For researchers
Is your paper here?
2,660 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.
80 matches for
UK Biobank,
showing the first 20.
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Coleman JRI,
Peyrot WJ,
Purves KL,
Davis KAS,
Rayner C,
Choi SW,
Hübel C,
Gaspar HA,
Kan C,
Van der Auwera S,
Adams MJ,
Lyall DM
and 14 more — show all
Choi KW,
Dunn EC,
Vassos E,
Danese A,
Maughan B,
Grabe HJ,
Lewis CM,
O'Reilly PF,
McIntosh AM,
Smith DJ,
Wray NR,
Hotopf M,
Eley TC,
Breen G
on the behalf of Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Molecular psychiatry · 2020 · PMID 31969693 · open access
2 pages
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network
Palmer MR,
Kim DS,
Crosslin DR,
Stanaway IB,
Rosenthal EA,
Carrell DS,
Cronkite DJ,
Gordon A,
Du X,
Li YK,
Williams MS,
Weng C
and 12 more — show all
Feng Q,
Li R,
Pendergrass SA,
Hakonarson H,
Fasel D,
Sohn S,
Sleiman P,
Handelman SK,
Speliotes E,
Kullo IJ,
Larson EB,
Jarvik GP
eMERGE Consortium
Genetic epidemiology · 2021 · PMID 32964493 · open access
2 pages
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies
Sun Q,
Graff M,
Rowland B,
Wen J,
Huang L,
Miller-Fleming TW,
Haessler J,
Preuss MH,
Chai JF,
Lee MP,
Avery CL,
Cheng CY
and 7 more — show all
Journal of human genetics · 2022 · PMID 34376796 · open access
2 pages
Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Guggenheim JA,
Clark R,
Cui J,
Terry L,
Patasova K,
Haarman AEG,
Musolf AM,
Verhoeven VJM,
Klaver CCW,
Bailey-Wilson JE,
Hysi PG,
Williams C
CREAM Consortium · UK Biobank Eye Vision Consortium
Human molecular genetics · 2022 · PMID 35022715 · open access
2 pages
Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank
McDonald MN,
Lakshman Kumar P,
Srinivasasainagendra V,
Nair A,
Rocco AP,
Wilson AC,
Chiles JW,
Richman JS,
Pinson SA,
Dennis RA,
Jagadale V,
Brown CJ
and 4 more — show all
Nature genetics · 2022 · PMID 36411363
2 pages
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease
Klarin D,
Zhu QM,
Emdin CA,
Chaffin M,
Horner S,
McMillan BJ,
Leed A,
Weale ME,
Spencer CCA,
Aguet F,
Segrè AV,
Ardlie KG
and 4 more — show all
CARDIoGRAMplusC4D Consortium
Nature genetics · 2017 · PMID 28714974 · open access
1 page
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank
Hall LS,
Adams MJ,
Arnau-Soler A,
Clarke TK,
Howard DM,
Zeng Y,
Davies G,
Hagenaars SP,
Maria Fernandez-Pujals A,
Gibson J,
Wigmore EM,
Boutin TS
and 7 more — show all
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Translational psychiatry · 2018 · PMID 29317602 · open access
1 page
Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort
Strawbridge RJ,
Ward J,
Cullen B,
Tunbridge EM,
Hartz S,
Bierut L,
Horton A,
Bailey MES,
Graham N,
Ferguson A,
Lyall DM,
Mackay D
and 7 more — show all
Translational psychiatry · 2018 · PMID 29391395 · open access
1 page
Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank
Valette K,
Li Z,
Bon-Baret V,
Chignon A,
Bérubé JC,
Eslami A,
Lamothe J,
Gaudreault N,
Joubert P,
Obeidat M,
van den Berge M,
Timens W
and 11 more — show all
Sin DD,
Nickle DC,
Hao K,
Labbé C,
Godbout K,
Côté A,
Laviolette M,
Boulet LP,
Mathieu P,
Thériault S,
Bossé Y
Communications biology · 2021 · PMID 34103634 · open access
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.