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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.
70 matches for
23andMe Research team,
showing the first 20.
The phenotypic and genetic association between endometriosis and immunological diseases
Shigesi N,
Harris HR,
Fang H,
Ndungu A,
Lincoln MR,
Cotsapas C,
Knight J,
Missmer SA,
Morris AP,
Becker CM,
Rahmioglu N,
Zondervan KT
International Endometriosis Genome Consortium · 23andMe Research Team
Human reproduction (Oxford, England) · 2025 · PMID 40262193 · open access
10 pages
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Demontis D,
Walters RK,
Martin J,
Mattheisen M,
Als TD,
Agerbo E,
Baldursson G,
Belliveau R,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Cerrato F,
Chambert K
and 69 more — show all
Churchhouse C,
Dumont A,
Eriksson N,
Gandal M,
Goldstein JI,
Grasby KL,
Grove J,
Gudmundsson OO,
Hansen CS,
Hauberg ME,
Hollegaard MV,
Howrigan DP,
Huang H,
Maller JB,
Martin AR,
Martin NG,
Moran J,
Pallesen J,
Palmer DS,
Pedersen CB,
Pedersen MG,
Poterba T,
Poulsen JB,
Ripke S,
Robinson EB,
Satterstrom FK,
Stefansson H,
Stevens C,
Turley P,
Walters GB,
Won H,
Wright MJ,
Andreassen OA,
Asherson P,
Burton CL,
Boomsma DI,
Cormand B,
Dalsgaard S,
Franke B,
Gelernter J,
Geschwind D,
Hakonarson H,
Haavik J,
Kranzler HR,
Kuntsi J,
Langley K,
Lesch KP,
Middeldorp C,
Reif A,
Rohde LA,
Roussos P,
Schachar R,
Sklar P,
Sonuga-Barke EJS,
Sullivan PF,
Thapar A,
Tung JY,
Waldman ID,
Medland SE,
Stefansson K,
Nordentoft M,
Hougaard DM,
Werge T,
Mors O,
Mortensen PB,
Daly MJ,
Faraone SV,
Børglum AD,
Neale BM
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 1 more consortia
Nature genetics · 2019 · PMID 30478444
8 pages
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
Ong JS,
An J,
Han X,
Law MH,
Nandakumar P,
Schumacher J,
Gockel I,
Bohmer A,
Jankowski J,
Palles C,
Olsen CM,
Neale RE
and 8 more — show all
23andMe Research team · Esophageal cancer consortium
Gut · 2022 · PMID 34187846 · open access
8 pages
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
and 121 more — show all
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
Sliz E,
Sobalska-Kwapis M,
Thorleifsson G,
Topbas-Selcuki NF,
Vitonis A,
Westergaard D,
Arnadottir R,
Burgdorf KS,
Campbell A,
Cheuk CSK,
Clementi C,
Cook J,
De Vivo I,
DiVasta A,
Dorien O,
Donoghue JF,
Edwards T,
Fontanillas P,
Fung JN,
Geirsson RT,
Girling JE,
Harkki P,
Harris HR,
Healey M,
Heikinheimo O,
Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
Jarvelin MR,
Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
Laivuori H,
Laufer MR,
Lindgren CM,
MacGregor S,
Mangino M,
Martin NG,
Matalliotaki C,
Matalliotakis M,
Murray AD,
Ndungu A,
Nezhat C,
Olsen CM,
Opoku-Anane J,
Padmanabhan S,
Paranjpe M,
Peters M,
Polak G,
Porteous DJ,
Rabban J,
Rexrode KM,
Romanowicz H,
Saare M,
Saavalainen L,
Schork AJ,
Sen S,
Shafrir AL,
Siewierska-Górska A,
Słomka M,
Smith BH,
Smolarz B,
Szaflik T,
Szyłło K,
Takahashi A,
Terry KL,
Tomassetti C,
Treloar SA,
Vanhie A,
Vincent K,
Vo KC,
Werring DJ,
Zeggini E,
Zervou MI,
Adachi S,
Buring JE,
Ridker PM,
D'Hooghe T,
Goulielmos GN,
Hapangama DK,
Hayward C,
Horne AW,
Low SK,
Martikainen H,
Chasman DI,
Rogers PAW,
Saunders PT,
Sirota M,
Spector T,
Strapagiel D,
Tung JY,
Whiteman DC,
Giudice LC,
Velez-Edwards DR,
Uimari O,
Kraft P,
Salumets A,
Nyholt DR,
Mägi R,
Stefansson K,
Becker CM,
Yurttas-Beim P,
Steinthorsdottir V,
Nyegaard M,
Missmer SA,
Montgomery GW,
Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
Ferreira MAR,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
Lu Y,
Grosche S,
Rüschendorf F
and 28 more — show all
Granell R,
Brumpton BM,
Fritsche LG,
Bhatta L,
Gabrielsen ME,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Emami NC,
Cavazos TB,
Witte JS,
Szwajda A,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PK,
Jorgenson E,
Karlsson R,
Paternoster L,
Boomsma DI,
Almqvist C,
Lee YA,
Koppelman GH
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
7 pages
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts
Sanchez-Roige S,
Palmer AA,
Fontanillas P,
Elson SL,
Adams MJ,
Howard DM,
Edenberg HJ,
Davies G,
Crist RC,
Deary IJ,
McIntosh AM,
Clarke TK
23andMe Research Team, the Substance Use Disorder Working Group of the Psychiatric Genomics Consortium
The American journal of psychiatry · 2019 · PMID 30336701
6 pages
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
Warrington NM,
Shevroja E,
Hemani G,
Hysi PG,
Jiang Y,
Auton A,
Boer CG,
Mangino M,
Wang CA,
Kemp JP,
McMahon G,
Medina-Gomez C
and 18 more — show all
Hickey M,
Trajanoska K,
Wolke D,
Ikram MA,
Montgomery GW,
Felix JF,
Wright MJ,
Mackey DA,
Jaddoe VW,
Martin NG,
Tung JY,
Davey Smith G,
Pennell CE,
Spector TD,
van Meurs J,
Rivadeneira F,
Medland SE,
Evans DM
23andMe Research Team
Human molecular genetics · 2018 · PMID 29659830 · open access
5 pages
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Simcoe M,
Valdes A,
Liu F,
Furlotte NA,
Evans DM,
Hemani G,
Ring SM,
Smith GD,
Duffy DL,
Zhu G,
Gordon SD,
Medland SE
and 32 more — show all
Vuckovic D,
Girotto G,
Sala C,
Catamo E,
Concas MP,
Brumat M,
Gasparini P,
Toniolo D,
Cocca M,
Robino A,
Yazar S,
Hewitt A,
Wu W,
Kraft P,
Hammond CJ,
Shi Y,
Chen Y,
Zeng C,
Klaver CCW,
Uitterlinden AG,
Ikram MA,
Hamer MA,
van Duijn CM,
Nijsten T,
Han J,
Mackey DA,
Martin NG,
Cheng CY,
Hinds DA,
Spector TD,
Kayser M,
Hysi PG
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
Liyanage UE,
MacGregor S,
Bishop DT,
Shi J,
An J,
Ong JS,
Han X,
Scolyer RA,
Martin NG,
Medland SE,
Byrne EM,
Green AC
and 14 more — show all
Saw RPM,
Thompson JF,
Stretch J,
Spillane A,
Jiang Y,
Tian C,
Gordon SG,
Duffy DL,
Olsen CM,
Whiteman DC,
Long GV,
Iles MM,
Landi MT,
Law MH
23andMe Research Team
The Journal of investigative dermatology · 2022 · PMID 34813871
5 pages
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Day F,
Karaderi T,
Jones MR,
Meun C,
He C,
Drong A,
Kraft P,
Lin N,
Huang H,
Broer L,
Magi R,
Saxena R
and 37 more — show all
Laisk T,
Urbanek M,
Hayes MG,
Thorleifsson G,
Fernandez-Tajes J,
Mahajan A,
Mullin BH,
Stuckey BGA,
Spector TD,
Wilson SG,
Goodarzi MO,
Davis L,
Obermayer-Pietsch B,
Uitterlinden AG,
Anttila V,
Neale BM,
Jarvelin MR,
Fauser B,
Kowalska I,
Visser JA,
Andersen M,
Ong K,
Stener-Victorin E,
Ehrmann D,
Legro RS,
Salumets A,
McCarthy MI,
Morin-Papunen L,
Thorsteinsdottir U,
Stefansson K,
Styrkarsdottir U,
Perry JRB,
Dunaif A,
Laven J,
Franks S,
Lindgren CM,
Welt CK
23andMe Research Team
PLoS genetics · 2018 · PMID 30566500 · open access
4 pages
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases
An J,
Gharahkhani P,
Law MH,
Ong JS,
Han X,
Olsen CM,
Neale RE,
Lai J,
Vaughan TL,
Gockel I,
Thieme R,
Böhmer AC
and 6 more — show all
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
4 pages
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Zheng T,
Ellinghaus D,
Juzenas S,
Cossais F,
Burmeister G,
Mayr G,
Jørgensen IF,
Teder-Laving M,
Skogholt AH,
Chen S,
Strege PR,
Ito G
and 73 more — show all
Banasik K,
Becker T,
Bokelmann F,
Brunak S,
Buch S,
Clausnitzer H,
Datz C,
Degenhardt F,
Doniec M,
Erikstrup C,
Esko T,
Forster M,
Frey N,
Fritsche LG,
Gabrielsen ME,
Gräßle T,
Gsur A,
Gross J,
Hampe J,
Hendricks A,
Hinz S,
Hveem K,
Jongen J,
Junker R,
Karlsen TH,
Hemmrich-Stanisak G,
Kruis W,
Kupcinskas J,
Laubert T,
Rosenstiel PC,
Röcken C,
Laudes M,
Leendertz FH,
Lieb W,
Limperger V,
Margetis N,
Mätz-Rensing K,
Németh CG,
Ness-Jensen E,
Nowak-Göttl U,
Pandit A,
Pedersen OB,
Peleikis HG,
Peuker K,
Rodriguez CL,
Rühlemann MC,
Schniewind B,
Schulzky M,
Skieceviciene J,
Tepel J,
Thomas L,
Uellendahl-Werth F,
Ullum H,
Vogel I,
Volzke H,
von Fersen L,
von Schönfels W,
Vanderwerff B,
Wilking J,
Wittig M,
Zeissig S,
Zobel M,
Zawistowski M,
Vacic V,
Sazonova O,
Noblin ES,
Farrugia G,
Beyder A,
Wedel T,
Kahlke V,
Schafmayer C,
D'Amato M,
Franke A
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
4 pages
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
and 25 more — show all
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Chang D,
Nalls MA,
Hallgrímsdóttir IB,
Hunkapiller J,
van der Brug M,
Cai F,
Kerchner GA,
Ayalon G,
Bingol B,
Sheng M,
Hinds D,
Behrens TW
and 3 more — show all
International Parkinson's Disease Genomics Consortium · 23andMe Research Team
Nature genetics · 2017 · PMID 28892059
3 pages
Discovery of 42 genome-wide significant loci associated with dyslexia
Doust C,
Fontanillas P,
Eising E,
Gordon SD,
Wang Z,
Alagöz G,
Molz B,
Pourcain BS,
Francks C,
Marioni RE,
Zhao J,
Paracchini S
and 15 more — show all
Talcott JB,
Monaco AP,
Stein JF,
Gruen JR,
Olson RK,
Willcutt EG,
DeFries JC,
Pennington BF,
Smith SD,
Wright MJ,
Martin NG,
Auton A,
Bates TC,
Fisher SE,
Luciano M
23andMe Research Team · Quantitative Trait Working Group of the GenLang Consortium
Nature genetics · 2022 · PMID 36266505 · open access
3 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.