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2,682 papers hold this site up. Every variant and condition page names
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8 matches for
Haas M.
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+
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Vujkovic M,
Ramdas S,
Lorenz KM,
Guo X,
Darlay R,
Cordell HJ,
He J,
Gindin Y,
Chung C,
Myers RP,
Schneider CV,
Park J
and 78 more — show all
Lee KM,
Serper M,
Carr RM,
Kaplan DE,
Haas ME,
MacLean MT,
Witschey WR,
Zhu X,
Tcheandjieu C,
Kember RL,
Kranzler HR,
Verma A,
Giri A,
Klarin DM,
Sun YV,
Huang J,
Huffman JE,
Creasy KT,
Hand NJ,
Liu CT,
Long MT,
Yao J,
Budoff M,
Tan J,
Li X,
Lin HJ,
Chen YI,
Taylor KD,
Chang RK,
Krauss RM,
Vilarinho S,
Brancale J,
Nielsen JB,
Locke AE,
Jones MB,
Verweij N,
Baras A,
Reddy KR,
Neuschwander-Tetri BA,
Schwimmer JB,
Sanyal AJ,
Chalasani N,
Ryan KA,
Mitchell BD,
Gill D,
Wells AD,
Manduchi E,
Saiman Y,
Mahmud N,
Miller DR,
Reaven PD,
Phillips LS,
Muralidhar S,
DuVall SL,
Lee JS,
Assimes TL,
Pyarajan S,
Cho K,
Edwards TL,
Damrauer SM,
Wilson PW,
Gaziano JM,
O'Donnell CJ,
Khera AV,
Grant SFA,
Brown CD,
Tsao PS,
Saleheen D,
Lotta LA,
Bastarache L,
Anstee QM,
Daly AK,
Meigs JB,
Rotter JI,
Lynch JA,
Rader DJ,
Voight BF,
Chang KM
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Klarin D,
Busenkell E,
Judy R,
Lynch J,
Levin M,
Haessler J,
Aragam K,
Chaffin M,
Haas M,
Lindström S,
Assimes TL,
Huang J
and 30 more — show all
Min Lee K,
Shao Q,
Huffman JE,
Kabrhel C,
Huang Y,
Sun YV,
Vujkovic M,
Saleheen D,
Miller DR,
Reaven P,
DuVall S,
Boden WE,
Pyarajan S,
Reiner AP,
Trégouët DA,
Henke P,
Kooperberg C,
Gaziano JM,
Concato J,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
Smith NL,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Obi A,
Damrauer SM,
Natarajan P
INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
7 pages
Biological and clinical insights from genetics of insomnia symptoms
Lane JM,
Jones SE,
Dashti HS,
Wood AR,
Aragam KG,
van Hees VT,
Strand LB,
Winsvold BS,
Wang H,
Bowden J,
Song Y,
Patel K
and 31 more — show all
Anderson SG,
Beaumont RN,
Bechtold DA,
Cade BE,
Haas M,
Kathiresan S,
Little MA,
Luik AI,
Loudon AS,
Purcell S,
Richmond RC,
Scheer FAJL,
Schormair B,
Tyrrell J,
Winkelman JW,
Winkelmann J,
Hveem K,
Zhao C,
Nielsen JB,
Willer CJ,
Redline S,
Spiegelhalder K,
Kyle SD,
Ray DW,
Zwart JA,
Brumpton B,
Frayling TM,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
Hindy G,
Tyrrell DJ,
Vasbinder A,
Wei C,
Presswalla F,
Wang H,
Blakely P,
Ozel AB,
Graham S,
Holton GH,
Dowsett J,
Fahed AC
and 30 more — show all
Amadi KM,
Erne GK,
Tekmulla A,
Ismail A,
Launius C,
Sotoodehnia N,
Pankow JS,
Thørner LW,
Erikstrup C,
Pedersen OB,
Banasik K,
Brunak S,
Ullum H,
Eugen-Olsen J,
Ostrowski SR,
Haas ME,
Nielsen JB,
Lotta LA,
Engström G,
Melander O,
Orho-Melander M,
Zhao L,
Murthy VL,
Pinsky DJ,
Willer CJ,
Heckbert SR,
Reiser J,
Goldstein DR,
Desch KC,
Hayek SS
DBDS Consortium · Regeneron Genetics Center
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
5 pages
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes
Akbari P,
Sosina OA,
Bovijn J,
Landheer K,
Nielsen JB,
Kim M,
Aykul S,
De T,
Haas ME,
Hindy G,
Lin N,
Dinsmore IR
and 48 more — show all
Luo JZ,
Hectors S,
Geraghty B,
Germino M,
Panagis L,
Parasoglou P,
Walls JR,
Halasz G,
Atwal GS,
Jones M,
LeBlanc MG,
Still CD,
Carey DJ,
Giontella A,
Orho-Melander M,
Berumen J,
Kuri-Morales P,
Alegre-Díaz J,
Torres JM,
Emberson JR,
Collins R,
Rader DJ,
Zambrowicz B,
Murphy AJ,
Balasubramanian S,
Overton JD,
Reid JG,
Shuldiner AR,
Cantor M,
Abecasis GR,
Ferreira MAR,
Sleeman MW,
Gusarova V,
Altarejos J,
Harris C,
Economides AN,
Idone V,
Karalis K,
Della Gatta G,
Mirshahi T,
Yancopoulos GD,
Melander O,
Marchini J,
Tapia-Conyer R,
Locke AE,
Baras A,
Verweij N,
Lotta LA
Regeneron Genetics Center · DiscovEHR Collaboration
Nature communications · 2022 · PMID 35999217 · open access
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
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
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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?
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It is rebuilt from the pages every hour. A paper appears the moment a page starts
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keep in step, because the citation lives on the page that makes the claim.