For researchers
Is your paper here?
2,662 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.
6 matches for
Yan C.
Whole-genome sequence-based analysis of thyroid function
Taylor PN,
Porcu E,
Chew S,
Campbell PJ,
Traglia M,
Brown SJ,
Mullin BH,
Shihab HA,
Min J,
Walter K,
Memari Y,
Huang J
and 38 more — show all
Barnes MR,
Beilby JP,
Charoen P,
Danecek P,
Dudbridge F,
Forgetta V,
Greenwood C,
Grundberg E,
Johnson AD,
Hui J,
Lim EM,
McCarthy S,
Muddyman D,
Panicker V,
Perry JR,
Bell JT,
Yuan W,
Relton C,
Gaunt T,
Schlessinger D,
Abecasis G,
Cucca F,
Surdulescu GL,
Woltersdorf W,
Zeggini E,
Zheng HF,
Toniolo D,
Dayan CM,
Naitza S,
Walsh JP,
Spector T,
Davey Smith G,
Durbin R,
Richards JB,
Sanna S,
Soranzo N,
Timpson NJ,
Wilson SG
UK0K Consortium
Nature communications · 2015 · PMID 25743335 · open access
7 pages
Trans-ancestry meta-analysis of genome-wide association study identifies eight novel genetic loci in type 1 diabetes: A multi-population study
Guo X,
Hu J,
Tian H,
Yan C,
Liu Q,
Zhou T,
Liu C,
Guo Y,
Wang N,
Ren Q,
Xu Y,
Wang C
and 10 more — show all
Diabetic medicine : a journal of the British Diabetic Association · 2026 · PMID 42594184
5 pages
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Wang Z,
Dai J,
Hu N,
Miao X,
Abnet CC,
Yang M,
Freedman ND,
Chen J,
Burdette L,
Zhu X,
Chung CC,
Ren C
and 35 more — show all
Dawsey SM,
Wang M,
Ding T,
Du J,
Gao YT,
Zhong R,
Giffen C,
Pan W,
Koh WP,
Dai N,
Liao LM,
Yan C,
Qiao YL,
Jiang Y,
Shu XO,
Chen J,
Wang C,
Ma H,
Su H,
Zhang Z,
Wang L,
Wu C,
Xiang YB,
Hu Z,
Yuan JM,
Xie L,
Zheng W,
Zheng W,
Lin D,
Chanock SJ,
Shi Y,
Goldstein AM,
Jin G,
Taylor PR,
Shen H
Gut · 2017 · PMID 26701879 · open access
3 pages
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
and 180 more — show all
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium and 2 more consortia
Nature genetics · 2021 · PMID 34873335 · open access
3 pages
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Yan C,
Zhu M,
Ding Y,
Yang M,
Wang M,
Li G,
Ren C,
Huang T,
Yang W,
He B,
Wang M,
Yu F
and 22 more — show all
Wang J,
Zhang R,
Wang T,
Ni J,
Chen J,
Jiang Y,
Dai J,
Zhang E,
Ma H,
Wang Y,
Xu D,
Wang S,
Chen Y,
Xu Z,
Zhou J,
Ji G,
Wang Z,
Zhang Z,
Hu Z,
Wei Q,
Shen H,
Jin G
Gut · 2020 · PMID 31383772
1 page
Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study
Jin G,
Lv J,
Yang M,
Wang M,
Zhu M,
Wang T,
Yan C,
Yu C,
Ding Y,
Li G,
Ren C,
Ni J
and 22 more — show all
Zhang R,
Guo Y,
Bian Z,
Zheng Y,
Zhang N,
Jiang Y,
Chen J,
Wang Y,
Xu D,
Zheng H,
Yang L,
Chen Y,
Walters R,
Millwood IY,
Dai J,
Ma H,
Chen K,
Chen Z,
Hu Z,
Wei Q,
Shen H,
Li L
The Lancet. Oncology · 2020 · PMID 33002439
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.