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2,662 papers hold this site up. Every variant and condition page names
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14 matches for
Wang B.
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+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
and 145 more — show all
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Bujnis MN,
Sterenborg RBTM,
Li Y,
Åsvold BO,
Brčić L,
Boraska Perica V,
Babbar A,
Denny JC,
Fritsche LG,
Kanai M,
Konrade I,
Leese G
and 22 more — show all
Marouli E,
Metspalu A,
Moksnes MR,
Mukherjee B,
Okada Y,
Palmer CNA,
Papadopoulou A,
Peculis R,
Rovite V,
Sauer PJ,
Soto-Pedre E,
Srinivasan S,
Steinbrenner I,
Teder-Laving M,
Wang B,
Weihs A,
Zeng C,
Zhou J,
Song X,
Jorde LB,
Medici M,
Teumer A
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
12 pages+
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium
Jiang MZ,
Gaynor SM,
Li X,
Van Buren E,
Stilp A,
Stilp A,
Buth E,
Wang FF,
Manansala R,
Gogarten SM,
Li Z,
Polfus LM
and 35 more — show all
Salimi S,
Bis JC,
Pankratz N,
Yanek LR,
Durda P,
Tracy RP,
Rich SS,
Rotter JI,
Mitchell BD,
Lewis JP,
Psaty BM,
Pratte KA,
Silverman EK,
Kaplan RC,
Avery C,
North KE,
Mathias RA,
Faraday N,
Lin H,
Wang B,
Carson AP,
Norwood AF,
Gibbs RA,
Kooperberg C,
Lundin J,
Peters U,
Dupuis J,
Hou L,
Fornage M,
Benjamin EJ,
Reiner AP,
Bowler RP,
Lin X,
Auer PL,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Inflammation Working Group
Human molecular genetics · 2024 · PMID 38747556
11 pages
A genome-wide association study of neonatal metabolites
He Q,
Liu H,
Lu L,
Zhang Q,
Wang Q,
Wang B,
Wu X,
Guan L,
Mao J,
Xue Y,
Zhang C,
Cao X
and 9 more — show all
Cell genomics · 2024 · PMID 39389019 · open access
9 pages
Whole-genome sequencing reveals host factors underlying critical COVID-19
Kousathanas A,
Pairo-Castineira E,
Rawlik K,
Stuckey A,
Odhams CA,
Walker S,
Russell CD,
Malinauskas T,
Wu Y,
Millar J,
Shen X,
Elliott KS
and 64 more — show all
Griffiths F,
Oosthuyzen W,
Morrice K,
Keating S,
Wang B,
Rhodes D,
Klaric L,
Zechner M,
Parkinson N,
Siddiq A,
Goddard P,
Donovan S,
Maslove D,
Nichol A,
Semple MG,
Zainy T,
Maleady-Crowe F,
Todd L,
Salehi S,
Knight J,
Elgar G,
Chan G,
Arumugam P,
Patch C,
Rendon A,
Bentley D,
Kingsley C,
Kosmicki JA,
Horowitz JE,
Baras A,
Abecasis GR,
Ferreira MAR,
Justice A,
Mirshahi T,
Oetjens M,
Rader DJ,
Ritchie MD,
Verma A,
Fowler TA,
Shankar-Hari M,
Summers C,
Hinds C,
Horby P,
Ling L,
McAuley D,
Montgomery H,
Openshaw PJM,
Elliott P,
Walsh T,
Tenesa A,
Fawkes A,
Murphy L,
Rowan K,
Ponting CP,
Vitart V,
Wilson JF,
Yang J,
Bretherick AD,
Scott RH,
Hendry SC,
Moutsianas L,
Law A,
Caulfield MJ,
Baillie JK
GenOMICC investigators · 23andMe investigators and 1 more consortia
Nature · 2022 · PMID 35255492 · open access
5 pages
Polygenic adaptation leads to a higher reproductive fitness of native Tibetans at high altitude
He Y,
Guo Y,
Zheng W,
Yue T,
Zhang H,
Wang B,
Feng Z,
Ouzhuluobu,
Cui C,
Liu K,
Zhou B,
Zeng X
and 7 more — show all
Current biology : CB · 2023 · PMID 37643619
3 pages
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Jiang L,
Yin J,
Ye L,
Yang J,
Hemani G,
Liu AJ,
Zou H,
He D,
Sun L,
Zeng X,
Li Z,
Zheng Y
and 61 more — show all
Lin Y,
Liu Y,
Fang Y,
Xu J,
Li Y,
Dai S,
Guan J,
Jiang L,
Wei Q,
Wang Y,
Li Y,
Huang C,
Zuo X,
Liu Y,
Wu X,
Zhang L,
Zhou L,
Zhang Q,
Li T,
Chen L,
Xu Z,
Yang X,
Qian F,
Xie W,
Liu W,
Guo Q,
Huang S,
Zhao J,
Li M,
Jin Y,
Gao J,
Lv Y,
Wang Y,
Lin L,
Guo A,
Danoy P,
Willner D,
Cremin C,
Hadler J,
Zhang F,
Zhao Y,
Li M,
Yue T,
Fan X,
Guo J,
Mu R,
Li J,
Wu C,
Zeng M,
Wang J,
Li S,
Jin L,
Wang B,
Wang J,
Ma X,
Sun L,
Zhang X,
Brown MA,
Visscher PM,
Su DF,
Xu H
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
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
Identification of new susceptibility loci associated with rheumatoid arthritis
Leng RX,
Di DS,
Ni J,
Wu XX,
Zhang LL,
Wang XF,
Liu RS,
Huang Q,
Fan YG,
Pan HF,
Wang B,
Ye DQ
Annals of the rheumatic diseases · 2020 · PMID 32868391
2 pages
Genetic mechanisms of critical illness in COVID-19
Pairo-Castineira E,
Clohisey S,
Klaric L,
Bretherick AD,
Rawlik K,
Pasko D,
Walker S,
Parkinson N,
Fourman MH,
Russell CD,
Furniss J,
Richmond A
and 54 more — show all
Gountouna E,
Wrobel N,
Harrison D,
Wang B,
Wu Y,
Meynert A,
Griffiths F,
Oosthuyzen W,
Kousathanas A,
Moutsianas L,
Yang Z,
Zhai R,
Zheng C,
Grimes G,
Beale R,
Millar J,
Shih B,
Keating S,
Zechner M,
Haley C,
Porteous DJ,
Hayward C,
Yang J,
Knight J,
Summers C,
Shankar-Hari M,
Klenerman P,
Turtle L,
Ho A,
Moore SC,
Hinds C,
Horby P,
Nichol A,
Maslove D,
Ling L,
McAuley D,
Montgomery H,
Walsh T,
Pereira AC,
Renieri A,
Shen X,
Ponting CP,
Fawkes A,
Tenesa A,
Caulfield M,
Scott R,
Rowan K,
Murphy L,
Openshaw PJM,
Semple MG,
Law A,
Vitart V,
Wilson JF,
Baillie JK
GenOMICC Investigators · ISARIC4C Investigators and 4 more consortia
Nature · 2021 · PMID 33307546
2 pages
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
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.