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580 matches for
An J,
showing the first 20.
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Nielsen JB,
Thorolfsdottir RB,
Fritsche LG,
Zhou W,
Skov MW,
Graham SE,
Herron TJ,
McCarthy S,
Schmidt EM,
Sveinbjornsson G,
Surakka I,
Mathis MR
and 37 more — show all
Yamazaki M,
Crawford RD,
Gabrielsen ME,
Skogholt AH,
Holmen OL,
Lin M,
Wolford BN,
Dey R,
Dalen H,
Sulem P,
Chung JH,
Backman JD,
Arnar DO,
Thorsteinsdottir U,
Baras A,
O'Dushlaine C,
Holst AG,
Wen X,
Hornsby W,
Dewey FE,
Boehnke M,
Kheterpal S,
Mukherjee B,
Lee S,
Kang HM,
Holm H,
Kitzman J,
Shavit JA,
Jalife J,
Brummett CM,
Teslovich TM,
Carey DJ,
Gudbjartsson DF,
Stefansson K,
Abecasis GR,
Hveem K,
Willer CJ
Nature genetics · 2018 · PMID 30061737
12 pages+
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Evangelou E,
Warren HR,
Mosen-Ansorena D,
Mifsud B,
Pazoki R,
Gao H,
Ntritsos G,
Dimou N,
Cabrera CP,
Karaman I,
Ng FL,
Evangelou M
and 268 more — show all
Witkowska K,
Tzanis E,
Hellwege JN,
Giri A,
Velez Edwards DR,
Sun YV,
Cho K,
Gaziano JM,
Wilson PWF,
Tsao PS,
Kovesdy CP,
Esko T,
Mägi R,
Milani L,
Almgren P,
Boutin T,
Debette S,
Ding J,
Giulianini F,
Holliday EG,
Jackson AU,
Li-Gao R,
Lin WY,
Luan J,
Mangino M,
Oldmeadow C,
Prins BP,
Qian Y,
Sargurupremraj M,
Shah N,
Surendran P,
Thériault S,
Verweij N,
Willems SM,
Zhao JH,
Amouyel P,
Connell J,
de Mutsert R,
Doney ASF,
Farrall M,
Menni C,
Morris AD,
Noordam R,
Paré G,
Poulter NR,
Shields DC,
Stanton A,
Thom S,
Abecasis G,
Amin N,
Arking DE,
Ayers KL,
Barbieri CM,
Batini C,
Bis JC,
Blake T,
Bochud M,
Boehnke M,
Boerwinkle E,
Boomsma DI,
Bottinger EP,
Braund PS,
Brumat M,
Campbell A,
Campbell H,
Chakravarti A,
Chambers JC,
Chauhan G,
Ciullo M,
Cocca M,
Collins F,
Cordell HJ,
Davies G,
de Borst MH,
de Geus EJ,
Deary IJ,
Deelen J,
Del Greco M F,
Demirkale CY,
Dörr M,
Ehret GB,
Elosua R,
Enroth S,
Erzurumluoglu AM,
Ferreira T,
Frånberg M,
Franco OH,
Gandin I,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Goel A,
Gow AJ,
Gudnason V,
Guo X,
Gyllensten U,
Hamsten A,
Harris TB,
Harris SE,
Hartman CA,
Havulinna AS,
Hicks AA,
Hofer E,
Hofman A,
Hottenga JJ,
Huffman JE,
Hwang SJ,
Ingelsson E,
James A,
Jansen R,
Jarvelin MR,
Joehanes R,
Johansson Å,
Johnson AD,
Joshi PK,
Jousilahti P,
Jukema JW,
Jula A,
Kähönen M,
Kathiresan S,
Keavney BD,
Khaw KT,
Knekt P,
Knight J,
Kolcic I,
Kooner JS,
Koskinen S,
Kristiansson K,
Kutalik Z,
Laan M,
Larson M,
Launer LJ,
Lehne B,
Lehtimäki T,
Liewald DCM,
Lin L,
Lind L,
Lindgren CM,
Liu Y,
Loos RJF,
Lopez LM,
Lu Y,
Lyytikäinen LP,
Mahajan A,
Mamasoula C,
Marrugat J,
Marten J,
Milaneschi Y,
Morgan A,
Morris AP,
Morrison AC,
Munson PJ,
Nalls MA,
Nandakumar P,
Nelson CP,
Niiranen T,
Nolte IM,
Nutile T,
Oldehinkel AJ,
Oostra BA,
O'Reilly PF,
Org E,
Padmanabhan S,
Palmas W,
Palotie A,
Pattie A,
Penninx BWJH,
Perola M,
Peters A,
Polasek O,
Pramstaller PP,
Nguyen QT,
Raitakari OT,
Ren M,
Rettig R,
Rice K,
Ridker PM,
Ried JS,
Riese H,
Ripatti S,
Robino A,
Rose LM,
Rotter JI,
Rudan I,
Ruggiero D,
Saba Y,
Sala CF,
Salomaa V,
Samani NJ,
Sarin AP,
Schmidt R,
Schmidt H,
Shrine N,
Siscovick D,
Smith AV,
Snieder H,
Sõber S,
Sorice R,
Starr JM,
Stott DJ,
Strachan DP,
Strawbridge RJ,
Sundström J,
Swertz MA,
Taylor KD,
Teumer A,
Tobin MD,
Tomaszewski M,
Toniolo D,
Traglia M,
Trompet S,
Tuomilehto J,
Tzourio C,
Uitterlinden AG,
Vaez A,
van der Most PJ,
van Duijn CM,
Vergnaud AC,
Verwoert GC,
Vitart V,
Völker U,
Vollenweider P,
Vuckovic D,
Watkins H,
Wild SH,
Willemsen G,
Wilson JF,
Wright AF,
Yao J,
Zemunik T,
Zhang W,
Attia JR,
Butterworth AS,
Chasman DI,
Conen D,
Cucca F,
Danesh J,
Hayward C,
Howson JMM,
Laakso M,
Lakatta EG,
Langenberg C,
Melander O,
Mook-Kanamori DO,
Palmer CNA,
Risch L,
Scott RA,
Scott RJ,
Sever P,
Spector TD,
van der Harst P,
Wareham NJ,
Zeggini E,
Levy D,
Munroe PB,
Newton-Cheh C,
Brown MJ,
Metspalu A,
Hung AM,
O'Donnell CJ,
Edwards TL,
Psaty BM,
Tzoulaki I,
Barnes MR,
Wain LV,
Elliott P,
Caulfield MJ
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Klarin D,
Damrauer SM,
Cho K,
Sun YV,
Teslovich TM,
Honerlaw J,
Gagnon DR,
DuVall SL,
Li J,
Peloso GM,
Chaffin M,
Small AM
and 33 more — show all
Huang J,
Tang H,
Lynch JA,
Ho YL,
Liu DJ,
Emdin CA,
Li AH,
Huffman JE,
Lee JS,
Natarajan P,
Chowdhury R,
Saleheen D,
Vujkovic M,
Baras A,
Pyarajan S,
Di Angelantonio E,
Neale BM,
Naheed A,
Khera AV,
Danesh J,
Chang KM,
Abecasis G,
Willer C,
Dewey FE,
Carey DJ,
Concato J,
Gaziano JM,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Rader DJ,
Wilson PWF,
Assimes TL
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium and 2 more consortia
Nature genetics · 2018 · PMID 30275531 · open access
12 pages+
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
van der Meer D,
Rokicki J,
Kaufmann T,
Córdova-Palomera A,
Moberget T,
Alnæs D,
Bettella F,
Frei O,
Doan NT,
Sønderby IE,
Smeland OB,
Agartz I
and 42 more — show all
Bertolino A,
Bralten J,
Brandt CL,
Buitelaar JK,
Djurovic S,
van Donkelaar M,
Dørum ES,
Espeseth T,
Faraone SV,
Fernández G,
Fisher SE,
Franke B,
Haatveit B,
Hartman CA,
Hoekstra PJ,
Håberg AK,
Jönsson EG,
Kolskår KK,
Le Hellard S,
Lund MJ,
Lundervold AJ,
Lundervold A,
Melle I,
Monereo Sánchez J,
Norbom LC,
Nordvik JE,
Nyberg L,
Oosterlaan J,
Papalino M,
Papassotiropoulos A,
Pergola G,
de Quervain DJF,
Richard G,
Sanders AM,
Selvaggi P,
Shumskaya E,
Steen VM,
Tønnesen S,
Ulrichsen KM,
Zwiers MP,
Andreassen OA,
Westlye LT
Alzheimer’s Disease Neuroimaging Initiative · Pediatric Imaging, Neurocognition and Genetics Study
Molecular psychiatry · 2020 · PMID 30279459 · open access
12 pages+
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Mahajan A,
Taliun D,
Thurner M,
Robertson NR,
Torres JM,
Rayner NW,
Payne AJ,
Steinthorsdottir V,
Scott RA,
Grarup N,
Cook JP,
Schmidt EM
and 103 more — show all
Wuttke M,
Sarnowski C,
Mägi R,
Nano J,
Gieger C,
Trompet S,
Lecoeur C,
Preuss MH,
Prins BP,
Guo X,
Bielak LF,
Below JE,
Bowden DW,
Chambers JC,
Kim YJ,
Ng MCY,
Petty LE,
Sim X,
Zhang W,
Bennett AJ,
Bork-Jensen J,
Brummett CM,
Canouil M,
Ec Kardt KU,
Fischer K,
Kardia SLR,
Kronenberg F,
Läll K,
Liu CT,
Locke AE,
Luan J,
Ntalla I,
Nylander V,
Schönherr S,
Schurmann C,
Yengo L,
Bottinger EP,
Brandslund I,
Christensen C,
Dedoussis G,
Florez JC,
Ford I,
Franco OH,
Frayling TM,
Giedraitis V,
Hackinger S,
Hattersley AT,
Herder C,
Ikram MA,
Ingelsson M,
Jørgensen ME,
Jørgensen T,
Kriebel J,
Kuusisto J,
Ligthart S,
Lindgren CM,
Linneberg A,
Lyssenko V,
Mamakou V,
Meitinger T,
Mohlke KL,
Morris AD,
Nadkarni G,
Pankow JS,
Peters A,
Sattar N,
Stančáková A,
Strauch K,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tuomilehto J,
Witte DR,
Dupuis J,
Peyser PA,
Zeggini E,
Loos RJF,
Froguel P,
Ingelsson E,
Lind L,
Groop L,
Laakso M,
Collins FS,
Jukema JW,
Palmer CNA,
Grallert H,
Metspalu A,
Dehghan A,
Köttgen A,
Abecasis GR,
Meigs JB,
Rotter JI,
Marchini J,
Pedersen O,
Hansen T,
Langenberg C,
Wareham NJ,
Stefansson K,
Gloyn AL,
Morris AP,
Boehnke M,
McCarthy MI
Nature genetics · 2018 · PMID 30297969
12 pages+
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Teumer A,
Chaker L,
Groeneweg S,
Li Y,
Di Munno C,
Barbieri C,
Schultheiss UT,
Traglia M,
Ahluwalia TS,
Akiyama M,
Appel EVR,
Arking DE
and 116 more — show all
Arnold A,
Astrup A,
Beekman M,
Beilby JP,
Bekaert S,
Boerwinkle E,
Brown SJ,
De Buyzere M,
Campbell PJ,
Ceresini G,
Cerqueira C,
Cucca F,
Deary IJ,
Deelen J,
Eckardt KU,
Ekici AB,
Eriksson JG,
Ferrrucci L,
Fiers T,
Fiorillo E,
Ford I,
Fox CS,
Fuchsberger C,
Galesloot TE,
Gieger C,
Gögele M,
De Grandi A,
Grarup N,
Greiser KH,
Haljas K,
Hansen T,
Harris SE,
van Heemst D,
den Heijer M,
Hicks AA,
den Hollander W,
Homuth G,
Hui J,
Ikram MA,
Ittermann T,
Jensen RA,
Jing J,
Jukema JW,
Kajantie E,
Kamatani Y,
Kasbohm E,
Kaufman JM,
Kiemeney LA,
Kloppenburg M,
Kronenberg F,
Kubo M,
Lahti J,
Lapauw B,
Li S,
Liewald DCM,
Lim EM,
Linneberg A,
Marina M,
Mascalzoni D,
Matsuda K,
Medenwald D,
Meisinger C,
Meulenbelt I,
De Meyer T,
Meyer Zu Schwabedissen HE,
Mikolajczyk R,
Moed M,
Netea-Maier RT,
Nolte IM,
Okada Y,
Pala M,
Pattaro C,
Pedersen O,
Petersmann A,
Porcu E,
Postmus I,
Pramstaller PP,
Psaty BM,
Ramos YFM,
Rawal R,
Redmond P,
Richards JB,
Rietzschel ER,
Rivadeneira F,
Roef G,
Rotter JI,
Sala CF,
Schlessinger D,
Selvin E,
Slagboom PE,
Soranzo N,
Sørensen TIA,
Spector TD,
Starr JM,
Stott DJ,
Taes Y,
Taliun D,
Tanaka T,
Thuesen B,
Tiller D,
Toniolo D,
Uitterlinden AG,
Visser WE,
Walsh JP,
Wilson SG,
Wolffenbuttel BHR,
Yang Q,
Zheng HF,
Cappola A,
Peeters RP,
Naitza S,
Völzke H,
Sanna S,
Köttgen A,
Visser TJ,
Medici M
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
Ligthart S,
Vaez A,
Võsa U,
Stathopoulou MG,
de Vries PS,
Prins BP,
Van der Most PJ,
Tanaka T,
Naderi E,
Rose LM,
Wu Y,
Karlsson R
and 274 more — show all
Barbalic M,
Lin H,
Pool R,
Zhu G,
Macé A,
Sidore C,
Trompet S,
Mangino M,
Sabater-Lleal M,
Kemp JP,
Abbasi A,
Kacprowski T,
Verweij N,
Smith AV,
Huang T,
Marzi C,
Feitosa MF,
Lohman KK,
Kleber ME,
Milaneschi Y,
Mueller C,
Huq M,
Vlachopoulou E,
Lyytikäinen LP,
Oldmeadow C,
Deelen J,
Perola M,
Zhao JH,
Feenstra B,
Amini M,
Lahti J,
Schraut KE,
Fornage M,
Suktitipat B,
Chen WM,
Li X,
Nutile T,
Malerba G,
Luan J,
Bak T,
Schork N,
Del Greco M F,
Thiering E,
Mahajan A,
Marioni RE,
Mihailov E,
Eriksson J,
Ozel AB,
Zhang W,
Nethander M,
Cheng YC,
Aslibekyan S,
Ang W,
Gandin I,
Yengo L,
Portas L,
Kooperberg C,
Hofer E,
Rajan KB,
Schurmann C,
den Hollander W,
Ahluwalia TS,
Zhao J,
Draisma HHM,
Ford I,
Timpson N,
Teumer A,
Huang H,
Wahl S,
Liu Y,
Huang J,
Uh HW,
Geller F,
Joshi PK,
Yanek LR,
Trabetti E,
Lehne B,
Vozzi D,
Verbanck M,
Biino G,
Saba Y,
Meulenbelt I,
O'Connell JR,
Laakso M,
Giulianini F,
Magnusson PKE,
Ballantyne CM,
Hottenga JJ,
Montgomery GW,
Rivadineira F,
Rueedi R,
Steri M,
Herzig KH,
Stott DJ,
Menni C,
Frånberg M,
St Pourcain B,
Felix SB,
Pers TH,
Bakker SJL,
Kraft P,
Peters A,
Vaidya D,
Delgado G,
Smit JH,
Großmann V,
Sinisalo J,
Seppälä I,
Williams SR,
Holliday EG,
Moed M,
Langenberg C,
Räikkönen K,
Ding J,
Campbell H,
Sale MM,
Chen YI,
James AL,
Ruggiero D,
Soranzo N,
Hartman CA,
Smith EN,
Berenson GS,
Fuchsberger C,
Hernandez D,
Tiesler CMT,
Giedraitis V,
Liewald D,
Fischer K,
Mellström D,
Larsson A,
Wang Y,
Scott WR,
Lorentzon M,
Beilby J,
Ryan KA,
Pennell CE,
Vuckovic D,
Balkau B,
Concas MP,
Schmidt R,
Mendes de Leon CF,
Bottinger EP,
Kloppenburg M,
Paternoster L,
Boehnke M,
Musk AW,
Willemsen G,
Evans DM,
Madden PAF,
Kähönen M,
Kutalik Z,
Zoledziewska M,
Karhunen V,
Kritchevsky SB,
Sattar N,
Lachance G,
Clarke R,
Harris TB,
Raitakari OT,
Attia JR,
van Heemst D,
Kajantie E,
Sorice R,
Gambaro G,
Scott RA,
Hicks AA,
Ferrucci L,
Standl M,
Lindgren CM,
Starr JM,
Karlsson M,
Lind L,
Li JZ,
Chambers JC,
Mori TA,
de Geus EJCN,
Heath AC,
Martin NG,
Auvinen J,
Buckley BM,
de Craen AJM,
Waldenberger M,
Strauch K,
Meitinger T,
Scott RJ,
McEvoy M,
Beekman M,
Bombieri C,
Ridker PM,
Mohlke KL,
Pedersen NL,
Morrison AC,
Boomsma DI,
Whitfield JB,
Strachan DP,
Hofman A,
Vollenweider P,
Cucca F,
Jarvelin MR,
Jukema JW,
Spector TD,
Hamsten A,
Zeller T,
Uitterlinden AG,
Nauck M,
Gudnason V,
Qi L,
Grallert H,
Borecki IB,
Rotter JI,
März W,
Wild PS,
Lokki ML,
Boyle M,
Salomaa V,
Melbye M,
Eriksson JG,
Wilson JF,
Penninx BWJH,
Becker DM,
Worrall BB,
Gibson G,
Krauss RM,
Ciullo M,
Zaza G,
Wareham NJ,
Oldehinkel AJ,
Palmer LJ,
Murray SS,
Pramstaller PP,
Bandinelli S,
Heinrich J,
Ingelsson E,
Deary IJ,
Mägi R,
Vandenput L,
van der Harst P,
Desch KC,
Kooner JS,
Ohlsson C,
Hayward C,
Lehtimäki T,
Shuldiner AR,
Arnett DK,
Beilin LJ,
Robino A,
Froguel P,
Pirastu M,
Jess T,
Koenig W,
Loos RJF,
Evans DA,
Schmidt H,
Smith GD,
Slagboom PE,
Eiriksdottir G,
Morris AP,
Psaty BM,
Tracy RP,
Nolte IM,
Boerwinkle E,
Visvikis-Siest S,
Reiner AP,
Gross M,
Bis JC,
Franke L,
Franco OH,
Benjamin EJ,
Chasman DI,
Dupuis J,
Snieder H,
Dehghan A,
Alizadeh BZ
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
Takeuchi F,
Akiyama M,
Matoba N,
Katsuya T,
Nakatochi M,
Tabara Y,
Narita A,
Saw WY,
Moon S,
Spracklen CN,
Chai JF,
Kim YJ
and 83 more — show all
Zhang L,
Wang C,
Li H,
Li H,
Wu JY,
Dorajoo R,
Nierenberg JL,
Wang YX,
He J,
Bennett DA,
Takahashi A,
Momozawa Y,
Hirata M,
Matsuda K,
Rakugi H,
Nakashima E,
Isono M,
Shirota M,
Hozawa A,
Ichihara S,
Matsubara T,
Yamamoto K,
Kohara K,
Igase M,
Han S,
Gordon-Larsen P,
Huang W,
Lee NR,
Adair LS,
Hwang MY,
Lee J,
Chee ML,
Sabanayagam C,
Zhao W,
Liu J,
Reilly DF,
Sun L,
Huo S,
Edwards TL,
Long J,
Chang LC,
Chen CH,
Yuan JM,
Koh WP,
Friedlander Y,
Kelly TN,
Bin Wei W,
Xu L,
Cai H,
Xiang YB,
Lin K,
Clarke R,
Walters RG,
Millwood IY,
Li L,
Chambers JC,
Kooner JS,
Elliott P,
van der Harst P,
Chen Z,
Sasaki M,
Shu XO,
Jonas JB,
He J,
Heng CK,
Chen YT,
Zheng W,
Zheng W,
Lin X,
Teo YY,
Tai ES,
Cheng CY,
Wong TY,
Sim X,
Mohlke KL,
Yamamoto M,
Kim BJ,
Miki T,
Nabika T,
Yokota M,
Kamatani Y,
Kubo M,
Kato N
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors
Lotta LA,
Wittemans LBL,
Zuber V,
Stewart ID,
Sharp SJ,
Luan J,
Day FR,
Li C,
Bowker N,
Cai L,
De Lucia Rolfe E,
Khaw KT
and 7 more — show all
JAMA · 2018 · PMID 30575882
12 pages+
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Giri A,
Hellwege JN,
Keaton JM,
Park J,
Qiu C,
Warren HR,
Torstenson ES,
Kovesdy CP,
Sun YV,
Wilson OD,
Robinson-Cohen C,
Roumie CL
and 86 more — show all
Chung CP,
Birdwell KA,
Damrauer SM,
DuVall SL,
Klarin D,
Cho K,
Wang Y,
Evangelou E,
Cabrera CP,
Wain LV,
Shrestha R,
Mautz BS,
Akwo EA,
Sargurupremraj M,
Debette S,
Boehnke M,
Scott LJ,
Luan J,
Zhao JH,
Willems SM,
Thériault S,
Shah N,
Oldmeadow C,
Almgren P,
Li-Gao R,
Verweij N,
Boutin TS,
Mangino M,
Ntalla I,
Feofanova E,
Surendran P,
Cook JP,
Karthikeyan S,
Lahrouchi N,
Liu C,
Sepúlveda N,
Richardson TG,
Kraja A,
Amouyel P,
Farrall M,
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Laakso M,
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Sever P,
Scott RA,
Langenberg C,
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Understanding Society Scientific Group · International Consortium for Blood Pressure and 2 more consortia
Nature genetics · 2019 · PMID 30578418 · open access
12 pages+
An atlas of genetic influences on osteoporosis in humans and mice
Morris JA,
Kemp JP,
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Chai RC,
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Forgetta V,
Kleinman A,
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Sergio CM,
Quinn J
and 47 more — show all
Nguyen-Yamamoto L,
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Lelliott CJ,
Hinds DA,
Ackert-Bicknell CL,
Hsu YH,
Maurano MT,
Croucher PI,
Williams GR,
Bassett JHD,
Evans DM,
Richards JB
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
12 pages+
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Morris AP,
Le TH,
Wu H,
Akbarov A,
van der Most PJ,
Hemani G,
Smith GD,
Mahajan A,
Gaulton KJ,
Nadkarni GN,
Valladares-Salgado A,
Wacher-Rodarte N
and 60 more — show all
Mychaleckyj JC,
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Kamatani Y,
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Zhu G,
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Bottinger EP,
Buchanan TA,
Cechova S,
Charchar FJ,
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Kiryluk K,
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Kubo M,
Larsson A,
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Lu Y,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
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Sacco RL,
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Taylor KD,
Xiang AH,
Zivkovic A,
Lind L,
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Martin NG,
Whitfield JB,
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Chen YI,
Rundek T,
Rich SS,
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Humphreys BD,
Franceschini N
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
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Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
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Choquet H
and 111 more — show all
Docherty AR,
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Gordon SD,
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Hottenga JJ,
Huang H,
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McMahon G,
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Zhao W,
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Esko T,
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Gudbjartsson DF,
Haller T,
Harris KM,
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Hickie IB,
Hokanson JE,
Hopfer CJ,
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Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
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Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
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Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
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Zuccolo L,
Bierut LJ,
Hveem K,
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23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Karlsson Linnér R,
Biroli P,
Kong E,
Meddens SFW,
Wedow R,
Fontana MA,
Lebreton M,
Tino SP,
Abdellaoui A,
Hammerschlag AR,
Nivard MG,
Okbay A
and 80 more — show all
Rietveld CA,
Timshel PN,
Trzaskowski M,
Vlaming R,
Zünd CL,
Bao Y,
Buzdugan L,
Caplin AH,
Chen CY,
Eibich P,
Fontanillas P,
Gonzalez JR,
Joshi PK,
Karhunen V,
Kleinman A,
Levin RZ,
Lill CM,
Meddens GA,
Muntané G,
Sanchez-Roige S,
Rooij FJV,
Taskesen E,
Wu Y,
Zhang F,
Auton A,
Boardman JD,
Clark DW,
Conlin A,
Dolan CC,
Fischbacher U,
Groenen PJF,
Harris KM,
Hasler G,
Hofman A,
Ikram MA,
Jain S,
Karlsson R,
Kessler RC,
Kooyman M,
MacKillop J,
Männikkö M,
Morcillo-Suarez C,
McQueen MB,
Schmidt KM,
Smart MC,
Sutter M,
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Uitterlinden AG,
White J,
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Yang J,
Bertram L,
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Johannesson M,
Kumari M,
Laibson D,
Magnusson PKE,
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Navarro A,
Palmer AA,
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Posthuma D,
Schunk D,
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Svento R,
Tiemeier H,
Timmers PRHJ,
Turley P,
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Wilson JF,
Gratten J,
Lee JJ,
Cesarini D,
Benjamin DJ,
Koellinger PD,
Beauchamp JP
23and Me Research Team · eQTLgen Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30643258
12 pages+
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population
Imaizumi A,
Adachi Y,
Kawaguchi T,
Higasa K,
Tabara Y,
Sonomura K,
Sato TA,
Takahashi M,
Mizukoshi T,
Yoshida HO,
Kageyama N,
Okamoto C
and 7 more — show all
European journal of human genetics : EJHG · 2019 · PMID 30659259 · open access
12 pages+
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data
Tachmazidou I,
Hatzikotoulas K,
Southam L,
Esparza-Gordillo J,
Haberland V,
Zheng J,
Johnson T,
Koprulu M,
Zengini E,
Steinberg J,
Wilkinson JM,
Bhatnagar S
and 9 more — show all
arcOGEN Consortium
Nature genetics · 2019 · PMID 30664745 · open access
12 pages+
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Kilpeläinen TO,
Bentley AR,
Noordam R,
Sung YJ,
Schwander K,
Winkler TW,
Jakupović H,
Chasman DI,
Manning A,
Ntalla I,
Aschard H,
Brown MR
and 217 more — show all
de las Fuentes L,
Franceschini N,
Guo X,
Vojinovic D,
Aslibekyan S,
Feitosa MF,
Kho M,
Musani SK,
Richard M,
Wang H,
Wang Z,
Bartz TM,
Bielak LF,
Campbell A,
Dorajoo R,
Fisher V,
Hartwig FP,
Horimoto ARVR,
Li C,
Lohman KK,
Marten J,
Sim X,
Smith AV,
Tajuddin SM,
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Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Graff M,
Harris SE,
He M,
Hsu FC,
Jackson AU,
Zhao JH,
Kraja AT,
Kühnel B,
Laguzzi F,
Lyytikäinen LP,
Nolte IM,
Rauramaa R,
Riaz M,
Robino A,
Rueedi R,
Stringham HM,
Takeuchi F,
van der Most PJ,
Varga TV,
Verweij N,
Ware EB,
Wen W,
Li X,
Yanek LR,
Amin N,
Arnett DK,
Boerwinkle E,
Brumat M,
Cade B,
Canouil M,
Chen YI,
Concas MP,
Connell J,
de Mutsert R,
de Silva HJ,
de Vries PS,
Demirkan A,
Ding J,
Eaton CB,
Faul JD,
Friedlander Y,
Gabriel KP,
Ghanbari M,
Giulianini F,
Gu CC,
Gu D,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hunt SC,
Ikram MA,
Jonas JB,
Koh WP,
Komulainen P,
Krieger JE,
Kritchevsky SB,
Kutalik Z,
Kuusisto J,
Langefeld CD,
Langenberg C,
Launer LJ,
Leander K,
Lemaitre RN,
Lewis CE,
Liang J,
Liu J,
Mägi R,
Manichaikul A,
Meitinger T,
Metspalu A,
Milaneschi Y,
Mohlke KL,
Mosley TH Jr,
Murray AD,
Nalls MA,
Nang EK,
Nelson CP,
Nona S,
Norris JM,
Nwuba CV,
O'Connell J,
Palmer ND,
Papanicolau GJ,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Porteous DJ,
Poveda A,
Raitakari OT,
Rich SS,
Risch N,
Robinson JG,
Rose LM,
Rudan I,
Schreiner PJ,
Scott RA,
Sidney SS,
Sims M,
Smith JA,
Snieder H,
Sofer T,
Starr JM,
Sternfeld B,
Strauch K,
Tang H,
Taylor KD,
Tsai MY,
Tuomilehto J,
Uitterlinden AG,
van der Ende MY,
van Heemst D,
Voortman T,
Waldenberger M,
Wennberg P,
Wilson G,
Xiang YB,
Yao J,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Kato N,
Laakso M,
Lakka TA,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Samani NJ,
Shu XO,
van der Harst P,
Van Vliet-Ostaptchouk JV,
Vollenweider P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Weir DR,
Wu T,
Zheng W,
Zhu X,
Evans MK,
Franks PW,
Gudnason V,
Hayward C,
Horta BL,
Kelly TN,
Liu Y,
North KE,
Pereira AC,
Ridker PM,
Tai ES,
van Dam RM,
Fox ER,
Kardia SLR,
Liu CT,
Mook-Kanamori DO,
Province MA,
Redline S,
van Duijn CM,
Rotter JI,
Kooperberg CB,
Gauderman WJ,
Psaty BM,
Rice K,
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Cupples LA,
Rotimi CN,
Morrison AC,
Rao DC,
Loos RJF
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
van Setten J,
Verweij N,
Mbarek H,
Niemeijer MN,
Trompet S,
Arking DE,
Brody JA,
Gandin I,
Grarup N,
Hall LM,
Hemerich D,
Lyytikäinen LP
and 49 more — show all
Mei H,
Müller-Nurasyid M,
Prins BP,
Robino A,
Smith AV,
Warren HR,
Asselbergs FW,
Boomsma DI,
Caulfield MJ,
Eijgelsheim M,
Ford I,
Hansen T,
Harris TB,
Heckbert SR,
Hottenga JJ,
Iorio A,
Kors JA,
Linneberg A,
MacFarlane PW,
Meitinger T,
Nelson CP,
Raitakari OT,
Silva Aldana CT,
Sinagra G,
Sinner M,
Soliman EZ,
Stoll M,
Uitterlinden A,
van Duijn CM,
Waldenberger M,
Alonso A,
Gasparini P,
Gudnason V,
Jamshidi Y,
Kääb S,
Kanters JK,
Lehtimäki T,
Munroe PB,
Peters A,
Samani NJ,
Sotoodehnia N,
Ulivi S,
Wilson JG,
de Geus EJC,
Jukema JW,
Stricker B,
van der Harst P,
de Bakker PIW,
Isaacs A
European journal of human genetics : EJHG · 2019 · PMID 30679814 · open access
12 pages+
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Howard DM,
Adams MJ,
Clarke TK,
Hafferty JD,
Gibson J,
Shirali M,
Coleman JRI,
Hagenaars SP,
Ward J,
Wigmore EM,
Alloza C,
Shen X
and 26 more — show all
Barbu MC,
Xu EY,
Whalley HC,
Marioni RE,
Porteous DJ,
Davies G,
Deary IJ,
Hemani G,
Berger K,
Teismann H,
Rawal R,
Arolt V,
Baune BT,
Dannlowski U,
Domschke K,
Tian C,
Hinds DA,
Trzaskowski M,
Byrne EM,
Ripke S,
Smith DJ,
Sullivan PF,
Wray NR,
Breen G,
Lewis CM,
McIntosh AM
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
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