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83 matches for
Kamatani Y,
showing the first 20.
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Okada Y,
Wu D,
Trynka G,
Raj T,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Yoshida S,
Graham RR,
Manoharan A
and 83 more — show all
Ortmann W,
Bhangale T,
Denny JC,
Carroll RJ,
Eyler AE,
Greenberg JD,
Kremer JM,
Pappas DA,
Jiang L,
Yin J,
Ye L,
Su DF,
Yang J,
Xie G,
Keystone E,
Westra HJ,
Esko T,
Metspalu A,
Zhou X,
Gupta N,
Mirel D,
Stahl EA,
Diogo D,
Cui J,
Liao K,
Guo MH,
Myouzen K,
Kawaguchi T,
Coenen MJ,
van Riel PL,
van de Laar MA,
Guchelaar HJ,
Huizinga TW,
Dieudé P,
Mariette X,
Bridges SL Jr,
Zhernakova A,
Toes RE,
Tak PP,
Miceli-Richard C,
Bang SY,
Lee HS,
Martin J,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Rantapää-Dahlqvist S,
Arlestig L,
Choi HK,
Kamatani Y,
Galan P,
Lathrop M,
Eyre S,
Bowes J,
Barton A,
de Vries N,
Moreland LW,
Criswell LA,
Karlson EW,
Taniguchi A,
Yamada R,
Kubo M,
Liu JS,
Bae SC,
Worthington J,
Padyukov L,
Klareskog L,
Gregersen PK,
Raychaudhuri S,
Stranger BE,
De Jager PL,
Franke L,
Visscher PM,
Brown MA,
Yamanaka H,
Mimori T,
Takahashi A,
Xu H,
Behrens TW,
Siminovitch KA,
Momohara S,
Matsuda F,
Yamamoto K,
Plenge RM
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
12 pages+
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
and 150 more — show all
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
Genome-wide association study identifies 112 new loci for body mass index in the Japanese population
Akiyama M,
Okada Y,
Kanai M,
Takahashi A,
Momozawa Y,
Ikeda M,
Iwata N,
Ikegawa S,
Hirata M,
Matsuda K,
Iwasaki M,
Yamaji T
and 10 more — show all
Nature genetics · 2017 · PMID 28892062
12 pages+
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Horikoshi M,
Day FR,
Akiyama M,
Hirata M,
Kamatani Y,
Matsuda K,
Ishigaki K,
Kanai M,
Wright H,
Toro CA,
Ojeda SR,
Lomniczi A
and 3 more — show all
Nature communications · 2018 · PMID 29773799 · open access
12 pages+
Multi-ethnic genome-wide association study for atrial fibrillation
Roselli C,
Chaffin MD,
Weng LC,
Aeschbacher S,
Ahlberg G,
Albert CM,
Almgren P,
Alonso A,
Anderson CD,
Aragam KG,
Arking DE,
Barnard J
and 206 more — show all
Bartz TM,
Benjamin EJ,
Bihlmeyer NA,
Bis JC,
Bloom HL,
Boerwinkle E,
Bottinger EB,
Brody JA,
Calkins H,
Campbell A,
Cappola TP,
Carlquist J,
Chasman DI,
Chen LY,
Chen YI,
Choi EK,
Choi SH,
Christophersen IE,
Chung MK,
Cole JW,
Conen D,
Cook J,
Crijns HJ,
Cutler MJ,
Damrauer SM,
Daniels BR,
Darbar D,
Delgado G,
Denny JC,
Dichgans M,
Dörr M,
Dudink EA,
Dudley SC,
Esa N,
Esko T,
Eskola M,
Fatkin D,
Felix SB,
Ford I,
Franco OH,
Geelhoed B,
Grewal RP,
Gudnason V,
Guo X,
Gupta N,
Gustafsson S,
Gutmann R,
Hamsten A,
Harris TB,
Hayward C,
Heckbert SR,
Hernesniemi J,
Hocking LJ,
Hofman A,
Horimoto ARVR,
Huang J,
Huang PL,
Huffman J,
Ingelsson E,
Ipek EG,
Ito K,
Jimenez-Conde J,
Johnson R,
Jukema JW,
Kääb S,
Kähönen M,
Kamatani Y,
Kane JP,
Kastrati A,
Kathiresan S,
Katschnig-Winter P,
Kavousi M,
Kessler T,
Kietselaer BL,
Kirchhof P,
Kleber ME,
Knight S,
Krieger JE,
Kubo M,
Launer LJ,
Laurikka J,
Lehtimäki T,
Leineweber K,
Lemaitre RN,
Li M,
Lim HE,
Lin HJ,
Lin H,
Lind L,
Lindgren CM,
Lokki ML,
London B,
Loos RJF,
Low SK,
Lu Y,
Lyytikäinen LP,
Macfarlane PW,
Magnusson PK,
Mahajan A,
Malik R,
Mansur AJ,
Marcus GM,
Margolin L,
Margulies KB,
März W,
McManus DD,
Melander O,
Mohanty S,
Montgomery JA,
Morley MP,
Morris AP,
Müller-Nurasyid M,
Natale A,
Nazarian S,
Neumann B,
Newton-Cheh C,
Niemeijer MN,
Nikus K,
Nilsson P,
Noordam R,
Oellers H,
Olesen MS,
Orho-Melander M,
Padmanabhan S,
Pak HN,
Paré G,
Pedersen NL,
Pera J,
Pereira A,
Porteous D,
Psaty BM,
Pulit SL,
Pullinger CR,
Rader DJ,
Refsgaard L,
Ribasés M,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rosand J,
Rosenberg MA,
Rost N,
Rotter JI,
Saba S,
Sandhu RK,
Schnabel RB,
Schramm K,
Schunkert H,
Schurman C,
Scott SA,
Seppälä I,
Shaffer C,
Shah S,
Shalaby AA,
Shim J,
Shoemaker MB,
Siland JE,
Sinisalo J,
Sinner MF,
Slowik A,
Smith AV,
Smith BH,
Smith JG,
Smith JD,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Stricker BH,
Sun A,
Sun H,
Svendsen JH,
Tanaka T,
Tanriverdi K,
Taylor KD,
Teder-Laving M,
Teumer A,
Thériault S,
Trompet S,
Tucker NR,
Tveit A,
Uitterlinden AG,
Van Der Harst P,
Van Gelder IC,
Van Wagoner DR,
Verweij N,
Vlachopoulou E,
Völker U,
Wang B,
Weeke PE,
Weijs B,
Weiss R,
Weiss S,
Wells QS,
Wiggins KL,
Wong JA,
Woo D,
Worrall BB,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Lubitz SA,
Lunetta KL,
Ellinor PT
Nature genetics · 2018 · PMID 29892015
12 pages+
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
Feitosa MF,
Kraja AT,
Chasman DI,
Sung YJ,
Winkler TW,
Ntalla I,
Guo X,
Franceschini N,
Cheng CY,
Sim X,
Vojinovic D,
Marten J
and 261 more — show all
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,
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
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect
Ikeda M,
Takahashi A,
Kamatani Y,
Momozawa Y,
Saito T,
Kondo K,
Shimasaki A,
Kawase K,
Sakusabe T,
Iwayama Y,
Toyota T,
Wakuda T
and 20 more — show all
Kikuchi M,
Kanahara N,
Yamamori H,
Yasuda Y,
Watanabe Y,
Hoya S,
Aleksic B,
Kushima I,
Arai H,
Takaki M,
Hattori K,
Kunugi H,
Okahisa Y,
Ohnuma T,
Ozaki N,
Someya T,
Hashimoto R,
Yoshikawa T,
Kubo M,
Iwata N
Schizophrenia bulletin · 2019 · PMID 30285260
12 pages+
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Teumer A,
Chaker L,
Groeneweg S,
Li Y,
Di Munno C,
Barbieri C,
Schultheiss UT,
Traglia M,
Ahluwalia TS,
Akiyama M,
Appel EVR,
Arking DE
and 116 more — show all
Arnold A,
Astrup A,
Beekman M,
Beilby JP,
Bekaert S,
Boerwinkle E,
Brown SJ,
De Buyzere M,
Campbell PJ,
Ceresini G,
Cerqueira C,
Cucca F,
Deary IJ,
Deelen J,
Eckardt KU,
Ekici AB,
Eriksson JG,
Ferrrucci L,
Fiers T,
Fiorillo E,
Ford I,
Fox CS,
Fuchsberger C,
Galesloot TE,
Gieger C,
Gögele M,
De Grandi A,
Grarup N,
Greiser KH,
Haljas K,
Hansen T,
Harris SE,
van Heemst D,
den Heijer M,
Hicks AA,
den Hollander W,
Homuth G,
Hui J,
Ikram MA,
Ittermann T,
Jensen RA,
Jing J,
Jukema JW,
Kajantie E,
Kamatani Y,
Kasbohm E,
Kaufman JM,
Kiemeney LA,
Kloppenburg M,
Kronenberg F,
Kubo M,
Lahti J,
Lapauw B,
Li S,
Liewald DCM,
Lim EM,
Linneberg A,
Marina M,
Mascalzoni D,
Matsuda K,
Medenwald D,
Meisinger C,
Meulenbelt I,
De Meyer T,
Meyer Zu Schwabedissen HE,
Mikolajczyk R,
Moed M,
Netea-Maier RT,
Nolte IM,
Okada Y,
Pala M,
Pattaro C,
Pedersen O,
Petersmann A,
Porcu E,
Postmus I,
Pramstaller PP,
Psaty BM,
Ramos YFM,
Rawal R,
Redmond P,
Richards JB,
Rietzschel ER,
Rivadeneira F,
Roef G,
Rotter JI,
Sala CF,
Schlessinger D,
Selvin E,
Slagboom PE,
Soranzo N,
Sørensen TIA,
Spector TD,
Starr JM,
Stott DJ,
Taes Y,
Taliun D,
Tanaka T,
Thuesen B,
Tiller D,
Toniolo D,
Uitterlinden AG,
Visser WE,
Walsh JP,
Wilson SG,
Wolffenbuttel BHR,
Yang Q,
Zheng HF,
Cappola A,
Peeters RP,
Naitza S,
Völzke H,
Sanna S,
Köttgen A,
Visser TJ,
Medici M
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
Takeuchi F,
Akiyama M,
Matoba N,
Katsuya T,
Nakatochi M,
Tabara Y,
Narita A,
Saw WY,
Moon S,
Spracklen CN,
Chai JF,
Kim YJ
and 83 more — show all
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,
Chen Z,
Sasaki M,
Shu XO,
Jonas JB,
He J,
Heng CK,
Chen YT,
Zheng W,
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
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Morris AP,
Le TH,
Wu H,
Akbarov A,
van der Most PJ,
Hemani G,
Smith GD,
Mahajan A,
Gaulton KJ,
Nadkarni GN,
Valladares-Salgado A,
Wacher-Rodarte N
and 60 more — show all
Mychaleckyj JC,
Dueker ND,
Guo X,
Hai Y,
Haessler J,
Kamatani Y,
Stilp AM,
Zhu G,
Cook JP,
Ärnlöv J,
Blanton SH,
de Borst MH,
Bottinger EP,
Buchanan TA,
Cechova S,
Charchar FJ,
Chu PL,
Damman J,
Eales J,
Gharavi AG,
Giedraitis V,
Heath AC,
Ipp E,
Kiryluk K,
Kramer HJ,
Kubo M,
Larsson A,
Lindgren CM,
Lu Y,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
Raffel LJ,
Sacco RL,
Sanchez E,
Stark H,
Sundstrom J,
Taylor KD,
Xiang AH,
Zivkovic A,
Lind L,
Ingelsson E,
Martin NG,
Whitfield JB,
Cai J,
Laurie CC,
Okada Y,
Matsuda K,
Kooperberg C,
Chen YI,
Rundek T,
Rich SS,
Loos RJF,
Parra EJ,
Cruz M,
Rotter JI,
Snieder H,
Tomaszewski M,
Humphreys BD,
Franceschini N
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
and 111 more — show all
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Wuttke M,
Li Y,
Li M,
Sieber KB,
Feitosa MF,
Gorski M,
Tin A,
Wang L,
Chu AY,
Hoppmann A,
Kirsten H,
Giri A
and 315 more — show all
Chai JF,
Sveinbjornsson G,
Tayo BO,
Nutile T,
Fuchsberger C,
Marten J,
Cocca M,
Ghasemi S,
Xu Y,
Horn K,
Noce D,
van der Most PJ,
Sedaghat S,
Yu Z,
Akiyama M,
Afaq S,
Ahluwalia TS,
Almgren P,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boehnke M,
Boerwinkle E,
Boissel M,
Bottinger EP,
Boutin TS,
Brenner H,
Brumat M,
Burkhardt R,
Butterworth AS,
Campana E,
Campbell A,
Campbell H,
Canouil M,
Carroll RJ,
Catamo E,
Chambers JC,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cheng Y,
Christensen K,
Cifkova R,
Ciullo M,
Concas MP,
Cook JP,
Coresh J,
Corre T,
Sala CF,
Cusi D,
Danesh J,
Daw EW,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Delgado G,
Demirkan A,
Di Angelantonio E,
Dittrich K,
Divers J,
Dorajoo R,
Eckardt KU,
Ehret G,
Elliott P,
Endlich K,
Evans MK,
Felix JF,
Foo VHX,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Friedlander Y,
Froguel P,
Gansevoort RT,
Gao H,
Gasparini P,
Gaziano JM,
Giedraitis V,
Gieger C,
Girotto G,
Giulianini F,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hartman CA,
Hayward C,
Hellwege JN,
Heng CK,
Hicks AA,
Hofer E,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Indridason OS,
Ingelsson E,
Ising M,
Jaddoe VWV,
Jakobsdottir J,
Jonas JB,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kammerer CM,
Kanai M,
Kastarinen M,
Kerr SM,
Khor CC,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Kraja AT,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
Kuokkanen M,
Kuusisto J,
La Bianca M,
Laakso M,
Lange LA,
Langefeld CD,
Lee JJ,
Lehne B,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Liu J,
Loeffler M,
Loos RJF,
Lucae S,
Lukas MA,
Lyytikäinen LP,
Mägi R,
Magnusson PKE,
Mahajan A,
Martin NG,
Martins J,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Melander O,
Metspalu A,
Mikaelsdottir EK,
Milaneschi Y,
Miliku K,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell J,
O'Donoghue ML,
Olafsson I,
Oldehinkel AJ,
Orho-Melander M,
Ouwehand WH,
Padmanabhan S,
Palmer ND,
Palsson R,
Penninx BWJH,
Perls T,
Perola M,
Pirastu M,
Pirastu N,
Pistis G,
Podgornaia AI,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Pramstaller PP,
Preuss MH,
Prins BP,
Province MA,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Ridker PM,
Rivadeneira F,
Rizzi F,
Roberts DJ,
Robino A,
Rossing P,
Rudan I,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Sabanayagam C,
Salomaa V,
Salvi E,
Saum KU,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Schupf N,
Shaffer CM,
Shi Y,
Smith AV,
Smith BH,
Soranzo N,
Spracklen CN,
Strauch K,
Stringham HM,
Stumvoll M,
Svensson PO,
Szymczak S,
Tai ES,
Tajuddin SM,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorleifsson G,
Toniolo D,
Tönjes A,
Tremblay J,
Tzoulaki I,
Uitterlinden AG,
Vaccargiu S,
van Dam RM,
van der Harst P,
van Duijn CM,
Velez Edward DR,
Verweij N,
Vogelezang S,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Wallentin L,
Wang YX,
Wang C,
Waterworth DM,
Bin Wei W,
White H,
Whitfield JB,
Wild SH,
Wilson JF,
Wojczynski MK,
Wong C,
Wong TY,
Xu L,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang W,
Zonderman AB,
Rotter JI,
Bochud M,
Psaty BM,
Vitart V,
Wilson JG,
Dehghan A,
Parsa A,
Chasman DI,
Ho K,
Morris AP,
Devuyst O,
Akilesh S,
Pendergrass SA,
Sim X,
Böger CA,
Okada Y,
Edwards TL,
Snieder H,
Stefansson K,
Hung AM,
Heid IM,
Scholz M,
Teumer A,
Köttgen A,
Pattaro C
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
and 213 more — show all
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
Okada Y,
Edwards TL,
Stefansson K,
Susztak K,
Scholz M,
Heid IM,
Hung AM,
Teumer A,
Pattaro C,
Woodward OM,
Vitart V,
Köttgen A
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation
Terao C,
Momozawa Y,
Ishigaki K,
Kawakami E,
Akiyama M,
Loh PR,
Genovese G,
Sugishita H,
Ohta T,
Hirata M,
Perry JRB,
Matsuda K
and 3 more — show all
Nature communications · 2019 · PMID 31624269 · open access
12 pages+
Transethnic Meta-Analysis of Genome-Wide Association Studies Identifies Three New Loci and Characterizes Population-Specific Differences for Coronary Artery Disease
Matsunaga H,
Ito K,
Akiyama M,
Takahashi A,
Koyama S,
Nomura S,
Ieki H,
Ozaki K,
Onouchi Y,
Sakaue S,
Suna S,
Ogishima S
and 24 more — show all
Yamamoto M,
Hozawa A,
Satoh M,
Sasaki M,
Yamaji T,
Sawada N,
Iwasaki M,
Tsugane S,
Tanaka K,
Arisawa K,
Ikezaki H,
Takashima N,
Naito M,
Wakai K,
Tanaka H,
Sakata Y,
Morita H,
Sakata Y,
Matsuda K,
Murakami Y,
Akazawa H,
Kubo M,
Kamatani Y,
Komuro I
Circulation. Genomic and precision medicine · 2020 · PMID 32469254
12 pages+
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Spracklen CN,
Horikoshi M,
Kim YJ,
Lin K,
Bragg F,
Moon S,
Suzuki K,
Tam CHT,
Tabara Y,
Kwak SH,
Takeuchi F,
Long J
and 101 more — show all
Lim VJY,
Chai JF,
Chen CH,
Nakatochi M,
Yao J,
Choi HS,
Iyengar AK,
Perrin HJ,
Brotman SM,
van de Bunt M,
Gloyn AL,
Below JE,
Boehnke M,
Bowden DW,
Chambers JC,
Mahajan A,
McCarthy MI,
Ng MCY,
Petty LE,
Zhang W,
Morris AP,
Adair LS,
Akiyama M,
Bian Z,
Chan JCN,
Chang LC,
Chee ML,
Chen YI,
Chen YT,
Chen Z,
Chuang LM,
Du S,
Gordon-Larsen P,
Gross M,
Guo X,
Guo Y,
Han S,
Howard AG,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Isono M,
Jang HM,
Jiang G,
Jonas JB,
Kamatani Y,
Katsuya T,
Kawaguchi T,
Khor CC,
Kohara K,
Lee MS,
Lee NR,
Li L,
Liu J,
Luk AO,
Lv J,
Okada Y,
Pereira MA,
Sabanayagam C,
Shi J,
Shin DM,
So WY,
Takahashi A,
Tomlinson B,
Tsai FJ,
van Dam RM,
Xiang YB,
Yamamoto K,
Yamauchi T,
Yoon K,
Yu C,
Yuan JM,
Zhang L,
Zheng W,
Zheng W,
Igase M,
Cho YS,
Rotter JI,
Wang YX,
Sheu WHH,
Yokota M,
Wu JY,
Cheng CY,
Wong TY,
Shu XO,
Kato N,
Park KS,
Tai ES,
Matsuda F,
Koh WP,
Ma RCW,
Maeda S,
Millwood IY,
Lee J,
Kadowaki T,
Walters RG,
Kim BJ,
Mohlke KL,
Sim X
Nature · 2020 · PMID 32499647 · open access
12 pages+
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Ishigaki K,
Akiyama M,
Kanai M,
Takahashi A,
Kawakami E,
Sugishita H,
Sakaue S,
Matoba N,
Low SK,
Okada Y,
Terao C,
Amariuta T
and 77 more — show all
Gazal S,
Kochi Y,
Horikoshi M,
Suzuki K,
Ito K,
Koyama S,
Ozaki K,
Niida S,
Sakata Y,
Sakata Y,
Kohno T,
Shiraishi K,
Momozawa Y,
Hirata M,
Matsuda K,
Ikeda M,
Iwata N,
Ikegawa S,
Kou I,
Tanaka T,
Nakagawa H,
Suzuki A,
Hirota T,
Tamari M,
Chayama K,
Miki D,
Mori M,
Nagayama S,
Daigo Y,
Miki Y,
Katagiri T,
Ogawa O,
Obara W,
Ito H,
Yoshida T,
Imoto I,
Takahashi T,
Tanikawa C,
Suzuki T,
Sinozaki N,
Minami S,
Yamaguchi H,
Asai S,
Takahashi Y,
Yamaji K,
Takahashi K,
Fujioka T,
Takata R,
Yanai H,
Masumoto A,
Koretsune Y,
Kutsumi H,
Higashiyama M,
Murayama S,
Minegishi N,
Suzuki K,
Tanno K,
Shimizu A,
Yamaji T,
Iwasaki M,
Sawada N,
Uemura H,
Tanaka K,
Naito M,
Sasaki M,
Wakai K,
Tsugane S,
Yamamoto M,
Yamamoto K,
Murakami Y,
Nakamura Y,
Raychaudhuri S,
Inazawa J,
Yamauchi T,
Kadowaki T,
Kubo M,
Kamatani Y
Nature genetics · 2020 · PMID 32514122
12 pages+
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen MH,
Raffield LM,
Mousas A,
Sakaue S,
Huffman JE,
Moscati A,
Trivedi B,
Jiang T,
Akbari P,
Vuckovic D,
Bao EL,
Zhong X
and 98 more — show all
Manansala R,
Laplante V,
Chen M,
Lo KS,
Qian H,
Lareau CA,
Beaudoin M,
Hunt KA,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala K,
Cho K,
Choquet H,
Correa A,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang QQ,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Lerch MM,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Martin HC,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nauck M,
Nikus K,
Ouwehand WH,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Roberts DJ,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Trembath RC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Zonderman AB,
Wilson PWF,
Li Y,
Butterworth AS,
Gauchat JF,
Chiang CWK,
Li B,
Loos RJF,
Astle WJ,
Evangelou E,
van Heel DA,
Sankaran VG,
Okada Y,
Soranzo N,
Johnson AD,
Reiner AP,
Auer PL,
Lettre G
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic D,
Bao EL,
Akbari P,
Lareau CA,
Mousas A,
Jiang T,
Chen MH,
Raffield LM,
Tardaguila M,
Huffman JE,
Ritchie SC,
Megy K
and 100 more — show all
Ponstingl H,
Penkett CJ,
Albers PK,
Wigdor EM,
Sakaue S,
Moscati A,
Manansala R,
Lo KS,
Qian H,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala KN,
Wilson PWF,
Choquet H,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Felix SB,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Guo Q,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nikus K,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Weiss S,
Cai N,
Kundu K,
Watt SB,
Walter K,
Zonderman AB,
Cho K,
Li Y,
Loos RJF,
Knight JC,
Georges M,
Stegle O,
Evangelou E,
Okada Y,
Roberts DJ,
Inouye M,
Johnson AD,
Auer PL,
Astle WJ,
Reiner AP,
Butterworth AS,
Ouwehand WH,
Lettre G,
Sankaran VG,
Soranzo N
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
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cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.