For researchers
Is your paper here?
2,682 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
87 matches for
Yang J,
showing the first 20.
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians
Yang W,
Tang H,
Zhang Y,
Tang X,
Zhang J,
Sun L,
Yang J,
Cui Y,
Zhang L,
Hirankarn N,
Cheng H,
Pan HF
and 66 more — show all
Pan HF,
Gao J,
Lee TL,
Sheng Y,
Lau CS,
Li Y,
Chan TM,
Yin X,
Ying D,
Lu Q,
Leung AM,
Zuo X,
Chen X,
Tong KL,
Zhou F,
Diao Q,
Tse NK,
Xie H,
Mok CC,
Hao F,
Wong SN,
Shi B,
Lee KW,
Hui Y,
Ho MH,
Liang B,
Lee PP,
Cui H,
Guo Q,
Chung BH,
Pu X,
Liu Q,
Zhang X,
Zhang C,
Chong CY,
Fang H,
Wong RW,
Sun Y,
Mok MY,
Li XP,
Avihingsanon Y,
Zhai Z,
Rianthavorn P,
Deekajorndej T,
Suphapeetiporn K,
Gao F,
Shotelersuk V,
Kang X,
Ying SK,
Zhang L,
Wong WH,
Zhu D,
Fung SK,
Zeng F,
Lai WM,
Wong CM,
Ng IO,
Garcia-Barceló MM,
Cherny SS,
Shen N,
Tam PK,
Sham PC,
Ye DQ,
Yang S,
Zhang X,
Lau YL
American journal of human genetics · 2013 · PMID 23273568
5 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
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
van Rooij FJA,
Qayyum R,
Smith AV,
Zhou Y,
Trompet S,
Tanaka T,
Keller MF,
Chang LC,
Schmidt H,
Yang ML,
Chen MH,
Hayes J
and 88 more — show all
Johnson AD,
Yanek LR,
Mueller C,
Lange L,
Floyd JS,
Ghanbari M,
Zonderman AB,
Jukema JW,
Hofman A,
van Duijn CM,
Desch KC,
Saba Y,
Ozel AB,
Snively BM,
Wu JY,
Schmidt R,
Fornage M,
Klein RJ,
Fox CS,
Matsuda K,
Kamatani N,
Wild PS,
Stott DJ,
Ford I,
Slagboom PE,
Yang J,
Chu AY,
Lambert AJ,
Uitterlinden AG,
Franco OH,
Hofer E,
Ginsburg D,
Hu B,
Keating B,
Schick UM,
Brody JA,
Li JZ,
Chen Z,
Zeller T,
Guralnik JM,
Chasman DI,
Peters LL,
Kubo M,
Becker DM,
Li J,
Eiriksdottir G,
Rotter JI,
Levy D,
Grossmann V,
Patel KV,
Chen CH,
Ridker PM,
Tang H,
Launer LJ,
Rice KM,
Li-Gao R,
Ferrucci L,
Evans MK,
Choudhuri A,
Trompouki E,
Abraham BJ,
Yang S,
Takahashi A,
Kamatani Y,
Kooperberg C,
Harris TB,
Jee SH,
Coresh J,
Tsai FJ,
Longo DL,
Chen YT,
Felix JF,
Yang Q,
Psaty BM,
Boerwinkle E,
Becker LC,
Mook-Kanamori DO,
Wilson JG,
Gudnason V,
O'Donnell CJ,
Dehghan A,
Cupples LA,
Nalls MA,
Morris AP,
Okada Y,
Reiner AP,
Zon LI,
Ganesh SK
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
Clinical Pharmacogenetics Implementation Consortium Guideline for Thiopurine Dosing Based on TPMT and NUDT15 Genotypes: 2018 Update
Relling MV,
Schwab M,
Whirl-Carrillo M,
Suarez-Kurtz G,
Pui CH,
Stein CM,
Moyer AM,
Evans WE,
Klein TE,
Antillon-Klussmann FG,
Caudle KE,
Kato M
and 3 more — show all
Clinical pharmacology and therapeutics · 2019 · PMID 30447069
5 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
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
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
Cortes A,
Hadler J,
Pointon JP,
Robinson PC,
Karaderi T,
Leo P,
Cremin K,
Pryce K,
Harris J,
Lee S,
Joo KB,
Shim SC
and 53 more — show all
Weisman M,
Ward M,
Zhou X,
Garchon HJ,
Chiocchia G,
Nossent J,
Lie BA,
Førre Ø,
Tuomilehto J,
Laiho K,
Jiang L,
Liu Y,
Wu X,
Bradbury LA,
Elewaut D,
Burgos-Vargas R,
Stebbings S,
Appleton L,
Farrah C,
Lau J,
Kenna TJ,
Haroon N,
Ferreira MA,
Yang J,
Mulero J,
Fernandez-Sueiro JL,
Gonzalez-Gay MA,
Lopez-Larrea C,
Deloukas P,
Donnelly P,
Bowness P,
Gafney K,
Gaston H,
Gladman DD,
Rahman P,
Maksymowych WP,
Xu H,
Crusius JB,
van der Horst-Bruinsma IE,
Chou CT,
Valle-Oñate R,
Romero-Sánchez C,
Hansen IM,
Pimentel-Santos FM,
Inman RD,
Videm V,
Martin J,
Breban M,
Reveille JD,
Evans DM,
Kim TH,
Wordsworth BP,
Brown MA
International Genetics of Ankylosing Spondylitis Consortium (IGAS) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 4 more consortia
Nature genetics · 2013 · PMID 23749187
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
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study
Yu H,
Yan H,
Wang L,
Li J,
Tan L,
Deng W,
Chen Q,
Yang G,
Zhang F,
Lu T,
Yang J,
Li K
and 12 more — show all
Lv L,
Tan Q,
Zhang H,
Xiao X,
Li M,
Ma X,
Yang F,
Li L,
Wang C,
Li T,
Zhang D,
Yue W
Chinese Antipsychotics Pharmacogenomics Consortium
The lancet. Psychiatry · 2018 · PMID 29503163
4 pages
Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus
Song Q,
Lei Y,
Shao L,
Li W,
Kong Q,
Lin Z,
Qin X,
Wei W,
Hou F,
Li J,
Guo X,
Mao Y
and 13 more — show all
Cao Y,
Liu Z,
Zheng L,
Liang R,
Jiang Y,
Liu Y,
Zhang L,
Yang J,
Lau YL,
Zhang Y,
Ban B,
Wang YF,
Yang W
Rheumatology (Oxford, England) · 2021 · PMID 33493351
4 pages
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
Todd JA,
Walker NM,
Cooper JD,
Smyth DJ,
Downes K,
Plagnol V,
Bailey R,
Nejentsev S,
Field SF,
Payne F,
Lowe CE,
Szeszko JS
and 28 more — show all
Hafler JP,
Zeitels L,
Yang JH,
Vella A,
Nutland S,
Stevens HE,
Schuilenburg H,
Coleman G,
Maisuria M,
Meadows W,
Smink LJ,
Healy B,
Burren OS,
Lam AA,
Ovington NR,
Allen J,
Adlem E,
Leung HT,
Wallace C,
Howson JM,
Guja C,
Ionescu-Tîrgovişte C,
Simmonds MJ,
Heward JM,
Gough SC,
Dunger DB,
Wicker LS,
Clayton DG
Genetics of Type 1 Diabetes in Finland · Wellcome Trust Case Control Consortium
Nature genetics · 2007 · PMID 17554260
3 pages
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
and 290 more — show all
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
and 247 more — show all
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
3 pages
Genetic signatures of high-altitude adaptation in Tibetans
Yang J,
Jin ZB,
Chen J,
Huang XF,
Li XM,
Liang YB,
Mao JY,
Chen X,
Zheng Z,
Bakshi A,
Zheng DD,
Zheng MQ
and 4 more — show all
Proceedings of the National Academy of Sciences of the United States of America · 2017 · PMID 28373541
3 pages
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
Jones G,
Trajanoska K,
Santanasto AJ,
Stringa N,
Kuo CL,
Atkins JL,
Lewis JR,
Duong T,
Hong S,
Biggs ML,
Luan J,
Sarnowski C
and 54 more — show all
Lunetta KL,
Tanaka T,
Wojczynski MK,
Cvejkus R,
Nethander M,
Ghasemi S,
Yang J,
Zillikens MC,
Walter S,
Sicinski K,
Kague E,
Ackert-Bicknell CL,
Arking DE,
Windham BG,
Boerwinkle E,
Grove ML,
Graff M,
Spira D,
Demuth I,
van der Velde N,
de Groot LCPGM,
Psaty BM,
Odden MC,
Fohner AE,
Langenberg C,
Wareham NJ,
Bandinelli S,
van Schoor NM,
Huisman M,
Tan Q,
Zmuda J,
Mellström D,
Karlsson M,
Bennett DA,
Buchman AS,
De Jager PL,
Uitterlinden AG,
Völker U,
Kocher T,
Teumer A,
Rodriguéz-Mañas L,
García FJ,
Carnicero JA,
Herd P,
Bertram L,
Ohlsson C,
Murabito JM,
Melzer D,
Kuchel GA,
Ferrucci L,
Karasik D,
Rivadeneira F,
Kiel DP,
Pilling LC
Nature communications · 2021 · PMID 33510174 · open access
3 pages
Genome-wide meta-analysis, functional genomics and integrative analyses implicate new risk genes and therapeutic targets for anxiety disorders
Li W,
Chen R,
Feng L,
Dang X,
Liu J,
Chen T,
Yang J,
Su X,
Lv L,
Li T,
Zhang Z,
Luo XJ
Nature human behaviour · 2024 · PMID 37945807
3 pages
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers
Zhang H,
Zhai Y,
Hu Z,
Wu C,
Qian J,
Jia W,
Ma F,
Huang W,
Yu L,
Yue W,
Wang Z,
Li P
and 20 more — show all
Zhang Y,
Liang R,
Wei Z,
Cui Y,
Xie W,
Cai M,
Yu X,
Yuan Y,
Xia X,
Zhang X,
Yang H,
Qiu W,
Yang J,
Gong F,
Chen M,
Shen H,
Lin D,
Zeng YX,
He F,
Zhou G
Nature genetics · 2010 · PMID 20676096
2 pages
ELF1 is associated with systemic lupus erythematosus in Asian populations
Yang J,
Yang W,
Hirankarn N,
Ye DQ,
Zhang Y,
Pan HF,
Pan HF,
Mok CC,
Chan TM,
Wong RW,
Mok MY,
Lee KW
and 24 more — show all
Wong SN,
Leung AM,
Li XP,
Avihingsanon Y,
Rianthavorn P,
Deekajorndej T,
Suphapeetiporn K,
Shotelersuk V,
Baum L,
Kwan P,
Lee TL,
Ho MH,
Lee PP,
Wong WH,
Zeng S,
Zhang J,
Wong CM,
Ng IO,
Garcia-Barceló MM,
Cherny SS,
Tam PK,
Sham PC,
Lau CS,
Lau YL
Human molecular genetics · 2011 · PMID 21044949
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.