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84 matches for
He P,
showing the first 20.
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts
Sanchez-Roige S,
Palmer AA,
Fontanillas P,
Elson SL,
Adams MJ,
Howard DM,
Edenberg HJ,
Davies G,
Crist RC,
Deary IJ,
McIntosh AM,
Clarke TK
23andMe Research Team, the Substance Use Disorder Working Group of the Psychiatric Genomics Consortium
The American journal of psychiatry · 2019 · PMID 30336701
6 pages
Genome-wide association study identifies 30 loci associated with bipolar disorder
Stahl EA,
Breen G,
Forstner AJ,
McQuillin A,
Ripke S,
Trubetskoy V,
Mattheisen M,
Wang Y,
Coleman JRI,
Gaspar HA,
de Leeuw CA,
Steinberg S
and 265 more — show all
Pavlides JMW,
Trzaskowski M,
Byrne EM,
Pers TH,
Holmans PA,
Richards AL,
Abbott L,
Agerbo E,
Akil H,
Albani D,
Alliey-Rodriguez N,
Als TD,
Anjorin A,
Antilla V,
Awasthi S,
Badner JA,
Bækvad-Hansen M,
Barchas JD,
Bass N,
Bauer M,
Belliveau R,
Bergen SE,
Pedersen CB,
Bøen E,
Boks MP,
Boocock J,
Budde M,
Bunney W,
Burmeister M,
Bybjerg-Grauholm J,
Byerley W,
Casas M,
Cerrato F,
Cervantes P,
Chambert K,
Charney AW,
Chen D,
Churchhouse C,
Clarke TK,
Coryell W,
Craig DW,
Cruceanu C,
Curtis D,
Czerski PM,
Dale AM,
de Jong S,
Degenhardt F,
Del-Favero J,
DePaulo JR,
Djurovic S,
Dobbyn AL,
Dumont A,
Elvsåshagen T,
Escott-Price V,
Fan CC,
Fischer SB,
Flickinger M,
Foroud TM,
Forty L,
Frank J,
Fraser C,
Freimer NB,
Frisén L,
Gade K,
Gage D,
Garnham J,
Giambartolomei C,
Pedersen MG,
Goldstein J,
Gordon SD,
Gordon-Smith K,
Green EK,
Green MJ,
Greenwood TA,
Grove J,
Guan W,
Guzman-Parra J,
Hamshere ML,
Hautzinger M,
Heilbronner U,
Herms S,
Hipolito M,
Hoffmann P,
Holland D,
Huckins L,
Jamain S,
Johnson JS,
Juréus A,
Kandaswamy R,
Karlsson R,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koller AC,
Kupka R,
Lavebratt C,
Lawrence J,
Lawson WB,
Leber M,
Lee PH,
Levy SE,
Li JZ,
Liu C,
Lucae S,
Maaser A,
MacIntyre DJ,
Mahon PB,
Maier W,
Martinsson L,
McCarroll S,
McGuffin P,
McInnis MG,
McKay JD,
Medeiros H,
Medland SE,
Meng F,
Milani L,
Montgomery GW,
Morris DW,
Mühleisen TW,
Mullins N,
Nguyen H,
Nievergelt CM,
Adolfsson AN,
Nwulia EA,
O'Donovan C,
Loohuis LMO,
Ori APS,
Oruc L,
Ösby U,
Perlis RH,
Perry A,
Pfennig A,
Potash JB,
Purcell SM,
Regeer EJ,
Reif A,
Reinbold CS,
Rice JP,
Rivas F,
Rivera M,
Roussos P,
Ruderfer DM,
Ryu E,
Sánchez-Mora C,
Schatzberg AF,
Scheftner WA,
Schork NJ,
Shannon Weickert C,
Shehktman T,
Shilling PD,
Sigurdsson E,
Slaney C,
Smeland OB,
Sobell JL,
Søholm Hansen C,
Spijker AT,
St Clair D,
Steffens M,
Strauss JS,
Streit F,
Strohmaier J,
Szelinger S,
Thompson RC,
Thorgeirsson TE,
Treutlein J,
Vedder H,
Wang W,
Watson SJ,
Weickert TW,
Witt SH,
Xi S,
Xu W,
Young AH,
Zandi P,
Zhang P,
Zöllner S,
Adolfsson R,
Agartz I,
Alda M,
Backlund L,
Baune BT,
Bellivier F,
Berrettini WH,
Biernacka JM,
Blackwood DHR,
Boehnke M,
Børglum AD,
Corvin A,
Craddock N,
Daly MJ,
Dannlowski U,
Esko T,
Etain B,
Frye M,
Fullerton JM,
Gershon ES,
Gill M,
Goes F,
Grigoroiu-Serbanescu M,
Hauser J,
Hougaard DM,
Hultman CM,
Jones I,
Jones LA,
Kahn RS,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Martin NG,
Mayoral F,
McElroy SL,
McIntosh AM,
McMahon FJ,
Melle I,
Metspalu A,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nimgaonkar V,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Owen MJ,
Paciga SA,
Pato C,
Pato MT,
Posthuma D,
Ramos-Quiroga JA,
Ribasés M,
Rietschel M,
Rouleau GA,
Schalling M,
Schofield PR,
Schulze TG,
Serretti A,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Sullivan PF,
Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Werge T,
Nurnberger JI,
Wray NR,
Di Florio A,
Edenberg HJ,
Cichon S,
Ophoff RA,
Scott LJ,
Andreassen OA,
Kelsoe J,
Sklar P
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
Minimal phenotyping yields genome-wide association signals of low specificity for major depression
Cai N,
Revez JA,
Adams MJ,
Andlauer TFM,
Breen G,
Byrne EM,
Clarke TK,
Forstner AJ,
Grabe HJ,
Hamilton SP,
Levinson DF,
Lewis CM
and 21 more — show all
Lewis G,
Martin NG,
Milaneschi Y,
Mors O,
Müller-Myhsok B,
Penninx BWJH,
Perlis RH,
Pistis G,
Potash JB,
Potash JB,
Preisig M,
Shi J,
Smoller JW,
Streit F,
Tiemeier H,
Uher R,
Van der Auwera S,
Viktorin A,
Weissman MM,
Kendler KS,
Flint J
MDD Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2020 · PMID 32231276
6 pages
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality
Soler Artigas M,
Sánchez-Mora C,
Rovira P,
Richarte V,
Garcia-Martínez I,
Pagerols M,
Demontis D,
Stringer S,
Vink JM,
Børglum AD,
Neale BM,
Franke B
and 4 more — show all
ADHD Group of the Psychiatric Genomics Consortium, International Cannabis Consortium
Molecular psychiatry · 2020 · PMID 30610198
5 pages
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Rietveld CA,
Esko T,
Davies G,
Pers TH,
Turley P,
Benyamin B,
Chabris CF,
Emilsson V,
Johnson AD,
Lee JJ,
de Leeuw C,
Marioni RE
and 48 more — show all
Medland SE,
Miller MB,
Rostapshova O,
van der Lee SJ,
Vinkhuyzen AA,
Amin N,
Conley D,
Derringer J,
van Duijn CM,
Fehrmann R,
Franke L,
Glaeser EL,
Hansell NK,
Hayward C,
Iacono WG,
Ibrahim-Verbaas C,
Jaddoe V,
Karjalainen J,
Laibson D,
Lichtenstein P,
Liewald DC,
Magnusson PK,
Martin NG,
McGue M,
McMahon G,
Pedersen NL,
Pinker S,
Porteous DJ,
Posthuma D,
Rivadeneira F,
Smith BH,
Smith BH,
Starr JM,
Tiemeier H,
Timpson NJ,
Trzaskowski M,
Uitterlinden AG,
Verhulst FC,
Ward ME,
Wright MJ,
Davey Smith G,
Deary IJ,
Johannesson M,
Plomin R,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
4 pages
Effect of genetic variations on ticagrelor plasma levels and clinical outcomes
Varenhorst C,
Eriksson N,
Johansson Å,
Barratt BJ,
Hagström E,
Åkerblom A,
Syvänen AC,
Becker RC,
James SK,
Katus HA,
Husted S,
Steg PG
and 5 more — show all
PLATO Investigators
European heart journal · 2015 · PMID 25935875
4 pages
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies
Tamm R,
Mägi R,
Tremmel R,
Winter S,
Mihailov E,
Smid A,
Möricke A,
Klein K,
Schrappe M,
Stanulla M,
Houlston R,
Weinshilboum R
and 5 more — show all
Clinical pharmacology and therapeutics · 2017 · PMID 27770449
4 pages
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
and 25 more — show all
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Demontis D,
Walters GB,
Athanasiadis G,
Walters R,
Therrien K,
Nielsen TT,
Farajzadeh L,
Voloudakis G,
Bendl J,
Zeng B,
Zhang W,
Grove J
and 35 more — show all
Als TD,
Duan J,
Satterstrom FK,
Bybjerg-Grauholm J,
Bækved-Hansen M,
Gudmundsson OO,
Magnusson SH,
Baldursson G,
Davidsdottir K,
Haraldsdottir GS,
Agerbo E,
Hoffman GE,
Dalsgaard S,
Martin J,
Ribasés M,
Boomsma DI,
Soler Artigas M,
Roth Mota N,
Howrigan D,
Medland SE,
Zayats T,
Rajagopal VM,
Nordentoft M,
Mors O,
Hougaard DM,
Mortensen PB,
Daly MJ,
Faraone SV,
Stefansson H,
Roussos P,
Franke B,
Werge T,
Neale BM,
Stefansson K,
Børglum AD
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
4 pages
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
Strawbridge RJ,
Dupuis J,
Prokopenko I,
Barker A,
Ahlqvist E,
Rybin D,
Petrie JR,
Travers ME,
Bouatia-Naji N,
Dimas AS,
Nica A,
Wheeler E
and 91 more — show all
Chen H,
Voight BF,
Taneera J,
Kanoni S,
Peden JF,
Turrini F,
Gustafsson S,
Zabena C,
Almgren P,
Barker DJ,
Barnes D,
Dennison EM,
Eriksson JG,
Eriksson P,
Eury E,
Folkersen L,
Fox CS,
Frayling TM,
Goel A,
Gu HF,
Horikoshi M,
Isomaa B,
Jackson AU,
Jameson KA,
Kajantie E,
Kerr-Conte J,
Kuulasmaa T,
Kuusisto J,
Loos RJ,
Luan J,
Makrilakis K,
Manning AK,
Martínez-Larrad MT,
Narisu N,
Nastase Mannila M,
Ohrvik J,
Osmond C,
Pascoe L,
Payne F,
Sayer AA,
Sennblad B,
Silveira A,
Stancáková A,
Stirrups K,
Swift AJ,
Syvänen AC,
Tuomi T,
van 't Hooft FM,
Walker M,
Weedon MN,
Xie W,
Zethelius B,
Ongen H,
Mälarstig A,
Hopewell JC,
Saleheen D,
Chambers J,
Parish S,
Danesh J,
Kooner J,
Ostenson CG,
Lind L,
Cooper CC,
Serrano-Ríos M,
Ferrannini E,
Forsen TJ,
Clarke R,
Franzosi MG,
Seedorf U,
Watkins H,
Froguel P,
Johnson P,
Deloukas P,
Collins FS,
Laakso M,
Dermitzakis ET,
Boehnke M,
McCarthy MI,
Wareham NJ,
Groop L,
Pattou F,
Gloyn AL,
Dedoussis GV,
Lyssenko V,
Meigs JB,
Barroso I,
Watanabe RM,
Ingelsson E,
Langenberg C,
Hamsten A,
Florez JC
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Diabetes · 2011 · PMID 21873549 · open access
3 pages
Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris
Navarini AA,
Simpson MA,
Weale M,
Knight J,
Carlavan I,
Reiniche P,
Burden DA,
Layton A,
Bataille V,
Allen M,
Pleass R,
Pink A
and 11 more — show all
Creamer D,
English J,
Munn S,
Walton S,
Willis C,
Déret S,
Voegel JJ,
Spector T,
Smith CH,
Trembath RC,
Barker JN
Acne Genetic Study Group
Nature communications · 2014 · PMID 24927181
3 pages
A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine
Nakajima M,
Takahashi A,
Tsuji T,
Karasugi T,
Baba H,
Uchida K,
Kawabata S,
Okawa A,
Shindo S,
Takeuchi K,
Taniguchi Y,
Maeda S
and 22 more — show all
Kashii M,
Seichi A,
Nakajima H,
Kawaguchi Y,
Fujibayashi S,
Takahata M,
Tanaka T,
Watanabe K,
Kida K,
Kanchiku T,
Ito Z,
Mori K,
Kaito T,
Kobayashi S,
Yamada K,
Takahashi M,
Chiba K,
Matsumoto M,
Furukawa K,
Kubo M,
Toyama Y,
Ikegawa S
Genetic Study Group of Investigation Committee on Ossification of the Spinal Ligaments
Nature genetics · 2014 · PMID 25064007
3 pages
A genome-wide analysis of the response to inhaled β2-agonists in chronic obstructive pulmonary disease
Hardin M,
Cho MH,
McDonald ML,
Wan E,
Lomas DA,
Coxson HO,
MacNee W,
Vestbo J,
Yates JC,
Agusti A,
Calverley PM,
Celli B
and 13 more — show all
Crim C,
Rennard S,
Wouters E,
Bakke P,
Bhatt SP,
Kim V,
Ramsdell J,
Regan EA,
Make BJ,
Hokanson JE,
Crapo JD,
Beaty TH,
Hersh CP
ECLIPSE and COPDGene Investigators · COPDGene Investigators—clinical centers
The pharmacogenomics journal · 2016 · PMID 26503814 · open access
3 pages
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures
Styrkarsdottir U,
Thorleifsson G,
Gudjonsson SA,
Sigurdsson A,
Center JR,
Lee SH,
Nguyen TV,
Kwok TCY,
Lee JSW,
Ho SC,
Woo J,
Leung PC
and 11 more — show all
Kim BJ,
Rafnar T,
Kiemeney LA,
Ingvarsson T,
Koh JM,
Tang NLS,
Eisman JA,
Christiansen C,
Sigurdsson G,
Thorsteinsdottir U,
Stefansson K
Nature communications · 2016 · PMID 26733130 · open access
3 pages
Multidimensional Bone Density Phenotyping Reveals New Insights Into Genetic Regulation of the Pediatric Skeleton
Mitchell JA,
Chesi A,
Cousminer DL,
McCormack SE,
Kalkwarf HJ,
Lappe JM,
Gilsanz V,
Oberfield SE,
Shepherd JA,
Kelly A,
Zemel BS,
Grant SF
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2018 · PMID 29240982
3 pages
Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of <i>FADS1</i> variants to arachidonic acid, a critical infant micronutrient
Mychaleckyj JC,
Nayak U,
Colgate ER,
Zhang D,
Carstensen T,
Ahmed S,
Ahmed T,
Mentzer AJ,
Alam M,
Kirkpatrick BD,
Haque R,
Faruque ASG
and 1 more — show all
Journal of medical genetics · 2018 · PMID 29514873 · open access
3 pages
Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder
Amare AT,
Schubert KO,
Tekola-Ayele F,
Hsu YH,
Sangkuhl K,
Jenkins G,
Whaley RM,
Barman P,
Batzler A,
Altman RB,
Arolt V,
Brockmöller J
and 25 more — show all
Chen CH,
Domschke K,
Hall-Flavin DK,
Hong CJ,
Illi A,
Ji Y,
Kampman O,
Kinoshita T,
Leinonen E,
Liou YJ,
Mushiroda T,
Nonen S,
Skime MK,
Wang L,
Kato M,
Liu YL,
Praphanphoj V,
Stingl JC,
Bobo WV,
Tsai SJ,
Kubo M,
Klein TE,
Weinshilboum RM,
Biernacka JM,
Baune BT
Frontiers in psychiatry · 2018 · PMID 29559929 · open access
3 pages
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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
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