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22 matches for
Xu L,
showing the first 20.
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+
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+
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
Zhou W,
Brumpton B,
Kabil O,
Gudmundsson J,
Thorleifsson G,
Weinstock J,
Zawistowski M,
Nielsen JB,
Chaker L,
Medici M,
Teumer A,
Naitza S
and 44 more — show all
Sanna S,
Schultheiss UT,
Cappola A,
Karjalainen J,
Kurki M,
Oneka M,
Taylor P,
Fritsche LG,
Graham SE,
Wolford BN,
Overton W,
Rasheed H,
Haug EB,
Gabrielsen ME,
Skogholt AH,
Surakka I,
Davey Smith G,
Pandit A,
Roychowdhury T,
Hornsby WE,
Jonasson JG,
Senter L,
Liyanarachchi S,
Ringel MD,
Xu L,
Kiemeney LA,
He H,
Netea-Maier RT,
Mayordomo JI,
Plantinga TS,
Hrafnkelsson J,
Hjartarson H,
Sturgis EM,
Palotie A,
Daly M,
Citterio CE,
Arvan P,
Brummett CM,
Boehnke M,
de la Chapelle A,
Stefansson K,
Hveem K,
Willer CJ,
Åsvold BO
Nature communications · 2020 · PMID 32769997 · open access
12 pages+
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
and 142 more — show all
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
Guo X,
Mazur J,
Huffman JE,
Williams KM,
Polasek O,
Campbell H,
Rudan I,
Vatavuk Z,
Wilson JF,
Joshi PK,
McMahon G,
St Pourcain B,
Evans DM,
Simpson CL,
Schwantes-An TH,
Igo RP,
Mirshahi A,
Cougnard-Gregoire A,
Bellenguez C,
Blettner M,
Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
Beuerman RW,
Siantar R,
Tai ES,
Vithana E,
Mihailov E,
Khor CC,
Hayward C,
Luben RN,
Foster PJ,
Klein BE,
Klein R,
Wong HS,
Mitchell P,
Metspalu A,
Aung T,
Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
Teo YY,
Mackey DA,
Oexle K,
Yoshimura N,
Paterson AD,
Pfeiffer N,
Wong TY,
Baird PN,
Stambolian D,
Wilson JE,
Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
Rahi JS,
Korobelnik JF,
Kemp JP,
Timpson NJ,
Smith GD,
Craig JE,
Burdon KP,
Fogarty RD,
Iyengar SK,
Chew E,
Janmahasatian S,
Martin NG,
MacGregor S,
Xu L,
Schache M,
Nangia V,
Panda-Jonas S,
Wright AF,
Fondran JR,
Lass JH,
Feng S,
Zhao JH,
Khaw KT,
Wareham NJ,
Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
Raffel LJ,
Cotch MF,
Li X,
Yip SP,
Yap MK,
Biino G,
Vaccargiu S,
Fossarello M,
Fleck B,
Yazar S,
Tideman JW,
Tedja M,
Deangelis MM,
Morrison M,
Farrer L,
Zhou X,
Chen W,
Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Verhoeven VJ,
Hysi PG,
Wojciechowski R,
Fan Q,
Guggenheim JA,
Höhn R,
MacGregor S,
Hewitt AW,
Nag A,
Cheng CY,
Yonova-Doing E,
Zhou X
and 96 more — show all
Ikram MK,
Buitendijk GH,
McMahon G,
Kemp JP,
Pourcain BS,
Simpson CL,
Mäkelä KM,
Lehtimäki T,
Kähönen M,
Paterson AD,
Hosseini SM,
Wong HS,
Xu L,
Jonas JB,
Pärssinen O,
Wedenoja J,
Yip SP,
Ho DW,
Pang CP,
Chen LJ,
Burdon KP,
Craig JE,
Klein BE,
Klein R,
Haller T,
Metspalu A,
Khor CC,
Tai ES,
Aung T,
Vithana E,
Tay WT,
Barathi VA,
Chen P,
Li R,
Liao J,
Zheng Y,
Ong RT,
Döring A,
Evans DM,
Timpson NJ,
Verkerk AJ,
Meitinger T,
Raitakari O,
Hawthorne F,
Spector TD,
Karssen LC,
Pirastu M,
Murgia F,
Ang W,
Mishra A,
Montgomery GW,
Pennell CE,
Cumberland PM,
Cotlarciuc I,
Mitchell P,
Wang JJ,
Schache M,
Janmahasatian S,
Igo RP Jr,
Lass JH,
Chew E,
Iyengar SK,
Gorgels TG,
Rudan I,
Hayward C,
Wright AF,
Polasek O,
Vatavuk Z,
Wilson JF,
Fleck B,
Zeller T,
Mirshahi A,
Müller C,
Uitterlinden AG,
Rivadeneira F,
Vingerling JR,
Hofman A,
Oostra BA,
Amin N,
Bergen AA,
Teo YY,
Rahi JS,
Vitart V,
Williams C,
Baird PN,
Wong TY,
Oexle K,
Pfeiffer N,
Mackey DA,
Young TL,
van Duijn CM,
Saw SM,
Bailey-Wilson JE,
Stambolian D,
Klaver CC,
Hammond CJ
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Lu X,
Wang L,
Lin X,
Huang J,
Charles Gu C,
He M,
Shen H,
He J,
Zhu J,
Li H,
Hixson JE,
Wu T
and 37 more — show all
Dai J,
Lu L,
Shen C,
Chen S,
He L,
Mo Z,
Hao Y,
Mo X,
Yang X,
Li J,
Cao J,
Chen J,
Fan Z,
Li Y,
Zhao L,
Li H,
Lu F,
Yao C,
Yu L,
Xu L,
Mu J,
Wu X,
Deng Y,
Hu D,
Zhang W,
Ji X,
Guo D,
Guo Z,
Zhou Z,
Yang Z,
Wang R,
Yang J,
Zhou X,
Yan W,
Sun N,
Gao P,
Gu D
Human molecular genetics · 2015 · PMID 25249183
5 pages
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
Springelkamp H,
Mishra A,
Hysi PG,
Gharahkhani P,
Höhn R,
Khor CC,
Cooke Bailey JN,
Luo X,
Ramdas WD,
Vithana E,
Koh V,
Yazar S
and 45 more — show all
Xu L,
Forward H,
Kearns LS,
Amin N,
Iglesias AI,
Sim KS,
van Leeuwen EM,
Demirkan A,
van der Lee S,
Loon SC,
Rivadeneira F,
Nag A,
Sanfilippo PG,
Schillert A,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Zhou T,
Burdon KP,
Spector TD,
Lackner KJ,
Saw SM,
Vingerling JR,
Teo YY,
Pasquale LR,
Wolfs RC,
Lemij HG,
Tai ES,
Jonas JB,
Cheng CY,
Aung T,
Jansonius NM,
Klaver CC,
Craig JE,
Young TL,
Haines JL,
MacGregor S,
Mackey DA,
Pfeiffer N,
Wong TY,
Wiggs JL,
Hewitt AW,
van Duijn CM,
Hammond CJ
NEIGHBORHOOD Consortium
Genetic epidemiology · 2015 · PMID 25631615
5 pages
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
Willems SM,
Wright DJ,
Day FR,
Trajanoska K,
Joshi PK,
Morris JA,
Matteini AM,
Garton FC,
Grarup N,
Oskolkov N,
Thalamuthu A,
Mangino M
and 64 more — show all
Liu J,
Demirkan A,
Lek M,
Xu L,
Wang G,
Oldmeadow C,
Gaulton KJ,
Lotta LA,
Miyamoto-Mikami E,
Rivas MA,
White T,
Loh PR,
Aadahl M,
Amin N,
Attia JR,
Austin K,
Benyamin B,
Brage S,
Cheng YC,
Cięszczyk P,
Derave W,
Eriksson KF,
Eynon N,
Linneberg A,
Lucia A,
Massidda M,
Mitchell BD,
Miyachi M,
Murakami H,
Padmanabhan S,
Pandey A,
Papadimitriou I,
Rajpal DK,
Sale C,
Schnurr TM,
Sessa F,
Shrine N,
Tobin MD,
Varley I,
Wain LV,
Wray NR,
Lindgren CM,
MacArthur DG,
Waterworth DM,
McCarthy MI,
Pedersen O,
Khaw KT,
Kiel DP,
Pitsiladis Y,
Fuku N,
Franks PW,
North KN,
van Duijn CM,
Mather KA,
Hansen T,
Hansson O,
Spector T,
Murabito JM,
Richards JB,
Rivadeneira F,
Langenberg C,
Perry JRB,
Wareham NJ,
Scott RA
GEFOS Any-Type of Fracture Consortium
Nature communications · 2017 · PMID 29313844 · open access
5 pages
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Hysi PG,
Cheng CY,
Springelkamp H,
Macgregor S,
Bailey JNC,
Wojciechowski R,
Vitart V,
Nag A,
Hewitt AW,
Höhn R,
Venturini C,
Mirshahi A
and 79 more — show all
Ramdas WD,
Thorleifsson G,
Vithana E,
Khor CC,
Stefansson AB,
Liao J,
Haines JL,
Amin N,
Wang YX,
Wild PS,
Ozel AB,
Li JZ,
Fleck BW,
Zeller T,
Staffieri SE,
Teo YY,
Cuellar-Partida G,
Luo X,
Allingham RR,
Richards JE,
Senft A,
Karssen LC,
Zheng Y,
Bellenguez C,
Xu L,
Iglesias AI,
Wilson JF,
Kang JH,
van Leeuwen EM,
Jonsson V,
Thorsteinsdottir U,
Despriet DDG,
Ennis S,
Moroi SE,
Martin NG,
Jansonius NM,
Yazar S,
Tai ES,
Amouyel P,
Kirwan J,
van Koolwijk LME,
Hauser MA,
Jonasson F,
Leo P,
Loomis SJ,
Fogarty R,
Rivadeneira F,
Kearns L,
Lackner KJ,
de Jong PTVM,
Simpson CL,
Pennell CE,
Oostra BA,
Uitterlinden AG,
Saw SM,
Lotery AJ,
Bailey-Wilson JE,
Hofman A,
Vingerling JR,
Maubaret C,
Pfeiffer N,
Wolfs RCW,
Lemij HG,
Young TL,
Pasquale LR,
Delcourt C,
Spector TD,
Klaver CCW,
Small KS,
Burdon KP,
Stefansson K,
Wong TY,
Viswanathan A,
Mackey DA,
Craig JE,
Wiggs JL,
van Duijn CM,
Hammond CJ,
Aung T
BMES GWAS Group · NEIGHBORHOOD Consortium and 1 more consortia
Nature genetics · 2014 · PMID 25173106 · open access
4 pages
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations
Lu X,
Huang J,
Mo Z,
He J,
Wang L,
Yang X,
Tan A,
Chen S,
Chen J,
Gu CC,
Chen J,
Li Y
and 26 more — show all
Zhao L,
Li H,
Hao Y,
Li J,
Hixson JE,
Li Y,
Cheng M,
Liu X,
Cao J,
Liu F,
Huang C,
Shen C,
Shen J,
Yu L,
Xu L,
Mu J,
Wu X,
Ji X,
Guo D,
Zhou Z,
Yang Z,
Wang R,
Yang J,
Yan W,
Peng X,
Gu D
Circulation. Cardiovascular genetics · 2016 · PMID 26582766
4 pages
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
Jin G,
Ma H,
Wu C,
Dai J,
Zhang R,
Shi Y,
Lu J,
Miao X,
Wang M,
Zhou Y,
Chen J,
Li H
and 21 more — show all
Pan S,
Chu M,
Lu F,
Yu D,
Jiang Y,
Dong J,
Hu L,
Chen Y,
Xu L,
Shu Y,
Pan S,
Tan W,
Zhou B,
Lu D,
Wu T,
Zhang Z,
Chen F,
Wang X,
Hu Z,
Lin D,
Shen H
American journal of human genetics · 2012 · PMID 23103227
2 pages
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
Dong J,
Jin G,
Wu C,
Guo H,
Zhou B,
Lv J,
Lu D,
Shi Y,
Shu Y,
Xu L,
Chu M,
Wang C
and 37 more — show all
Zhang R,
Dai J,
Jiang Y,
Yu D,
Ma H,
Zhao X,
Yin Z,
Yang L,
Li Z,
Deng Q,
Cao S,
Qin Z,
Gong J,
Sun C,
Wang J,
Wu W,
Zhou G,
Chen H,
Guan P,
Chen Y,
Liu X,
Liu L,
Xu P,
Han B,
Bai C,
Zhao Y,
Zhang H,
Yan Y,
Liu J,
Amos CI,
Chen F,
Tan W,
Jin L,
Wu T,
Hu Z,
Lin D,
Shen H
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
Hysi PG,
Bailey-Wilson JE
and 96 more — show all
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
van Duijn CM,
de Jong PT,
Vingerling JR,
Zhou X,
Chen P,
Li R,
Tay WT,
Zheng Y,
Chew M,
Burdon KP,
Craig JE,
Iyengar SK,
Igo RP Jr,
Lass JH Jr,
Chew EY,
Haller T,
Mihailov E,
Metspalu A,
Wedenoja J,
Simpson CL,
Wojciechowski R,
Höhn R,
Mirshahi A,
Zeller T,
Pfeiffer N,
Lackner KJ,
Bettecken T,
Meitinger T,
Oexle K,
Pirastu M,
Portas L,
Nag A,
Williams KM,
Yonova-Doing E,
Klein R,
Klein BE,
Hosseini SM,
Paterson AD,
Makela KM,
Lehtimaki T,
Kahonen M,
Raitakari O,
Yoshimura N,
Matsuda F,
Chen LJ,
Pang CP,
Yip SP,
Yap MK,
Meguro A,
Mizuki N,
Inoko H,
Foster PJ,
Zhao JH,
Vithana E,
Tai ES,
Fan Q,
Xu L,
Campbell H,
Fleck B,
Rudan I,
Aung T,
Hofman A,
Uitterlinden AG,
Bencic G,
Khor CC,
Forward H,
Pärssinen O,
Mitchell P,
Rivadeneira F,
Hewitt AW,
Williams C,
Oostra BA,
Teo YY,
Hammond CJ,
Stambolian D,
Mackey DA,
Klaver CC,
Wong TY,
Saw SM,
Baird PN
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract
Liao J,
Su X,
Chen P,
Wang X,
Xu L,
Li X,
Thean L,
Tan C,
Tan AG,
Tay WT,
Jun G,
Zheng Y
and 17 more — show all
Chew M,
Wang YX,
Tan QS,
Barathi VA,
Klein BE,
Saw SM,
Vithana EN,
Tai ES,
Iyengar SK,
Mitchell P,
Khor CC,
Aung T,
Wang JJ,
Jonas JB,
Teo YY,
Wong TY,
Cheng CY
Human molecular genetics · 2014 · PMID 24951543
2 pages
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
and 66 more — show all
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
Spector TD,
Mirshahi A,
Saw SM,
Vingerling JR,
Teo YY,
Haines JL,
Wolfs RC,
Lemij HG,
Tai ES,
Jansonius NM,
Jonas JB,
Cheng CY,
Aung T,
Viswanathan AC,
Klaver CC,
Craig JE,
Macgregor S,
Mackey DA,
Lotery AJ,
Stefansson K,
Bergen AA,
Young TL,
Wiggs JL,
Pfeiffer N,
Wong TY,
Pasquale LR,
Hewitt AW,
van Duijn CM,
Hammond CJ
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
2 pages
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis
Ogura Y,
Kou I,
Miura S,
Takahashi A,
Xu L,
Takeda K,
Takahashi Y,
Kono K,
Kawakami N,
Uno K,
Ito M,
Minami S
and 23 more — show all
Yonezawa I,
Yanagida H,
Taneichi H,
Zhu Z,
Tsuji T,
Suzuki T,
Sudo H,
Kotani T,
Watanabe K,
Hosogane N,
Okada E,
Iida A,
Nakajima M,
Sudo A,
Chiba K,
Hiraki Y,
Toyama Y,
Qiu Y,
Shukunami C,
Kamatani Y,
Kubo M,
Matsumoto M,
Ikegawa S
American journal of human genetics · 2015 · PMID 26211971
2 pages
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Zhu Z,
Tang NL,
Xu L,
Qin X,
Mao S,
Song Y,
Liu L,
Li F,
Liu P,
Yi L,
Chang J,
Jiang L
and 25 more — show all
Ng BK,
Shi B,
Zhang W,
Qiao J,
Sun X,
Qiu X,
Wang Z,
Wang F,
Xie D,
Chen L,
Chen Z,
Jin M,
Han X,
Hu Z,
Zhang Z,
Liu Z,
Zhu F,
Qian BP,
Yu Y,
Wang B,
Lee KM,
Lee WYW,
Lam TP,
Qiu Y,
Cheng JC
Nature communications · 2015 · PMID 26394188 · open access
2 pages
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Hu Z,
Wu C,
Shi Y,
Guo H,
Zhao X,
Yin Z,
Yang L,
Dai J,
Hu L,
Tan W,
Li Z,
Deng Q
and 33 more — show all
Wang J,
Wu W,
Jin G,
Jiang Y,
Yu D,
Zhou G,
Chen H,
Guan P,
Chen Y,
Shu Y,
Xu L,
Liu X,
Liu L,
Xu P,
Han B,
Bai C,
Zhao Y,
Zhang H,
Yan Y,
Ma H,
Chen J,
Chu M,
Lu F,
Zhang Z,
Chen F,
Wang X,
Jin L,
Lu J,
Zhou B,
Lu D,
Wu T,
Lin D,
Shen H
Nature genetics · 2011 · PMID 21725308
1 page
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Lu X,
Wang L,
Chen S,
He L,
Yang X,
Shi Y,
Cheng J,
Zhang L,
Gu CC,
Huang J,
Wu T,
Ma Y
and 68 more — show all
Li J,
Cao J,
Chen J,
Ge D,
Fan Z,
Li Y,
Zhao L,
Li H,
Zhou X,
Chen L,
Liu D,
Chen J,
Duan X,
Hao Y,
Wang L,
Lu F,
Liu Z,
Yao C,
Shen C,
Pu X,
Yu L,
Fang X,
Xu L,
Mu J,
Wu X,
Zheng R,
Wu N,
Zhao Q,
Li Y,
Liu X,
Wang M,
Yu D,
Hu D,
Ji X,
Guo D,
Sun D,
Wang Q,
Yang Y,
Liu F,
Mao Q,
Liang X,
Ji J,
Chen P,
Mo X,
Li D,
Chai G,
Tang Y,
Li X,
Du Z,
Liu X,
Dou C,
Yang Z,
Meng Q,
Wang D,
Wang R,
Yang J,
Schunkert H,
Samani NJ,
Kathiresan S,
Reilly MP,
Erdmann J,
Peng X,
Wu X,
Liu D,
Yang Y,
Chen R,
Qiang B,
Gu D
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
1 page
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma
Nongpiur ME,
Khor CC,
Jia H,
Cornes BK,
Chen LJ,
Qiao C,
Nair KS,
Cheng CY,
Xu L,
George R,
Tan D,
Abu-Amero K
and 61 more — show all
Perera SA,
Ozaki M,
Mizoguchi T,
Kurimoto Y,
Low S,
Tajudin LS,
Ho CL,
Tham CC,
Soto I,
Chew PT,
Wong HT,
Shantha B,
Kuroda M,
Osman EA,
Tang G,
Fan S,
Meng H,
Wang H,
Feng B,
Yong VH,
Ting SM,
Li Y,
Wang YX,
Li Z,
Lavanya R,
Wu RY,
Zheng YF,
Su DH,
Loon SC,
Yong VK,
Allingham RR,
Hauser MA,
Soumittra N,
Ramprasad VL,
Waseem N,
Yaakub A,
Chia KS,
Kumaramanickavel G,
Wong TT,
How AC,
Chau TN,
Simmons CP,
Bei JX,
Zeng YX,
Bhattacharya SS,
Zhang M,
Tan DT,
Teo YY,
Al-Obeidan SA,
Hon DN,
Tai ES,
Saw SM,
Foster PJ,
Vijaya L,
Jonas JB,
Wong TY,
John SW,
Pang CP,
Vithana EN,
Wang N,
Aung T
PLoS genetics · 2014 · PMID 24603532 · open access
1 page
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