For researchers
Is your paper here?
2,661 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.
7 matches for
Pan C.
Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma
Han Y,
Jia Q,
Jahani PS,
Hurrell BP,
Pan C,
Huang P,
Gukasyan J,
Woodward NC,
Eskin E,
Gilliland FD,
Akbari O,
Hartiala JA
and 1 more — show all
Nature communications · 2020 · PMID 32296059 · open access
12 pages+
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Klarin D,
Verma SS,
Judy R,
Dikilitas O,
Wolford BN,
Paranjpe I,
Levin MG,
Pan C,
Tcheandjieu C,
Spin JM,
Lynch J,
Assimes TL
and 41 more — show all
Åldstedt Nyrønning L,
Mattsson E,
Edwards TL,
Denny J,
Larson E,
Lee MTM,
Carrell D,
Zhang Y,
Jarvik GP,
Gharavi AG,
Harley J,
Mentch F,
Pacheco JA,
Hakonarson H,
Skogholt AH,
Thomas L,
Gabrielsen ME,
Hveem K,
Nielsen JB,
Zhou W,
Fritsche L,
Huang J,
Natarajan P,
Sun YV,
DuVall SL,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Scali ST,
Berceli SA,
Willer C,
Jones GT,
Bown MJ,
Nadkarni G,
Kullo IJ,
Ritchie M,
Damrauer SM,
Tsao PS
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
Kolz M,
Johnson T,
Sanna S,
Teumer A,
Vitart V,
Perola M,
Mangino M,
Albrecht E,
Wallace C,
Farrall M,
Johansson A,
Nyholt DR
and 44 more — show all
Aulchenko Y,
Beckmann JS,
Bergmann S,
Bochud M,
Brown M,
Campbell H,
Connell J,
Dominiczak A,
Homuth G,
Lamina C,
McCarthy MI,
Meitinger T,
Mooser V,
Munroe P,
Nauck M,
Peden J,
Prokisch H,
Salo P,
Salomaa V,
Samani NJ,
Schlessinger D,
Uda M,
Völker U,
Waeber G,
Waterworth D,
Wang-Sattler R,
Wright AF,
Adamski J,
Whitfield JB,
Gyllensten U,
Wilson JF,
Rudan I,
Pramstaller P,
Watkins H,
Doering A,
Wichmann HE,
Spector TD,
Peltonen L,
Völzke H,
Nagaraja R,
Vollenweider P,
Caulfield M,
Illig T,
Gieger C
EUROSPAN Consortium · ENGAGE Consortium and 3 more consortia
PLoS genetics · 2009 · PMID 19503597 · open access
3 pages
Host control of persistent Epstein-Barr virus infection
Schmidt A,
Alawathurage TM,
David FS,
Ogawa Y,
Frach L,
Richter S,
Schaefer M,
Mathey CM,
Henne SK,
Forstner AJ,
Dilthey AT,
Pröbstel AK
and 6 more — show all
Japan COVID-19 Task Force
Nature · 2026 · PMID 41714741 · open access
3 pages
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
Hartiala JA,
Han Y,
Jia Q,
Hilser JR,
Huang P,
Gukasyan J,
Schwartzman WS,
Cai Z,
Biswas S,
Trégouët DA,
Smith NL,
Seldin M
and 47 more — show all
Pan C,
Mehrabian M,
Lusis AJ,
Bazeley P,
Sun YV,
Liu C,
Quyyumi AA,
Scholz M,
Thiery J,
Delgado GE,
Kleber ME,
März W,
Howe LJ,
Asselbergs FW,
van Vugt M,
Vlachojannis GJ,
Patel RS,
Lyytikäinen LP,
Kähönen M,
Lehtimäki T,
Nieminen TVM,
Kuukasjärvi P,
Laurikka JO,
Chang X,
Heng CK,
Jiang R,
Kraus WE,
Hauser ER,
Ferguson JF,
Reilly MP,
Ito K,
Koyama S,
Kamatani Y,
Komuro I,
Stolze LK,
Romanoski CE,
Khan MD,
Turner AW,
Miller CL,
Aherrahrou R,
Civelek M,
Ma L,
Björkegren JLM,
Kumar SR,
Tang WHW,
Hazen SL,
Allayee H
INVENT Consortium · CHARGE Consortium Hemostasis Working Group and 2 more consortia
European heart journal · 2021 · PMID 33532862
2 pages
A genome-wide association study identifies two new risk loci for Graves' disease
Chu X,
Pan CM,
Zhao SX,
Liang J,
Gao GQ,
Zhang XM,
Yuan GY,
Li CG,
Xue LQ,
Shen M,
Liu W,
Xie F
and 36 more — show all
Yang SY,
Wang HF,
Shi JY,
Sun WW,
Du WH,
Zuo CL,
Shi JX,
Liu BL,
Guo CC,
Zhan M,
Gu ZH,
Zhang XN,
Sun F,
Wang ZQ,
Song ZY,
Zou CY,
Sun WH,
Guo T,
Cao HM,
Ma JH,
Han B,
Li P,
Jiang H,
Huang QH,
Liang L,
Liu LB,
Chen G,
Su Q,
Peng YD,
Zhao JJ,
Ning G,
Chen Z,
Chen JL,
Chen SJ,
Huang W,
Song HD
China Consortium for Genetics of Autoimmune Thyroid Disease
Nature genetics · 2011 · PMID 21841780
1 page
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations
Zhan M,
Chen G,
Pan CM,
Gu ZH,
Zhao SX,
Liu W,
Wang HN,
Ye XP,
Xie HJ,
Yu SS,
Liang J,
Gao GQ
and 9 more — show all
China Consortium for Genetics of Autoimmune Thyroid Disease
Human molecular genetics · 2014 · PMID 24852370
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.