For researchers
Is your paper here?
2,662 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 10.
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Krohn L,
Heilbron K,
Blauwendraat C,
Reynolds RH,
Yu E,
Senkevich K,
Rudakou U,
Estiar MA,
Gustavsson EK,
Brolin K,
Ruskey JA,
Freeman K
and 46 more — show all
Asayesh F,
Chia R,
Arnulf I,
Hu MTM,
Montplaisir JY,
Gagnon JF,
Desautels A,
Dauvilliers Y,
Gigli GL,
Valente M,
Janes F,
Bernardini A,
Högl B,
Stefani A,
Ibrahim A,
Šonka K,
Kemlink D,
Oertel W,
Janzen A,
Plazzi G,
Biscarini F,
Antelmi E,
Figorilli M,
Puligheddu M,
Mollenhauer B,
Trenkwalder C,
Sixel-Döring F,
Cochen De Cock V,
Monaca CC,
Heidbreder A,
Ferini-Strambi L,
Dijkstra F,
Viaene M,
Abril B,
Boeve BF,
Scholz SW,
Ryten M,
Bandres-Ciga S,
Noyce A,
Cannon P,
Pihlstrøm L,
Nalls MA,
Singleton AB,
Rouleau GA,
Postuma RB,
Gan-Or Z
23andMe Research Team
Nature communications · 2022 · PMID 36470867 · open access
2 pages
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction
Braun A,
Shekhar S,
Levey DF,
Straub P,
Kraft J,
Panagiotaropoulou GM,
Heilbron K,
Awasthi S,
Meleka Hanna R,
Hoffmann S,
Stein M,
Lehnerer S
and 28 more — show all
Mergenthaler P,
Elnahas AG,
Topaloudi A,
Koromina M,
Palviainen T,
Asbjornsdottir B,
Stefansson H,
Skuladóttir AT,
Jónsdóttir I,
Stefansson K,
Reis K,
Esko T,
Palotie A,
Leypoldt F,
Stein MB,
Fontanillas P,
Kaprio J,
Gelernter J,
Davis LK,
Paschou P,
Tannemaat MR,
Verschuuren JJGM,
Kuhlenbäumer G,
Gregersen PK,
Huijbers MG,
Stascheit F,
Meisel A,
Ripke S
Estonian Biobank Research Team · 23andMe Research Team
Nature communications · 2024 · PMID 39537604 · open access
2 pages
Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry
Sanchez-Roige S,
Fontanillas P,
Elson SL,
Pandit A,
Schmidt EM,
Foerster JR,
Abecasis GR,
Gray JC,
de Wit H,
Davis LK,
MacKillop J,
Palmer AA
23andMe Research Team
Nature neuroscience · 2018 · PMID 29230059
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
Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder
Li X,
Luo Z,
Gu C,
Hall LS,
McIntosh AM,
Zeng Y,
Porteous DJ,
Hayward C,
Li M,
Yao YG,
Zhang C,
Luo XJ
23andMe Research Team7
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018 · PMID 29728651
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
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
Liao C,
Castonguay CE,
Heilbron K,
Vuokila V,
Medeiros M,
Houle G,
Akçimen F,
Ross JP,
Catoire H,
Diez-Fairen M,
Kang J,
Mueller SH
and 36 more — show all
Girard SL,
Hopfner F,
Lorenz D,
Clark LN,
Soto-Beasley AI,
Klebe S,
Hallett M,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Seppi K,
Berg D,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Dupré N,
Jankovic J,
Testa CM,
Ross OA,
Arzberger T,
Chouinard S,
Louis ED,
Mandich P,
Vitale C,
Barone P,
García-Martín E,
Alonso-Navarro H,
Agúndez JAG,
Jiménez-Jiménez FJ,
Pastor P,
Rajput A,
Deuschl G,
Kuhlenbaümer G,
Meijer IA,
Dion PA,
Rouleau GA
23andMe Research Team
JAMA neurology · 2022 · PMID 34982113 · 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.