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54 matches for
Shi Y,
showing the first 20.
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Li Z,
Chen J,
Yu H,
He L,
Xu Y,
Zhang D,
Yi Q,
Li C,
Li X,
Shen J,
Song Z,
Ji W
and 26 more — show all
Wang M,
Zhou J,
Chen B,
Liu Y,
Wang J,
Wang P,
Yang P,
Wang Q,
Feng G,
Liu B,
Sun W,
Li B,
He G,
Li W,
Wan C,
Xu Q,
Li W,
Wen Z,
Liu K,
Huang F,
Ji J,
Ripke S,
Yue W,
Sullivan PF,
O'Donovan MC,
Shi Y
Nature genetics · 2017 · PMID 28991256
12 pages+
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Iglesias AI,
Mishra A,
Vitart V,
Bykhovskaya Y,
Höhn R,
Springelkamp H,
Cuellar-Partida G,
Gharahkhani P,
Bailey JNC,
Willoughby CE,
Li X,
Yazar S
and 47 more — show all
Nag A,
Khawaja AP,
Polašek O,
Siscovick D,
Mitchell P,
Tham YC,
Haines JL,
Kearns LS,
Hayward C,
Shi Y,
van Leeuwen EM,
Taylor KD,
Bonnemaijer P,
Rotter JI,
Martin NG,
Zeller T,
Mills RA,
Souzeau E,
Staffieri SE,
Jonas JB,
Schmidtmann I,
Boutin T,
Kang JH,
Lucas SEM,
Wong TY,
Beutel ME,
Wilson JF,
Uitterlinden AG,
Vithana EN,
Foster PJ,
Hysi PG,
Hewitt AW,
Khor CC,
Pasquale LR,
Montgomery GW,
Klaver CCW,
Aung T,
Pfeiffer N,
Mackey DA,
Hammond CJ,
Cheng CY,
Craig JE,
Rabinowitz YS,
Wiggs JL,
Burdon KP,
van Duijn CM,
MacGregor S
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2018 · PMID 29760442 · open access
12 pages+
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Tedja MS,
Wojciechowski R,
Hysi PG,
Eriksson N,
Furlotte NA,
Verhoeven VJM,
Iglesias AI,
Meester-Smoor MA,
Tompson SW,
Fan Q,
Khawaja AP,
Cheng CY
and 86 more — show all
Höhn R,
Yamashiro K,
Wenocur A,
Grazal C,
Haller T,
Metspalu A,
Wedenoja J,
Jonas JB,
Wang YX,
Xie J,
Mitchell P,
Foster PJ,
Klein BEK,
Klein R,
Paterson AD,
Hosseini SM,
Shah RL,
Williams C,
Teo YY,
Tham YC,
Gupta P,
Zhao W,
Shi Y,
Saw WY,
Tai ES,
Sim XL,
Huffman JE,
Polašek O,
Hayward C,
Bencic G,
Rudan I,
Wilson JF,
Joshi PK,
Tsujikawa A,
Matsuda F,
Whisenhunt KN,
Zeller T,
van der Spek PJ,
Haak R,
Meijers-Heijboer H,
van Leeuwen EM,
Iyengar SK,
Lass JH,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Vingerling JR,
Lehtimäki T,
Raitakari OT,
Biino G,
Concas MP,
Schwantes-An TH,
Igo RP Jr,
Cuellar-Partida G,
Martin NG,
Craig JE,
Gharahkhani P,
Williams KM,
Nag A,
Rahi JS,
Cumberland PM,
Delcourt C,
Bellenguez C,
Ried JS,
Bergen AA,
Meitinger T,
Gieger C,
Wong TY,
Hewitt AW,
Mackey DA,
Simpson CL,
Pfeiffer N,
Pärssinen O,
Baird PN,
Vitart V,
Amin N,
van Duijn CM,
Bailey-Wilson JE,
Young TL,
Saw SM,
Stambolian D,
MacGregor S,
Guggenheim JA,
Tung JY,
Hammond CJ,
Klaver CCW
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
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+
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+
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer A,
Li Y,
Ghasemi S,
Prins BP,
Wuttke M,
Hermle T,
Giri A,
Sieber KB,
Qiu C,
Kirsten H,
Tin A,
Chu AY
and 174 more — show all
Bansal N,
Feitosa MF,
Wang L,
Chai JF,
Cocca M,
Fuchsberger C,
Gorski M,
Hoppmann A,
Horn K,
Li M,
Marten J,
Noce D,
Nutile T,
Sedaghat S,
Sveinbjornsson G,
Tayo BO,
van der Most PJ,
Xu Y,
Yu Z,
Gerstner L,
Ärnlöv J,
Bakker SJL,
Baptista D,
Biggs ML,
Boerwinkle E,
Brenner H,
Burkhardt R,
Carroll RJ,
Chee ML,
Chee ML,
Chen M,
Cheng CY,
Cook JP,
Coresh J,
Corre T,
Danesh J,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Dittrich K,
Divers J,
Eckardt KU,
Ehret G,
Endlich K,
Felix JF,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Gansevoort RT,
Giedraitis V,
Gögele M,
Grundner-Culemann F,
Gudbjartsson DF,
Gudnason V,
Hamet P,
Harris TB,
Hicks AA,
Holm H,
Foo VHX,
Hwang SJ,
Ikram MA,
Ingelsson E,
Jaddoe VWV,
Jakobsdottir J,
Josyula NS,
Jung B,
Kähönen M,
Khor CC,
Kiess W,
Koenig W,
Körner A,
Kovacs P,
Kramer H,
Krämer BK,
Kronenberg F,
Lange LA,
Langefeld CD,
Lee JJ,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Mahajan A,
Maranville JC,
Mascalzoni D,
McMullen B,
Meisinger C,
Meitinger T,
Miliku K,
Mook-Kanamori DO,
Müller-Nurasyid M,
Mychaleckyj JC,
Nauck M,
Nikus K,
Ning B,
Noordam R,
Connell JO,
Olafsson I,
Palmer ND,
Peters A,
Podgornaia AI,
Ponte B,
Poulain T,
Pramstaller PP,
Rabelink TJ,
Raffield LM,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Rivadeneira F,
Runz H,
Ryan KA,
Sabanayagam C,
Saum KU,
Schöttker B,
Shaffer CM,
Shi Y,
Smith AV,
Strauch K,
Stumvoll M,
Sun BB,
Szymczak S,
Tai ES,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorsteinsdottir U,
Tönjes A,
Tremblay J,
Uitterlinden AG,
van der Harst P,
Verweij N,
Vogelezang S,
Völker U,
Waldenberger M,
Wang C,
Wilson OD,
Wong C,
Wong TY,
Yang Q,
Yasuda M,
Akilesh S,
Bochud M,
Böger CA,
Devuyst O,
Edwards TL,
Ho K,
Morris AP,
Parsa A,
Pendergrass SA,
Psaty BM,
Rotter JI,
Stefansson K,
Wilson JG,
Susztak K,
Snieder H,
Heid IM,
Scholz M,
Butterworth AS,
Hung AM,
Pattaro C,
Köttgen A
Nature communications · 2019 · PMID 31511532 · 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+
A cross-population atlas of genetic associations for 220 human phenotypes
Sakaue S,
Kanai M,
Tanigawa Y,
Karjalainen J,
Kurki M,
Koshiba S,
Narita A,
Konuma T,
Yamamoto K,
Akiyama M,
Ishigaki K,
Suzuki A
and 34 more — show all
Suzuki K,
Obara W,
Yamaji K,
Takahashi K,
Asai S,
Takahashi Y,
Suzuki T,
Shinozaki N,
Yamaguchi H,
Minami S,
Murayama S,
Yoshimori K,
Nagayama S,
Obata D,
Higashiyama M,
Masumoto A,
Koretsune Y,
Ito K,
Terao C,
Yamauchi T,
Komuro I,
Kadowaki T,
Tamiya G,
Yamamoto M,
Nakamura Y,
Kubo M,
Murakami Y,
Yamamoto K,
Kamatani Y,
Palotie A,
Rivas MA,
Daly MJ,
Matsuda K,
Okada Y
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Trubetskoy V,
Pardiñas AF,
Qi T,
Panagiotaropoulou G,
Awasthi S,
Bigdeli TB,
Bryois J,
Chen CY,
Dennison CA,
Hall LS,
Lam M,
Watanabe K
and 422 more — show all
Frei O,
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Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
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and 15 more — show all
Duan S,
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Xu H,
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PLoS genetics · 2019 · PMID 31609978 · open access
5 pages
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Simcoe M,
Valdes A,
Liu F,
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Hemani G,
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Zhu G,
Gordon SD,
Medland SE
and 32 more — show all
Vuckovic D,
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Spector TD,
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Hysi PG
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Chen ZJ,
Zhao H,
He L,
Shi Y,
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Shi Y,
Li Z,
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Zhao J,
Liu J,
Liang X,
Zhao X
and 22 more — show all
Zhao J,
Sun Y,
Zhang B,
Jiang H,
Zhao D,
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Gao X,
Geng L,
Li Y,
Zhu D,
Sun X,
Xu JE,
Hao C,
Ren CE,
Zhang Y,
Chen S,
Zhang W,
Yang A,
Yan J,
Li Y,
Ma J,
Zhao Y
Nature genetics · 2011 · PMID 21151128
4 pages
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Shi Y,
Zhao H,
Shi Y,
Cao Y,
Yang D,
Li Z,
Zhang B,
Liang X,
Li T,
Chen J,
Shen J,
Zhao J
and 41 more — show all
You L,
Gao X,
Zhu D,
Zhao X,
Yan Y,
Qin Y,
Li W,
Yan J,
Wang Q,
Zhao J,
Geng L,
Ma J,
Zhao Y,
He G,
Zhang A,
Zou S,
Yang A,
Liu J,
Li W,
Li B,
Wan C,
Qin Y,
Shi J,
Yang J,
Jiang H,
Xu JE,
Qi X,
Sun Y,
Zhang Y,
Hao C,
Ju X,
Zhao D,
Ren CE,
Li X,
Zhang W,
Zhang Y,
Zhang J,
Wu D,
Zhang C,
He L,
Chen ZJ
Nature genetics · 2012 · PMID 22885925
4 pages
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