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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.
70 matches for
23andMe Research team,
showing the first 20.
Multi-trait analysis of genome-wide association summary statistics using MTAG
Turley P,
Walters RK,
Maghzian O,
Okbay A,
Lee JJ,
Fontana MA,
Nguyen-Viet TA,
Wedow R,
Zacher M,
Furlotte NA,
Magnusson P,
Oskarsson S
and 6 more — show all
23andMe Research Team · Social Science Genetic Association Consortium
Nature genetics · 2018 · PMID 29292387 · 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+
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Tedja MS,
Wojciechowski R,
Hysi PG,
Eriksson N,
Furlotte NA,
Verhoeven VJM,
Iglesias AI,
Meester-Smoor MA,
Tompson SW,
Fan Q,
Khawaja AP,
Cheng CY
and 86 more — show all
Höhn R,
Yamashiro K,
Wenocur A,
Grazal C,
Haller T,
Metspalu A,
Wedenoja J,
Jonas JB,
Wang YX,
Xie J,
Mitchell P,
Foster PJ,
Klein BEK,
Klein R,
Paterson AD,
Hosseini SM,
Shah RL,
Williams C,
Teo YY,
Tham YC,
Gupta P,
Zhao W,
Shi Y,
Saw WY,
Tai ES,
Sim XL,
Huffman JE,
Polašek O,
Hayward C,
Bencic G,
Rudan I,
Wilson JF,
Joshi PK,
Tsujikawa A,
Matsuda F,
Whisenhunt KN,
Zeller T,
van der Spek PJ,
Haak R,
Meijers-Heijboer H,
van Leeuwen EM,
Iyengar SK,
Lass JH,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Vingerling JR,
Lehtimäki T,
Raitakari OT,
Biino G,
Concas MP,
Schwantes-An TH,
Igo RP Jr,
Cuellar-Partida G,
Martin NG,
Craig JE,
Gharahkhani P,
Williams KM,
Nag A,
Rahi JS,
Cumberland PM,
Delcourt C,
Bellenguez C,
Ried JS,
Bergen AA,
Meitinger T,
Gieger C,
Wong TY,
Hewitt AW,
Mackey DA,
Simpson CL,
Pfeiffer N,
Pärssinen O,
Baird PN,
Vitart V,
Amin N,
van Duijn CM,
Bailey-Wilson JE,
Young TL,
Saw SM,
Stambolian D,
MacGregor S,
Guggenheim JA,
Tung JY,
Hammond CJ,
Klaver CCW
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
Nagel M,
Jansen PR,
Stringer S,
Watanabe K,
de Leeuw CA,
Bryois J,
Savage JE,
Hammerschlag AR,
Skene NG,
Muñoz-Manchado AB,
White T,
Tiemeier H
and 6 more — show all
23andMe Research Team
Nature genetics · 2018 · PMID 29942085
12 pages+
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
Waage J,
Standl M,
Curtin JA,
Jessen LE,
Thorsen J,
Tian C,
Schoettler N,
Flores C,
Abdellaoui A,
Ahluwalia TS,
Alves AC,
Amaral AFS
and 76 more — show all
Antó JM,
Arnold A,
Barreto-Luis A,
Baurecht H,
van Beijsterveldt CEM,
Bleecker ER,
Bonàs-Guarch S,
Boomsma DI,
Brix S,
Bunyavanich S,
Burchard EG,
Chen Z,
Curjuric I,
Custovic A,
den Dekker HT,
Dharmage SC,
Dmitrieva J,
Duijts L,
Ege MJ,
Gauderman WJ,
Georges M,
Gieger C,
Gilliland F,
Granell R,
Gui H,
Hansen T,
Heinrich J,
Henderson J,
Hernandez-Pacheco N,
Holt P,
Imboden M,
Jaddoe VWV,
Jarvelin MR,
Jarvis DL,
Jensen KK,
Jónsdóttir I,
Kabesch M,
Kaprio J,
Kumar A,
Lee YA,
Levin AM,
Li X,
Lorenzo-Diaz F,
Melén E,
Mercader JM,
Meyers DA,
Myers R,
Nicolae DL,
Nohr EA,
Palviainen T,
Paternoster L,
Pennell CE,
Pershagen G,
Pino-Yanes M,
Probst-Hensch NM,
Rüschendorf F,
Simpson A,
Stefansson K,
Sunyer J,
Sveinbjornsson G,
Thiering E,
Thompson PJ,
Torrent M,
Torrents D,
Tung JY,
Wang CA,
Weidinger S,
Weiss S,
Willemsen G,
Williams LK,
Ober C,
Hinds DA,
Ferreira MA,
Bisgaard H,
Strachan DP,
Bønnelykke K
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Lee JJ,
Wedow R,
Okbay A,
Kong E,
Maghzian O,
Zacher M,
Nguyen-Viet TA,
Bowers P,
Sidorenko J,
Karlsson Linnér R,
Fontana MA,
Kundu T
and 65 more — show all
Lee C,
Li H,
Li R,
Royer R,
Timshel PN,
Walters RK,
Willoughby EA,
Yengo L,
Alver M,
Bao Y,
Clark DW,
Day FR,
Furlotte NA,
Joshi PK,
Kemper KE,
Kleinman A,
Langenberg C,
Mägi R,
Trampush JW,
Verma SS,
Wu Y,
Lam M,
Zhao JH,
Zheng Z,
Boardman JD,
Campbell H,
Freese J,
Harris KM,
Hayward C,
Herd P,
Kumari M,
Lencz T,
Luan J,
Malhotra AK,
Metspalu A,
Milani L,
Ong KK,
Perry JRB,
Porteous DJ,
Ritchie MD,
Smart MC,
Smith BH,
Tung JY,
Wareham NJ,
Wilson JF,
Beauchamp JP,
Conley DC,
Esko T,
Lehrer SF,
Magnusson PKE,
Oskarsson S,
Pers TH,
Robinson MR,
Thom K,
Watson C,
Chabris CF,
Meyer MN,
Laibson DI,
Yang J,
Johannesson M,
Koellinger PD,
Turley P,
Visscher PM,
Benjamin DJ,
Cesarini D
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
An atlas of genetic influences on osteoporosis in humans and mice
Morris JA,
Kemp JP,
Youlten SE,
Laurent L,
Logan JG,
Chai RC,
Vulpescu NA,
Forgetta V,
Kleinman A,
Mohanty ST,
Sergio CM,
Quinn J
and 47 more — show all
Nguyen-Yamamoto L,
Luco AL,
Vijay J,
Simon MM,
Pramatarova A,
Medina-Gomez C,
Trajanoska K,
Ghirardello EJ,
Butterfield NC,
Curry KF,
Leitch VD,
Sparkes PC,
Adoum AT,
Mannan NS,
Komla-Ebri DSK,
Pollard AS,
Dewhurst HF,
Hassall TAD,
Beltejar MG,
Adams DJ,
Vaillancourt SM,
Kaptoge S,
Baldock P,
Cooper C,
Reeve J,
Ntzani EE,
Evangelou E,
Ohlsson C,
Karasik D,
Rivadeneira F,
Kiel DP,
Tobias JH,
Gregson CL,
Harvey NC,
Grundberg E,
Goltzman D,
Adams DJ,
Lelliott CJ,
Hinds DA,
Ackert-Bicknell CL,
Hsu YH,
Maurano MT,
Croucher PI,
Williams GR,
Bassett JHD,
Evans DM,
Richards JB
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
12 pages+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
and 111 more — show all
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Howard DM,
Adams MJ,
Clarke TK,
Hafferty JD,
Gibson J,
Shirali M,
Coleman JRI,
Hagenaars SP,
Ward J,
Wigmore EM,
Alloza C,
Shen X
and 26 more — show all
Barbu MC,
Xu EY,
Whalley HC,
Marioni RE,
Porteous DJ,
Davies G,
Deary IJ,
Hemani G,
Berger K,
Teismann H,
Rawal R,
Arolt V,
Baune BT,
Dannlowski U,
Domschke K,
Tian C,
Hinds DA,
Trzaskowski M,
Byrne EM,
Ripke S,
Smith DJ,
Sullivan PF,
Wray NR,
Breen G,
Lewis CM,
McIntosh AM
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
Jansen PR,
Watanabe K,
Stringer S,
Skene N,
Bryois J,
Hammerschlag AR,
de Leeuw CA,
Benjamins JS,
Muñoz-Manchado AB,
Nagel M,
Savage JE,
Tiemeier H
and 12 more — show all
White T,
Tung JY,
Hinds DA,
Vacic V,
Wang X,
Sullivan PF,
van der Sluis S,
Polderman TJC,
Smit AB,
Hjerling-Leffler J,
Van Someren EJW,
Posthuma D
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
12 pages+
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci
Dudding T,
Haworth S,
Lind PA,
Sathirapongsasuti JF,
Tung JY,
Mitchell R,
Colodro-Conde L,
Medland SE,
Gordon S,
Elsworth B,
Paternoster L,
Franks PW
and 3 more — show all
23andMe Research Team
Nature communications · 2019 · PMID 30837455 · open access
12 pages+
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct
Ferreira MAR,
Mathur R,
Vonk JM,
Szwajda A,
Brumpton B,
Granell R,
Brew BK,
Ullemar V,
Lu Y,
Jiang Y,
Magnusson PKE,
Karlsson R
and 4 more — show all
23andMe Research Team · eQTLGen Consortium and 1 more consortia
American journal of human genetics · 2019 · PMID 30929738
12 pages+
Combined analysis of keratinocyte cancers identifies novel genome-wide loci
Liyanage UE,
Law MH,
Han X,
An J,
Ong JS,
Gharahkhani P,
Gordon S,
Neale RE,
Olsen CM,
MacGregor S,
Whiteman DC
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
12 pages+
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Gallagher CS,
Mäkinen N,
Harris HR,
Rahmioglu N,
Uimari O,
Cook JP,
Shigesi N,
Ferreira T,
Velez-Edwards DR,
Edwards TL,
Mortlock S,
Ruhioglu Z
and 24 more — show all
Day F,
Becker CM,
Karhunen V,
Martikainen H,
Järvelin MR,
Cantor RM,
Ridker PM,
Terry KL,
Buring JE,
Gordon SD,
Medland SE,
Montgomery GW,
Nyholt DR,
Hinds DA,
Tung JY,
Perry JRB,
Lind PA,
Painter JN,
Martin NG,
Morris AP,
Chasman DI,
Missmer SA,
Zondervan KT,
Morton CC
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
12 pages+
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
Kia DA,
Noyce AJ,
Xue A,
Bras J,
Young E
and 39 more — show all
von Coelln R,
Simón-Sánchez J,
Schulte C,
Sharma M,
Krohn L,
Pihlstrøm L,
Siitonen A,
Iwaki H,
Leonard H,
Faghri F,
Gibbs JR,
Hernandez DG,
Scholz SW,
Botia JA,
Martinez M,
Corvol JC,
Lesage S,
Jankovic J,
Shulman LM,
Sutherland M,
Tienari P,
Majamaa K,
Toft M,
Andreassen OA,
Bangale T,
Brice A,
Yang J,
Gan-Or Z,
Gasser T,
Heutink P,
Shulman JM,
Wood NW,
Hinds DA,
Hardy JA,
Morris HR,
Gratten J,
Visscher PM,
Graham RR,
Singleton AB
23andMe Research Team · System Genomics of Parkinson's Disease Consortium and 1 more consortia
The Lancet. Neurology · 2019 · PMID 31701892
12 pages+
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan
Hollis B,
Day FR,
Busch AS,
Thompson DJ,
Soares ALG,
Timmers PRHJ,
Kwong A,
Easton DF,
Joshi PK,
Timpson NJ,
Ong KK,
Perry JRB
PRACTICAL Consortium · 23andMe Research Team
Nature communications · 2020 · PMID 32210231 · open access
12 pages+
Genetic determinants of daytime napping and effects on cardiometabolic health
Dashti HS,
Daghlas I,
Lane JM,
Huang Y,
Udler MS,
Wang H,
Ollila HM,
Jones SE,
Kim J,
Wood AR,
Weedon MN,
Aslibekyan S
and 2 more — show all
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
12 pages+
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression
Thorp JG,
Campos AI,
Grotzinger AD,
Gerring ZF,
An J,
Ong JS,
Wang W,
Shringarpure S,
Byrne EM,
MacGregor S,
Martin NG,
Medland SE
and 2 more — show all
23andMe Research Team
Nature human behaviour · 2021 · PMID 33859377
12 pages+
Genetic analyses identify widespread sex-differential participation bias
Pirastu N,
Cordioli M,
Nandakumar P,
Mignogna G,
Abdellaoui A,
Hollis B,
Kanai M,
Rajagopal VM,
Parolo PDB,
Baya N,
Carey CE,
Karjalainen J
and 17 more — show all
Als TD,
Van der Zee MD,
Day FR,
Ong KK,
Morisaki T,
de Geus E,
Bellocco R,
Okada Y,
Børglum AD,
Joshi P,
Auton A,
Hinds D,
Neale BM,
Walters RK,
Nivard MG,
Perry JRB,
Ganna A
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects
Choquet H,
Melles RB,
Anand D,
Yin J,
Cuellar-Partida G,
Wang W,
Hoffmann TJ,
Nair KS,
Hysi PG,
Lachke SA,
Jorgenson E
23andMe Research Team
Nature communications · 2021 · PMID 34127677 · open access
12 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.