For researchers
Is your paper here?
2,663 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.
4 matches for
Hou S.
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases
Chen Y,
Lu T,
Pettersson-Kymmer U,
Stewart ID,
Butler-Laporte G,
Nakanishi T,
Cerani A,
Liang KYH,
Yoshiji S,
Willett JDS,
Su CY,
Raina P
and 7 more — show all
Nature genetics · 2023 · PMID 36635386
12 pages+
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Bakker MK,
van der Spek RAA,
van Rheenen W,
Morel S,
Bourcier R,
Hostettler IC,
Alg VS,
van Eijk KR,
Koido M,
Akiyama M,
Terao C,
Matsuda K
and 62 more — show all
Walters RG,
Lin K,
Li L,
Millwood IY,
Chen Z,
Rouleau GA,
Zhou S,
Rannikmäe K,
Sudlow CLM,
Houlden H,
van den Berg LH,
Dina C,
Naggara O,
Gentric JC,
Shotar E,
Eugène F,
Desal H,
Winsvold BS,
Børte S,
Johnsen MB,
Brumpton BM,
Sandvei MS,
Willer CJ,
Hveem K,
Zwart JA,
Verschuren WMM,
Friedrich CM,
Hirsch S,
Schilling S,
Dauvillier J,
Martin O,
Jones GT,
Bown MJ,
Ko NU,
Kim H,
Coleman JRI,
Breen G,
Zaroff JG,
Klijn CJM,
Malik R,
Dichgans M,
Sargurupremraj M,
Tatlisumak T,
Amouyel P,
Debette S,
Rinkel GJE,
Worrall BB,
Pera J,
Slowik A,
Gaál-Paavola EI,
Niemelä M,
Jääskeläinen JE,
von Und Zu Fraunberg M,
Lindgren A,
Broderick JP,
Werring DJ,
Woo D,
Redon R,
Bijlenga P,
Kamatani Y,
Veldink JH,
Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker KB,
Ramus SJ,
Tyrer J,
Lee A,
Shen HC,
Beesley J,
Lawrenson K,
McGuffog L,
Healey S,
Lee JM,
Spindler TJ,
Lin YG
and 277 more — show all
Pejovic T,
Bean Y,
Li Q,
Coetzee S,
Hazelett D,
Miron A,
Southey M,
Terry MB,
Goldgar DE,
Buys SS,
Janavicius R,
Dorfling CM,
van Rensburg EJ,
Neuhausen SL,
Ding YC,
Hansen TV,
Jønson L,
Gerdes AM,
Ejlertsen B,
Barrowdale D,
Dennis J,
Benitez J,
Osorio A,
Garcia MJ,
Komenaka I,
Weitzel JN,
Ganschow P,
Peterlongo P,
Bernard L,
Viel A,
Bonanni B,
Peissel B,
Manoukian S,
Radice P,
Papi L,
Ottini L,
Fostira F,
Konstantopoulou I,
Garber J,
Frost D,
Perkins J,
Platte R,
Ellis S,
Godwin AK,
Schmutzler RK,
Meindl A,
Engel C,
Sutter C,
Sinilnikova OM,
Damiola F,
Mazoyer S,
Stoppa-Lyonnet D,
Claes K,
De Leeneer K,
Kirk J,
Rodriguez GC,
Piedmonte M,
O'Malley DM,
de la Hoya M,
Caldes T,
Aittomäki K,
Nevanlinna H,
Collée JM,
Rookus MA,
Oosterwijk JC,
Tihomirova L,
Tung N,
Hamann U,
Isaccs C,
Tischkowitz M,
Imyanitov EN,
Caligo MA,
Campbell IG,
Hogervorst FB,
Olah E,
Diez O,
Blanco I,
Brunet J,
Lazaro C,
Pujana MA,
Jakubowska A,
Gronwald J,
Lubinski J,
Sukiennicki G,
Barkardottir RB,
Plante M,
Simard J,
Soucy P,
Montagna M,
Tognazzo S,
Teixeira MR,
Pankratz VS,
Wang X,
Lindor N,
Szabo CI,
Kauff N,
Vijai J,
Aghajanian CA,
Pfeiler G,
Berger A,
Singer CF,
Tea MK,
Phelan CM,
Greene MH,
Mai PL,
Rennert G,
Mulligan AM,
Tchatchou S,
Andrulis IL,
Glendon G,
Toland AE,
Jensen UB,
Kruse TA,
Thomassen M,
Bojesen A,
Zidan J,
Friedman E,
Laitman Y,
Soller M,
Liljegren A,
Arver B,
Einbeigi Z,
Stenmark-Askmalm M,
Olopade OI,
Nussbaum RL,
Rebbeck TR,
Nathanson KL,
Domchek SM,
Lu KH,
Karlan BY,
Walsh C,
Lester J,
Hein A,
Ekici AB,
Beckmann MW,
Fasching PA,
Lambrechts D,
Van Nieuwenhuysen E,
Vergote I,
Lambrechts S,
Dicks E,
Doherty JA,
Wicklund KG,
Rossing MA,
Rudolph A,
Chang-Claude J,
Wang-Gohrke S,
Eilber U,
Moysich KB,
Odunsi K,
Sucheston L,
Lele S,
Wilkens LR,
Goodman MT,
Thompson PJ,
Shvetsov YB,
Runnebaum IB,
Dürst M,
Hillemanns P,
Dörk T,
Antonenkova N,
Bogdanova N,
Leminen A,
Pelttari LM,
Butzow R,
Modugno F,
Kelley JL,
Edwards RP,
Ness RB,
du Bois A,
Heitz F,
Schwaab I,
Harter P,
Matsuo K,
Hosono S,
Orsulic S,
Jensen A,
Kjaer SK,
Hogdall E,
Hasmad HN,
Azmi MA,
Teo SH,
Woo YL,
Fridley BL,
Goode EL,
Cunningham JM,
Vierkant RA,
Bruinsma F,
Giles GG,
Liang D,
Hildebrandt MA,
Wu X,
Levine DA,
Bisogna M,
Berchuck A,
Iversen ES,
Schildkraut JM,
Concannon P,
Weber RP,
Cramer DW,
Terry KL,
Poole EM,
Tworoger SS,
Bandera EV,
Orlow I,
Olson SH,
Krakstad C,
Salvesen HB,
Tangen IL,
Bjorge L,
van Altena AM,
Aben KK,
Kiemeney LA,
Massuger LF,
Kellar M,
Brooks-Wilson A,
Kelemen LE,
Cook LS,
Le ND,
Cybulski C,
Yang H,
Lissowska J,
Brinton LA,
Wentzensen N,
Hogdall C,
Lundvall L,
Nedergaard L,
Baker H,
Song H,
Eccles D,
McNeish I,
Paul J,
Carty K,
Siddiqui N,
Glasspool R,
Whittemore AS,
Rothstein JH,
McGuire V,
Sieh W,
Ji BT,
Zheng W,
Shu XO,
Gao YT,
Rosen B,
Risch HA,
McLaughlin JR,
Narod SA,
Monteiro AN,
Chen A,
Lin HY,
Permuth-Wey J,
Sellers TA,
Tsai YY,
Chen Z,
Ziogas A,
Anton-Culver H,
Gentry-Maharaj A,
Menon U,
Harrington P,
Lee AW,
Wu AH,
Pearce CL,
Coetzee G,
Pike MC,
Dansonka-Mieszkowska A,
Timorek A,
Rzepecka IK,
Kupryjanczyk J,
Freedman M,
Noushmehr H,
Easton DF,
Offit K,
Couch FJ,
Gayther S,
Pharoah PP,
Antoniou AC,
Chenevix-Trench G
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3
Hou S,
Du L,
Lei B,
Pang CP,
Zhang M,
Zhuang W,
Zhang M,
Huang L,
Gong B,
Wang M,
Zhang Q,
Hu K
and 17 more — show all
Zhou Q,
Qi J,
Wang C,
Tian Y,
Ye Z,
Liang L,
Yu H,
Li H,
Zhou Y,
Cao Q,
Liu Y,
Bai L,
Liao D,
Kijlstra A,
Xu J,
Yang Z,
Yang P
Nature genetics · 2014 · PMID 25108386
2 pages
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.