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2,665 papers hold this site up. Every variant and condition page names
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15 matches for
Polimanti R.
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+
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
Watanabe K,
Jansen PR,
Savage JE,
Nandakumar P,
Wang X,
Hinds DA,
Gelernter J,
Levey DF,
Polimanti R,
Stein MB,
Van Someren EJW,
Smit AB
and 1 more — show all
23andMe Research Team
Nature genetics · 2022 · PMID 35835914
12 pages+
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Meng X,
Navoly G,
Giannakopoulou O,
Levey DF,
Koller D,
Pathak GA,
Koen N,
Lin K,
Adams MJ,
Rentería ME,
Feng Y,
Gaziano JM
and 66 more — show all
Stein DJ,
Zar HJ,
Campbell ML,
van Heel DA,
Trivedi B,
Finer S,
McQuillin A,
Bass N,
Chundru VK,
Martin HC,
Huang QQ,
Valkovskaya M,
Chu CY,
Kanjira S,
Kuo PH,
Chen HC,
Tsai SJ,
Liu YL,
Kendler KS,
Peterson RE,
Cai N,
Fang Y,
Sen S,
Scott LJ,
Burmeister M,
Loos RJF,
Preuss MH,
Actkins KV,
Davis LK,
Uddin M,
Wani AH,
Wildman DE,
Aiello AE,
Ursano RJ,
Kessler RC,
Kanai M,
Okada Y,
Sakaue S,
Rabinowitz JA,
Maher BS,
Uhl G,
Eaton W,
Cruz-Fuentes CS,
Martinez-Levy GA,
Campos AI,
Millwood IY,
Chen Z,
Li L,
Wassertheil-Smoller S,
Jiang Y,
Tian C,
Martin NG,
Mitchell BL,
Byrne EM,
Awasthi S,
Coleman JRI,
Ripke S,
Sofer T,
Walters RG,
McIntosh AM,
Polimanti R,
Dunn EC,
Stein MB,
Gelernter J,
Lewis CM,
Kuchenbaecker K
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
Nievergelt CM,
Maihofer AX,
Atkinson EG,
Chen CY,
Choi KW,
Coleman JRI,
Daskalakis NP,
Duncan LE,
Polimanti R,
Aaronson C,
Amstadter AB,
Andersen SB
and 223 more — show all
Andreassen OA,
Arbisi PA,
Ashley-Koch AE,
Austin SB,
Avdibegoviç E,
Babić D,
Bacanu SA,
Baker DG,
Batzler A,
Beckham JC,
Belangero S,
Benjet C,
Bergner C,
Bierer LM,
Biernacka JM,
Bierut LJ,
Bisson JI,
Boks MP,
Bolger EA,
Brandolino A,
Breen G,
Bressan RA,
Bryant RA,
Bustamante AC,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Børglum AD,
Børte S,
Cahn L,
Calabrese JR,
Caldas-de-Almeida JM,
Chatzinakos C,
Cheema S,
Clouston SAP,
Colodro-Conde L,
Coombes BJ,
Cruz-Fuentes CS,
Dale AM,
Dalvie S,
Davis LK,
Deckert J,
Delahanty DL,
Dennis MF,
Desarnaud F,
DiPietro CP,
Disner SG,
Docherty AR,
Domschke K,
Dyb G,
Kulenović AD,
Edenberg HJ,
Evans A,
Fabbri C,
Fani N,
Farrer LA,
Feder A,
Feeny NC,
Flory JD,
Forbes D,
Franz CE,
Galea S,
Garrett ME,
Gelaye B,
Gelernter J,
Geuze E,
Gillespie CF,
Goleva SB,
Gordon SD,
Goçi A,
Grasser LR,
Guindalini C,
Haas M,
Hagenaars S,
Hauser MA,
Heath AC,
Hemmings SMJ,
Hesselbrock V,
Hickie IB,
Hogan K,
Hougaard DM,
Huang H,
Huckins LM,
Hveem K,
Jakovljević M,
Javanbakht A,
Jenkins GD,
Johnson J,
Jones I,
Jovanovic T,
Karstoft KI,
Kaufman ML,
Kennedy JL,
Kessler RC,
Khan A,
Kimbrel NA,
King AP,
Koen N,
Kotov R,
Kranzler HR,
Krebs K,
Kremen WS,
Kuan PF,
Lawford BR,
Lebois LAM,
Lehto K,
Levey DF,
Lewis C,
Liberzon I,
Linnstaedt SD,
Logue MW,
Lori A,
Lu Y,
Luft BJ,
Lupton MK,
Luykx JJ,
Makotkine I,
Maples-Keller JL,
Marchese S,
Marmar C,
Martin NG,
Martínez-Levy GA,
McAloney K,
McFarlane A,
McLaughlin KA,
McLean SA,
Medland SE,
Mehta D,
Meyers J,
Michopoulos V,
Mikita EA,
Milani L,
Milberg W,
Miller MW,
Morey RA,
Morris CP,
Mors O,
Mortensen PB,
Mufford MS,
Nelson EC,
Nordentoft M,
Norman SB,
Nugent NR,
O'Donnell M,
Orcutt HK,
Pan PM,
Panizzon MS,
Pathak GA,
Peters ES,
Peterson AL,
Peverill M,
Pietrzak RH,
Polusny MA,
Porjesz B,
Powers A,
Qin XJ,
Ratanatharathorn A,
Risbrough VB,
Roberts AL,
Rothbaum AO,
Rothbaum BO,
Roy-Byrne P,
Ruggiero KJ,
Rung A,
Runz H,
Rutten BPF,
de Viteri SS,
Salum GA,
Sampson L,
Sanchez SE,
Santoro M,
Seah C,
Seedat S,
Seng JS,
Shabalin A,
Sheerin CM,
Silove D,
Smith AK,
Smoller JW,
Sponheim SR,
Stein DJ,
Stensland S,
Stevens JS,
Sumner JA,
Teicher MH,
Thompson WK,
Tiwari AK,
Trapido E,
Uddin M,
Ursano RJ,
Valdimarsdóttir U,
Van Hooff M,
Vermetten E,
Vinkers CH,
Voisey J,
Wang Y,
Wang Z,
Waszczuk M,
Weber H,
Wendt FR,
Werge T,
Williams MA,
Williamson DE,
Winsvold BS,
Winternitz S,
Wolf C,
Wolf EJ,
Xia Y,
Xiong Y,
Yehuda R,
Young KA,
Young RM,
Zai CC,
Zai GC,
Zervas M,
Zhao H,
Zoellner LA,
Zwart JA,
deRoon-Cassini T,
van Rooij SJH,
van den Heuvel LL,
Stein MB,
Ressler KJ,
Koenen KC
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A,
Huffman JE,
Rodriguez A,
Conery M,
Liu M,
Ho YL,
Kim Y,
Heise DA,
Guare L,
Panickan VA,
Garcon H,
Linares F
and 59 more — show all
Costa L,
Goethert I,
Tipton R,
Honerlaw J,
Davies L,
Whitbourne S,
Cohen J,
Posner DC,
Sangar R,
Murray M,
Wang X,
Dochtermann DR,
Devineni P,
Shi Y,
Nandi TN,
Assimes TL,
Brunette CA,
Carroll RJ,
Clifford R,
Duvall S,
Gelernter J,
Hung A,
Iyengar SK,
Joseph J,
Kember R,
Kranzler H,
Kripke CM,
Levey D,
Luoh SW,
Merritt VC,
Overstreet C,
Deak JD,
Grant SFA,
Polimanti R,
Roussos P,
Shakt G,
Sun YV,
Tsao N,
Venkatesh S,
Voloudakis G,
Justice A,
Begoli E,
Ramoni R,
Tourassi G,
Pyarajan S,
Tsao P,
O'Donnell CJ,
Muralidhar S,
Moser J,
Casas JP,
Bick AG,
Zhou W,
Cai T,
Voight BF,
Cho K,
Gaziano JM,
Madduri RK,
Damrauer S,
Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
Multi-ancestry genome-wide association and integrated multi-omics analyses of endometriosis and its clinical manifestations
Koller D,
He J,
Løkhammer S,
Aranda S,
Qiu D,
Davtian D,
Chen Q,
Xu Z,
Mao Z,
Friligkou E,
Karaca S,
Cormand B
and 5 more — show all
Nature genetics · 2026 · PMID 42056605
12 pages+
Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder
Wendt FR,
Pathak GA,
Deak JD,
De Angelis F,
Koller D,
Cabrera-Mendoza B,
Lebovitch DS,
Levey DF,
Stein MB,
Kranzler HR,
Koenen KC,
Gelernter J
and 2 more — show all
Molecular psychiatry · 2022 · PMID 35181757 · open access
7 pages
Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program
Stein MB,
Levey DF,
Cheng Z,
Wendt FR,
Harrington K,
Pathak GA,
Cho K,
Quaden R,
Radhakrishnan K,
Girgenti MJ,
Ho YA,
Posner D
and 6 more — show all
Department of Veterans Affairs Cooperative Studies Program (no. 575B) · VA Million Veteran Program
Nature genetics · 2021 · PMID 33510476 · open access
5 pages
Gene discovery and biological insights into anxiety disorders from a large-scale multi-ancestry genome-wide association study
Friligkou E,
Løkhammer S,
Cabrera-Mendoza B,
Shen J,
He J,
Deiana G,
Zanoaga MD,
Asgel Z,
Pilcher A,
Di Lascio L,
Makharashvili A,
Koller D
and 3 more — show all
Nature genetics · 2024 · PMID 39294497
5 pages
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations
Kranzler HR,
Zhou H,
Kember RL,
Vickers Smith R,
Justice AC,
Damrauer S,
Tsao PS,
Klarin D,
Baras A,
Reid J,
Overton J,
Rader DJ
and 8 more — show all
Nature communications · 2019 · PMID 30940813 · open access
4 pages
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications
Levey DF,
Galimberti M,
Deak JD,
Wendt FR,
Bhattacharya A,
Koller D,
Harrington KM,
Quaden R,
Johnson EC,
Gupta P,
Biradar M,
Lam M
and 18 more — show all
Cooke M,
Rajagopal VM,
Empke SLL,
Zhou H,
Nunez YZ,
Kranzler HR,
Edenberg HJ,
Agrawal A,
Smoller JW,
Lencz T,
Hougaard DM,
Børglum AD,
Demontis D,
Gaziano JM,
Gandal MJ,
Polimanti R,
Stein MB,
Gelernter J
Veterans Affairs Million Veteran Program
Nature genetics · 2023 · PMID 37985822 · open access
4 pages
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
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.