For researchers
Is your paper here?
2,671 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.
47 matches for
Andreassen O,
showing the first 7.
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis
van Hulzen KJE,
Scholz CJ,
Franke B,
Ripke S,
Klein M,
McQuillin A,
Sonuga-Barke EJ,
Kelsoe JR,
Landén M,
Andreassen OA,
Lesch KP,
Weber H
and 3 more — show all
PGC ADHD Working Group · PGC Bipolar Disorder Working Group
Biological psychiatry · 2017 · PMID 27890468
1 page
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Lo MT,
Hinds DA,
Tung JY,
Franz C,
Fan CC,
Wang Y,
Smeland OB,
Schork A,
Holland D,
Kauppi K,
Sanyal N,
Escott-Price V
and 10 more — show all
Nature genetics · 2017 · PMID 27918536
1 page
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Vojinovic D,
Adams HH,
Jian X,
Yang Q,
Smith AV,
Bis JC,
Teumer A,
Scholz M,
Armstrong NJ,
Hofer E,
Saba Y,
Luciano M
and 79 more — show all
Bernard M,
Trompet S,
Yang J,
Gillespie NA,
van der Lee SJ,
Neumann A,
Ahmad S,
Andreassen OA,
Ames D,
Amin N,
Arfanakis K,
Bastin ME,
Becker DM,
Beiser AS,
Beyer F,
Brodaty H,
Bryan RN,
Bülow R,
Dale AM,
De Jager PL,
Deary IJ,
DeCarli C,
Fleischman DA,
Gottesman RF,
van der Grond J,
Gudnason V,
Harris TB,
Homuth G,
Knopman DS,
Kwok JB,
Lewis CE,
Li S,
Loeffler M,
Lopez OL,
Maillard P,
El Marroun H,
Mather KA,
Mosley TH,
Muetzel RL,
Nauck M,
Nyquist PA,
Panizzon MS,
Pausova Z,
Psaty BM,
Rice K,
Rotter JI,
Royle N,
Satizabal CL,
Schmidt R,
Schofield PR,
Schreiner PJ,
Sidney S,
Stott DJ,
Thalamuthu A,
Uitterlinden AG,
Valdés Hernández MC,
Vernooij MW,
Wen W,
White T,
Witte AV,
Wittfeld K,
Wright MJ,
Yanek LR,
Tiemeier H,
Kremen WS,
Bennett DA,
Jukema JW,
Paus T,
Wardlaw JM,
Schmidt H,
Sachdev PS,
Villringer A,
Grabe HJ,
Longstreth WT,
van Duijn CM,
Launer LJ,
Seshadri S,
Ikram MA,
Fornage M
Nature communications · 2018 · PMID 30258056 · open access
1 page
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Watson HJ,
Yilmaz Z,
Thornton LM,
Hübel C,
Coleman JRI,
Gaspar HA,
Bryois J,
Hinney A,
Leppä VM,
Mattheisen M,
Medland SE,
Ripke S
and 198 more — show all
Yao S,
Giusti-Rodríguez P,
Hanscombe KB,
Purves KL,
Adan RAH,
Alfredsson L,
Ando T,
Andreassen OA,
Baker JH,
Berrettini WH,
Boehm I,
Boni C,
Perica VB,
Buehren K,
Burghardt R,
Cassina M,
Cichon S,
Clementi M,
Cone RD,
Courtet P,
Crow S,
Crowley JJ,
Danner UN,
Davis OSP,
de Zwaan M,
Dedoussis G,
Degortes D,
DeSocio JE,
Dick DM,
Dikeos D,
Dina C,
Dmitrzak-Weglarz M,
Docampo E,
Duncan LE,
Egberts K,
Ehrlich S,
Escaramís G,
Esko T,
Estivill X,
Farmer A,
Favaro A,
Fernández-Aranda F,
Fichter MM,
Fischer K,
Föcker M,
Foretova L,
Forstner AJ,
Forzan M,
Franklin CS,
Gallinger S,
Giegling I,
Giuranna J,
Gonidakis F,
Gorwood P,
Mayora MG,
Guillaume S,
Guo Y,
Hakonarson H,
Hatzikotoulas K,
Hauser J,
Hebebrand J,
Helder SG,
Herms S,
Herpertz-Dahlmann B,
Herzog W,
Huckins LM,
Hudson JI,
Imgart H,
Inoko H,
Janout V,
Jiménez-Murcia S,
Julià A,
Kalsi G,
Kaminská D,
Kaprio J,
Karhunen L,
Karwautz A,
Kas MJH,
Kennedy JL,
Keski-Rahkonen A,
Kiezebrink K,
Kim YR,
Klareskog L,
Klump KL,
Knudsen GPS,
La Via MC,
Le Hellard S,
Levitan RD,
Li D,
Lilenfeld L,
Lin BD,
Lissowska J,
Luykx J,
Magistretti PJ,
Maj M,
Mannik K,
Marsal S,
Marshall CR,
Mattingsdal M,
McDevitt S,
McGuffin P,
Metspalu A,
Meulenbelt I,
Micali N,
Mitchell K,
Monteleone AM,
Monteleone P,
Munn-Chernoff MA,
Nacmias B,
Navratilova M,
Ntalla I,
O'Toole JK,
Ophoff RA,
Padyukov L,
Palotie A,
Pantel J,
Papezova H,
Pinto D,
Rabionet R,
Raevuori A,
Ramoz N,
Reichborn-Kjennerud T,
Ricca V,
Ripatti S,
Ritschel F,
Roberts M,
Rotondo A,
Rujescu D,
Rybakowski F,
Santonastaso P,
Scherag A,
Scherer SW,
Schmidt U,
Schork NJ,
Schosser A,
Seitz J,
Slachtova L,
Slagboom PE,
Slof-Op 't Landt MCT,
Slopien A,
Sorbi S,
Świątkowska B,
Szatkiewicz JP,
Tachmazidou I,
Tenconi E,
Tortorella A,
Tozzi F,
Treasure J,
Tsitsika A,
Tyszkiewicz-Nwafor M,
Tziouvas K,
van Elburg AA,
van Furth EF,
Wagner G,
Walton E,
Widen E,
Zeggini E,
Zerwas S,
Zipfel S,
Bergen AW,
Boden JM,
Brandt H,
Crawford S,
Halmi KA,
Horwood LJ,
Johnson C,
Kaplan AS,
Kaye WH,
Mitchell JE,
Olsen CM,
Pearson JF,
Pedersen NL,
Strober M,
Werge T,
Whiteman DC,
Woodside DB,
Stuber GD,
Gordon S,
Grove J,
Henders AK,
Juréus A,
Kirk KM,
Larsen JT,
Parker R,
Petersen L,
Jordan J,
Kennedy M,
Montgomery GW,
Wade TD,
Birgegård A,
Lichtenstein P,
Norring C,
Landén M,
Martin NG,
Mortensen PB,
Sullivan PF,
Breen G,
Bulik CM
Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2019 · PMID 31308545
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
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.