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2,673 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.
14 matches for
Davis LK.
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Jansen IE,
Savage JE,
Watanabe K,
Bryois J,
Williams DM,
Steinberg S,
Sealock J,
Karlsson IK,
Hägg S,
Athanasiu L,
Voyle N,
Proitsi P
and 41 more — show all
Witoelar A,
Stringer S,
Aarsland D,
Almdahl IS,
Andersen F,
Bergh S,
Bettella F,
Bjornsson S,
Brækhus A,
Bråthen G,
de Leeuw C,
Desikan RS,
Djurovic S,
Dumitrescu L,
Fladby T,
Hohman TJ,
Jonsson PV,
Kiddle SJ,
Rongve A,
Saltvedt I,
Sando SB,
Selbæk G,
Shoai M,
Skene NG,
Snaedal J,
Stordal E,
Ulstein ID,
Wang Y,
White LR,
Hardy J,
Hjerling-Leffler J,
Sullivan PF,
van der Flier WM,
Dobson R,
Davis LK,
Stefansson H,
Stefansson K,
Pedersen NL,
Ripke S,
Andreassen OA,
Posthuma D
Nature genetics · 2019 · PMID 30617256
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+
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+
Genome-wide association study of Tourette's syndrome
Scharf JM,
Yu D,
Mathews CA,
Neale BM,
Stewart SE,
Fagerness JA,
Evans P,
Gamazon E,
Edlund CK,
Service SK,
Tikhomirov A,
Osiecki L
and 86 more — show all
Illmann C,
Pluzhnikov A,
Konkashbaev A,
Davis LK,
Han B,
Crane J,
Moorjani P,
Crenshaw AT,
Parkin MA,
Reus VI,
Lowe TL,
Rangel-Lugo M,
Chouinard S,
Dion Y,
Girard S,
Cath DC,
Smit JH,
King RA,
Fernandez TV,
Leckman JF,
Kidd KK,
Kidd JR,
Pakstis AJ,
State MW,
Herrera LD,
Romero R,
Fournier E,
Sandor P,
Barr CL,
Phan N,
Gross-Tsur V,
Benarroch F,
Pollak Y,
Budman CL,
Bruun RD,
Erenberg G,
Naarden AL,
Lee PC,
Weiss N,
Kremeyer B,
Berrío GB,
Campbell DD,
Cardona Silgado JC,
Ochoa WC,
Mesa Restrepo SC,
Muller H,
Valencia Duarte AV,
Lyon GJ,
Leppert M,
Morgan J,
Weiss R,
Grados MA,
Anderson K,
Davarya S,
Singer H,
Walkup J,
Jankovic J,
Tischfield JA,
Heiman GA,
Gilbert DL,
Hoekstra PJ,
Robertson MM,
Kurlan R,
Liu C,
Gibbs JR,
Singleton A,
Hardy J,
Strengman E,
Ophoff RA,
Wagner M,
Moessner R,
Mirel DB,
Posthuma D,
Sabatti C,
Eskin E,
Conti DV,
Knowles JA,
Ruiz-Linares A,
Rouleau GA,
Purcell S,
Heutink P,
Oostra BA,
McMahon WM,
Freimer NB,
Cox NJ,
Pauls DL
North American Brain Expression Consortium · UK Human Brain Expression Database
Molecular psychiatry · 2013 · PMID 22889924 · open access
2 pages
A genome-wide association study of polycystic ovary syndrome identified from electronic health records
Zhang Y,
Ho K,
Keaton JM,
Hartzel DN,
Day F,
Justice AE,
Josyula NS,
Pendergrass SA,
Actkins K,
Davis LK,
Velez Edwards DR,
Holohan B
and 8 more — show all
American journal of obstetrics and gynecology · 2020 · PMID 32289280
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 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
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Burns K,
Mullin BH,
Moolhuijsen LME,
Laisk T,
Tyrmi JS,
Cui J,
Actkins KV,
Louwers YV,
Davis LK,
Dudbridge F,
Azziz R,
Goodarzi MO
and 7 more — show all
Estonian Biobank Research Team · FinnGen and 1 more consortia
BMC genomics · 2024 · PMID 38408933 · 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.