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2,657 papers hold this site up. Every variant and condition page names
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12 matches for
King A.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
Brazel DM,
Jiang Y,
Hughey JM,
Turcot V,
Zhan X,
Gong J,
Batini C,
Weissenkampen JD,
Liu M,
Barnes DR,
Bertelsen S,
Chou YL
and 59 more — show all
Erzurumluoglu AM,
Faul JD,
Haessler J,
Hammerschlag AR,
Hsu C,
Kapoor M,
Lai D,
Le N,
de Leeuw CA,
Loukola A,
Mangino M,
Melbourne CA,
Pistis G,
Qaiser B,
Rohde R,
Shao Y,
Stringham H,
Wetherill L,
Zhao W,
Agrawal A,
Bierut L,
Chen C,
Eaton CB,
Goate A,
Haiman C,
Heath A,
Iacono WG,
Martin NG,
Polderman TJ,
Reiner A,
Rice J,
Schlessinger D,
Scholte HS,
Smith JA,
Tardif JC,
Tindle HA,
van der Leij AR,
Boehnke M,
Chang-Claude J,
Cucca F,
David SP,
Foroud T,
Howson JMM,
Kardia SLR,
Kooperberg C,
Laakso M,
Lettre G,
Madden P,
McGue M,
North K,
Posthuma D,
Spector T,
Stram D,
Tobin MD,
Weir DR,
Kaprio J,
Abecasis GR,
Liu DJ,
Vrieze S
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
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+
Environmental and genetic predictors of human cardiovascular ageing
Shah M,
de A Inácio MH,
Lu C,
Schiratti PR,
Zheng SL,
Clement A,
de Marvao A,
Bai W,
King AP,
Ware JS,
Wilkins MR,
Mielke J
and 6 more — show all
Nature communications · 2023 · PMID 37604819 · open access
3 pages
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Wang Z,
Seow WJ,
Shiraishi K,
Hsiung CA,
Matsuo K,
Liu J,
Chen K,
Yamji T,
Yang Y,
Chang IS,
Wu C,
Hong YC
and 138 more — show all
Burdett L,
Wyatt K,
Chung CC,
Li SA,
Yeager M,
Hutchinson A,
Hu W,
Caporaso N,
Landi MT,
Chatterjee N,
Song M,
Fraumeni JF Jr,
Kohno T,
Yokota J,
Kunitoh H,
Ashikawa K,
Momozawa Y,
Daigo Y,
Mitsudomi T,
Yatabe Y,
Hida T,
Hu Z,
Dai J,
Ma H,
Jin G,
Song B,
Wang Z,
Cheng S,
Yin Z,
Li X,
Ren Y,
Guan P,
Chang J,
Tan W,
Chen CJ,
Chang GC,
Tsai YH,
Su WC,
Chen KY,
Huang MS,
Chen YM,
Zheng H,
Li H,
Cui P,
Guo H,
Xu P,
Liu L,
Iwasaki M,
Shimazu T,
Tsugane S,
Zhu J,
Jiang G,
Fei K,
Park JY,
Kim YH,
Sung JS,
Park KH,
Kim YT,
Jung YJ,
Kang CH,
Park IK,
Kim HN,
Jeon HS,
Choi JE,
Choi YY,
Kim JH,
Oh IJ,
Kim YC,
Sung SW,
Kim JS,
Yoon HI,
Kweon SS,
Shin MH,
Seow A,
Chen Y,
Lim WY,
Liu J,
Wong MP,
Lee VH,
Bassig BA,
Tucker M,
Berndt SI,
Chow WH,
Ji BT,
Wang J,
Xu J,
Sihoe AD,
Ho JC,
Chan JK,
Wang JC,
Lu D,
Zhao X,
Zhao Z,
Wu J,
Chen H,
Jin L,
Wei F,
Wu G,
An SJ,
Zhang XC,
Su J,
Wu YL,
Gao YT,
Xiang YB,
He X,
Li J,
Zheng W,
Shu XO,
Cai Q,
Klein R,
Pao W,
Lawrence C,
Hosgood HD 3rd,
Hsiao CF,
Chien LH,
Chen YH,
Chen CH,
Wang WC,
Chen CY,
Wang CL,
Yu CJ,
Chen HL,
Su YC,
Tsai FY,
Chen YS,
Li YJ,
Yang TY,
Lin CC,
Yang PC,
Wu T,
Lin D,
Zhou B,
Yu J,
Shen H,
Kubo M,
Chanock SJ,
Rothman N,
Lan Q
Human molecular genetics · 2016 · PMID 26732429
1 page
Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism
Pardiñas AF,
Nalmpanti M,
Pocklington AJ,
Legge SE,
Medway C,
King A,
Jansen J,
Helthuis M,
Zammit S,
MacCabe J,
Owen MJ,
O'Donovan MC
and 1 more — show all
The American journal of psychiatry · 2019 · PMID 30922102
1 page
Association of Variants Near the Bradykinin Receptor B<sub>2</sub> Gene With Angioedema in Patients Taking ACE Inhibitors
Ghouse J,
Ahlberg G,
Andreasen L,
Banasik K,
Brunak S,
Schwinn M,
Larsen IH,
Petersen O,
Sørensen E,
Ullum H,
Rasmussen ER,
Eriksson N
and 4 more — show all
Journal of the American College of Cardiology · 2021 · PMID 34384552
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
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation
Adlam D,
Berrandou TE,
Georges A,
Nelson CP,
Giannoulatou E,
Henry J,
Ma L,
Blencowe M,
Turley TN,
Yang ML,
Chopade S,
Finan C
and 40 more — show all
Braund PS,
Sadeg-Sayoud I,
Iismaa SE,
Kosel ML,
Zhou X,
Hamby SE,
Cheng J,
Liu L,
Tarr I,
Muller DWM,
d'Escamard V,
King A,
Brunham LR,
Baranowska-Clarke AA,
Debette S,
Amouyel P,
Olin JW,
Patil S,
Hesselson SE,
Junday K,
Kanoni S,
Aragam KG,
Butterworth AS,
Tweet MS,
Gulati R,
Combaret N,
Kadian-Dodov D,
Kalman JM,
Fatkin D,
Hingorani AD,
Saw J,
Webb TR,
Hayes SN,
Yang X,
Ganesh SK,
Olson TM,
Kovacic JC,
Graham RM,
Samani NJ,
Bouatia-Naji N
CARDIoGRAMPlusC4D · MEGASTROKE and 2 more consortia
Nature genetics · 2023 · PMID 37248441 · 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?
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.