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Is your paper here?
2,671 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.
13 matches for
Hao C.
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Schormair B,
Zhao C,
Bell S,
Didriksen M,
Nawaz MS,
Schandra N,
Stefani A,
Högl B,
Dauvilliers Y,
Bachmann CG,
Kemlink D,
Sonka K
and 55 more — show all
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek ZK,
Ibrahim A,
Bergmann M,
Kittke V,
Harrer P,
Dowsett J,
Chenini S,
Ostrowski SR,
Sørensen E,
Erikstrup C,
Pedersen OB,
Topholm Bruun M,
Nielsen KR,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Burchell B,
Furlotte NA,
Nandakumar P,
Earley CJ,
Ondo WG,
Xiong L,
Desautels A,
Perola M,
Vodicka P,
Dina C,
Stoll M,
Franke A,
Lieb W,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rye DB,
Rouleau GA,
Berger K,
Stefansson H,
Ullum H,
Stefansson K,
Hinds DA,
Di Angelantonio E,
Oexle K,
Winkelmann J
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
12 pages+
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Schormair B,
Zhao C,
Bell S,
Tilch E,
Salminen AV,
Pütz B,
Dauvilliers Y,
Stefani A,
Högl B,
Poewe W,
Kemlink D,
Sonka K
and 39 more — show all
Bachmann CG,
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek Z,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Allen RP,
Earley CJ,
Ondo WG,
Xiong L,
Montplaisir J,
Gan-Or Z,
Perola M,
Vodicka P,
Dina C,
Franke A,
Tittmann L,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rouleau GA,
Berger K,
Oexle K,
Di Angelantonio E,
Hinds DA,
Müller-Myhsok B,
Winkelmann J
23andMe Research Team · DESIR study group
The Lancet. Neurology · 2017 · PMID 29029846 · open access
10 pages
Biological and clinical insights from genetics of insomnia symptoms
Lane JM,
Jones SE,
Dashti HS,
Wood AR,
Aragam KG,
van Hees VT,
Strand LB,
Winsvold BS,
Wang H,
Bowden J,
Song Y,
Patel K
and 31 more — show all
Anderson SG,
Beaumont RN,
Bechtold DA,
Cade BE,
Haas M,
Kathiresan S,
Little MA,
Luik AI,
Loudon AS,
Purcell S,
Richmond RC,
Scheer FAJL,
Schormair B,
Tyrrell J,
Winkelman JW,
Winkelmann J,
Hveem K,
Zhao C,
Nielsen JB,
Willer CJ,
Redline S,
Spiegelhalder K,
Kyle SD,
Ray DW,
Zwart JA,
Brumpton B,
Frayling TM,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer
Hoffmann TJ,
Passarelli MN,
Graff RE,
Emami NC,
Sakoda LC,
Jorgenson E,
Habel LA,
Shan J,
Ranatunga DK,
Quesenberry CP,
Chao CR,
Ghai NR
and 17 more — show all
Aaronson D,
Presti J,
Nordström T,
Wang Z,
Berndt SI,
Chanock SJ,
Mosley JD,
Klein RJ,
Middha M,
Lilja H,
Melander O,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Van Den Eeden SK,
Witte JS
Nature communications · 2017 · PMID 28139693 · open access
5 pages
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Chen ZJ,
Zhao H,
He L,
Shi Y,
Qin Y,
Shi Y,
Li Z,
You L,
Zhao J,
Liu J,
Liang X,
Zhao X
and 22 more — show all
Zhao J,
Sun Y,
Zhang B,
Jiang H,
Zhao D,
Bian Y,
Gao X,
Geng L,
Li Y,
Zhu D,
Sun X,
Xu JE,
Hao C,
Ren CE,
Zhang Y,
Chen S,
Zhang W,
Yang A,
Yan J,
Li Y,
Ma J,
Zhao Y
Nature genetics · 2011 · PMID 21151128
4 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
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Hoffmann TJ,
Van Den Eeden SK,
Sakoda LC,
Jorgenson E,
Habel LA,
Graff RE,
Passarelli MN,
Cario CL,
Emami NC,
Chao CR,
Ghai NR,
Shan J
and 23 more — show all
Ranatunga DK,
Quesenberry CP,
Aaronson D,
Presti J,
Wang Z,
Berndt SI,
Chanock SJ,
McDonnell SK,
French AJ,
Schaid DJ,
Thibodeau SN,
Li Q,
Freedman ML,
Penney KL,
Mucci LA,
Haiman CA,
Henderson BE,
Seminara D,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Witte JS
Cancer discovery · 2015 · PMID 26034056
3 pages
Genome wide association analysis and association of genetic risk and lifestyle with upper gastrointestinal cancer among an endoscopy-screened cohort in China
He F,
Ran X,
Jiang H,
Fan Z,
Zhang Y,
Wang J,
Hao C,
Song G,
Gong Y,
Li Y,
Li X,
Chen R
and 5 more — show all
Science bulletin · 2026 · PMID 41963194
3 pages
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Li Y,
Zhang K,
Chen H,
Sun F,
Xu J,
Wu Z,
Li P,
Zhang L,
Du Y,
Luan H,
Li X,
Wu L
and 64 more — show all
Li H,
Wu H,
Li X,
Li X,
Zhang X,
Gong L,
Dai L,
Sun L,
Zuo X,
Xu J,
Gong H,
Li Z,
Tong S,
Wu M,
Li X,
Xiao W,
Wang G,
Zhu P,
Shen M,
Liu S,
Zhao D,
Liu W,
Wang Y,
Huang C,
Jiang Q,
Liu G,
Liu B,
Hu S,
Zhang W,
Zhang Z,
You X,
Li M,
Hao W,
Zhao C,
Leng X,
Bi L,
Wang Y,
Zhang F,
Shi Q,
Qi W,
Zhang X,
Jia Y,
Su J,
Li Q,
Hou Y,
Wu Q,
Xu D,
Zheng W,
Zhang M,
Wang Q,
Fei Y,
Zhang X,
Li J,
Jiang Y,
Tian X,
Zhao L,
Wang L,
Zhou B,
Li Y,
Zhao Y,
Zeng X,
Ott J,
Wang J,
Zhang F
Nature genetics · 2013 · PMID 24097066
1 page
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility
Emami NC,
Cavazos TB,
Rashkin SR,
Cario CL,
Graff RE,
Tai CG,
Mefford JA,
Kachuri L,
Wan E,
Wong S,
Aaronson D,
Presti J
and 14 more — show all
Habel LA,
Shan J,
Ranatunga DK,
Chao CR,
Ghai NR,
Jorgenson E,
Sakoda LC,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Hoffmann TJ,
Van Den Eeden SK,
Witte JS
Cancer research · 2021 · PMID 33293427
1 page
ExomeChip-based rare variant association study in restless legs syndrome
Tilch E,
Schormair B,
Zhao C,
Högl B,
Stefani A,
Berger K,
Trenkwalder C,
Bachmann CG,
Hornyak M,
Fietze I,
Müller-Nurasyid M,
Peters A
and 5 more — show all
Sleep medicine · 2022 · PMID 35489115
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.