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84 matches for
He P,
showing the first 20.
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans
Guggenheim JA,
McMahon G,
Kemp JP,
Akhtar S,
St Pourcain B,
Northstone K,
Ring SM,
Evans DM,
Smith GD,
Timpson NJ,
Williams C
Molecular vision · 2013 · PMID 23401653 · open access
1 page
Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries
Futema M,
Shah S,
Cooper JA,
Li K,
Whittall RA,
Sharifi M,
Goldberg O,
Drogari E,
Mollaki V,
Wiegman A,
Defesche J,
D'Agostino MN
and 14 more — show all
D'Angelo A,
Rubba P,
Fortunato G,
Waluś-Miarka M,
Hegele RA,
Aderayo Bamimore M,
Durst R,
Leitersdorf E,
Mulder MT,
Roeters van Lennep JE,
Sijbrands EJ,
Whittaker JC,
Talmud PJ,
Humphries SE
Clinical chemistry · 2015 · PMID 25414277
1 page
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Power RA,
Tansey KE,
Buttenschøn HN,
Cohen-Woods S,
Bigdeli T,
Hall LS,
Kutalik Z,
Lee SH,
Ripke S,
Steinberg S,
Teumer A,
Viktorin A
and 64 more — show all
Wray NR,
Arolt V,
Baune BT,
Boomsma DI,
Børglum AD,
Byrne EM,
Castelao E,
Craddock N,
Craig IW,
Dannlowski U,
Deary IJ,
Degenhardt F,
Forstner AJ,
Gordon SD,
Grabe HJ,
Grove J,
Hamilton SP,
Hayward C,
Heath AC,
Hocking LJ,
Homuth G,
Hottenga JJ,
Kloiber S,
Krogh J,
Landén M,
Lang M,
Levinson DF,
Lichtenstein P,
Lucae S,
MacIntyre DJ,
Madden P,
Magnusson PKE,
Martin NG,
McIntosh AM,
Middeldorp CM,
Milaneschi Y,
Montgomery GW,
Mors O,
Müller-Myhsok B,
Nyholt DR,
Oskarsson H,
Owen MJ,
Padmanabhan S,
Penninx BWJH,
Pergadia ML,
Porteous DJ,
Potash JB,
Preisig M,
Rivera M,
Shi J,
Shyn SI,
Sigurdsson E,
Smit JH,
Smith BH,
Stefansson H,
Stefansson K,
Strohmaier J,
Sullivan PF,
Thomson P,
Thorgeirsson TE,
Van der Auwera S,
Weissman MM,
Breen G,
Lewis CM
CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium
Biological psychiatry · 2017 · PMID 27519822 · 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
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
Martin J,
Walters RK,
Demontis D,
Mattheisen M,
Lee SH,
Robinson E,
Brikell I,
Ghirardi L,
Larsson H,
Lichtenstein P,
Eriksson N,
Werge T
and 13 more — show all
Mortensen PB,
Pedersen MG,
Mors O,
Nordentoft M,
Hougaard DM,
Bybjerg-Grauholm J,
Wray NR,
Franke B,
Faraone SV,
O'Donovan MC,
Thapar A,
Børglum AD,
Neale BM
23andMe Research Team · Psychiatric Genomics Consortium: ADHD Subgroup and 1 more consortia
Biological psychiatry · 2018 · PMID 29325848 · open access
1 page
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia
Pasman JA,
Verweij KJH,
Gerring Z,
Stringer S,
Sanchez-Roige S,
Treur JL,
Abdellaoui A,
Nivard MG,
Baselmans BML,
Ong JS,
Ip HF,
van der Zee MD
and 36 more — show all
Bartels M,
Day FR,
Fontanillas P,
Elson SL,
de Wit H,
Davis LK,
MacKillop J,
Derringer JL,
Branje SJT,
Hartman CA,
Heath AC,
van Lier PAC,
Madden PAF,
Mägi R,
Meeus W,
Montgomery GW,
Oldehinkel AJ,
Pausova Z,
Ramos-Quiroga JA,
Paus T,
Ribases M,
Kaprio J,
Boks MPM,
Bell JT,
Spector TD,
Gelernter J,
Boomsma DI,
Martin NG,
MacGregor S,
Perry JRB,
Palmer AA,
Posthuma D,
Munafò MR,
Gillespie NA,
Derks EM,
Vink JM
23andMe Research Team · Substance Use Disorders Working Group of the Psychiatric Genomics Consortium and 1 more consortia
Nature neuroscience · 2018 · PMID 30150663
1 page
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Watson HJ,
Yilmaz Z,
Thornton LM,
Hübel C,
Coleman JRI,
Gaspar HA,
Bryois J,
Hinney A,
Leppä VM,
Mattheisen M,
Medland SE,
Ripke S
and 198 more — show all
Yao S,
Giusti-Rodríguez P,
Hanscombe KB,
Purves KL,
Adan RAH,
Alfredsson L,
Ando T,
Andreassen OA,
Baker JH,
Berrettini WH,
Boehm I,
Boni C,
Perica VB,
Buehren K,
Burghardt R,
Cassina M,
Cichon S,
Clementi M,
Cone RD,
Courtet P,
Crow S,
Crowley JJ,
Danner UN,
Davis OSP,
de Zwaan M,
Dedoussis G,
Degortes D,
DeSocio JE,
Dick DM,
Dikeos D,
Dina C,
Dmitrzak-Weglarz M,
Docampo E,
Duncan LE,
Egberts K,
Ehrlich S,
Escaramís G,
Esko T,
Estivill X,
Farmer A,
Favaro A,
Fernández-Aranda F,
Fichter MM,
Fischer K,
Föcker M,
Foretova L,
Forstner AJ,
Forzan M,
Franklin CS,
Gallinger S,
Giegling I,
Giuranna J,
Gonidakis F,
Gorwood P,
Mayora MG,
Guillaume S,
Guo Y,
Hakonarson H,
Hatzikotoulas K,
Hauser J,
Hebebrand J,
Helder SG,
Herms S,
Herpertz-Dahlmann B,
Herzog W,
Huckins LM,
Hudson JI,
Imgart H,
Inoko H,
Janout V,
Jiménez-Murcia S,
Julià A,
Kalsi G,
Kaminská D,
Kaprio J,
Karhunen L,
Karwautz A,
Kas MJH,
Kennedy JL,
Keski-Rahkonen A,
Kiezebrink K,
Kim YR,
Klareskog L,
Klump KL,
Knudsen GPS,
La Via MC,
Le Hellard S,
Levitan RD,
Li D,
Lilenfeld L,
Lin BD,
Lissowska J,
Luykx J,
Magistretti PJ,
Maj M,
Mannik K,
Marsal S,
Marshall CR,
Mattingsdal M,
McDevitt S,
McGuffin P,
Metspalu A,
Meulenbelt I,
Micali N,
Mitchell K,
Monteleone AM,
Monteleone P,
Munn-Chernoff MA,
Nacmias B,
Navratilova M,
Ntalla I,
O'Toole JK,
Ophoff RA,
Padyukov L,
Palotie A,
Pantel J,
Papezova H,
Pinto D,
Rabionet R,
Raevuori A,
Ramoz N,
Reichborn-Kjennerud T,
Ricca V,
Ripatti S,
Ritschel F,
Roberts M,
Rotondo A,
Rujescu D,
Rybakowski F,
Santonastaso P,
Scherag A,
Scherer SW,
Schmidt U,
Schork NJ,
Schosser A,
Seitz J,
Slachtova L,
Slagboom PE,
Slof-Op 't Landt MCT,
Slopien A,
Sorbi S,
Świątkowska B,
Szatkiewicz JP,
Tachmazidou I,
Tenconi E,
Tortorella A,
Tozzi F,
Treasure J,
Tsitsika A,
Tyszkiewicz-Nwafor M,
Tziouvas K,
van Elburg AA,
van Furth EF,
Wagner G,
Walton E,
Widen E,
Zeggini E,
Zerwas S,
Zipfel S,
Bergen AW,
Boden JM,
Brandt H,
Crawford S,
Halmi KA,
Horwood LJ,
Johnson C,
Kaplan AS,
Kaye WH,
Mitchell JE,
Olsen CM,
Pearson JF,
Pedersen NL,
Strober M,
Werge T,
Whiteman DC,
Woodside DB,
Stuber GD,
Gordon S,
Grove J,
Henders AK,
Juréus A,
Kirk KM,
Larsen JT,
Parker R,
Petersen L,
Jordan J,
Kennedy M,
Montgomery GW,
Wade TD,
Birgegård A,
Lichtenstein P,
Norring C,
Landén M,
Martin NG,
Mortensen PB,
Sullivan PF,
Breen G,
Bulik CM
Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2019 · PMID 31308545
1 page
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder
Demontis D,
Walters RK,
Rajagopal VM,
Waldman ID,
Grove J,
Als TD,
Dalsgaard S,
Ribasés M,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Werge T,
Nordentoft M
and 8 more — show all
ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
Nature communications · 2021 · PMID 33495439 · open access
1 page
Longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis: a genome-wide association study
Allen RJ,
Oldham JM,
Jenkins DA,
Leavy OC,
Guillen-Guio B,
Melbourne CA,
Ma SF,
Jou J,
Kim JS,
Fahy WA,
Oballa E,
Hubbard RB
and 19 more — show all
Navaratnam V,
Braybrooke R,
Saini G,
Roach KM,
Tobin MD,
Hirani N,
Whyte MKB,
Kaminski N,
Zhang Y,
Martinez FJ,
Linderholm AL,
Adegunsoye A,
Strek ME,
Maher TM,
Molyneaux PL,
Flores C,
Noth I,
Gisli Jenkins R,
Wain LV
CleanUP-IPF Investigators of the Pulmonary Trials Cooperative
The Lancet. Respiratory medicine · 2023 · PMID 35985358 · open access
1 page
Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions
Lindström S,
Wang L,
Feng H,
Majumdar A,
Huo S,
Macdonald J,
Harrison T,
Turman C,
Chen H,
Mancuso N,
Bammler T,
Gallinger S
and 49 more — show all
Gruber SB,
Gunter MJ,
Le Marchand L,
Moreno V,
Offit K,
De Vivo I,
O'Mara TA,
Spurdle AB,
Tomlinson I,
Fitzgerald R,
Gharahkhani P,
Gockel I,
Jankowski J,
Macgregor S,
Schumacher J,
Barnholtz-Sloan J,
Bondy ML,
Houlston RS,
Jenkins RB,
Melin B,
Wrensch M,
Brennan P,
Christiani DC,
Johansson M,
Mckay J,
Aldrich MC,
Amos CI,
Landi MT,
Tardon A,
Bishop DT,
Demenais F,
Goldstein AM,
Iles MM,
Kanetsky PA,
Law MH,
Amundadottir LT,
Stolzenberg-Solomon R,
Wolpin BM,
Klein A,
Petersen G,
Risch H,
Chanock SJ,
Purdue MP,
Scelo G,
Pharoah P,
Kar S,
Hung RJ,
Pasaniuc B,
Kraft P
Breast Cancer Association Consortium (BCAC) · Colorectal Transdisciplinary Study (CORECT), Colon Cancer Family Registry Study (CCFR), Genetics And Epidemiology Of Colorectal Cancer Consortium (GECCO) and 5 more consortia
Journal of the National Cancer Institute · 2023 · PMID 36929942
1 page
Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders
Hatoum AS,
Colbert SMC,
Johnson EC,
Huggett SB,
Deak JD,
Pathak G,
Jennings MV,
Paul SE,
Karcher NR,
Hansen I,
Baranger DAA,
Edwards A
and 10 more — show all
Substance Use Disorder Working Group of the Psychiatric Genomics Consortium
Nature. Mental health · 2023 · PMID 37250466
1 page
Meta-GWAS on PCSK9 concentrations reveals associations of novel loci outside the PCSK9 locus in White populations
Kheirkhah A,
Schachtl-Riess JF,
Lamina C,
Di Maio S,
Koller A,
Schönherr S,
Coassin S,
Forer L,
Sekula P,
Gieger C,
Peters A,
Köttgen A
and 2 more — show all
Atherosclerosis · 2023 · PMID 37989062
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
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.