For researchers
Is your paper here?
2,657 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.
7 matches for
Haley C.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants
Nagy R,
Boutin TS,
Marten J,
Huffman JE,
Kerr SM,
Campbell A,
Evenden L,
Gibson J,
Amador C,
Howard DM,
Navarro P,
Morris A
and 13 more — show all
Deary IJ,
Hocking LJ,
Padmanabhan S,
Smith BH,
Joshi P,
Wilson JF,
Hastie ND,
Wright AF,
McIntosh AM,
Porteous DJ,
Haley CS,
Vitart V,
Hayward C
Genome medicine · 2017 · PMID 28270201 · open access
12 pages+
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Howard DM,
Adams MJ,
Shirali M,
Clarke TK,
Marioni RE,
Davies G,
Coleman JRI,
Alloza C,
Shen X,
Barbu MC,
Wigmore EM,
Gibson J
and 9 more — show all
23andMe Research Team
Nature communications · 2018 · PMID 29662059 · open access
12 pages+
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Folkersen L,
Gustafsson S,
Wang Q,
Hansen DH,
Hedman ÅK,
Schork A,
Page K,
Zhernakova DV,
Wu Y,
Peters J,
Eriksson N,
Bergen SE
and 71 more — show all
Boutin TS,
Bretherick AD,
Enroth S,
Kalnapenkis A,
Gådin JR,
Suur BE,
Chen Y,
Matic L,
Gale JD,
Lee J,
Zhang W,
Quazi A,
Ala-Korpela M,
Choi SH,
Claringbould A,
Danesh J,
Davey Smith G,
de Masi F,
Elmståhl S,
Engström G,
Fauman E,
Fernandez C,
Franke L,
Franks PW,
Giedraitis V,
Haley C,
Hamsten A,
Ingason A,
Johansson Å,
Joshi PK,
Lind L,
Lindgren CM,
Lubitz S,
Palmer T,
Macdonald-Dunlop E,
Magnusson M,
Melander O,
Michaelsson K,
Morris AP,
Mägi R,
Nagle MW,
Nilsson PM,
Nilsson J,
Orho-Melander M,
Polasek O,
Prins B,
Pålsson E,
Qi T,
Sjögren M,
Sundström J,
Surendran P,
Võsa U,
Werge T,
Wernersson R,
Westra HJ,
Yang J,
Zhernakova A,
Ärnlöv J,
Fu J,
Smith JG,
Esko T,
Hayward C,
Gyllensten U,
Landen M,
Siegbahn A,
Wilson JF,
Wallentin L,
Butterworth AS,
Holmes MV,
Ingelsson E,
Mälarstig A
Nature metabolism · 2020 · PMID 33067605
12 pages+
Genetic architecture reconciles linkage and association studies of complex traits
Sidorenko J,
Couvy-Duchesne B,
Kemper KE,
Moen GH,
Bhatta L,
Åsvold BO,
Mägi R,
Ani A,
Wang R,
Nolte IM,
Gordon S,
Hayward C
and 15 more — show all
Campbell A,
Benjamin DJ,
Cesarini D,
Evans DM,
Goddard ME,
Haley CS,
Porteous D,
Medland SE,
Martin NG,
Snieder H,
Metspalu A,
Hveem K,
Brumpton B,
Visscher PM,
Yengo L
Estonian Biobank Research Team · Lifelines Cohort Study
Nature genetics · 2024 · PMID 39375568
12 pages+
Genetic mechanisms of critical illness in COVID-19
Pairo-Castineira E,
Clohisey S,
Klaric L,
Bretherick AD,
Rawlik K,
Pasko D,
Walker S,
Parkinson N,
Fourman MH,
Russell CD,
Furniss J,
Richmond A
and 54 more — show all
Gountouna E,
Wrobel N,
Harrison D,
Wang B,
Wu Y,
Meynert A,
Griffiths F,
Oosthuyzen W,
Kousathanas A,
Moutsianas L,
Yang Z,
Zhai R,
Zheng C,
Grimes G,
Beale R,
Millar J,
Shih B,
Keating S,
Zechner M,
Haley C,
Porteous DJ,
Hayward C,
Yang J,
Knight J,
Summers C,
Shankar-Hari M,
Klenerman P,
Turtle L,
Ho A,
Moore SC,
Hinds C,
Horby P,
Nichol A,
Maslove D,
Ling L,
McAuley D,
Montgomery H,
Walsh T,
Pereira AC,
Renieri A,
Shen X,
Ponting CP,
Fawkes A,
Tenesa A,
Caulfield M,
Scott R,
Rowan K,
Murphy L,
Openshaw PJM,
Semple MG,
Law A,
Vitart V,
Wilson JF,
Baillie JK
GenOMICC Investigators · ISARIC4C Investigators and 4 more consortia
Nature · 2021 · PMID 33307546
2 pages
Modulation of genetic associations with serum urate levels by body-mass-index in humans
Huffman JE,
Albrecht E,
Teumer A,
Mangino M,
Kapur K,
Johnson T,
Kutalik Z,
Pirastu N,
Pistis G,
Lopez LM,
Haller T,
Salo P
and 108 more — show all
Goel A,
Li M,
Tanaka T,
Dehghan A,
Ruggiero D,
Malerba G,
Smith AV,
Nolte IM,
Portas L,
Phipps-Green A,
Boteva L,
Navarro P,
Johansson A,
Hicks AA,
Polasek O,
Esko T,
Peden JF,
Harris SE,
Murgia F,
Wild SH,
Tenesa A,
Tin A,
Mihailov E,
Grotevendt A,
Gislason GK,
Coresh J,
D'Adamo P,
Ulivi S,
Vollenweider P,
Waeber G,
Campbell S,
Kolcic I,
Fisher K,
Viigimaa M,
Metter JE,
Masciullo C,
Trabetti E,
Bombieri C,
Sorice R,
Döring A,
Reischl E,
Strauch K,
Hofman A,
Uitterlinden AG,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Dalbeth N,
Stamp L,
Smit JH,
Kirin M,
Nagaraja R,
Nauck M,
Schurmann C,
Budde K,
Farrington SM,
Theodoratou E,
Jula A,
Salomaa V,
Sala C,
Hengstenberg C,
Burnier M,
Mägi R,
Klopp N,
Kloiber S,
Schipf S,
Ripatti S,
Cabras S,
Soranzo N,
Homuth G,
Nutile T,
Munroe PB,
Hastie N,
Campbell H,
Rudan I,
Cabrera C,
Haley C,
Franco OH,
Merriman TR,
Gudnason V,
Pirastu M,
Penninx BW,
Snieder H,
Metspalu A,
Ciullo M,
Pramstaller PP,
van Duijn CM,
Ferrucci L,
Gambaro G,
Deary IJ,
Dunlop MG,
Wilson JF,
Gasparini P,
Gyllensten U,
Spector TD,
Wright AF,
Hayward C,
Watkins H,
Perola M,
Bochud M,
Kao WH,
Caulfield M,
Toniolo D,
Völzke H,
Gieger C,
Köttgen A,
Vitart V
PloS one · 2015 · PMID 25811787 · 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
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.