacking estrogen receptor alpha. Eur J Pharmacol. 2010 Sep 1;641(2-3):168-78. PMID: 20639141
  83. Nakashima E, Watarai A, Tsukahara T, Hamada Y, Naruse K, Kamiya H, Kato J, Kato N ,Tomita M, Oiso Y, Nakamura J. Association of resistin polymorphism, its serum levels and prevalence of stroke in Japanese type 2 diabetic patients. J Diabetes Invest. 2010; 1(4):154-58.
  84. Takeuchi F, Serizawa M, Yamamoto K, Fujisawa T, Nakashima E, Ohnaka K, Ikegami H, Sugiyama T, Katsuya T, Miyagishi M, Nakashima N, Nawata H, Nakamura J, Kono S, Takayanagi R, Kato N*. Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. Diabetes. 2009, 58(7):1690-9. PMID: 19401414
  85. Takeuchi F, Katsuya T, Charkrewarthy S, Yamamoto K, Fujioka A, Serizawa M, Fujisawa T, Nakashima E, Ohnaka K, Ikegami H, Sugiyama T, Nabika T, Kasturiratne A, Yamaguchi S, Kono S, Takayanagi R, Yamori Y, Kobayashi S, Ogihara T, de Silva A, Wickremasinghe R, Kato N*. Common variants at the GCK, GCKR, G6PC2-ABCB11,and MTNR1B lociare associatedwith fasting glucose in two Asian populations. Diabetologia. 2010, 53(2):299-308. PMID: 19937311
  86. Konoshita T, Kato N, Fuchs S, Mizuno S, Aoyama C, Motomura M, Makino Y, Wakahara S, Inoki I, Miyamori I, Pinet F; the Genomic Disease Outcome Consortium (G-DOC) Study Investigators. Genetic Variant of the Renin-Angiotensin System and Diabetes Influences Blood Pressure Response to Angiotensin Receptor Blocker. Diabetes Care. 2009, 32(8):1485-90. PMID: 19509012
  87. Takeuchi F, Nabika T, Isono M, Katsuya T, Sugiyama T, Yamaguchi S, Kobayashi S, Yamori Y, Ogihara T, Kato N*. Evaluation of genetic loci influencing adult height in the Japanese population. J Hum Genet. 2009, 54(12):749-52. PMID: 19834501
  88. Tsuchihashi-Makaya M, Serizawa M, Yanai K, Katsuya T, Takeuchi F, Fujioka A, Yamori Y, Ogihara T, Kato N. Gene-environmental interaction regarding alcohol metabolizing enzymes in the Japanese general population. Hypertens Res. 2009, 32(3):207-13.
  89. Fujimoto T, Miyasaka K, Koyanagi M, Tsunoda T, Baba I, Doi K, Ohta M, Kato N, Sasazuki T, Shirasawa S. Altered energy homeostasis and resistance to diet-induced obesity in KRAP-deficient mice. PLoS One. 2009, 4:e4240. PMID: 19156225
  90. Tsuchihashi-Makaya M, Hamaguchi S, Kinugawa S, Yokota T, Goto D, Yokoshiki H, Kato N, Takeshita A, Tsutsui H; JCARE-CARD Investigators. Characteristics and outcomes of hospitalized patients with heart failure and reduced vs preserved ejection fraction. Report from the Japanese Cardiac Registry of Heart Failure in Cardiology (JCARE-CARD). Circ J. 2009, 73(10):1893-900. PMID: 19644216
  91. Dassanayake AS, Kasthuriratne A, Rajindrajith S, Kalubowila U, Chakrawarthi S, De Silva AP, Makaya M, Mizoue T, Kato N. Wickremasinghe AR, de Silva HJ. Prevalence and risk factors for non-alcoholic fatty liver disease (NAFLD) among adults in an urban Sri Lankan population. J Gastroenterol Hepatol. 2009, 24(7):1284-8. PMID: 19476560
  92. Morii T, Ohno Y, Kato N, Hirose H, Kawabe H, Hirao K, Eguchi T, Maruyama T, Hayashi M, Saito I, Yazaki Y, Saruta T. CD36 SNP is associated with variation in LDL-cholesterol in young Japanese men. Biomarkers. 2009, 14(4):207-12. PMID: 19489681
  93. Tsuchihashi-Makaya M, Kato N, Chishaki A, Takeshita A, Tsutsui H. Anxiety and poor social support are independently associated with adverse outcomes in patients with mild heart failure. Circ J. 2009, 73(2):280-7. PMID: 19096191
  94. Tsukahara T, Nakashima E, Watarai A, Hamada Y, Naruse K, Kamiya H, Nakamura N, Kato N, Hamajima N, Sekido Y, Niwa T, Tomita M, Oiso Y, Nakamura J. Polymorphism in resistin promoter region at -420 determines the serum resistin levels and may be a risk marker of stroke in Japanese type 2 diabetic patients. Diabetes Res Clin Pract. 2009, 84(2):179-86. PMID: 19269054
  95. Hanasaki H, Takemura Y, Fukuo K, Ohishi M, Onishi M, Yasuda O, Katsuya T, Awata N, Kato N, Ogihara T, Rakugi H. Fas Promoter Region Gene Polymorphism Is Associated With An Increased Risk For Myocardial Infarction. Hypertens Res. 2009, 32(4):261-4. PMID: 19262492
  96. Kato N*, Miyata T, Tabara Y, Katsuya T, Yanai K, Hanada H, Kamide K, Nakura J, Kohara K, Takeuchi F, Mano H, Yasunami M, Kimura A, Kita Y, Ueshima H, Nakayama T, Soma M, Hata A, Fujioka A, Kawano Y, Nakao K, Sekine A, Yoshida T, Nakamura Y, Saruta T, Ogihara T, Sugano S, Miki T, Tomoike H. High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project. Hum Mol Genet. 2008, 17:617-27. PMID: 18003638
  97. Ochiai Y, Liang YQ, Serizawa M, Kato N*. Dynamic changes of the renin-angiotensin and associated systems in the rat after pharmacological and dietary interventions in vivo. Physiol Genomics. 2008, 35:330-40. PMID: 18796534
  98. Takeuchi F, Ochiai Y, Serizawa M, Yanai K, Kuzuya N, Kajio H, Honjo S, Takeda N, Kaburagi Y, Yasuda K, Shirasawa S, Sasazuki T, Kato N*. Search for type 2 diabetes susceptibility genes on chromosomes 1q, 3q and 12q. J Hum Genet. 2008, 53:314-24. PMID: 18259684
  99. Takeuchi F, Serizawa M, Kato N*. HapMap coverage for SNPs in the Japanese population. J Hum Genet. 2008, 53:96-9. PMID: 18043864
  100. Serizawa M, Nabika T, Ochiai Y, Takahashi K, Yamaguchi S, Makaya M, Kobayashi S, Kato N*. Association between PRKCH gene polymorphisms and subcortical silent brain infarction. Atherosclerosis. 2008, 199:340-5. PMID: 18164711
  101. Kato N*, Liang YQ, Ochiai Y, Birukawa N, Serizawa M, Jesmin S. Candesartan-induced gene expression in five organs of stroke-prone spontaneously hypertensive rats. Hypertens Res. 2008, 31:1963-75. PMID: 19015604
  102. Kato N*, Liang YQ, Ochiai Y, Jesmin S. Systemic evaluation of gene expression changes in major target organs induced by atorvastatin. Eur J Pharmacol. 2008, 584:376-89. PMID: 18295756
  103. Koyanagi M, Nakabayashi K, Fujimoto T, Gu N, Baba I, Takashima Y, Doi K, Harada H, Kato N, Sasazuki T, Shirasawa S. ZFAT expression in B and T lymphocytes and identification of ZFAT-regulated genes. Genomics. 2008, 91:451-7. PMID: 18329245
  104. Takeuchi F, Yanai K, Inomata H, Kuzuya N, Kajio H, Honjo S, Takeda N, Kaburagi Y, Yasuda K, Shirasawa S, Sasazuki T, Kato N*. Search of type 2 diabetes susceptibility gene on chromosome 20q. Biochem Biophys Res Commun. 2007, 357:1100-6. PMID: 17466274
  105. Jesmin S, Maeda S, Mowa CN, Zaedi S, Togashi H, Prodhan SH, Yamaguchi T, Yoshioka M, Sakuma I, Miyauchi T, Kato N. Antagonism of endothelin action normalizes altered levels of VEGF and its signaling in the brain of stroke-prone spontaneously hypertensive rat. Eur J Pharmacol. 2007, 574:158-71. PMID: 17689527
  106. Fujimoto T, Koyanagi M, Baba I, Nakabayashi K, Kato N, Sasazuki T, Shirasawa S. Analysis of KRAP expression and localization, and genes regulated by KRAP in a human colon cancer cell line. J Hum Genet. 2007, 52:978-84. PMID: 17934691
  107. Wakahara S, Konoshita T, Mizuno S, Motomura M, Aoyama C, Makino Y, Kato N, Koni I, Miyamori I. Synergistic expression of angiotensin-converting enzyme (ACE) and ACE2 in human renal tissue and confounding effects of hypertension on the ACE to ACE2 ratio. Endocrinology. 2007, 148:2453-7. PMID: 17303661
  108. Konoshita T, Wakahara S, Mizuno S, Motomura M, Aoyama C, Makino Y, Kawai Y, Kato N, Koni I, Miyamori I, Mabuchi H. Tissue gene expression of renin-angiotensin system in human type 2 diabetic nephropathy. Diabetes Care. 2006, 29:848-52. PMID: 16567826
  109. Manabe N, Hoshino A, Liang YQ, Goto T, Kato N, Yamamoto K. Quantum dot as a drug tracer in vivo. IEEE Trans Nanobioscience. 2006, 5:263-7. PMID: 17181025
  110. Takeuchi F, Yanai K, Morii T, Ishinaga Y, Taniguchi-Yanai K, Nagano S, Kato N. Linkage disequilibrium grouping of single nucleotide polymorphisms (SNPs) reflecting haplotype phylogeny for efficient selection of tag SNPs. Genetics. 2005, 170:291-304. PMID: 15716494
  111. Watanabe T, Iizuka Y, Liang Y-Q, Inomata H, Gotoda T, Yanai K, Isobe M, Kato N*. Evaluation of insulin resistance linkage to rat chromosome 4 in SHR of a Japanese colony Biochem Biophys Res Commun. 2005, 329: 879-87. PMID: 15752738
  112. Inomata H, Watanabe T, Iizuka Y, Liang Y-Q, Mashimo T, Nabika T, Ikeda K, Yanai K, Gotoda T, Yamori Y, Isobe M, Kato N*. Identification of quantitative trait loci for cardiac hypertrophy in two different strains of the spontaneously hypertensive rat. Hypertens Res. 2005, 28: 273-81. PMID: 16097372
  113. Nawata H, Shirasawa S, Nakashima N, 他38人, Kato N. Yasuda K, Yamamoto K, Sasazuki T. Genome-wide linkage analysis of type 2 diabetes mellitus reconfirms the susceptibility locus on 11p13-p12 in Japanese. J Hum Genet. 2004, 49:629-34. PMID: 15490285
  114. Kato N*, Nabika T, Liang YQ, Mashimo T, Inomata H, Watanabe T, Yanai K, Yamori Y, Yazaki Y, Sasazuki T. Isolation of a chromosome 1 region affecting blood pressure and vascular disease traits in the stroke-prone rat model. Hypertension. 2003, 42:1191-7. PMID: 14623828
  115. Kato N*, Mashimo T, Nabika T, Cui ZH, Ikeda K, Yamori Y. Genome-wide searches for blood pressure quantitative trait loci in the stroke-prone spontaneously hypertensive rat of a Japanese colony. J Hypertens. 2003, 21:295-303. PMID: 12569259
  116. Nanko S, Kunugi H, Hirasawa H, Kato N, Nabika T, Kobayashi S. Brain-derived neurotrophic factor gene and schizophrenia: polymorphism screening and association analysis. Schizophr Res. 2003, 62:281-3. PMID: 12837526
  117. Kato N*, Ikeda K, Nabika T, Morita H, Sugiyama T, Gotoda T, Kurihara H, Kobayashi S, Yazaki Y, Yamori Y. Evaluation of the atrial natriuretic peptide gene in stroke. Atherosclerosis. 2002, 163:279-86. PMID: 12052474
  118. Kato N*, Kanda T, Sagara M, Bos A, Moriguchi EH, Moriguchi Y, Yamori Y. Proposition of a feasible protocol to evaluate salt sensitivity in a population-based setting. Hypertens Res. 2002, 25:801-9. PMID: 12484501
  119. Kato N*. Genetic analysis in human hypertension. Hypertens Res. 2002, 25:319-27. PMID: 12135308
  120. Sugiyama T, Kato N*, Ishinaga Y, Yamori Y, Yazaki Y. Evaluation of selected polymorphisms of the Mendelian hypertensive disease genes in the Japanese population. Hypertens Res. 2001, 24:515-21. PMID: 11675945
  121. Kato N*, Sugiyama T, Morita H, Kurihara H, Sato T, Yamori Y, Yazaki Y. Association analysis of beta(2)-adrenergic receptor polymorphisms with hypertension in Japanese. Hypertension. 2001, 37:286-92. PMID: 11230287
  122. Kunugi H, Ueki A, Otsuka M, Isse K, Hirasawa H, Kato N, Nabika T, Kobayashi S, Nanko S. A novel polymorphism of the brain-derived neurotrophic factor (BDNF) gene associated with late-onset Alzheimer's disease. Mol Psychiatry. 2001, 6:83-6. PMID: 11244490
  123. Kato N*, Sugiyama T, Morita H, Kurihara H, Furukawa T, Isshiki T, Sato T, Yamori Y, Yazaki Y. Comprehensive analysis of the renin-angiotensin gene polymorphisms with relation to hypertension in the Japanese. J Hypertens. 2000, 18:1025-32. PMID: 10953993
  124. Kunugi H, Akahane A, Ueki A, Otsuka M, Isse K, Hirasawa H, Kato N, Nabika T, Kobayashi S, Nanko S. No evidence for an association between the Glu298Asp polymorphism of the NOS3 gene and Alzheimer's disease. J Neural Transm. 2000, 107:1081-4. PMID: 11041283
  125. Kunugi H, Ueki A, Otsuka M, Isse K, Hirasawa H, Kato N, Nabika T, Kobayashi S, Nanko S. Alzheimer's disease and 5-HTTLPR polymorphism of the serotonin transporter gene: no evidence for an association. Am J Med Genet. 2000, 96:307-9. PMID: 10898905
  126. Imai Y, Morita H, Kurihara H, Sugiyama T, Kato N, Ebihara A, Hamada C, Kurihara Y, Shindo T, Oh-hashi Y, Yazaki Y. Evidence for association between paraoxonase gene polymorphisms and atherosclerotic diseases. Atherosclerosis. 2000, 149:435-42. PMID: 10729395
  127. Kato N*, Sugiyama T, Morita H, Nabika T, Kurihara H, Yamori Y, Yazaki Y. Genetic analysis of the atrial natriuretic peptide gene in essential hypertension. Clin Sci (Lond). 2000, 98:251-8. PMID: 10677382
  128. Kato N*, Morita H, Sugiyama T, Kurihara H, Tsubaki S, Nabika T, Kitamura K, Yamori Y, Yazaki Y. Evaluation of the poly(ADP-ribose) polymerase gene in human stroke. Atherosclerosis. 2000, 148:345-52. PMID: 10657571
  129. Kato N*, Tamada T, Nabika T, Ueno K, Gotoda T, Matsumoto C, Mashimo T, Sawamura M, Ikeda K, Nara Y, Yamori Y. Identification of quantitative trait loci for serum cholesterol levels in stroke-prone spontaneously hypertensive rats. Arterioscler Thromb Vasc Biol. 2000, 20:223-9. PMID: 10634822
  130. Mashimo T, Nabika T, Matsumoto C, Tamada T, Ueno K, Sawamura M, Ikeda K, Kato N, Nara Y, Yamori Y. Aging and salt-loading modulate blood pressure QTLs in rats. Am J Hypertens. 1999, 12:1098-104. PMID: 10604486
  131. Kato N*, Sugiyama T, Morita H, Kurihara H, Yamori Y, Yazaki Y. Angiotensinogen gene and essential hypertension in the Japanese: extensive association study and meta-analysis on six reported studies. J Hypertens. 1999, 17:757-63. PMID: 10459872
  132. Gotoda T, Iizuka Y, Kato N, Osuga J, Bihoreau MT, Murakami T, Yamori Y, Shimano H, Ishibashi S, Yamada N. Absence of Cd36 mutation in the original spontaneously hypertensive rats with insulin resistance. Nat Genet. 1999, 22:226-8. PMID: 10391208
  133. Kato N*. Genetic analysis in Dahl salt-sensitive rats. Clin Exp Pharmacol Physiol. 1999, 26:539-40. PMID: 10405783
  134. Kato N*, Sugiyama T, Morita H, Nabika T, Kurihara H, Yamori Y, Yazaki Y. Lack of evidence for association between the endothelial nitric oxide synthase gene and hypertension. Hypertension. 1999, 33:933-6. PMID: 10205226
  135. Kato N*, Hyne G, Bihoreau MT, Gauguier D, Lathrop GM, Rapp JP. Complete genome searches for quantitative trait loci controlling blood pressure and related traits in four segregating populations derived from Dahl hypertensive rats. Mamm Genome. 1999, 10:259-65. PMID: 10051321
  136. Sugiyama T, Morita H, Kato N*, Kurihara H, Yamori Y, Yazaki Y. Lack of sex-specific effects on the association between angiotensin-converting enzyme gene polymorphism and hypertension in Japanese. Hypertens Res. 1999, 22:55-9. PMID: 10221352
  137. Kato N*, Julier C. Linkage mapping for hypertension susceptibility genes. Curr Hypertens Rep. 1999, 1:15-24. PMID: 10981038
  138. Kato N*, Sugiyama T, Morita H, Kurihara H, Yamori Y, Yazaki Y. G protein beta3 subunit variant and essential hypertension in Japanese. Hypertension. 1998, 32:935-8. PMID: 9822456
  139. Brand E, Kato N, Chatelain N, Krozowski ZS, Jeunemaitre X, Corvol P, Plouin PF, Cambien F, Pascoe L, Soubrier F. Structural analysis and evaluation of the 11beta-hydroxysteroid dehydrogenase type 2 (11beta-HSD2) gene in human essential hypertension. J Hypertens. 1998, 16:1627-33. PMID: 9856363
  140. Matsumoto C, Nabika T, Mashimo T, Kato N, Yamori Y, Masuda J. Construction of a rat genetic map by using randomly amplified microsatellite polymorphism (RAMP) markers. Mamm Genome. 1998, 9:531-5. PMID: 9657849
  141. Kato N*, Sugiyama T, Nabika T, Morita H, Kurihara H, Yazaki Y, Yamori Y. Lack of association between the alpha-adducin locus and essential hypertension in the Japanese population. Hypertension. 1998, 31:730-3. PMID: 9495254
  142. Kato N*, Hyne G, Rapp JP, Lathrop GM. Practicable approaches to targeted comparative mapping of rat chromosome regions: linkage mapping of five genes on rat chromosome 13. Cytogenet Cell Genet. 1998, 81:42-5. PMID: 9691173
  143. Bihoreau MT, Gauguier D, Kato N, Hyne G, Lindpaintner K, Rapp JP, James MR, Lathrop GM. A linkage map of the rat genome derived from three F2 crosses. Genome Res. 1997, 7:434-40. PMID: 9149940
  144. Satsangi J, Parkes M, Louis E, Hashimoto L, Kato N, Welsh K, Terwilliger JD, Lathrop GM, Bell JI, Jewell DP. Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12. Nat Genet. 1996, 14:199-202. PMID: 8841195
  145. Kato N*, Bihoreau M, Lathrop GM, Rapp JP. Localization of the rat stimulatory G-protein alpha subunit (GNPAS) gene to rat chromosome 3 by linkage analysis. Mamm Genome. 1996, 7:628-9. PMID: 8679006
  146. Deng AY, Rapp JP, Kato N, Bihoreau MT. Linkage mapping of the neuronal nitric oxide synthase gene (Nos1) to rat chromosome 12. Mamm Genome. 1995, 6:824. PMID: 8597645
  147. Tanaka T, Nakahara K, Kato N, Imai T, Yamazaki T, Tomita H, Shimokawa H, Matsuhashi H, Sato N, Matsui M, et al. Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families. Hum Genet. 1994, 94:380-4. PMID: 7927333
  148. Kobayashi T, Tamemoto K, Nakanishi K, Kato N, Okubo M, Kajio H, Sugimoto T, Murase T, Kosaka K. Immunogenetic and clinical characterization of slowly progressive IDDM. Diabetes Care. 1993, 16:780-8. PMID: 8098691

□以下は2005年度以後分を抜粋

II. 和文総説・書籍

2019（平成31-令和元）年度

  • 加藤規弘．次世代シークエンサーを用いた原因遺伝子探索研究と臨床ゲノム情報統合データベースの構築．病理と臨床. vol. 37 No.6, 528-534, 2019.
  • 加藤規弘．ゲノムと高血圧．循環器内科. vol. 85 No.6, 812-816, 2019.
  • 加藤規弘．冠動脈疾患のリスク管理のフロントライン〜遺伝子解析でどう評価する〜．循環器ジャーナル. 印刷中, 2019.

2018（平成30）年度

  • 加藤規弘．ゲノム医療における多因子疾患の位置付けと国際的動向．遺伝子医学MOOK別冊「多因子遺伝性疾患 研究と遺伝カウンセリング」．シリーズ3. 櫻井晃洋 編. メディカルドゥ. 大阪. 260-265, 2018.
  • 加藤規弘．生活習慣病におけるゲノム医療とは．日本医師会雑誌 2018；第147巻7号：1413-7.
  • 加藤規弘. ゲノム医療実用化に関する国際動向. 南山堂. 印刷中.
  • 加藤規弘．高血圧のゲノムワイド関連解析．血圧 2019 印刷中.

2017（平成29）年度

  • 加藤規弘．ゲノム医療の国際動向と我が国の取り組み．臨床レビュー「ゲノム医療をめぐる最近の動向2017-2018」．vol 158. 21-27, 2017.
  • 加藤規弘．高血圧および関連疾患のゲノム研究．血圧．vol 24 No.9. 18-22, 2017.
  • 加藤規弘．臨床ゲノム情報統合データベース整備事業の構想と展望．実験医学増刊．vol 35 No.17. 84-89, 2017.
  • 加藤規弘．高血圧・血圧のゲノムワイド関連解析の現状と展望．医学のあゆみ．vol 26１ No.8. 813-817, 2017
  • 加藤規弘．臨床ゲノム情報統合データベース整備事業が目指すもの．医学のあゆみ．vol 260 No.11. 949-954, 2017.
  • 加藤規弘．ゲノム医療を支える統合データベースの構築．BIO Clinica．vol. 32 No.6, 18-22, 2017.
  • 加藤規弘．臨床ゲノム情報統合データベースの構築．BIO Clinica．vol 32 No.2. 43-46, 2017.
  • 加藤規弘．高血圧のゲノミクスと個別化医療．腎臓内科・泌尿器科．vol 5 No.1. 63-69, 2017.

2016（平成28）年度

  • 加藤規弘．序〜遺伝子検査の新たな時代〜：遺伝子検査の実用化と課題. 血液フロンティア, vol. 26 No.7, 17-20, 2016.
  • 加藤規弘．ゲノム医療における遺伝子検査：遺伝子検査の実用化と課題. 血液フロンティア, vol. 26 No.7, 43-50, 2016.
  • 加藤規弘．Current Topics複数祖先集団のゲノムワイド関連解析から血圧を左右する12の遺伝的座位が同定され、DNAメチル化の役割が示唆された. 実験医学, vol. 34 No.4, 583-586, 2016.
  • 加藤規弘．ゲノムと予防医学. アニムス Spring 2016, No.87, 13-16, 2016.
  • 加藤規弘．東アジア人の高血圧関連遺伝子の同定. 臨床免疫・アレルギー科, vol. 66 No.1, 77-81, 2016.

2014（平成26）年度

  • 加藤規弘．高血圧関連遺伝子のGWAS． 最新臨床高血圧学—高血圧治療の最前線．日本臨牀．東京, 35-40, 2014.

2013（平成25）年度

  • 加藤規弘．ゲノムと循環器病．カラー版循環器病学—基礎と臨床—アップデート版．西村書店．東京, 25-33, 2014.
  • 加藤規弘．ポストヒトゲノムプロジェクト時代の心脈管ゲノミクス．日本心脈管作動物質学会誌, 第36巻4号, 129-138, 2013.
  • 加藤規弘．疾病の遺伝機構と遺伝性疾患への対策．内科学第１０版. 朝倉書店, 東京 12-18, 2013.
  • 加藤規弘．高血圧診療のすべて. 疫学・遺伝「高血圧関連遺伝子」．日本医師会雑誌第142巻特別号, 東京 49-52, 2013.

2012（平成24）年度

  • 加藤規弘．医学のあゆみ 高血圧のすべて2012-研究と診療の最前線. 高血圧関連遺伝子のゲノムワイド関連解析．医歯薬出版, 東京 966-970, 2012.
  • 加藤規弘．Progress in Medicine. 食塩感受性と高血圧. 食塩感受性の関連遺伝子．ライフサイエンス, 東京. 21-25, 2012.
  • 加藤規弘．第４８回高血圧関連疾患モデル学会学術集会．東京, 先端医学社. 84-85, 2012.
  • 加藤規弘．EBM循環器疾患の治療 2012-2013. 高血圧・脂質異常症：高血圧関連遺伝子の解明はどこまで進み何処へ向かうのか？ 中外医学社．東京, 2012.

2011（平成23）年度

  • 加藤規弘．ゲノムワイド関連解析（GWAS）．動脈硬化予防. メディカルレビュー社．東京, 2011: 10 (3); 98-99.
  • 加藤規弘．高血圧の遺伝子解析の現状．進歩する心臓研究—Tokyo Heart Journal．東京, 2011: 29 (2); 27-30.

2010（平成22）年度

  • 加藤規弘．高血圧のゲノムワイド関連解析．Annual Review 循環器2011．中外医学社．印刷中.
  • 加藤規弘．高血圧の遺伝子座が位置する染色体領域．Medical Practice．文光堂．印刷中.

2009（平成21）年度

  • 加藤規弘．ゲノムと循環器病．カラー版循環器病学—基礎と臨床—．西村書店．東京、p111-120、2010
  • 加藤規弘．高血圧研究における遺伝子解析の現状と展望．高血圧（上）第4版—基礎編—．日本臨床2009年増刊．22-28.

2008（平成20）年度

  • 加藤規弘．メタボリックシンドロームの理解．「メタボリックシンドローム概論：生活習慣病ナーシング1」（加藤規弘　編）．東京、メヂカルフレンド社、2008：2-28.
  • 加藤規弘．遺伝子とアンチエイジング（抗加齢）医学：動脈硬化関連遺伝子．アンチアンチエイジング医学の基礎と臨床（日本抗加齢医学会専門医・指導士認定委員会編）改訂2版. 東京、Medical View、2008: 26-28.
  • 加藤規弘．ゲノム研究の進展と診断への応用．Nature Asia-Pacific．2008年11月号冊子別添．3.

2007（平成19）年度

  • 加藤規弘．高血圧研究における遺伝子解析の意義．臨床高血圧．2007；12：14-28．メディカルレビュー社
  • 加藤規弘．臨床研究と個人情報保護：ゲノム・遺伝子解析研究を中心に．学術の動向．2007；12：42-47．日本学術協力財団．
  • 加藤規弘．疾病の遺伝機構と遺伝性疾患への対策．内科学第９版（矢崎義雄、小俣政男、水野美邦ら　編）. 東京、朝倉書店、2007：11-17.
  • 加藤規弘．高血圧の成因を識る：遺伝的素因の重要性．新・心臓病診療プラクティス．2007；11：45-49．文光堂

2006（平成18）年度

  • 加藤規弘．概論：ゲノムワイドスキャン．高血圧（上）—最新の研究動向—．日本臨床2006年増刊．324-330.
  • 加藤規弘．高血圧治療の変遷と将来展望：高血圧遺伝子と治療への応用．内科．2006；98(3)．467-470．南光堂
  • 加藤規弘．食塩感受性と遺伝子．ゲノム医科学NOW（文部科学省特定領域研究「ゲノム」4領域　編）．2006：119-134.

2005（平成1７）年度

  • 加藤規弘．RA系遺伝子多型と循環器疾患． Cardiac Practice．2005；16(1): 83-88.
  • 加藤規弘．高血圧関連疾患におけるゲノム疫学．「ゲノム疫学」 BIO Clinica．2005；20(4)：31-37.
  • 笹月健彦, 加藤規弘．ゲノム疫学から予防医学へ．「ゲノム疫学」 BIO Clinica．2005；20(4)：16-17.
  • 加藤規弘．高血圧遺伝子解析の進歩：大規模候補遺伝子解析から．Molecular Medicine増刊号「生活習慣病2005」 2005；42：202-207.
  • 加藤規弘．候補遺伝子アプローチ（国際医療センター方式）．血圧．2005；12(8)：41-45.
  • 加藤規弘．疾患ゲノム解析—レニン・アンジオテンシン系を中心として—．進歩する心臓研究（Tokyo Heart Journal）．2005; 25(2)：28-32.
  • 加藤規弘．SHRおよびSHRSPにおける高血圧関連疾患の量的形質遺伝子座同定．SHR等疾患モデル共同研究会News Letter．2005；20：12-13.
  • 加藤規弘．心血管系疾患と遺伝子診断学．心血管病学（矢崎義雄、永井良三　編）．東京、朝倉書店．2005；864-873.

III. 学術集会発表−国際学会・研究会

  1. Niriella MA, Kasturiratna KATT, De Silva ST, Ranasinghe A, Perera KR, Subasinghe SKCE, Kodisinghe SK, Piyaratna TACL, Vithiya K, Dassanayaka AS, De Silva AP, Pathmeswaran A, Wickramasinghe AR, Kato N, de Silva HJ. Non-resolution of non-alcoholic fatty liver disease (NAFLD) among urban, adult Sri Lankans: a prospective 7-year follow-up study. American Association for the Study of Liver Diseases, The liver meeting, San Francisco, USA, November 2018.
  2. Imai-Okazaki A, Takeuchi F, Arakawa R, Miyo K, Saito K, Ott J, Kato N. Incorporation of originally-developed statistical genetics methods into a clinical sequencing platform to improve the efficiency and quality of variant annotation. Keystone Symposia. One million genomes: from discovery to health, Hanover, Germany, June 2018.
  3. Niriella MA, De Silva ST, Kasturiratna A, Perera KR, Subasinghe SKCE, Kodisinghe SK, Piyaratna TACL, Vithiya K, Dassanayaka AS, De Silva AP, Pathmeswaran A, Wickramasinghe AR, Takeuchi F, Kato N, de Silva HJ. Lean-NAFLD is the strongest predictor of future obesity among urban adult Sri Lankans: results from a prospective, community cohort follow-up study. UEG week 2017, Barcelona, Spain, October 2017.
  4. Spracklen CN, Kim Y.J, Chen P, Sim X, Cai H, Li S, Long J, Wu Y, Wang X, Wang YX, Takeuchi F, Jung KJ, Wu JY, Johnson T.A, Li H, Dorajoo R, He M, Akiyama K, Zhang Y, Hou X, Hu C, Moon S, Salfati E, AGEN Consortium. Association analyses of up to 72,043 East Asian individuals and trans-ancestry analyses with up to 186,265 European individuals reveal new loci associated with cholesterol and triglyceride levels. 61st annual meeting of the American Society of Human Genetics, Vancouver, Canada, October, 2016.
  5. Shimizu-Furusawa H, Takeuchi F, Isono M, Akiyama K, Liang Y-Q, Kato N. Epigenetic changes in the brain with high-salt intervention in SHR. Cardiovascular Genetics, Satellite Symposium of ISH 2016. Tokyo, Japan, September 2016.
  6. Shimizu-Furusawa H, Takeuchi F, Isono M, Akiyama K, Liang Y-Q, Kato N. Epigenetic changes in the liver with high-fat-diet intervention in SHR. Cardiovascular Genetics, Satellite Symposium of ISH 2016. Tokyo, Japan, September 2016.
  7. Shimizu-Furusawa H, Takeuchi F, Isono M, Akiyama K, Liang Y-Q, Kato N. Epigenetic changes in the liver with dexamethasone administration in SHR. Cardiovascular Genetics, Satellite Symposium of ISH 2016. Tokyo, Japan, September 2016.
  8. Shimizu-Furusawa H, Takeuchi F, Isono M, Akiyama K, Liang Y-Q, Kato N. Comparison of epigenetic changes in the liver between Tg-CETP rat and SHR. Cardiovascular Genetics, Satellite Symposium of ISH 2016. Tokyo, Japan, September 2016.
  9. Shimizu-Furusawa H, Takeuchi F, Isono M, Akiyama K, Liang Y-Q, Kato N. Comparison of epigenetic changes in the liver between RNO4-derived congenic rat and progenitor strains. Cardiovascular Genetics, Satellite Symposium of ISH 2016. Tokyo, Japan, September 2016.
  10. Konoshita T, Sakai A, Kaeriyama S, Urabe M, Nakaya T, Yamada M, Ichikawa M, Sato S, Yamamoto K, Imagawa M, Fujii M, Zenimaru Y, Suzuki J, Makino Y, Ishizuka T, Kato N. Association study of angiotensinase A (ENPEP) genotype with diabetic nephropathy. 26th European Meeting onHypertension and Cardiovascular Protection. Paris, France, June, 2016.
  11. Niriella MA, De Silva ST, Kasturiratna A, Perera KR, Subasinghe SKCE, Kodisinghe SK, Piyaratna TACL, Vithiya K, Dassanayaka AS, De Silva AP, Pathmeswaran A, Wickramasinghe AR, Kato N, de Silva HJ. Lean non-alcoholic fatty liver disease (Lean-NAFLD): characteristics and risk factors from a community cohort follow up study. UEG week 2016, Vienna, Austria, October 2016.
  12. Niriella M, Kasturiratna A, De Silva S, Perera R, Subasinghe C, Kodisinghe K, Piyarathna C, Rishikeshavan V, Dassanayake A, De Silva A, Pathmeswaran A, Kato N, de Silva J. Incidence and risk factors for non-alcoholic fatty liver disease in an urban, adult Sri Lankan population – a community cohort follow-up study. UEG week 2015, Barcelona, Spain, October 2015.
  13. Takeuchi F, Katsuya T, Kimura R, Nabika T, Okubo T, Tabara Y, Yamamoto K, Yokota M, Saw W-Y, Teo YY, Kato N. The fine-scale genetic structure of the Japanese population: estimation of genetic materials derived from Asians and the basis of genetic differentiation. 60th annual meeting of the American Society of Human Genetics, Baltimore, USA, October, 2015.
  14. Kawamura R, Tabara Y, Igase M, Takata Y, Kawamoto R, Saito I, Onuma H, Kohara K, Tanigawa T, Yamada K, Kato N, Miki M, Osawa H. Rs10401670 was identified as a possible functional quantitative trait locus for circulating resistin by a genome-wide association study in Japanese. 75th Scientific Session of American Diabetic Association. Boston, USA, June 2015.
  15. Loh M, et al. on behalf of iGEN-BP. Trans-ethnic genome-wide association study identifies 15 new genetic loci influencing blood pressure traits, and implicates a role for DNA methylation: the International Genetics of Blood Pressure (iGEN-BP) Study. 59th annual meeting of the American Society of Human Genetics, San Diego, USA, October, 2014.
  16. Kawamura R, Tabara Y, Igase M, Takata Y, Kawamoto R, Saito I, Tanigawa T, Onuma H, Kohara K, Kato N, Miki M, Osawa H. Resistin SNP-358, SNP-420, and rs1423096 were identified as major quantitative trait loci for serum resistin by a genome-wide association study in Japanese. 74th Scientific Session of American Diabetic Association. San Francisco, USA, June 2014.
  17. Konoshita T, Yamada M, Ichikawa M, Sato S, Imagawa M, Makino Y, Fujii M, Wakahara S, Zenimaru Y, Arakawa K, Suzuki J, Kato N. Measurement of soluble angiotensin-IV receptor (s-AT4), identified through systemic transcriptome analysis of hypertensive and diabetic renal tissue. 23rd European Meeting on Hypertension and Cardiovascular Protection. Milan, Italy, June, 2013.
  18. Akiyama K, Liang Y-Q, Kato N. Evaluation of human lipid-associated genes and methylation in SHR fed on high lipid diet. Cardiovascular Genetics Satellite 2012. Melbourne, Australia, September 2012.
  19. Akiyama K, Liang Y-Q, Kato N. Identification of "neutralizing" gene-gene interaction in the regulation of blood pressure in the SHR-related strains. Exploration of genetic loci controlling serum cholesterol concentration in the SHR-related strains: identification of two novel cholesterol loci. Cardiovascular Genetics Satellite 2012. Melbourne, Australia, September 2012.
  20. Liang Y-Q, Akiyama K, Kato N. Exploration of genetic loci controlling serum cholesterol concentration in the SHR-related strains: identification of two novel cholesterol loci. Cardiovascular Genetics Satellite 2012. Melbourne, Australia, September 2012.
  21. Liang Y-Q, Akiyama K, Kato N. Exploration of cardiac hypertrophy loci in the SHR-related strains: confirmation of the endonuclease G locus and identification of novel loci. Cardiovascular Genetics Satellite 2012. Melbourne, Australia, September 2012.
  22. Konoshita T, Kimura T, Fujii M, Makino Y, Wakahara S, Inaba S, Miyamori I, Kato N. A systematic review of pharmacogenetics in the renin angiotensin system – the genetic variants and inter-individual variation in blood pressure response to the blocking agents. 22nd European Meeting on Hypertension and Cardiovascular Protection. London, UK, April, 2012.
  23. Matsushita Y, Kishimoto M, Takahashi Y, Kanagawa S, Noda M, Thai SP, Ngoc QN, Hong HPT, Doan LD, Lan VN, Zeng Z-P, Wickremasinghe AR, Naruse M, Kato N, Kajio H. The Cutoff Levels of Waist Circumference for Predicting the Presence of the Clustering of Metabolic Risk Factors in some Asian Populations. IDF World Diabetes Congress 2011. Dubai, UAE, December, 2011.
  24. Horikoshi M, Wiltshire S, Kato N, Asimit J, Rayner N, Robertson N, Takeuchi F, Mahajan A, Teo Y-Y, Zeggini E, Morris A, McCarthy M, T2D-GENES. Trans-ethnic fine-mapping of Type 2 Diabetes susceptibility loci using a “Cosmopolitan” reference panel for imputation. 61st annual meeting of the American Society of Human Genetics and the International Congress of Human Genetics 2011, Montreal, Canada, Oct 14, 2011.
  25. Horikoshi M, Wiltshire S, Kato N, Asimit J, Rayner N, Robertson N, Takeuchi F, Mahajan A, Teo Y-Y, Zeggini E, Morris A, McCarthy M, T2D-GENES. Trans-ethnic fine-mapping of Type 2 Diabetes susceptibility loci using a “Cosmopolitan” reference panel for imputation. 61st annual meeting of the American Society of Human Genetics and the International Congress of Human Genetics 2011, Montreal, Canada, Oct 14, 2011.
  26. Takeuchi F, Kato N. Testing heterogeneity of quantitative trait variance among genotype classes guides fine mapping of association signals. 60th annual meeting of the American Society of Human Genetics, Washington DC, USA, November, 2010.
  27. Takeuchi F, Isono M, Katsuya T, Yamamoto K, Yokota M, Sugiyama T, Nabika T, Fujioka A, Ohnaka K, Asano H, Yamori Y, Yamaguchi S, Kobayashi S, Takayanagi R, Ogihara T, Kato N. Blood pressure and hypertension are associated with seven loci in the Japanese population. 23rd Scientific Meeting International Society of Hypertension. Vancouver, Canada, September, 2010.
  28. Takeuchi F, Katsuya T, Yamamoto K, Nabika T, Ranawaka U, Sugiyama T, Fujioka A, Yamori Y, Yamaguchi S, Kobayashi S, Ogihara T, Chakrewarthy S, Wickremasinghe R, and Kato N, for the NIBIO GWA Study and Ragama Health Study. Confirmation of eight loci associated with measures of obesity in two Asian populations with substantial ethnic heterogeneity. 27th annual scientific meeting of the Obesity Society, Washington DC, USA, October, 2009.
  29. Takeuchi F, Katsuya T, Chakrewarthy S, Yamamoto K, Fujisawa T, Nakashima E, Ohnaka K, Ikegami H, Sugiyama T, Nabika T, Kasturiratne A, Yamaguchi S, Kono S, Takayanagi R, Yamori Y, Kobayashi S, Ogihara T, de Silva A, Wickremasinghe R, Kato N for the NIBIO GWA Study. Ethnic diversity in fine mapping of the susceptibility loci G6PC2-ABCB11 for fasting glucose and CDKAL1 for type 2 diabetes. 59th annual meeting of the American Society of Human Genetics, Honolulu, USA, October, 2009.
  30. Konoshita T, Kato N, Fuchs S, Mizuno S, Aoyama C, Motomura M, Kimura T, Fujii M, Makino Y, Wakahara S, Arakawa K, Inoki I, Miyamori I, Pinet P. Genetic Variant of the Renin Angiotensin System Influences Blood Pressure Response to Angiotensin Receptor Blocker. 19th European Meeting on Hypertension, Milan, Italy, June, 2009.
  31. Kato N, Liang Y-Q, Ochiai Y, Serizawa M. Dissection of phenotypic traits associated with metabolic syndrome and positional cloning in the spontaneously hypertensive rat. The 22nd Scientific Meeting International Society of Hypertension, Berlin, Germany, June, 2008.
  32. Kato N, Liang Y-Q, Ochiai Y, Jesmin S. Systemic evaluation of gene expression changes in major target organs induced by atorvastatin. The 22nd Scientific Meeting International Society of Hypertension, Berlin, Germany, June, 2008.
  33. Ochiai Y, Liang Y-Q, Serizawa M, Birukawa N, Jesmin S, Kato N. Exploration of adipose tissue transcriptome network triggered in vivo by an insulin sensitizing agent, pioglitazone. 21st International Mammalian Genome Conference, Kyoto, Japan, October, 2007.
  34. Serizawa M, Liang Y-Q, Yanai K, Ochiai Y, Birukawa N, Jesmin S, Kato N. Compartmentalization of genome network downstream of the glucocorticoid receptor in cultured insulinoma cells and hepatoma cell. 21st International Mammalian Genome Conference, Kyoto, Japan, October, 2007.
  35. Manabe N, Hoshino A, Liang Y-Q, Fujioka K, Kato N, Yamamoto K. Quantum dot as a drug-tracer in vivo. Third International Conference on Advanced Materials and Nanotechnology, Wellington, New Zealand, February, 2007.
  36. Makaya M, Yanai K, Katsuya T, Fujioka A, Yamori Y, Ogihara T, Kato N. Gene-environment interaction regarding ethanol metabolizing enzymes in the Japanese general population. American Heart Association, Scientific Sessions 2006, Chicago, IL, November, 2006.
  37. Ochiai Y, Liang Y-Q, Serizawa M, Yanai K, Kato N. Systematic expression profiling in the major end-organs after pharmacological intervention. 12th International SHR Symposium, Kyoto, Japan, October, 2006.
  38. Makaya M, Yanai K, Katsuya T, Fujioka A, Yamori Y, Ogihara T, Kato N. Gene-environment interaction regarding ethanol metabolizing enzymes in the Japanese general population. 12th International SHR Symposium, Kyoto, Japan, October, 2006.
  39. Kato N, Yanai K, Makaya M, Nabika T, Katsuya T, Fujioka A, Yasuda K, Yamori Y, Kobayashi S, Ogihara T, Yazaki Y. Integrative large-scale candidate gene analysis of atherosclerotic diseases. 21st Scientific Meeting of the International Society of Hypertension, Fukuoka, October, 2006.
  40. Ochiai Y, Liang Y-Q, Serizawa M, Yanai K, Kato N. Dynamic changes of the renin-angiotensin and associated systems in the rat after pharmacological and dietary interventions in vivo. 21st Scientific Meeting of the International Society of Hypertension, Fukuoka, October, 2006.
  41. Kohara Y, Inomata H, Liang Y-Q, Y Ochiai Y, Serizawa M, Yanai K, Kato N. Unraveling genetic susceptibility by constructing 14 consomic strains derived from the spontaneously hypertensive rat strains. 21st Scientific Meeting of the International Society of Hypertension, Fukuoka, October, 2006.
  42. Makaya M, Yanai K, Katsuya T, Fujioka A, Yamori Y, Ogihara T, Kato N. Gene-environment interaction regarding ethanol metabolizing enzymes in the japanese general population. 21st Scientific Meeting of the International Society of Hypertension, Fukuoka, October, 2006.
  43. Inomata H, Yanai K, Nabika T, Nagano S, Isobe M, Kobayashi S, Kato N. Large-scale genetic analysis of stroke in the Japanese. International Stroke Conference 2006, Kissimmee, FL, February, 2006.
  44. Inomata H, Liang YQ, Yanai K, Isobe M, Kato N. Unraveling genetic susceptibility by the construction of eight consomic strains derived from the stroke-prone spontaneously hypertensive rat. International Stroke Conference 2006, Kissimmee, FL, February, 2006.
  45. Manabe N, Hoshino A, Liang Y-Q, Goto T Kato N, Yamamoto K. Quantum dots conjugated with captoril while remained effective in vivo. 2nd International Conference on Advanced Materials and Nanotechnology, Queenstown, February, 2005.

IV. 学術集会発表−国内学会・研究会

  1. 清水 華、梁 一強、磯野正人、竹内史比古、加藤規弘. 高脂肪食負荷によるラット肝臓エピゲノム変動の検討.第54回高血圧関連疾患モデル学会学術総会, 熊本, 12月, 2018.
  2. 梁 一強、清水 華、松坂恭成、磯野正人、竹内史比古、加藤規弘. 高脂質食成分の違いによる脂肪沈着の評価と肝臓microRNA変動の検討. 第54回高血圧関連疾患モデル学会学術総会, 熊本, 12月, 2018.
  3. 梁 一強、松坂恭成、清水 華、磯野正人、竹内史比古、加藤規弘. 食塩負荷に伴う心腎の線維化と血中miRNA変動の探究. 第54回高血圧関連疾患モデル学会学術総会, 熊本, 12月, 2018.
  4. 島貫秀之、北島浩二、葉山いずみ、田中真寿美、野口倫生、永井秀明、波多野賢二、服部功太郎、松村亮、美代賢吾、小南亮太、野口貴史、渡辺浩、新谷幸子、三上礼子、加藤規弘. ナショナルセンター・バイオバンクネットワーク・カタログデータベースの活用状況. 第38回医療情報学連合大会, 福岡, 11月, 2018.
  5. 宮本恵成, 美代賢吾, 石井雅通、斎藤加代子, 山内玲, 長澤直人, 奥村恭平, 加藤規弘：電子カルテシステムにおけるゲノム医療対応機能の開発と運用.　第63回日本人類遺伝学会. 横浜, 10月, 2018.
  6. Atsuko Imai-Okazaki, Fumihiko Takeuchi, Reiko Arakawa, Kengo Miyo, Kayoko Saito, Jurg Ott, Norihiro Kato. Incorporation of originally-developed statistical genetics methods into a clinical sequencing platform to improve efficiency and quality of variant annotation. 第63回日本人類遺伝学会. 横浜, 10月, 2018.
  7. 竹内史比古、加藤規弘. 高血圧のゲノムワイド関連解析. 第41回日本高血圧学会総会, 旭川, 9月, 2018.
  8. 梁一強、垣野明美、松坂恭成、竹内史比古、沢村達也、加藤規弘. ZFN法により作成したLOX-1 knockout SHRSPにおける脳卒中発症遅延とその機序の探究. 第41回日本高血圧学会総会, 旭川, 9月, 2018.
  9. 山内玲、美代賢吾、宮本恵成、長澤直人、奥村恭平、石割大範、小南亮太、中川陽介、加藤規弘. 効率・効果的な診療とプライバシーを両立したゲノム診療用電子カルテ機能の開発. 第37回医療情報学連合大会, 大阪, 11月, 2017.
  10. 竹内史比古、加藤規弘. ヒト集団における高血圧の遺伝的成因. 第53回高血圧関連疾患モデル学会学術総会, 福岡, 11月, 2017.
  11. 梁一強、垣野明美、磯野正人、竹内史比古、沢村達也、加藤規弘. LOX-1遺伝子ノックアウトラットにおける脳卒中発症の検討. 第53回高血圧関連疾患モデル学会学術総会, 福岡, 11月, 2017.
  12. 宮本恵成、美代賢吾、斎藤加代子、山内玲、長澤直人、奥村恭平、加藤規弘. 個人情報保護に配慮したゲノム医療対応電子カルテシステムの開発. 日本人類遺伝学会第62回大会, 神戸, 11月, 2017.
  13. 島貫秀之、池田仁子、西本寛、若尾文彦、平松治彦、大塚文之、東山綾、高田彰、永井秀明、波多野賢二、松村亮、菊池嘉、秋山純一、廣井透雄、美代賢吾、野口貴史、渡辺浩、武田美江、岩田悟、峯有佳、渡邉裕司、三上礼子、加藤規弘. ナショナルセンター・バイオバンクネットワークのカタログデータベースの現状とこれから. 第36回医療情報学連合大会, 横浜, 11月, 2016.
  14. 竹内史比古、清水華、加藤規弘. ゲノムワイド関連解析とエピゲノム解析による高血圧の機序解明. 第39回日本高血圧学会総会, 仙台, 10月, 2016.
  15. 清水華、竹内史比古、磯野正人、秋山康一、梁一強、加藤規弘. 高血圧自然発症ラットの脳における、食塩負荷に伴うエピジェネティック変化. 第39回日本高血圧学会総会, 仙台, 10月, 2016.
  16. 清水華、竹内史比古、磯野正人、秋山康一、梁一強、加藤規弘. 高血圧自然発症ラットの肝臓における、デキサメタゾン投与に伴うエピジェネティック変化. 第39回日本高血圧学会総会, 仙台, 10月, 2016.
  17. 大澤春彦、田原康玄、川村良一、塚田晃子、伊賀瀬道也、大橋順、山田亮、高田康徳、川本龍一、斉藤功、大沼裕、小原克彦、谷川武、大八木保政、山田一哉、加藤規弘、三木哲郎. レジスチン遺伝子プロモーターSNPとは独立して、新たな機能的SNPとして3’のrs1423096とrs10401670を同定した. 第59回日本糖尿病学会年次学術集会. 京都. 5月. 2016.
  18. 島貫秀之、佐藤泉美、田中康博、新保卓郎、西本寛、若尾文彦、原口亮、大塚文之、東山綾、高田彰、永井秀明、波多野賢二、松村亮、菊池嘉、日ノ下文彦、廣井透雄、美代賢吾、小塚和人、渡辺浩、岩田悟、丹藤昌治、望月修一、加藤規弘. ナショナルセンター・バイオバンクネットワークのカタログデータベースシステム構築. 第35回医療情報学連合大会, 沖縄, 11月, 2015.
  19. 竹内史比古、磯野正人、梁一強、秋山康一、加藤規弘. 6クラスの降圧剤間での、ラットにおける心肥大抑制と遺伝子発現変動の比較：続報. 第51回高血圧関連疾患モデル学会総会, 大阪, 10月, 2015.
  20. 竹内史比古、磯野正人、梁一強、秋山康一、加藤規弘. 3種のレニン–アンジオテンシン系関連降圧剤間での、ラットにおける降圧効果と腎臓での遺伝子発現変動の比較. 第51回高血圧関連疾患モデル学会総会, 大阪, 10月, 2015.
  21. 梁一強、秋山康一、磯野正人、竹内史比古、加藤規弘. ラット染色体1番上の、心血管合併症遺伝子座の同定とその病態機序の探究.第51回高血圧関連疾患モデル学会総会, 大阪, 10月, 2015.
  22. 梁一強、磯野正人、秋山康一、岡村匡史、竹内史比古、加藤規弘. ヒトCholesteryl ester transfer proteinのトランスジェニックラットにおける肝臓での脂質代謝解析. 第51回高血圧関連疾患モデル学会総会, 大阪, 10月, 2015.
  23. 竹内史比古、勝谷友宏、木村亮介、並河徹、大久保孝義、田原康玄、山本健、横田充弘、SAW, Woei-Yuh、TEO, Yik-Ying、加藤規弘. 日本人の精密な遺伝的構造の検討：アジア人の中での遺伝的由来及び遺伝的差異の起源の推定. 第60回日本人類遺伝学会. 東京, 10月, 2015.
  24. Woei-Yuh Saw, Xuanyao Liu, Chiea-Chuen Khor, 竹内史比古, 勝谷友宏, 木村亮介, 並河徹, 大久保孝義, 田原康玄, 山本健, 横田充弘, Yik-Ying Teo, 加藤規弘. Mapping the genetic diversity of HLA haplotypes in the Japanese populations. 第60回日本人類遺伝学会. 東京, 10月, 2015.
  25. Yik-Ying Teo for the Asian Diversity Project Group. Characterising private and shared signatures of positive selection in 37 Asian populations. 第60回日本人類遺伝学会. 東京, 10月, 2015.
  26. 坂井亜衣、帰山沙織、古谷真知、中屋隆裕、山田実夏、市川麻衣、佐藤さつき、今川美智子、山本勝司、藤井美紀、銭丸康夫、鈴木仁弥、牧野耕和、石塚 全、加藤規弘、此下忠志. アンジオテンシンII分解酵素、ENPEP遺伝子型と糖尿病性腎症の関連解析. 第38回日本高血圧学会総会, 松山, 10月, 2015.
  27. 竹内史比古、勝谷友宏、木村亮介、並河徹、大久保孝義、田原康玄、山本健、横田充弘、SAW, Woei-Yuh、TEO, Yik-Ying、加藤規弘. 日本人の精密な遺伝的構造の検討：アジア人の中での遺伝的由来及び遺伝的差異の起源の推定. 日本進化学会第17回大会. 東京, 8月, 2015.
  28. 竹内史比古、勝谷友宏、木村亮介、並河徹、大久保孝義、田原康玄、山本健、横田充弘、SAW, Woei-Yuh、TEO, Yik-Ying、加藤規弘. 日本人の精密な遺伝的構造の検討：アジア人の中での遺伝的由来及び遺伝的差異の起源の推定. 日本進化学会第17回大会. 東京, 8月, 2015.
  29. Sugiyama K, Sasano T, Tamura N, Okamura T, Kato N, Isobe M, Tetsushi Furukawa. Oxidative Stress Induced Ventricular Arrhythmias and Impaired Cardiac Function in Nos1ap Deleted Mice. 第79回日本循環器学会学術集会. 大阪. 4月. 2015.
  30. 磯野正人、梁一強、秋山康一、竹内. 史比古、加藤規弘. 降圧、心肥大抑制と遺伝子発現変動に関する、6クラスの降圧剤間での比較. 第50回高血圧関連疾患モデル学会総会, 和歌山, 12月, 2014.
  31. 坂井亜衣、中屋隆裕、山本勝司、山田実夏、市川麻衣、今川美智子、牧野耕和、藤井美紀、鈴木仁弥、石塚全、シャギデジャ ムードレイ、加藤規弘、此下忠志. ENPEP（angiotensinase A）遺伝子多型と高血圧症の相関解析. 第37回日本高血圧学会総会, 横浜, 10月, 2014.
  32. 梁一強、Nitish Mehta、秋山康一、磯野正人、加藤規弘. ラット染色体1番における、心血管合併症遺伝子座の多面的探索. 第37回日本高血圧学会総会, 横浜, 10月, 2014.
  33. 磯野正人、竹内史比古、山本健、横田充弘、勝谷友宏、秋山康一、加藤規弘. 東アジア人での遺伝的関連に関する、血圧と冠動脈疾患の間の不均一性. 第37回日本高血圧学会総会, 横浜, 10月, 2014.015.
  34. 秋山康一、梁一強、磯野正人、加藤規弘. 高血圧自然発症ラット（SHR）系統での腎臓mRNA発現解析を用いた高血圧感受性遺伝子の探索. 第36回日本高血圧学会総会, 大阪, 10月, 2013..
  35. 秋山康一、梁一強、磯野正人、加藤規弘. ヒトGWASで同定された脂質関連遺伝子のラット高脂肪食負荷における病態的意義の探究. 第36回日本高血圧学会総会, 大阪, 10月, 2013.
  36. 梁一強、秋山康一、磯野正人、岡村匡史、加藤規弘. ヒトcholesteryl ester transfer proteinの高血圧ラットへの遺伝子導入と代謝関連形質に対する影響の評価：続報. 第36回日本高血圧学会総会, 大阪, 10月, 2013.
  37. 梁一強、秋山康一、磯野正人、加藤規弘. ラット染色体１番における、血圧とは独立した心血管合併症遺伝子座の同定. 第36回日本高血圧学会総会, 大阪, 10月, 2013..
  38. 秋山康一、梁一強、磯野正人、加藤規弘. 高血圧自然発症ラット（SHR）系統での腎臓mRNA発現解析を用いた高血圧感受性遺伝子の探索. 第49回高血圧関連疾患モデル学会総会, 東京, 9月, 2013.
  39. 秋山康一、梁一強、磯野正人、加藤規弘. ヒトGWASで同定された脂質関連遺伝子のラット高脂肪食負荷における病態的意義の探究. 第49回高血圧関連疾患モデル学会総会, 東京, 9月, 2013.
  40. 梁一強、秋山康一、磯野正人、岡村匡史、加藤規弘. ヒトcholesteryl ester transfer proteinの高血圧ラットへの遺伝子導入と代謝関連形質に対する影響の評価：続報. 第49回高血圧関連疾患モデル学会総会, 東京, 9月, 2013.
  41. 梁一強、秋山康一、芹澤昌邦、尾留川直子、宮岸真、下川和郎、磯野正人、加藤規弘. デキサメサゾン負荷に伴う遺伝子発現変動に関する、in vivoとin vitroの統合的解析. 第49回高血圧関連疾患モデル学会総会, 東京, 9月, 2013.
  42. 梁一強、秋山康一、磯野正人、加藤規弘. ラット染色体１番における、血圧とは独立した心血管合併症遺伝子座の同定. 第49回高血圧関連疾患モデル学会総会, 東京, 9月, 2013..
  43. 秋山康一、梁一強、磯野正人、竹内史比古、加藤規弘. 高血圧自然発症ラット（SHR）系統を用いた、遺伝的血圧制御における中和的な遺伝子間相互作用の同定. 第35回日本高血圧学会総会, 名古屋, 9月, 2012.
  44. 秋山康一、梁一強、磯野正人、加藤規弘. 高血圧自然発症ラット（SHR）系統を用いた、高脂肪食負荷時の脂質制御におけるヒト脂質関連遺伝子群及びメチル化機序の関与の検討. 第35回日本高血圧学会総会, 名古屋, 9月, 2012.
  45. 梁一強、秋山康一、磯野正人、加藤規弘. 高血圧自然発症ラット（SHR）系統における心肥大遺伝子の探索：Endonuclease G遺伝子の確証と新規遺伝子座の同定. 第35回日本高血圧学会総会, 名古屋, 9月, 2012.
  46. 梁一強、秋山康一、磯野正人、加藤規弘. 高血圧自然発症ラット（SHR）系統での、動脈硬化の多面的効果に関わる遺伝的機序の探索：血圧遺伝子座SHR-Bp4-1〜Bp4-3の同定. 第35回日本高血圧学会総会, 名古屋, 9月, 2012.
  47. 梁一強、秋山康一、磯野正人、加藤規弘. 高血圧自然発症ラット（SHR）系統における高コレステロール血症責任遺伝子の探索：コレステロール遺伝子座TC15-1及びTC15-2の同定. 第35回日本高血圧学会総会, 名古屋, 9月, 2012.
  48. 梁一強、秋山康一、磯野正人、岡村匡史、加藤規弘. ヒトcholesteryl ester transfer proteinの高血圧ラットへの遺伝子導入と代謝関連形質に対する影響の評価：第１報. 第35回日本高血圧学会総会, 名古屋, 9月, 2012.
  49. 青山千賀子, 加藤規弘, 小川佳宏, 河内正治. 当院における術前の抗血小板薬休薬と術後の動脈血栓性合併症発症の実態報告. 第34回日本臨床麻酔学会, 東京, 6月, 2012..
  50. 青山千賀子, 加藤規弘, 小川佳宏, 志賀由佳, 河内正治. 当院での術前の抗血小板薬休薬と術後血栓性合併症の実態報告. 第31回日本臨床麻酔学会, 沖縄, 11月, 2011.
  51. 此下忠志, 加藤規弘, 木村朋子, 藤井美紀, 牧野耕和, 若原成行, 宮森勇. レニン-アンジオテンシン系(RAS)遺伝子型は同系抑制薬の効果を予測し得るか? -RASファルマコジェノミクスのシステマティックレビュー-. 第34回日本高血圧学会総会, 宇都宮, 10月, 2011.
  52. 加藤規弘, 竹内史比古, 山本健, 磯野正人, 勝谷友宏, 杉山卓郎, 並河徹, 藤岡晨宏, 大中佳三, 家森幸男, 山口修平, 小林祥泰, 高柳涼一, 荻原俊男. 日本人での大規模追試研究による、7つの候補遺伝子と血圧値/高血圧との関連の検討. 第34回日本高血圧学会総会, 宇都宮, 10月, 2011.
  53. 此下忠志, 加藤規弘, 宮森勇. 網羅的発現遺伝子解析により抽出された高血圧特異的遺伝子クラスター -高血圧とア ンジオテンシンII消去系遺伝子群発現低下との関連-. 第34回日本高血圧学会総会, 宇都宮, 10月, 2011.
  54. 此下忠志、加藤規弘、宮森 勇. 網羅的解析による高血圧特異的発現遺伝子の抽出－RAS抑制系遺伝子群の意義. 第84回日本内分泌学会総会, 神戸, 4月, 2011.
  55. 竹内史比古, 並河徹, 磯野正人, 勝谷友宏, 杉山卓郎, 山口修平, 小林祥泰, 家森幸男, 荻原俊男, 加藤規弘. 日本人において7つの新規遺伝子座が血圧値および高血圧と関連している. 第33回日本高血圧学会総会, 福岡, 10月, 2010.
  56. 竹内史比古, 加藤規弘. 遺伝子型間での量的形質の異分散性を活用した精密マッピング. 第55回日本人類遺伝学会, 大宮, 10月, 2010.
  57. 此下忠志, 加藤規弘, 高橋芳徳, 水野真一, 木村朋子, 藤井美紀, 牧野耕和, 荒川健一郎, 若原成行, 居軒 功, 宮森 勇、G-DOC Study Investigators. 網羅的解析による糖尿病腎症特異的発現遺伝子の抽出-Insulin Regulated Aminopeptidase (IRAP/AT4)の発現低下. 第53回日本糖尿病学会年次学術集会, 岡山, 5月, 2010.
  58. 加藤規弘, 梁一強, Zaidi Ali, 竹内史比古. 劇症型脳卒中易発症モデルラットの作成とポジショナルクローニング. 第32回日本高血圧学会総会, 大津, 10月, 2009.
  59. 此下忠志, 加藤規弘, 水野真一, 本村 誠, 青山千賀子, 木村朋子, 藤井美紀, 牧野耕和, 荒川健一郎, 若原成行, 居軒 功, Sebastien Fuchs, Florence Pinet, 宮森 勇、G-DOC Study Investigators. アンジオテンシン遮断薬responder決定因子としてのレニンアンジオテンシン系遺伝子. 第32回日本高血圧学会総会, 大津, 10月, 2009.
  60. 竹内史比古, 並河徹, 磯野正人, 勝谷友宏, 杉山卓郎, 山口修平, 小林祥泰, 家森幸男, 荻原俊男, 加藤規弘日本人の身長に影響する遺伝子多型の検証. 第54回日本人類遺伝学会, 東京, 9月,　2009.
  61. 弥富寿麻子, 岡野美江, 加賀朋子, 目﨑悦子, 田中めぐみ, 髙嶋美和, 橋本千草, 堀愛, 小林信之, 加藤規弘. 国立国際医療センターでの臨床研究コーディネーター（MRC）による臨床研究支援の試み. 第9回ＣＲＣと臨床試験のあり方を考える会議 2009, 横浜, 9月,　2009.
  62. 此下忠志, 加藤規弘, 牧野耕和, Sebastien Fuchs, Florence Pinet,宮森 勇, G-DOC Study Investigators. レニン遺伝子多型C-5312Tはアンジオテンシン遮断薬の降圧効果に影響する. 第52回日本腎臓学会, 横浜, 6月, 2009.
  63. 竹内史比古, 山本健, 藤澤智巳, 中島英太郎, 大中佳三, 池上博司, 杉山卓郎, 勝谷友宏, 宮岸真, 中島直樹, 名和田新, 中村二郎, 古野純典, 高柳涼一, 加藤規弘. 550Kアレイを用いた日本人2型糖尿病のGenome-Wide Association Studyと遺伝的効果の検証. 第52回日本糖尿病学会年次学術集会, 大阪, 5月,　2009.
  64. 此下忠志, 加藤規弘, 水野真一, 本村 誠, 青山千賀子, 木村朋子, 藤井美紀, 牧野耕和, 荒川健一郎, 若原成行, 居軒 功, Sebastien Fuchs, Florence Pinet, 宮森 勇、G-DOC Study Investigators. アンジオテンシン遮断薬responder決定因子としてのレニンアンジオテンシン系遺伝子と糖尿病. 第52回日本糖尿病学会年次学術集会, 大阪, 5月,　2009.
  65. 加藤規弘, 竹内史比古, 芹澤昌邦, 並河徹, 杉山卓郎, 勝谷友宏, 大久保孝義, 山口修平, 今井潤, 小林祥泰. Genome-Wide Association Studyによるラクナ梗塞と高血圧の感受性遺伝子探索. 第31回日本高血圧学会総会, 札幌, 10月, 2008
  66. 尾留川直子, 梁一強, 王涛, 張燕, 加藤規弘.　SHRSP由来のサブコンジェニッック系統を用いた腎障害QTLのポジショナルクローニング. 第31回日本高血圧学会総会, 札幌, 10月, 2008.
  67. Zhang Y, Makaya M, Kastriratne A, Wang T, Miyagishi M, de Silva J, Wickremasinghe AR, Kato N. Type 2 Diabetes is associated with decreased plasma adiponectin levels independently of insulin resistance in South Asians. 第31回日本高血圧学会総会, 札幌, 10月, 2008.
  68. Wang T, Liang Y-Q, Zhang Y, Birukawa N, Kato N. Detection of a rat chromosome 4 region that influences blood pressure using a combination approach. 第31回日本高血圧学会総会, 札幌, 10月, 2008.
  69. Wang T, Liang Y-Q, Zhang Y, Birukawa N, Zhang Y. Kato N. Comprehensive evaluation of gene expression profile induced by six antihypertensive drugs on three end-organs. 第31回日本高血圧学会総会, 札幌, 10月, 2008.
  70. 此下忠志, 木村朋子, 藤井美紀, 牧野耕和, 若原成行, 居軒功, 宮森勇, 加藤規弘, Sebastien Fuchs. 糖尿病性腎症におけるレニン-アンジオテンシン系. 第20回日本糖尿病性腎症研究会, 東京, 12月, 2008.
  71. 此下忠志, 加藤規弘, 牧野耕和, 宮森勇. DNAチップを用いた糖尿病性腎症発現遺伝子の網羅的解析. 第77回北陸糖尿病集談会, 金沢, 12月, 2008.
  72. 此下忠志, 加藤規弘, 水野真一, 本村誠, 青山千賀子, 木村朋子, 牧野耕和, 若原成行, Sebastien Fuch, Florence Pinet, 宮森　勇. アンジオテンシン遮断薬レスポンダー決定因子－レニンアンジオテンシン系遺伝子と糖尿病－. 第76回北陸糖尿病集談会, 金沢, 7月, 2008.
  73. 此下忠志, 牧野耕和, 若原成行, 加藤規弘, 宮森勇. メタボリックシンドロームにおける循環系・組織レニン-アンジオテンシン系亢進. 第51回日本糖尿病学会, 東京, 5月, 2008.
  74. 眞茅みゆき, 三田村昌泰, 笠原茂, 古殿次郎, 上村直実, 加藤規弘. 臨床研究の推進を目的とした臨床研究レジストリおよび臨床データブックの開発と実用. 第9回日本医療情報学会学術大会, 横浜, 11月,　2008.
  75. 岡野美江, 眞茅みゆき, 加藤規弘. 遺伝情報をも対象とした臨床研究における臨床研究コーディネーターの役割. 第7回日本遺伝看護学会,　東京, 9月, 2008.
  76. 田邉真紀人、成瀬光栄、鈴木知子、Zheng-pei Zeng、加藤規弘、岡嶋泰一郎. 中国における肥満症・メタホリックシントロームの実態調査(第2報). 第16回西日本肥満研究会, 宮崎, 7月, 2008.
  77. 眞茅みゆき, 岩嶋義雄, 加藤規弘. 専門医療機関受診者におけるリスクの重積した非メタボリックシンドローム（MS）症例とMS症例の心血管イベント発生率の比較. 第44回日本循環器予防学会・日本循環器管理研究協議会総会, 秋田, 5月, 2008.
  78. 加賀朋子, 今田香, 川路美子, 立入朋子, 目崎悦子, 眞茅みゆき, 上村直実, 加藤規弘. 医師主導型臨床研究を支援する臨床研究コーディネーターの役割：国立国際医療センターでの取り組み. 第72回日本循環器学会総会, 福岡, 3月, 2008.
  79. 加藤規弘, ミレニアムプロジェクト高血圧コンソーシアム. 高密度SNP association studyによる高血圧感受性遺伝子の同定. 第30回日本高血圧学会総会, 那覇, 10月, 2007.
  80. 加藤規弘, 梁一強, 落合義徳, 尾留川直子, 芹澤昌邦, 眞茅みゆき. SHRをモデルとしたメタボリック・シンドローム関連形質の分断化とポジショナル・クローニング. 第30回日本高血圧学会総会, 那覇, 10月, 2007.
  81. 眞茅みゆき, 藤岡晨宏, 勝谷友宏, 荻原俊男, 家森幸男, 加藤規弘. コレステロール逆転送系に関連する14遺伝子と脂質代謝との関連：高血圧罹患の有無と一般集団中での遺伝的効果の検証. 第30回日本高血圧学会総会, 那覇, 10月, 2007.
  82. 河原申弥, 富樫廣子, Subrina Jesmin, Sohel Zaedi, 山口拓, 吉岡充弘, 加藤規弘. エンドセリン受容体遮断はSHRSP大脳皮質における脳血流低下を改善する. 第41回高血圧関連疾患モデル学会学術総会, 大阪, 9月, 2007.
  83. Subrina Jesmin, 富樫廣子, 河原申弥, Sohel Zaedi, 下條信武, 山口直人, 宮内孝, 加藤規弘. Normalization of impairment in VEGF signaling, coronary collateral development and cardiac function in early diabetic rat heart by dual endothelin antagonism. 第41回高血圧関連疾患モデル学会学術総会, 大阪, 9月, 2007.
  84. 中林一彦, 藤本崇弘, 馬場賀, 小柳緑, 顧寧, 土井佳子, 加藤規弘，笹月健彦, 白澤専二. Towards elucidating the transcription network regulated by a novel immune-related transcription factor ZFAT. 第52回日本人類遺伝学会, 9月, 2007.
  85. Serizawa M, Yanai K, Nabika T, Inomata H, Ochiai Y, Makaya M, Kobayashi S, Kato N. Genetic signature for the prevention of stroke in the Japanese population. 第71回日本循環器学会学術集会, 神戸, 3月, 2007.
  86. Ochiai Y, Kohara Y, Inomata H, Liang Y-Q, Serizawa M, Yanai K, Kato N. Unraveling genetic susceptibility by constructing 14 consomic strains derived from the spontaneously hypertensive rat strains. 第71回日本循環器学会学術集会, 神戸, 3月, 2007.
  87. Makaya M, Yanai K, Katsuya T, Fujioka A, Yamori Y, Ogihara T, Kato N. Evaluation of 14 genes involved in reverse cholesterol transport in the Japanese general population. 第71回日本循環器学会学術集会, 神戸, 3月, 2007.
  88. 柳内和幸, 柳内圭子, 芹澤昌邦, 小池淑子, 落合義徳, 加藤規弘. ゲノムスケールでの転写因子標的配列の系統的な同定法の開発. 日本分子生物学会2006フォーラム, 名古屋, 12月, 2006.
  89. 芹澤昌邦, 柳内和幸, 柳内圭子, 小池淑子, 加藤規弘. ラットゲノムからのグルココルチコイド受容体結合配列の系統的な同定と解析. 日本分子生物学会2006フォーラム, 名古屋, 12月, 2006.
  90. 柳内圭子, 柳内和幸, 小池淑子, 芹澤昌邦, 加藤規弘. ヒトゲノムからのエストロゲン受容体結合配列の系統的な同定と解析. 日本分子生物学会2006フォーラム, 名古屋, 12月, 2006.
  91. 藤岡晨宏, 眞茅みゆき, 加藤規弘. 尼崎市民健康開発センターの検診受診者における高血圧の発症頻度および発症関連要因の検討. 第65回日本公衆衛生学会総会、富山,　10月, 2006.
  92. 落合義徳, 梁一強, 猪又兵衛, 芹澤昌邦, 柳内和幸, 加藤規弘, 矢崎義雄. レニン-アンジオテンシン-アルドステロン系遺伝子群の臓器および外的刺激に特異的な発現変動. 第14回分子高血圧研究会, 東京, 10月, 2005.
  93. 猪又兵衛, 梁一強, 落合義徳, 芹澤昌邦, 磯部光章, ,柳内和幸, 加藤規弘. コンジェニックラットにおけるQTLの検証とfine mappingのための戦略的アプローチ. 第41回高血圧関連疾患モデル学会学術総会, 札幌, 9月, 2005.
  94. 落合義徳, 梁一強, 猪又兵衛, 芹澤昌邦, 柳内和幸, 加藤規弘. DNAマイクロアレイ法を用いた降圧剤応答性遺伝子群の検出—ファーマコゲノミクスへの展開. 第41回高血圧関連疾患モデル学会学術総会, 札幌, 9月, 2005.
  95. 加藤規弘, 柳内和幸, 竹内史比古, 猪又兵衛, 眞茅みゆき, 柳内圭子, 長野忍, 並河徹, 勝谷友宏, 藤岡晨宏, 安田和基, 家森幸男, 小林祥泰, 荻原俊男, 矢崎義雄. 動脈硬化性疾患に関する複合的かつ大規模な候補遺伝子解析. 第28回日本高血圧学会総会, 旭川, 9月, 2005.
  96. 猪又兵衛, 梁一強, 落合義徳, 芹澤昌邦, 磯部光章, 柳内和幸, 加藤規弘. SHRSP由来の8コンソミック系統を用いた、高血圧関連疾患の組織的遺、解析. 第28回日本高血圧学会総会, 旭川, 9月, 2005.
  97. 猪又兵衛, 梁一強, 落合義徳,芹澤昌邦, 磯部光章, 柳内和幸, 加藤規弘. コンジェニックラットにおけるQTLの検証とfine mappingのための戦略的アプローチ. 第28回日本高血圧学会総会, 旭川, 9月, 2005.
  98. 落合義徳, 梁一強, 猪又兵衛, 芹澤昌邦, 柳内和幸, 加藤規弘. DNAマイクロアレイ法を用いた降圧剤応答性遺伝子群の検出：ファーマコゲノミクスへの展開. 第28回日本高血圧学会総会, 旭川, 9月, 2005.
  99. 落合義徳, 梁一強, 猪又兵衛, 芹澤昌邦, 柳内和幸, 加藤規弘. レニンーアンジオテンシン系遺伝子の網羅的発現解析. 第28回日本高血圧学会総会, 旭川, 9月, 2005.
  100. 柳内和幸, 長野忍, 芹澤昌邦, 小池淑子, 落合義徳, 柳内圭子 竹内史比古, 加藤規弘. 代謝性疾患の個別化医療に向けた統合データベース構築：JMDBase. 第28回日本高血圧学会総会, 旭川, 9月, 2005.
  101. 柳内和幸, 並河徹, 竹内史比古, 猪又兵衛, 小林祥泰, 加藤規弘. ２つの新規な脳卒中感受性遺伝子—PDE4DとALOX5AP—の脳硬塞の病型分類を考慮した日本人での評価. 第28回日本高血圧学会総会, 旭川, 9月, 2005.
  102. 真鍋法義、星野昭芳、梁一強、後藤知将、加藤規弘、山本健二. Quantum dotsと薬剤の結合によるn vivoでの効果. 日本薬学会第125年会, 東京, 3月, 2005.

V. シンポジウム・講演

  1. 加藤規弘. 脳梗塞のゲノム解析とビッグデータ医療 第28回日本脳ドック学会総会, 松江, 6月, 2019.
  2. 加藤規弘. 高血圧のゲノム疫学研究：総論. 第41回日本高血圧学会総会, 旭川, 9月, 2018.
  3. Kato N. Role of epigenome in hypertension. 27th Scientific Meeting of the International Society of Hypertension. Beijing, China, September 2018.
  4. Kato N. Genetics/genomics of hypertension with consideration of ethnic differences. Cardiovascular Genetics, Satellite Symposium of ISH 2018. Shanghai, China, September 2018.
  5. 加藤規弘. ビッグデータ医療に関わるイノベーションと国際動向. 日本オミックス医療学会大会〜AI創薬フォーラム, 東京, 6月, 2018
  6. 加藤規弘. 高血圧とprecision medicine総論. 第41回日本高血圧学会総会, 松山, 10月, 2017
  7. 加藤規弘. 臨床ゲノム情報統合データベース整備事業が目指すもの：ゲノム医療を支える統合データベースの構築.　 第23回日本家族性腫瘍学会学術集会, 札幌, 8月, 2017
  8. 加藤規弘. 臨床ゲノム情報統合データベース整備事業が目指すもの：ゲノム医療を支える統合データベースの構築.　 第3回クリニカルバイオバンク研究会シンポジウム, 千葉, 7月, 2017
  9. 加藤規弘. ゲノム医療を支える統合データベースの構築.　日本オミックス医療学会シンポジウム, 東京, 6月, 2017
  10. 加藤規弘. 臨床ゲノム情報統合データベース整備事業が目指すもの.　 第59回日本老年医学会学術集会, 名古屋, 6月, 2017
  11. Kato N. Medical Genomics Japan Database: Introduction of Global picture and somatic cancer group. ICBI Seminar Series. Washington DC, USA, February, 2017.
  12. 加藤規弘. ゲノム医療の国際連携と我が国の取り組み. 日本遺伝子診療学会：遺伝子診断・検査技術推進フォーラム　公開シンポジウム2016, 東京, 12月, 2016.
  13. 加藤規弘. 国内外のバイオバンクの動向やNCBNの取組みについて. 第22回日本薬剤疫学会, 京都, 11月, 2016.
  14. Kato N. DNA methylation and hypertension. Cardiovascular Genetics, Satellite Symposium of ISH 2016. Tokyo, Japan, September 2016.
  15. Kato N. Genomic medicine in NCDs: findings from Asians/ South Asians to global collaboration. 25th Anniversary International Scientific Conference University of Kelaniya. Ragama, Sri Lanka, April 2016.
  16. 加藤規弘. 高血圧および関連疾患のゲノム研究. 第39回日本高血圧学会総会, 仙台, 10月, 2016.
  17. 加藤規弘. 高血圧等の生活習慣病のゲノム／エピゲノム解析. 第4回低酸素研究会, 東京, 7月, 2016.
  18. 加藤規弘. 人種横断的ゲノムワイド関連解析による、新規の高血圧関連遺伝子座の同定とDNAメチル化の役割の推定：iGEN-BP国際共同研究での知見. 第38回日本高血圧学会総会, 松山, 10月, 2015.
  19. 加藤規弘. コンジェニック系統解析による新たな臓器障害QTLの同定. 第50回高血圧関連疾患モデル学会総会, 和歌山, 12月, 2014.
  20. Kato N. Towards elucidation of pathological basis of intractable tumors. International Symposium on Pheochromocytoma and Paraganglioma 2014. Kyoto, Japan, September 2014.
  21. Kato N. Genetics of NAFLD/ NASH. 127th Anniversary International Medical Congress of Sri Lanka Medical Association. Colombo, Sri Lanka, July 2014.
  22. Kato N. Can rat genetics help to improve human genetics? Cardiovascular Genetics Satellite 2014. Rome, Italy, June 2014.
  23. 加藤規弘. 高血圧および関連疾患のゲノム解析研究と展望. OKN summit 2014, 名古屋, １月, 2014.
  24. 加藤規弘. 高血圧および関連疾患のゲノム解析と展望. 第４回九州血圧研究会, 福岡, ９月, 2013.
  25. 加藤規弘. ゲノムワイドから遺伝子機能解析への展開に係る見通し. 第49回高血圧関連疾患モデル学会総会, 東京, ９月, 2013.
  26. 加藤規弘. 高血圧関連疾患のゲノム解析と展望. 島根大学高齢者難治性疾患予防研究 公開講演会. 出雲, 2月, 2013.
  27. Kato N. Global genomics of BP. Cardiovascular Genetics Satellite 2012. Melbourne, Australia, September 2012.
  28. 加藤規弘. 高血圧関連疾患のゲノム解析と展望. 動脈硬化Update2012, 東京, 9月, 2012.
  29. 加藤規弘. 高血圧関連疾患のゲノム解析と展望. 第49回日本臨床分子医学会学術集会, 京都, 4月, 2012.
  30. 加藤規弘. Common diseaseの遺伝子マッピング：成果と課題. 東京大学22世紀医療センターセミナー, 東京, 2月, 2012.
  31. 加藤規弘. 高血圧のゲノムワイド関連解析と展望. 第8回京都レニンアルドステロンフォーラム, 京都, 1月, 2012..
  32. 加藤規弘. Pathogenesis of Primary Aldosteronism. Primary Aldosteronism Symposium 2011, 東京, 12月, 2011.
  33. 加藤規弘. 高血圧のゲノムワイド関連解析と展望. 第48回日本臨床生理学会総会ランチョンセミナー, 東京, 11月, 2011.
  34. 加藤規弘, CAGE network. 全ゲノム関連解析による、東アジア人での高血圧関連遺伝子の探索:新規メカニズムと人種特異性の同定. 第34回日本高血圧学会総会, 宇都宮, 10月, 2011.
  35. Kato N. GWAS of hypertension-associated disease in the Japanese. 20th KOGO Conference. Osong, Korea, September, 2011.
  36. 加藤規弘. 日本人にみられる高血圧関連遺伝子多型. 第51回新潟高血圧談話会, 新潟, 7月, 2011.
  37. 加藤規弘. 高血圧の遺伝子解析の現状. 第73回東京心臓の会, 東京, 6月, 2011.
  38. Kato N. Genome-wide exploration of genetic susceptibility to hypertension and associated diseases. 5th Oriental Congress of Cardiology, Shanghai, China, May, 2011.
  39. Kato N. Genome-wide exploration of genetic susceptibility to hypertension and associated diseases. The National University of Singapore, Advanced genomics symposium, Singapore, February, 2011.
  40. 加藤規弘. 動脈硬化性疾患に対する予防戦略. 第81回日本衛生学会学術総会, 東京, 3月, 2011.
  41. 加藤規弘. 世界の稀少疾患対策の動向. 第14回日本内分泌病理学会学術総会, 京都, 10月, 2010.
  42. 加藤規弘. Post-GWAS時代における高血圧研究の世界的潮流と我が国からの提言. 第33回日本高血圧学会総会, 福岡, 10月, 2010.
  43. Kato N. Genetic susceptibility to diabetes and associated diseases in the Japanese. 8th IDF WPR Congress. Busan, Korea, October, 2010.
  44. Kato N. Genome-wide exploration of genetic susceptibility to cardiometabolic diseases. International Congress of Pathophysiology & International SHR Symposium 2010. Montreal, Canada, September, 2010.
  45. Kato N. Genetic susceptibility to cardiovascular disease and its risk factors in the Japanese. 19th KOGO Conference. Seoul, Korea, September, 2010.
  46. 加藤規弘. 「統合的生命システム実証学」としてのゲノム疫学研究. 第80回日本衛生学会学術総会, 仙台、5月, 2010.
  47. Kato N. Risk of myocardial infarction and stroke among Asians. 10th South East Asia Regional Scientific Meeting of the International Epidemiological Association, Colombo, Sri Lanka, May, 2010.
  48. Kato N. Genome-wide association study of cardiovascular disease in the Japanese. 3rd Annual Illumina Asia Pacific & Japan User Symposium. Phuket, Thailand, April, 2010.
  49. Kato N. Variations in the incidence of CVD in Asia and steps to contain the epidemic. 14th Annual Academic Sessions, College of Community Physicians of Sri Lanka. Colombo, Sri Lanka. September, 2009.
  50. 加藤規弘. SHR/SHRSPを用いた分子薬理学の展望. 第45回高血圧関連疾患モデル学会学術総会. 東京, 10月, 2009.
  51. 加藤規弘. 遺伝-環境因子からみた高血圧個別治療. 第57回日本心臓病学会学術集会教育プログラム. 札幌, 9月, 2009.
  52. 加藤規弘. 生活習慣病と遺伝子. 伏見内分泌代謝ネットワーク講演会. 京都, 7月, 2009.
  53. 加藤規弘.　生活習慣病に関する遺伝的リスクと疫学的意義の検討. 島根大学疾病予知予防研究拠点キックオフシンポジウム. 出雲, 3月, 2009.
  54. 加藤規弘. Full genomic signature：SHR、SHRSPとは一体どういうモデルなのか？ 第44回高血圧関連疾患モデル学会学術総会, 出雲, 11月, 2008.
  55. Kato N. Dissection of Phenotypic Traits Associated with Metabolic Syndrome and Cardiovascular Complications in SHR and SHRSP of Japanese Colony. 13th International. SHR Symposium. Prague, Czech Republic , June, 2008.
  56. 加藤規弘. 高血圧疾患のオーダーメイド治療. 北海道医師会認定生涯教育講座ARBの臓器保護を考える会. 札幌, 12月, 2007.
  57. Kato N. Metabolic syndrome, a public health burden in Japan. Topical Workshop-Metabolic Syndrome in Asia. 6th Asian-Pacific Congress of Hypertension, 9th International Symposium on Hypertension and Related Diseases, Beijing, China, November, 2007.
  58. 加藤規弘.高血圧疾患のオーダーメイド治療. 第15回愛媛血管病態研究会, 松山, 9月, 2007.
  59. Kato N. Genetic mechanisms underlying hypertension: transferabiity from rat to human. 北京協和医院内分泌科主催カンファレンス, Beijing, China, July, 2007.
  60. Kato N. Overview of our international collaborative research regarding metabolic syndrome. Health Education Course：代謝症候群の予防と制御に関する中日カンファレンス. 中国山西省太原市, July, 2007.
  61. 加藤規弘.臨床研究における医療情報活用と基礎研究との連携.　 情報システム研究機構シンポジウム「情報とシステム2007」.　東京, 3月, 2007.
  62. Kato N. Rat as a model to analyze genetic mechanisms underlying hypertension. 12th International SHR Symposium, Kyoto, Japan, October, 2006.
  63. Kato N. Genetic mechanisms underlying hypertension: Transferability from rat to human. 21st Scientific Meeting of the International Society of Hypertension, Fukuoka, October, 2006.
  64. Kato N. Genetic epidemiology of life-style related diseases. 20th IUBMB International Congress of Biochemistry and Molecular Biology, Kyoto, Japan, June, 2006.
  65. 加藤規弘. 心血管系疾患のゲノム解析とファーマコゲノミクス. 第２回ファルマハプロタイプ研究会. 東京, 3月, 2006.
  66. 加藤規弘. 心血管疾患のゲノム解析とテーラーメイド医療への応用. 第75回東京女子医大高血圧研究会. 東京, 3月, 2006.
  67. 加藤規弘. 心血管系疾患のゲノム解析の現状と個別化医療推進への課題. 品川研究開発センターセミナー. 東京, 3月, 2006.
  68. 加藤規弘. 高血圧のゲノム解析：モデル動物からヒトへの展開. 第7回高血圧を考える会. 東京, 2月, 2006.
  69. 加藤規弘. 不摂生と生活習慣病：長く健康な生活を送るために心がけること. 第65回日本未来科学館「展示の前で研究者に会おう」. 東京, 1月, 2006.
  70. 加藤規弘.　糖尿病の個別化医療実現に向けた統合的ゲノム解析研究. 医薬基盤研究所シンポジウム：疾病対策・創薬—ゲノム・蛋白研究の成果. 大阪, 12月, 2005.
  71. 加藤規弘.　心血管系疾患のゲノム解析の現状と個別化医療推進への課題. 九州大学血管病カンファランス. 福岡, 10月, 2005.
  72. 加藤規弘.　オーダーメード医療の必要性・意義に関する調査. 株）科学技術文明研究所・NTT データ共催 第1回フォーラム. 東京, 9月, 2005.
  73. 加藤規弘.　メタボリックシンドロームの遺伝学的アプローチ. 第26回ヒューマンサイエンス基礎研究講習会. 東京, 9月, 2005.
  74. 加藤規弘.　疾病ゲノム解析：レニン・アンギオテンシン系を中心として. 第61回東京心臓の会：心血管系のポストゲノムの現状と将来. 東京, 6月, 2005.
  75. 加藤規弘.　生活習慣病のテーラーメイド医療. 日本抗加齢医学会専門医・指導士認定委員会主催講習会. 大阪, 2月, 2005.
  76. 加藤規弘.　高血圧の感受性遺伝子探索：その成果と展望. 文科省特定領域研究 ゲノム医科学シンポジウム『多因子疾患のゲノム解析』. 東京, 2月, 2005.