For researchers
Is your paper here?
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.
9 matches for
Sanchez-Roige S.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Karlsson Linnér R,
Biroli P,
Kong E,
Meddens SFW,
Wedow R,
Fontana MA,
Lebreton M,
Tino SP,
Abdellaoui A,
Hammerschlag AR,
Nivard MG,
Okbay A
and 80 more — show all
Rietveld CA,
Timshel PN,
Trzaskowski M,
Vlaming R,
Zünd CL,
Bao Y,
Buzdugan L,
Caplin AH,
Chen CY,
Eibich P,
Fontanillas P,
Gonzalez JR,
Joshi PK,
Karhunen V,
Kleinman A,
Levin RZ,
Lill CM,
Meddens GA,
Muntané G,
Sanchez-Roige S,
Rooij FJV,
Taskesen E,
Wu Y,
Zhang F,
Auton A,
Boardman JD,
Clark DW,
Conlin A,
Dolan CC,
Fischbacher U,
Groenen PJF,
Harris KM,
Hasler G,
Hofman A,
Ikram MA,
Jain S,
Karlsson R,
Kessler RC,
Kooyman M,
MacKillop J,
Männikkö M,
Morcillo-Suarez C,
McQueen MB,
Schmidt KM,
Smart MC,
Sutter M,
Thurik AR,
Uitterlinden AG,
White J,
Wit H,
Yang J,
Bertram L,
Boomsma DI,
Esko T,
Fehr E,
Hinds DA,
Johannesson M,
Kumari M,
Laibson D,
Magnusson PKE,
Meyer MN,
Navarro A,
Palmer AA,
Pers TH,
Posthuma D,
Schunk D,
Stein MB,
Svento R,
Tiemeier H,
Timmers PRHJ,
Turley P,
Ursano RJ,
Wagner GG,
Wilson JF,
Gratten J,
Lee JJ,
Cesarini D,
Benjamin DJ,
Koellinger PD,
Beauchamp JP
23and Me Research Team · eQTLgen Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30643258
12 pages+
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits
Zhou H,
Sealock JM,
Sanchez-Roige S,
Clarke TK,
Levey DF,
Cheng Z,
Li B,
Polimanti R,
Kember RL,
Smith RV,
Thygesen JH,
Morgan MY
and 15 more — show all
Atkinson SR,
Thursz MR,
Nyegaard M,
Nyegaard M,
Mattheisen M,
Børglum AD,
Johnson EC,
Justice AC,
Palmer AA,
McQuillin A,
Davis LK,
Edenberg HJ,
Agrawal A,
Kranzler HR,
Gelernter J
Nature neuroscience · 2020 · PMID 32451486 · open access
12 pages+
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
Karlsson Linnér R,
Mallard TT,
Barr PB,
Sanchez-Roige S,
Madole JW,
Driver MN,
Poore HE,
de Vlaming R,
Grotzinger AD,
Tielbeek JJ,
Johnson EC,
Liu M
and 17 more — show all
Rosenthal SB,
Ideker T,
Zhou H,
Kember RL,
Pasman JA,
Verweij KJH,
Liu DJ,
Vrieze S,
Kranzler HR,
Gelernter J,
Harris KM,
Tucker-Drob EM,
Waldman ID,
Palmer AA,
Harden KP,
Koellinger PD,
Dick DM
COGA Collaborators
Nature neuroscience · 2021 · PMID 34446935 · open access
12 pages+
Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample
Kember RL,
Vickers-Smith R,
Zhou H,
Xu H,
Jennings M,
Dao C,
Davis L,
Sanchez-Roige S,
Justice AC,
Gelernter J,
Vujkovic M,
Kranzler HR
The American journal of psychiatry · 2023 · PMID 37282553
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
Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction
Kember RL,
Vickers-Smith R,
Xu H,
Toikumo S,
Niarchou M,
Zhou H,
Hartwell EE,
Crist RC,
Rentsch CT,
Davis LK,
Justice AC,
Sanchez-Roige S
and 3 more — show all
Million Veteran Program
Nature neuroscience · 2022 · PMID 36171425
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
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
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
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.