For researchers
Is your paper here?
2,665 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.
10 matches for
Hou C.
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
Li YR,
Li J,
Zhao SD,
Bradfield JP,
Mentch FD,
Maggadottir SM,
Hou C,
Abrams DJ,
Chang D,
Gao F,
Guo Y,
Wei Z
and 54 more — show all
Connolly JJ,
Cardinale CJ,
Bakay M,
Glessner JT,
Li D,
Kao C,
Thomas KA,
Qiu H,
Chiavacci RM,
Kim CE,
Wang F,
Snyder J,
Richie MD,
Flatø B,
Førre Ø,
Denson LA,
Thompson SD,
Becker ML,
Guthery SL,
Latiano A,
Perez E,
Resnick E,
Russell RK,
Wilson DC,
Silverberg MS,
Annese V,
Lie BA,
Punaro M,
Dubinsky MC,
Monos DS,
Strisciuglio C,
Staiano A,
Miele E,
Kugathasan S,
Ellis JA,
Munro JE,
Sullivan KE,
Wise CA,
Chapel H,
Cunningham-Rundles C,
Grant SF,
Orange JS,
Sleiman PM,
Behrens EM,
Griffiths AM,
Satsangi J,
Finkel TH,
Keinan A,
Prak ET,
Polychronakos C,
Baldassano RN,
Li H,
Keating BJ,
Hakonarson H
Nature medicine · 2015 · PMID 26301688
12 pages+
Your height affects your health: genetic determinants and health-related outcomes in Taiwan
Chiou JS,
Cheng CF,
Liang WM,
Chou CH,
Wang CH,
Lin WD,
Chiu ML,
Cheng WC,
Lin CW,
Lin TH,
Liao CC,
Huang SM
and 3 more — show all
BMC medicine · 2022 · PMID 35831902 · open access
12 pages+
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
Kany S,
Rämö JT,
Hou C,
Jurgens SJ,
Khurshid S,
Nauffal V,
Cunningham JW,
Lau ES,
Koyama S,
Ho JE,
Olgin JE,
Elmariah S
and 4 more — show all
FinnGen
Nature genetics · 2026 · PMID 41419685 · open access
12 pages+
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children
Li J,
Glessner JT,
Zhang H,
Hou C,
Wei Z,
Bradfield JP,
Mentch FD,
Guo Y,
Kim C,
Xia Q,
Chiavacci RM,
Thomas KA
and 5 more — show all
Human molecular genetics · 2013 · PMID 23263863
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
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma
Diskin SJ,
Capasso M,
Schnepp RW,
Cole KA,
Attiyeh EF,
Hou C,
Diamond M,
Carpenter EL,
Winter C,
Lee H,
Jagannathan J,
Latorre V
and 4 more — show all
Nature genetics · 2012 · PMID 22941191 · open access
3 pages
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma
McDaniel LD,
Conkrite KL,
Chang X,
Capasso M,
Vaksman Z,
Oldridge DA,
Zachariou A,
Horn M,
Diamond M,
Hou C,
Iolascon A,
Hakonarson H
and 3 more — show all
PLoS genetics · 2017 · PMID 28545128 · open access
2 pages
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk
Chang X,
Zhao Y,
Hou C,
Glessner J,
McDaniel L,
Diamond MA,
Thomas K,
Li J,
Wei Z,
Liu Y,
Guo Y,
Mentch FD
and 9 more — show all
Nature communications · 2017 · PMID 28924153 · open access
2 pages
Common variants at 5q33.1 predispose to migraine in African-American children
Chang X,
Pellegrino R,
Garifallou J,
March M,
Snyder J,
Mentch F,
Li J,
Hou C,
Liu Y,
Sleiman PMA,
Hakonarson H
Journal of medical genetics · 2018 · PMID 30266756
2 pages
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity
Rämö JT,
Kany S,
Hou CR,
Friedman SF,
Roselli C,
Nauffal V,
Koyama S,
Karjalainen J,
Maddah M,
Palotie A,
Ellinor PT,
Pirruccello JP
FinnGen
JAMA cardiology · 2024 · PMID 38477908
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.