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2,671 papers hold this site up. Every variant and condition page names
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31 matches for
Ke T,
showing the first 11.
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
Radstake TR,
Gorlova O,
Rueda B,
Martin JE,
Alizadeh BZ,
Palomino-Morales R,
Coenen MJ,
Vonk MC,
Voskuyl AE,
Schuerwegh AJ,
Broen JC,
van Riel PL
and 51 more — show all
van 't Slot R,
Italiaander A,
Ophoff RA,
Riemekasten G,
Hunzelmann N,
Simeon CP,
Ortego-Centeno N,
González-Gay MA,
González-Escribano MF,
Airo P,
van Laar J,
Herrick A,
Worthington J,
Hesselstrand R,
Smith V,
de Keyser F,
Houssiau F,
Chee MM,
Madhok R,
Shiels P,
Westhovens R,
Kreuter A,
Kiener H,
de Baere E,
Witte T,
Padykov L,
Klareskog L,
Beretta L,
Scorza R,
Lie BA,
Hoffmann-Vold AM,
Carreira P,
Varga J,
Hinchcliff M,
Gregersen PK,
Lee AT,
Ying J,
Han Y,
Weng SF,
Amos CI,
Wigley FM,
Hummers L,
Nelson JL,
Agarwal SK,
Assassi S,
Gourh P,
Tan FK,
Koeleman BP,
Arnett FC,
Martin J,
Mayes MD
Spanish Scleroderma Group
Nature genetics · 2010 · PMID 20383147
3 pages
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Schumann G,
Liu C,
O'Reilly P,
Gao H,
Song P,
Xu B,
Ruggeri B,
Amin N,
Jia T,
Preis S,
Segura Lepe M,
Akira S
and 115 more — show all
Barbieri C,
Baumeister S,
Cauchi S,
Clarke TK,
Enroth S,
Fischer K,
Hällfors J,
Harris SE,
Hieber S,
Hofer E,
Hottenga JJ,
Johansson Å,
Joshi PK,
Kaartinen N,
Laitinen J,
Lemaitre R,
Loukola A,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Mbarek H,
Milaneschi Y,
Moayyeri A,
Mukamal K,
Nelson C,
Nettleton J,
Partinen E,
Rawal R,
Robino A,
Rose L,
Sala C,
Satoh T,
Schmidt R,
Schraut K,
Scott R,
Smith AV,
Starr JM,
Teumer A,
Trompet S,
Uitterlinden AG,
Venturini C,
Vergnaud AC,
Verweij N,
Vitart V,
Vuckovic D,
Wedenoja J,
Yengo L,
Yu B,
Zhang W,
Zhao JH,
Boomsma DI,
Chambers J,
Chasman DI,
Daniela T,
de Geus E,
Deary I,
Eriksson JG,
Esko T,
Eulenburg V,
Franco OH,
Froguel P,
Gieger C,
Grabe HJ,
Gudnason V,
Gyllensten U,
Harris TB,
Hartikainen AL,
Heath AC,
Hocking L,
Hofman A,
Huth C,
Jarvelin MR,
Jukema JW,
Kaprio J,
Kooner JS,
Kutalik Z,
Lahti J,
Langenberg C,
Lehtimäki T,
Liu Y,
Madden PA,
Martin N,
Morrison A,
Penninx B,
Pirastu N,
Psaty B,
Raitakari O,
Ridker P,
Rose R,
Rotter JI,
Samani NJ,
Schmidt H,
Spector TD,
Stott D,
Strachan D,
Tzoulaki I,
van der Harst P,
van Duijn CM,
Marques-Vidal P,
Vollenweider P,
Wareham NJ,
Whitfield JB,
Wilson J,
Wolffenbuttel B,
Bakalkin G,
Evangelou E,
Liu Y,
Rice KM,
Desrivières S,
Kliewer SA,
Mangelsdorf DJ,
Müller CP,
Levy D,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
López-Isac E,
Acosta-Herrera M,
Kerick M,
Assassi S,
Satpathy AT,
Granja J,
Mumbach MR,
Beretta L,
Simeón CP,
Carreira P,
Ortego-Centeno N,
Castellvi I
and 30 more — show all
Bossini-Castillo L,
Carmona FD,
Orozco G,
Hunzelmann N,
Distler JHW,
Franke A,
Lunardi C,
Moroncini G,
Gabrielli A,
de Vries-Bouwstra J,
Wijmenga C,
Koeleman BPC,
Nordin A,
Padyukov L,
Hoffmann-Vold AM,
Lie B,
Proudman S,
Stevens W,
Nikpour M,
Vyse T,
Herrick AL,
Worthington J,
Denton CP,
Allanore Y,
Brown MA,
Radstake TRDJ,
Fonseca C,
Chang HY,
Mayes MD,
Martin J
European Scleroderma Group† · Australian Scleroderma Interest Group (ASIG)
Nature communications · 2019 · PMID 31672989 · open access
3 pages
A meta-analysis of genome-wide association studies of epigenetic age acceleration
Gibson J,
Russ TC,
Clarke TK,
Howard DM,
Hillary RF,
Evans KL,
Walker RM,
Bermingham ML,
Morris SW,
Campbell A,
Hayward C,
Murray AD
and 6 more — show all
PLoS genetics · 2019 · PMID 31738745 · open access
3 pages
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
Stahl EA,
Raychaudhuri S,
Remmers EF,
Xie G,
Eyre S,
Thomson BP,
Li Y,
Kurreeman FA,
Zhernakova A,
Hinks A,
Guiducci C,
Chen R
and 56 more — show all
Alfredsson L,
Amos CI,
Ardlie KG,
Barton A,
Bowes J,
Brouwer E,
Burtt NP,
Catanese JJ,
Coblyn J,
Coenen MJ,
Costenbader KH,
Criswell LA,
Crusius JB,
Cui J,
de Bakker PI,
De Jager PL,
Ding B,
Emery P,
Flynn E,
Harrison P,
Hocking LJ,
Huizinga TW,
Kastner DL,
Ke X,
Lee AT,
Liu X,
Martin P,
Morgan AW,
Padyukov L,
Posthumus MD,
Radstake TR,
Reid DM,
Seielstad M,
Seldin MF,
Shadick NA,
Steer S,
Tak PP,
Thomson W,
van der Helm-van Mil AH,
van der Horst-Bruinsma IE,
van der Schoot CE,
van Riel PL,
Weinblatt ME,
Wilson AG,
Wolbink GJ,
Wordsworth BP,
Wijmenga C,
Karlson EW,
Toes RE,
de Vries N,
Begovich AB,
Worthington J,
Siminovitch KA,
Gregersen PK,
Klareskog L,
Plenge RM
BIRAC Consortium · YEAR Consortium
Nature genetics · 2010 · PMID 20453842
2 pages
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Schumann G,
Coin LJ,
Lourdusamy A,
Charoen P,
Berger KH,
Stacey D,
Desrivières S,
Aliev FA,
Khan AA,
Amin N,
Aulchenko YS,
Bakalkin G
and 104 more — show all
Bakker SJ,
Balkau B,
Beulens JW,
Bilbao A,
de Boer RA,
Beury D,
Bots ML,
Breetvelt EJ,
Cauchi S,
Cavalcanti-Proença C,
Chambers JC,
Clarke TK,
Dahmen N,
de Geus EJ,
Dick D,
Ducci F,
Easton A,
Edenberg HJ,
Esko T,
Fernández-Medarde A,
Foroud T,
Freimer NB,
Girault JA,
Grobbee DE,
Guarrera S,
Gudbjartsson DF,
Hartikainen AL,
Heath AC,
Hesselbrock V,
Hofman A,
Hottenga JJ,
Isohanni MK,
Kaprio J,
Khaw KT,
Kuehnel B,
Laitinen J,
Lobbens S,
Luan J,
Mangino M,
Maroteaux M,
Matullo G,
McCarthy MI,
Mueller C,
Navis G,
Numans ME,
Núñez A,
Nyholt DR,
Onland-Moret CN,
Oostra BA,
O'Reilly PF,
Palkovits M,
Penninx BW,
Polidoro S,
Pouta A,
Prokopenko I,
Ricceri F,
Santos E,
Smit JH,
Soranzo N,
Song K,
Sovio U,
Stumvoll M,
Surakk I,
Thorgeirsson TE,
Thorsteinsdottir U,
Troakes C,
Tyrfingsson T,
Tönjes A,
Uiterwaal CS,
Uitterlinden AG,
van der Harst P,
van der Schouw YT,
Staehlin O,
Vogelzangs N,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Whitfield JB,
Wichmann EH,
Willemsen G,
Witteman JC,
Yuan X,
Zhai G,
Zhao JH,
Zhang W,
Martin NG,
Metspalu A,
Doering A,
Scott J,
Spector TD,
Loos RJ,
Boomsma DI,
Mooser V,
Peltonen L,
Stefansson K,
van Duijn CM,
Vineis P,
Sommer WH,
Kooner JS,
Spanagel R,
Heberlein UA,
Jarvelin MR,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
2 pages
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese
Okada Y,
Shimane K,
Kochi Y,
Tahira T,
Suzuki A,
Higasa K,
Takahashi A,
Horita T,
Atsumi T,
Ishii T,
Okamoto A,
Fujio K
and 32 more — show all
Hirakata M,
Amano H,
Kondo Y,
Ito S,
Takada K,
Mimori A,
Saito K,
Kamachi M,
Kawaguchi Y,
Ikari K,
Mohammed OW,
Matsuda K,
Terao C,
Ohmura K,
Myouzen K,
Hosono N,
Tsunoda T,
Nishimoto N,
Mimori T,
Matsuda F,
Tanaka Y,
Sumida T,
Yamanaka H,
Takasaki Y,
Koike T,
Horiuchi T,
Hayashi K,
Kubo M,
Kamatani N,
Yamada R,
Nakamura Y,
Yamamoto K
PLoS genetics · 2012 · PMID 22291604 · open access
1 page
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
Rothwell S,
Cooper RG,
Lundberg IE,
Miller FW,
Gregersen PK,
Bowes J,
Vencovsky J,
Danko K,
Limaye V,
Selva-O'Callaghan A,
Hanna MG,
Machado PM
and 24 more — show all
Pachman LM,
Reed AM,
Rider LG,
Cobb J,
Platt H,
Molberg Ø,
Benveniste O,
Mathiesen P,
Radstake T,
Doria A,
De Bleecker J,
De Paepe B,
Maurer B,
Ollier WE,
Padyukov L,
O'Hanlon TP,
Lee A,
Amos CI,
Gieger C,
Meitinger T,
Winkelmann J,
Wedderburn LR,
Chinoy H,
Lamb JA
Myositis Genetics Consortium
Annals of the rheumatic diseases · 2016 · PMID 26362759
1 page
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank
Hall LS,
Adams MJ,
Arnau-Soler A,
Clarke TK,
Howard DM,
Zeng Y,
Davies G,
Hagenaars SP,
Maria Fernandez-Pujals A,
Gibson J,
Wigmore EM,
Boutin TS
and 7 more — show all
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Translational psychiatry · 2018 · PMID 29317602 · open access
1 page
Factors associated with sharing e-mail information and mental health survey participation in large population cohorts
Adams MJ,
Hill WD,
Howard DM,
Dashti HS,
Davis KAS,
Campbell A,
Clarke TK,
Deary IJ,
Hayward C,
Porteous D,
Hotopf M,
McIntosh AM
International journal of epidemiology · 2020 · PMID 31263887 · open access
1 page
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.