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Is your paper here?
2,665 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.
34 matches for
Gelernter J,
showing the first 14.
Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression
Zhou H,
Polimanti R,
Yang BZ,
Wang Q,
Han S,
Sherva R,
Nuñez YZ,
Zhao H,
Farrer LA,
Kranzler HR,
Gelernter J
JAMA psychiatry · 2017 · PMID 29071344
2 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 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 alcohol dependence:significant findings in African- and European-Americans including novel risk loci
Gelernter J,
Kranzler HR,
Sherva R,
Almasy L,
Koesterer R,
Smith AH,
Anton R,
Preuss UW,
Ridinger M,
Rujescu D,
Wodarz N,
Zill P
and 2 more — show all
Molecular psychiatry · 2014 · PMID 24166409
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 analyses of psychological resilience in U.S. Army soldiers
Stein MB,
Choi KW,
Jain S,
Campbell-Sills L,
Chen CY,
Gelernter J,
He F,
Heeringa SG,
Maihofer AX,
Nievergelt C,
Nock MK,
Ripke S
and 4 more — show all
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2019 · PMID 31081985
1 page
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes
Chen J,
Loukola A,
Gillespie NA,
Peterson R,
Jia P,
Riley B,
Maes H,
Dick DM,
Kendler KS,
Damaj MI,
Miles MF,
Zhao Z
and 34 more — show all
Li MD,
Vink JM,
Minica CC,
Willemsen G,
Boomsma DI,
Qaiser B,
Madden PAF,
Korhonen T,
Jousilahti P,
Hällfors J,
Gelernter J,
Kranzler HR,
Sherva R,
Farrer L,
Maher B,
Vanyukov M,
Taylor M,
Ware JJ,
Munafò MR,
Lutz SM,
Hokanson JE,
Gu F,
Landi MT,
Caporaso NE,
Hancock DB,
Gaddis NC,
Baker TB,
Bierut LJ,
Johnson EO,
Chenoweth M,
Lerman C,
Tyndale R,
Kaprio J,
Chen X
Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2020 · PMID 31294817
1 page
Systematic review and meta-analysis of the moderating effect of rs1799971 in OPRM1, the mu-opioid receptor gene, on response to naltrexone treatment of alcohol use disorder
Hartwell EE,
Feinn R,
Morris PE,
Gelernter J,
Krystal J,
Arias AJ,
Hoffman M,
Petrakis I,
Gueorguieva R,
Schacht JP,
Oslin D,
Anton RF
and 1 more — show all
Addiction (Abingdon, England) · 2020 · PMID 31961981
1 page
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Maihofer AX,
Choi KW,
Coleman JRI,
Daskalakis NP,
Denckla CA,
Ketema E,
Morey RA,
Polimanti R,
Ratanatharathorn A,
Torres K,
Wingo AP,
Zai CC
and 169 more — show all
Aiello AE,
Almli LM,
Amstadter AB,
Andersen SB,
Andreassen OA,
Arbisi PA,
Ashley-Koch AE,
Austin SB,
Avdibegović E,
Borglum AD,
Babić D,
Bækvad-Hansen M,
Baker DG,
Beckham JC,
Bierut LJ,
Bisson JI,
Boks MP,
Bolger EA,
Bradley B,
Brashear M,
Breen G,
Bryant RA,
Bustamante AC,
Bybjerg-Grauholm J,
Calabrese JR,
Caldas-de-Almeida JM,
Chen CY,
Dale AM,
Dalvie S,
Deckert J,
Delahanty DL,
Dennis MF,
Disner SG,
Domschke K,
Duncan LE,
Džubur Kulenović A,
Erbes CR,
Evans A,
Farrer LA,
Feeny NC,
Flory JD,
Forbes D,
Franz CE,
Galea S,
Garrett ME,
Gautam A,
Gelaye B,
Gelernter J,
Geuze E,
Gillespie CF,
Goçi A,
Gordon SD,
Guffanti G,
Hammamieh R,
Hauser MA,
Heath AC,
Hemmings SMJ,
Hougaard DM,
Jakovljević M,
Jett M,
Johnson EO,
Jones I,
Jovanovic T,
Qin XJ,
Karstoft KI,
Kaufman ML,
Kessler RC,
Khan A,
Kimbrel NA,
King AP,
Koen N,
Kranzler HR,
Kremen WS,
Lawford BR,
Lebois LAM,
Lewis C,
Liberzon I,
Linnstaedt SD,
Logue MW,
Lori A,
Lugonja B,
Luykx JJ,
Lyons MJ,
Maples-Keller JL,
Marmar C,
Martin NG,
Maurer D,
Mavissakalian MR,
McFarlane A,
McGlinchey RE,
McLaughlin KA,
McLean SA,
Mehta D,
Mellor R,
Michopoulos V,
Milberg W,
Miller MW,
Morris CP,
Mors O,
Mortensen PB,
Nelson EC,
Nordentoft M,
Norman SB,
O'Donnell M,
Orcutt HK,
Panizzon MS,
Peters ES,
Peterson AL,
Peverill M,
Pietrzak RH,
Polusny MA,
Rice JP,
Risbrough VB,
Roberts AL,
Rothbaum AO,
Rothbaum BO,
Roy-Byrne P,
Ruggiero KJ,
Rung A,
Rutten BPF,
Saccone NL,
Sanchez SE,
Schijven D,
Seedat S,
Seligowski AV,
Seng JS,
Sheerin CM,
Silove D,
Smith AK,
Smoller JW,
Sponheim SR,
Stein DJ,
Stevens JS,
Teicher MH,
Thompson WK,
Trapido E,
Uddin M,
Ursano RJ,
van den Heuvel LL,
Van Hooff M,
Vermetten E,
Vinkers CH,
Voisey J,
Wang Y,
Wang Z,
Werge T,
Williams MA,
Williamson DE,
Winternitz S,
Wolf C,
Wolf EJ,
Yehuda R,
Young KA,
Young RM,
Zhao H,
Zoellner LA,
Haas M,
Lasseter H,
Provost AC,
Salem RM,
Sebat J,
Shaffer RA,
Wu T,
Ripke S,
Daly MJ,
Ressler KJ,
Koenen KC,
Stein MB,
Nievergelt CM
Biological psychiatry · 2022 · PMID 34865855 · open access
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.