For researchers
Is your paper here?
2,681 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.
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Burns K,
Mullin BH,
Moolhuijsen LME,
Laisk T,
Tyrmi JS,
Cui J,
Actkins KV,
Louwers YV,
Davis LK,
Dudbridge F,
Azziz R,
Goodarzi MO
and 7 more — show all
Estonian Biobank Research Team · FinnGen and 1 more consortia
BMC genomics · 2024 · PMID 38408933 · open access
1 page
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
Comprehensive Association Analyses of Extraintestinal Manifestations in Inflammatory Bowel Disease
Khrom M,
Long M,
Dube S,
Robbins L,
Botwin GJ,
Yang S,
Mengesha E,
Li D,
Naito T,
Bonthala NN,
Ha C,
Melmed G
and 23 more — show all
Rabizadeh S,
Syal G,
Vasiliauskas E,
Ziring D,
Brant SR,
Cho J,
Duerr RH,
Rioux J,
Schumm P,
Silverberg M,
Ananthakrishnan AN,
Faubion WA,
Jabri B,
Lira SA,
Newberry RD,
Sandler RS,
Xavier RJ,
Kugathasan S,
Hercules D,
Targan SR,
Sartor RB,
Haritunians T,
McGovern DPB
Gastroenterology · 2024 · PMID 38490347
1 page
Genome-wide analysis of spina bifida risk variants in a case-control study from Bangladesh
Tindula G,
Issac B,
Mukherjee SK,
Ekramullah SM,
Arman DM,
Islam J,
Suchanda HS,
Sun L,
Rockowitz S,
Christiani DC,
Warf BC,
Mazumdar M
Birth defects research · 2024 · PMID 38526198
1 page
A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children
Lin YP,
Shi Y,
Zhang R,
Xue X,
Rao S,
Yin L,
Lui KFH,
Pan DJ,
Maurer U,
Choy KW,
Paracchini S,
McBride C
and 1 more — show all
NPJ science of learning · 2024 · PMID 38538593 · open access
1 page
A genomic association study revealing subphenotypes of childhood steroid-sensitive nephrotic syndrome in a larger genomic sequencing cohort
Chan H,
Ni F,
Zhao B,
Jiang H,
Ding J,
Wang L,
Wang X,
Cui J,
Feng S,
Gao X,
Yang X,
Chi H
and 11 more — show all
Lee H,
Chen X,
Li X,
Jiao J,
Wu D,
Zhang G,
Wang M,
Cun Y,
Ruan X,
Yang H,
Li Q
Genes & diseases · 2024 · PMID 38560502 · open access
1 page
APOE4 homozygozity represents a distinct genetic form of Alzheimer's disease
Fortea J,
Pegueroles J,
Alcolea D,
Belbin O,
Dols-Icardo O,
Vaqué-Alcázar L,
Videla L,
Gispert JD,
Suárez-Calvet M,
Johnson SC,
Sperling R,
Bejanin A
and 2 more — show all
Nature medicine · 2024 · PMID 38710950
1 page
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
Dareng EO,
Coetzee SG,
Tyrer JP,
Peng PC,
Rosenow W,
Chen S,
Davis BD,
Dezem FS,
Seo JH,
Nameki R,
Reyes AL,
Aben KKH
and 141 more — show all
Anton-Culver H,
Antonenkova NN,
Aravantinos G,
Bandera EV,
Beane Freeman LE,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernardini MQ,
Bjorge L,
Black A,
Bogdanova NV,
Bolton KL,
Brenton JD,
Budzilowska A,
Butzow R,
Cai H,
Campbell I,
Cannioto R,
Chang-Claude J,
Chanock SJ,
Chen K,
Chenevix-Trench G,
Chiew YE,
Cook LS,
DeFazio A,
Dennis J,
Doherty JA,
Dörk T,
du Bois A,
Dürst M,
Eccles DM,
Ene G,
Fasching PA,
Flanagan JM,
Fortner RT,
Fostira F,
Gentry-Maharaj A,
Giles GG,
Goodman MT,
Gronwald J,
Haiman CA,
Håkansson N,
Heitz F,
Hildebrandt MAT,
Høgdall E,
Høgdall CK,
Huang RY,
Jensen A,
Jones ME,
Kang D,
Karlan BY,
Karnezis AN,
Kelemen LE,
Kennedy CJ,
Khusnutdinova EK,
Kiemeney LA,
Kjaer SK,
Kupryjanczyk J,
Labrie M,
Lambrechts D,
Larson MC,
Le ND,
Lester J,
Li L,
Lubiński J,
Lush M,
Marks JR,
Matsuo K,
May T,
McLaughlin JR,
McNeish IA,
Menon U,
Missmer S,
Modugno F,
Moffitt M,
Monteiro AN,
Moysich KB,
Narod SA,
Nguyen-Dumont T,
Odunsi K,
Olsson H,
Onland-Moret NC,
Park SK,
Pejovic T,
Permuth JB,
Piskorz A,
Prokofyeva D,
Riggan MJ,
Risch HA,
Rodríguez-Antona C,
Rossing MA,
Sandler DP,
Setiawan VW,
Shan K,
Song H,
Southey MC,
Steed H,
Sutphen R,
Swerdlow AJ,
Teo SH,
Terry KL,
Thompson PJ,
Vestrheim Thomsen LC,
Titus L,
Trabert B,
Travis R,
Tworoger SS,
Valen E,
Van Nieuwenhuysen E,
Edwards DV,
Vierkant RA,
Webb PM,
Weinberg CR,
Weise RM,
Wentzensen N,
White E,
Winham SJ,
Wolk A,
Woo YL,
Wu AH,
Yan L,
Yannoukakos D,
Zeinomar N,
Zheng W,
Ziogas A,
Berchuck A,
Goode EL,
Huntsman DG,
Pearce CL,
Ramus SJ,
Sellers TA,
Freedman ML,
Lawrenson K,
Schildkraut JM,
Hazelett D,
Plummer JT,
Kar S,
Jones MR,
Pharoah PDP,
Gayther SA
AOCS Group · OPAL Study Group and 1 more consortia
American journal of human genetics · 2024 · PMID 38723632
1 page
Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study
Borrego-Yaniz G,
Ortiz-Fernández L,
Madrid-Paredes A,
Kerick M,
Hernández-Rodríguez J,
Mackie SL,
Vaglio A,
Castañeda S,
Solans R,
Mestre-Torres J,
Khalidi N,
Langford CA
and 39 more — show all
Ytterberg S,
Beretta L,
Govoni M,
Emmi G,
Cimmino MA,
Witte T,
Neumann T,
Holle J,
Schönau V,
Pugnet G,
Papo T,
Haroche J,
Mahr A,
Mouthon L,
Molberg Ø,
Diamantopoulos AP,
Voskuyl A,
Daikeler T,
Berger CT,
Molloy ES,
Blockmans D,
van Sleen Y,
Iles M,
Sorensen L,
Luqmani R,
Reynolds G,
Bukhari M,
Bhagat S,
Ortego-Centeno N,
Brouwer E,
Lamprecht P,
Klapa S,
Salvarani C,
Merkel PA,
Cid MC,
González-Gay MA,
Morgan AW,
Martin J,
Márquez A
Spanish GCA Group · UK GCA Consortium and 1 more consortia
The Lancet. Rheumatology · 2024 · PMID 38734017 · open access
1 page
Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry
Brandenburg JT,
Chen WC,
Boua PR,
Govender MA,
Agongo G,
Micklesfield LK,
Sorgho H,
Tollman S,
Asiki G,
Mashinya F,
Hazelhurst S,
Morris AP
and 2 more — show all
Frontiers in genetics · 2024 · PMID 38812969 · open access
1 page
Vitamin D for the Prevention of Disease: An Endocrine Society Clinical Practice Guideline
Demay MB,
Pittas AG,
Bikle DD,
Diab DL,
Kiely ME,
Lazaretti-Castro M,
Lips P,
Mitchell DM,
Murad MH,
Powers S,
Rao SD,
Scragg R
and 4 more — show all
The Journal of clinical endocrinology and metabolism · 2024 · PMID 38828931
1 page
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer
Sun X,
Verma SP,
Jia G,
Wang X,
Ping J,
Guo X,
Shu XO,
Chen J,
Derkach A,
Cai Q,
Liang X,
Long J
and 34 more — show all
Offit K,
Oh JH,
Reiner AS,
Watt GP,
Woods M,
Yang Y,
Ambrosone CB,
Ambs S,
Chen Y,
Concannon P,
Garcia-Closas M,
Gu J,
Haiman CA,
Hu JJ,
Huo D,
John EM,
Knight JA,
Li CI,
Lynch CF,
Mellemkjær L,
Nathanson KL,
Nemesure B,
Olopade OI,
Olshan AF,
Pal T,
Palmer JR,
Press MF,
Sanderson M,
Sandler DP,
Troester MA,
Zheng W,
Bernstein JL,
Buas MF,
Shu X
Cancer research · 2024 · PMID 38832928
1 page
Showing the most-cited first. The list is rebuilt from the pages every hour, so a paper
appears here the moment a page starts resting on it — and disappears if that page stops.
Not finding yours is not a judgement. This catalogue is assembled from what a small team
could read, and it is thinnest outside European-ancestry cohorts — which we say on the
pages themselves, in the
graph and in each
condition's open questions.
Tell us what we are missing →
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.