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Chen S,
showing the first 20.
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
Willems SM,
Ng NHJ,
Fernandez J,
Fine RS,
Wheeler E,
Wessel J,
Kitajima H,
Marenne G,
Sim X,
Yaghootkar H,
Wang S,
Chen S
and 228 more — show all
Chen Y,
Chen YI,
Grarup N,
Li-Gao R,
Varga TV,
Asimit JL,
Feng S,
Strawbridge RJ,
Kleinbrink EL,
Ahluwalia TS,
An P,
Appel EV,
Arking DE,
Auvinen J,
Bielak LF,
Bihlmeyer NA,
Bork-Jensen J,
Brody JA,
Campbell A,
Chu AY,
Davies G,
Demirkan A,
Floyd JS,
Giulianini F,
Guo X,
Gustafsson S,
Jackson AU,
Jakobsdottir J,
Järvelin MR,
Jensen RA,
Kanoni S,
Keinanen-Kiukaanniemi S,
Li M,
Lu Y,
Luan J,
Manning AK,
Marten J,
Meidtner K,
Mook-Kanamori DO,
Muka T,
Pistis G,
Prins B,
Rice KM,
Sanna S,
Smith AV,
Smith JA,
Southam L,
Stringham HM,
Tragante V,
van der Laan SW,
Warren HR,
Yao J,
Yiorkas AM,
Zhang W,
Zhao W,
Graff M,
Highland HM,
Justice AE,
Marouli E,
Medina-Gomez C,
Afaq S,
Alhejily WA,
Amin N,
Asselbergs FW,
Bonnycastle LL,
Bots ML,
Brandslund I,
Chen J,
Danesh J,
de Mutsert R,
Dehghan A,
Ebeling T,
Elliott P,
Farmaki AE,
Faul JD,
Franks PW,
Franks S,
Fritsche A,
Gjesing AP,
Goodarzi MO,
Gudnason V,
Hallmans G,
Harris TB,
Herzig KH,
Hivert MF,
Jørgensen T,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Karaleftheri M,
Kardia SLR,
Kinnunen L,
Koistinen HA,
Komulainen P,
Kovacs P,
Kuusisto J,
Laakso M,
Lange LA,
Launer LJ,
Leong A,
Lindström J,
Manning Fox JE,
Männistö S,
Maruthur NM,
Moilanen L,
Mulas A,
Nalls MA,
Neville M,
Pankow JS,
Pattie A,
Petersen ERB,
Puolijoki H,
Rasheed A,
Redmond P,
Renström F,
Roden M,
Saleheen D,
Saltevo J,
Savonen K,
Sebert S,
Skaaby T,
Small KS,
Stančáková A,
Stokholm J,
Strauch K,
Tai ES,
Taylor KD,
Thuesen BH,
Tönjes A,
Tsafantakis E,
Tuomi T,
Tuomilehto J,
Uusitupa M,
Vääräsmäki M,
Vaartjes I,
Zoledziewska M,
Abecasis G,
Balkau B,
Bisgaard H,
Blakemore AI,
Blüher M,
Boeing H,
Boerwinkle E,
Bønnelykke K,
Bottinger EP,
Caulfield MJ,
Chambers JC,
Chasman DI,
Cheng CY,
Collins FS,
Coresh J,
Cucca F,
de Borst GJ,
Deary IJ,
Dedoussis G,
Deloukas P,
den Ruijter HM,
Dupuis J,
Evans MK,
Ferrannini E,
Franco OH,
Grallert H,
Hansen T,
Hattersley AT,
Hayward C,
Hirschhorn JN,
Ikram A,
Ingelsson E,
Karpe F,
Kaw KT,
Kiess W,
Kooner JS,
Körner A,
Lakka T,
Langenberg C,
Lind L,
Lindgren CM,
Linneberg A,
Lipovich L,
Liu CT,
Liu J,
Liu Y,
Loos RJF,
MacDonald PE,
Mohlke KL,
Morris AD,
Munroe PB,
Murray A,
Padmanabhan S,
Palmer CNA,
Pasterkamp G,
Pedersen O,
Peyser PA,
Polasek O,
Porteous D,
Province MA,
Psaty BM,
Rauramaa R,
Ridker PM,
Rolandsson O,
Rorsman P,
Rosendaal FR,
Rudan I,
Salomaa V,
Schulze MB,
Sladek R,
Smith BH,
Spector TD,
Starr JM,
Stumvoll M,
van Duijn CM,
Walker M,
Wareham NJ,
Weir DR,
Wilson JG,
Wong TY,
Zeggini E,
Zonderman AB,
Rotter JI,
Morris AP,
Boehnke M,
Florez JC,
McCarthy MI,
Meigs JB,
Mahajan A,
Scott RA,
Gloyn AL,
Barroso I
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
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
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy
Liu H,
Irwanto A,
Fu X,
Yu G,
Yu Y,
Sun Y,
Wang C,
Wang Z,
Okada Y,
Low H,
Li Y,
Liany H
and 20 more — show all
Chen M,
Bao F,
Li J,
You J,
Zhang Q,
Liu J,
Chu T,
Andiappan AK,
Wang N,
Niu G,
Liu D,
Yu X,
Zhang L,
Tian H,
Zhou G,
Rotzschke O,
Chen S,
Zhang X,
Liu J,
Zhang F
Nature genetics · 2015 · PMID 25642632
5 pages
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Huyghe JR,
Harrison TA,
Bien SA,
Hampel H,
Figueiredo JC,
Schmit SL,
Conti DV,
Chen S,
Qu C,
Lin Y,
Barfield R,
Baron JA
and 129 more — show all
Cross AJ,
Diergaarde B,
Duggan D,
Harlid S,
Imaz L,
Kang HM,
Levine DM,
Perduca V,
Perez-Cornago A,
Sakoda LC,
Schumacher FR,
Slattery ML,
Toland AE,
van Duijnhoven FJB,
Van Guelpen B,
Agudo A,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Banbury BL,
Bassik MC,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Boutron-Ruault MC,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Caan BJ,
Campbell PT,
Carr PR,
Castells A,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Curtis KR,
de la Chapelle A,
Easton DF,
English DR,
Feskens EJM,
Gala M,
Gallinger SJ,
Gauderman WJ,
Giles GG,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Jenab M,
Jenkins MA,
Joshi AD,
Keku TO,
Kooperberg C,
Kühn T,
Küry S,
Le Marchand L,
Lejbkowicz F,
Li CI,
Li L,
Lieb W,
Lindblom A,
Lindor NM,
Männistö S,
Markowitz SD,
Milne RL,
Moreno L,
Murphy N,
Nassir R,
Offit K,
Ogino S,
Panico S,
Parfrey PS,
Pearlman R,
Pharoah PDP,
Phipps AI,
Platz EA,
Potter JD,
Prentice RL,
Qi L,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Schafmayer C,
Schoen RE,
Seminara D,
Song M,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Trichopoulou A,
Ulrich CM,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Wolk A,
Woods MO,
Wu AH,
Abecasis GR,
Nickerson DA,
Scacheri PC,
Kundaje A,
Casey G,
Gruber SB,
Hsu L,
Moreno V,
Hayes RB,
Newcomb PA,
Peters U
Gut · 2021 · PMID 33632709 · open access
5 pages
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Degenhardt F,
Ellinghaus D,
Juzenas S,
Lerga-Jaso J,
Wendorff M,
Maya-Miles D,
Uellendahl-Werth F,
ElAbd H,
Rühlemann MC,
Arora J,
Özer O,
Lenning OB
and 317 more — show all
Myhre R,
Vadla MS,
Wacker EM,
Wienbrandt L,
Blandino Ortiz A,
de Salazar A,
Garrido Chercoles A,
Palom A,
Ruiz A,
Garcia-Fernandez AE,
Blanco-Grau A,
Mantovani A,
Zanella A,
Holten AR,
Mayer A,
Bandera A,
Cherubini A,
Protti A,
Aghemo A,
Gerussi A,
Ramirez A,
Braun A,
Nebel A,
Barreira A,
Lleo A,
Teles A,
Kildal AB,
Biondi A,
Caballero-Garralda A,
Ganna A,
Gori A,
Glück A,
Lind A,
Tanck A,
Hinney A,
Carreras Nolla A,
Fracanzani AL,
Peschuck A,
Cavallero A,
Dyrhol-Riise AM,
Ruello A,
Julià A,
Muscatello A,
Pesenti A,
Voza A,
Rando-Segura A,
Solier A,
Schmidt A,
Cortes B,
Mateos B,
Nafria-Jimenez B,
Schaefer B,
Jensen B,
Bellinghausen C,
Maj C,
Ferrando C,
de la Horra C,
Quereda C,
Skurk C,
Thibeault C,
Scollo C,
Herr C,
Spinner CD,
Gassner C,
Lange C,
Hu C,
Paccapelo C,
Lehmann C,
Angelini C,
Cappadona C,
Azuure C,
Bianco C,
Cea C,
Sancho C,
Hoff DAL,
Galimberti D,
Prati D,
Haschka D,
Jiménez D,
Pestaña D,
Toapanta D,
Muñiz-Diaz E,
Azzolini E,
Sandoval E,
Binatti E,
Scarpini E,
Helbig ET,
Casalone E,
Urrechaga E,
Paraboschi EM,
Pontali E,
Reverter E,
Calderón EJ,
Navas E,
Solligård E,
Contro E,
Arana-Arri E,
Aziz F,
Garcia F,
García Sánchez F,
Ceriotti F,
Martinelli-Boneschi F,
Peyvandi F,
Kurth F,
Blasi F,
Malvestiti F,
Medrano FJ,
Mesonero F,
Rodriguez-Frias F,
Hanses F,
Müller F,
Hemmrich-Stanisak G,
Bellani G,
Grasselli G,
Pezzoli G,
Costantino G,
Albano G,
Cardamone G,
Bellelli G,
Citerio G,
Foti G,
Lamorte G,
Matullo G,
Baselli G,
Kurihara H,
Neb H,
My I,
Kurth I,
Hernández I,
Pink I,
de Rojas I,
Galván-Femenia I,
Holter JC,
Afset JE,
Heyckendorf J,
Kässens J,
Damås JK,
Rybniker J,
Altmüller J,
Ampuero J,
Martín J,
Erdmann J,
Banales JM,
Badia JR,
Dopazo J,
Schneider J,
Bergan J,
Barretina J,
Walter J,
Hernández Quero J,
Goikoetxea J,
Delgado J,
Guerrero JM,
Fazaal J,
Kraft J,
Schröder J,
Risnes K,
Banasik K,
Müller KE,
Gaede KI,
Garcia-Etxebarria K,
Tonby K,
Heggelund L,
Izquierdo-Sanchez L,
Bettini LR,
Sumoy L,
Sander LE,
Lippert LJ,
Terranova L,
Nkambule L,
Knopp L,
Gustad LT,
Garbarino L,
Santoro L,
Téllez L,
Roade L,
Ostadreza M,
Intxausti M,
Kogevinas M,
Riveiro-Barciela M,
Berger MM,
Schaefer M,
Niemi MEK,
Gutiérrez-Stampa MA,
Carrabba M,
Figuera Basso ME,
Valsecchi MG,
Hernandez-Tejero M,
Vehreschild MJGT,
Manunta M,
Acosta-Herrera M,
D'Angiò M,
Baldini M,
Cazzaniga M,
Grimsrud MM,
Cornberg M,
Nöthen MM,
Marquié M,
Castoldi M,
Cordioli M,
Cecconi M,
D'Amato M,
Augustin M,
Tomasi M,
Boada M,
Dreher M,
Seilmaier MJ,
Joannidis M,
Wittig M,
Mazzocco M,
Ciccarelli M,
Rodríguez-Gandía M,
Bocciolone M,
Miozzo M,
Imaz Ayo N,
Blay N,
Chueca N,
Montano N,
Braun N,
Ludwig N,
Marx N,
Martínez N,
Cornely OA,
Witzke O,
Palmieri O,
Faverio P,
Preatoni P,
Bonfanti P,
Omodei P,
Tentorio P,
Castro P,
Rodrigues PM,
España PP,
Hoffmann P,
Rosenstiel P,
Schommers P,
Suwalski P,
de Pablo R,
Ferrer R,
Bals R,
Gualtierotti R,
Gallego-Durán R,
Nieto R,
Carpani R,
Morilla R,
Badalamenti S,
Haider S,
Ciesek S,
May S,
Bombace S,
Marsal S,
Pigazzini S,
Klein S,
Pelusi S,
Wilfling S,
Bosari S,
Volland S,
Brunak S,
Raychaudhuri S,
Schreiber S,
Heilmann-Heimbach S,
Aliberti S,
Ripke S,
Dudman S,
Wesse T,
Zheng T,
Bahmer T,
Eggermann T,
Illig T,
Brenner T,
Pumarola T,
Feldt T,
Folseraas T,
Gonzalez Cejudo T,
Landmesser U,
Protzer U,
Hehr U,
Rimoldi V,
Monzani V,
Skogen V,
Keitel V,
Kopfnagel V,
Friaza V,
Andrade V,
Moreno V,
Albrecht W,
Peter W,
Poller W,
Farre X,
Yi X,
Wang X,
Khodamoradi Y,
Karadeniz Z,
Latiano A,
Goerg S,
Bacher P,
Koehler P,
Tran F,
Zoller H,
Schulte EC,
Heidecker B,
Ludwig KU,
Fernández J,
Romero-Gómez M,
Albillos A,
Invernizzi P,
Buti M,
Duga S,
Bujanda L,
Hov JR,
Lenz TL,
Asselta R,
de Cid R,
Valenti L,
Karlsen TH,
Cáceres M,
Franke A
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group and 2 more consortia
Human molecular genetics · 2022 · PMID 35848942 · open access
5 pages
Genomewide association study of leprosy
Zhang FR,
Huang W,
Chen SM,
Sun LD,
Liu H,
Li Y,
Cui Y,
Yan XX,
Yang HT,
Yang RD,
Chu TS,
Zhang C
and 55 more — show all
Zhang L,
Han JW,
Yu GQ,
Quan C,
Yu YX,
Zhang Z,
Shi BQ,
Zhang LH,
Cheng H,
Wang CY,
Lin Y,
Zheng HF,
Fu XA,
Zuo XB,
Wang Q,
Long H,
Sun YP,
Cheng YL,
Tian HQ,
Zhou FS,
Liu HX,
Lu WS,
He SM,
Du WL,
Shen M,
Jin QY,
Wang Y,
Low HQ,
Erwin T,
Yang NH,
Li JY,
Zhao X,
Jiao YL,
Mao LG,
Yin G,
Jiang ZX,
Wang XD,
Yu JP,
Hu ZH,
Gong CH,
Liu YQ,
Liu RY,
Wang DM,
Wei D,
Liu JX,
Cao WK,
Cao HZ,
Li YP,
Yan WG,
Wei SY,
Wang KJ,
Hibberd ML,
Yang S,
Zhang XJ,
Liu JJ
The New England journal of medicine · 2009 · PMID 20018961
4 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,
Qin Y,
Shi Y,
Li Z,
You L,
Zhao J,
Liu J,
Liang X,
Zhao X
and 22 more — show all
Zhao J,
Sun Y,
Zhang B,
Jiang H,
Zhao D,
Bian Y,
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
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy
Zhang F,
Liu H,
Chen S,
Low H,
Sun L,
Cui Y,
Chu T,
Li Y,
Fu X,
Yu Y,
Yu G,
Shi B
and 25 more — show all
Tian H,
Liu D,
Yu X,
Li J,
Lu N,
Bao F,
Yuan C,
Liu J,
Liu H,
Zhang L,
Sun Y,
Chen M,
Yang Q,
Yang H,
Yang R,
Zhang L,
Wang Q,
Liu H,
Zuo F,
Zhang H,
Khor CC,
Hibberd ML,
Yang S,
Liu J,
Zhang X
Nature genetics · 2011 · PMID 22019778
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
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Zheng T,
Ellinghaus D,
Juzenas S,
Cossais F,
Burmeister G,
Mayr G,
Jørgensen IF,
Teder-Laving M,
Skogholt AH,
Chen S,
Strege PR,
Ito G
and 73 more — show all
Banasik K,
Becker T,
Bokelmann F,
Brunak S,
Buch S,
Clausnitzer H,
Datz C,
Degenhardt F,
Doniec M,
Erikstrup C,
Esko T,
Forster M,
Frey N,
Fritsche LG,
Gabrielsen ME,
Gräßle T,
Gsur A,
Gross J,
Hampe J,
Hendricks A,
Hinz S,
Hveem K,
Jongen J,
Junker R,
Karlsen TH,
Hemmrich-Stanisak G,
Kruis W,
Kupcinskas J,
Laubert T,
Rosenstiel PC,
Röcken C,
Laudes M,
Leendertz FH,
Lieb W,
Limperger V,
Margetis N,
Mätz-Rensing K,
Németh CG,
Ness-Jensen E,
Nowak-Göttl U,
Pandit A,
Pedersen OB,
Peleikis HG,
Peuker K,
Rodriguez CL,
Rühlemann MC,
Schniewind B,
Schulzky M,
Skieceviciene J,
Tepel J,
Thomas L,
Uellendahl-Werth F,
Ullum H,
Vogel I,
Volzke H,
von Fersen L,
von Schönfels W,
Vanderwerff B,
Wilking J,
Wittig M,
Zeissig S,
Zobel M,
Zawistowski M,
Vacic V,
Sazonova O,
Noblin ES,
Farrugia G,
Beyder A,
Wedel T,
Kahlke V,
Schafmayer C,
D'Amato M,
Franke A
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
4 pages
Genome-wide meta-analysis identifies ancestry-specific loci for Alzheimer's disease
Ge YJ,
Chen SD,
Wu BS,
Zhang YR,
Wang J,
He XY,
Liu WS,
Chen YL,
Ou YN,
Shen XN,
Huang YY,
Gan YH
and 12 more — show all
Yang L,
Ma LZ,
Ma YH,
Chen KL,
Chen SF,
Cui M,
Tan L,
Dong Q,
Zhao QH,
Wang YJ,
Jia JP,
Yu JT
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024 · PMID 39023044 · open access
4 pages
Genome-wide analysis implicates inner ear development in Ménière disease
Shi Z,
Mandla R,
Li J,
Li X,
Zhang ZE,
Chen S,
Lapinska S,
Flynn-Carroll AO,
Pasaniuc B,
Epstein DJ,
Mathieson I
American journal of human genetics · 2026 · PMID 42302782 · open access
3 pages
Genome-wide association study in Han Chinese identifies three novel loci for human height
Hao Y,
Liu X,
Lu X,
Yang X,
Wang L,
Chen S,
Li H,
Li J,
Cao J,
Chen J,
Li Y,
Zhao L
and 6 more — show all
Human genetics · 2013 · PMID 23456168
2 pages
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Shi Y,
Li L,
Hu Z,
Li S,
Wang S,
Liu J,
Wu C,
He L,
Zhou J,
Li Z,
Hu T,
Chen Y
and 72 more — show all
Jia Y,
Wang S,
Wu L,
Cheng X,
Yang Z,
Yang R,
Li X,
Huang K,
Zhang Q,
Zhou H,
Tang F,
Chen Z,
Shen J,
Jiang J,
Ding H,
Xing H,
Zhang S,
Qu P,
Song X,
Lin Z,
Deng D,
Xi L,
Lv W,
Han X,
Tao G,
Yan L,
Han Z,
Li Z,
Miao X,
Pan S,
Shen Y,
Wang H,
Liu D,
Gong E,
Li Z,
Zhou L,
Luan X,
Wang C,
Song Q,
Wu S,
Xu H,
Shen J,
Qiang F,
Ma G,
Liu L,
Chen X,
Liu J,
Wu J,
Shen Y,
Wen Y,
Chu M,
Yu J,
Hu X,
Fan Y,
He H,
Jiang Y,
Lei Z,
Liu C,
Chen J,
Zhang Y,
Yi C,
Chen S,
Li W,
Wang D,
Wang Z,
Di W,
Shen K,
Lin D,
Shen H,
Feng Y,
Xie X,
Ma D
Nature genetics · 2013 · PMID 23817570
2 pages
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
Chen PL,
Shih SR,
Wang PW,
Lin YC,
Chu CC,
Lin JH,
Chen SC,
Chang CC,
Huang TS,
Tsai KS,
Tseng FY,
Wang CY
and 8 more — show all
Nature communications · 2015 · PMID 26151496 · open access
2 pages
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Qiu F,
Tang R,
Zuo X,
Shi X,
Wei Y,
Zheng X,
Dai Y,
Gong Y,
Wang L,
Xu P,
Zhu X,
Wu J
and 78 more — show all
Han C,
Gao Y,
Zhang K,
Jiang Y,
Zhou J,
Shao Y,
Hu Z,
Tian Y,
Zhang H,
Dai N,
Liu L,
Wu X,
Zhao W,
Zhang X,
Zang Z,
Nie J,
Sun W,
Zhao Y,
Mao Y,
Jiang P,
Ji H,
Dong Q,
Li J,
Li Z,
Bai X,
Li L,
Lin M,
Dong M,
Li J,
Zhu P,
Wang C,
Zhang Y,
Jiang P,
Wang Y,
Jawed R,
Xu J,
Zhang Y,
Wang Q,
Yang Y,
Yang F,
Lian M,
Jiang X,
Xiao X,
Li Y,
Fang J,
Qiu D,
Zhu Z,
Qiu H,
Zhang J,
Tian W,
Chen S,
Jiang L,
Ji B,
Li P,
Chen G,
Wu T,
Sun Y,
Yu J,
Tang H,
He M,
Xia M,
Pei H,
Huang L,
Qing Z,
Wu J,
Huang Q,
Han J,
Xie W,
Sun Z,
Guo J,
He G,
Eric Gershwin M,
Lian Z,
Liu X,
Seldin MF,
Liu X,
Chen W,
Ma X
Nature communications · 2017 · PMID 28425483 · open access
2 pages
Genome-Wide Association and Functional Studies Identify <i>SCML4</i> and <i>THSD7A</i> as Novel Susceptibility Genes for Coronary Artery Disease
Li Y,
Wang DW,
Chen Y,
Chen C,
Guo J,
Zhang S,
Sun Z,
Ding H,
Yao Y,
Zhou L,
Xu K,
Song C
and 30 more — show all
Yang F,
Zhao B,
Yan H,
Wang WJ,
Wu C,
Lu X,
Yang X,
Dong J,
Zheng G,
Tian S,
Cui Y,
Jin L,
Liu G,
Cui H,
Wang S,
Jiang F,
Wang C,
Erdmann J,
Zeng L,
Huang S,
Zhong J,
Ma Y,
Chen W,
Sun J,
Lei W,
Chen S,
Rao S,
Gu D,
Schunkert H,
Tian XL
Arteriosclerosis, thrombosis, and vascular biology · 2018 · PMID 29472232
2 pages
Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
Gao J,
Zhu C,
Zhang Y,
Sheng Y,
Yang F,
Wang W,
Qian W,
Chen S,
Zhu Q,
Zuo X,
Tang H,
Tang X
and 13 more — show all
Li Y,
Cheng H,
Zhou F,
Liu S,
Chen G,
Zheng X,
Zhu Z,
Wang Z,
Yang S,
Luo X,
Ye D,
Zhang X,
Sun L
The Journal of investigative dermatology · 2018 · PMID 29857070
2 pages
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