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Martin N,
showing the first 20.
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Evangelou E,
Gao H,
Chu C,
Ntritsos G,
Ntritsos G,
Blakeley P,
Butts AR,
Pazoki R,
Suzuki H,
Koskeridis F,
Yiorkas AM,
Karaman I
and 88 more — show all
Elliott J,
Luo Q,
Aeschbacher S,
Bartz TM,
Baumeister SE,
Braund PS,
Brown MR,
Brody JA,
Clarke TK,
Dimou N,
Faul JD,
Homuth G,
Jackson AU,
Kentistou KA,
Joshi PK,
Lemaitre RN,
Lind PA,
Lyytikäinen LP,
Mangino M,
Milaneschi Y,
Nelson CP,
Nolte IM,
Perälä MM,
Polasek O,
Porteous D,
Ratliff SM,
Smith JA,
Stančáková A,
Teumer A,
Tuominen S,
Thériault S,
Vangipurapu J,
Whitfield JB,
Wood A,
Yao J,
Yu B,
Zhao W,
Zhao W,
Arking DE,
Auvinen J,
Liu C,
Männikkö M,
Risch L,
Rotter JI,
Snieder H,
Veijola J,
Blakemore AI,
Boehnke M,
Campbell H,
Conen D,
Eriksson JG,
Grabe HJ,
Guo X,
van der Harst P,
Hartman CA,
Hayward C,
Heath AC,
Jarvelin MR,
Kähönen M,
Kardia SLR,
Kühne M,
Kuusisto J,
Laakso M,
Lahti J,
Lehtimäki T,
McIntosh AM,
Mohlke KL,
Morrison AC,
Martin NG,
Oldehinkel AJ,
Penninx BWJH,
Psaty BM,
Raitakari OT,
Rudan I,
Samani NJ,
Scott LJ,
Spector TD,
Verweij N,
Weir DR,
Wilson JF,
Levy D,
Tzoulaki I,
Bell JD,
Matthews PM,
Rothenfluh A,
Desrivières S,
Schumann G,
Elliott P
Nature human behaviour · 2019 · PMID 31358974
9 pages
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
van der Laan CM,
Ip HF,
Schipper M,
Hottenga JJ,
St Pourcain B,
Zayats T,
Pool R,
Krapohl EML,
Brikell I,
Soler Artigas M,
Cabana-Domínguez J,
Llonga N
and 117 more — show all
Nolte IM,
Bolhuis K,
Palviainen T,
Zafarmand H,
Gordon S,
Aliev F,
Burt SA,
Wang CA,
Saunders G,
Karhunen V,
Adkins DE,
Border R,
Peterson RE,
Prinz JA,
Thiering E,
Vilor-Tejedor N,
Ahluwalia TS,
Allegrini A,
Rimfeld K,
Chen Q,
Lu Y,
Martin J,
Bosch R,
Ramos-Quiroga JA,
Neumann A,
Ensink J,
Grasby KL,
Morosoli JJ,
Tong X,
Marrington S,
Scott JG,
Shabalin AA,
Corley R,
Evans LM,
Sugden K,
Alemany S,
Sass L,
Vinding R,
Ehli EA,
Hagenbeek FA,
Derks EM,
Larsson H,
Snieder H,
Cecil C,
Whipp AM,
Korhonen T,
Vuoksimaa E,
Rose RJ,
Uitterlinden AG,
Haavik J,
Harris JR,
Helgeland Ø,
Johansson S,
Knudsen GPS,
Njolstad PR,
Lu Q,
Rodriguez A,
Henders AK,
Mamun A,
Najman JM,
Brown S,
Hopfer C,
Krauter K,
Reynolds CA,
Smolen A,
Stallings M,
Wadsworth S,
Wall TL,
Eaves L,
Silberg JL,
Miller A,
Havdahl A,
Llop S,
Lopez-Espinosa MJ,
Bønnelykke K,
Sunyer J,
Arseneault L,
Standl M,
Heinrich J,
Boden J,
Pearson J,
Horwood J,
Kennedy M,
Poulton R,
Maes HH,
Hewitt J,
Copeland WE,
Middeldorp CM,
Williams GM,
Wray N,
Järvelin MR,
McGue M,
Iacono W,
Caspi A,
Moffitt TE,
Whitehouse AJO,
Pennell CE,
Klump KL,
Jiang C,
Dick DM,
Reichborn-Kjennerud T,
Martin NG,
Medland SE,
Vrijkotte T,
Kaprio J,
Tiemeier H,
Davey Smith G,
Hartman CA,
Oldehinkel AJ,
Casas M,
Ribasés M,
Lichtenstein P,
Lundström S,
Plomin R,
Bartels M,
Nivard MG,
Boomsma DI
Nature genetics · 2025 · PMID 40962958
9 pages
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
Stolk L,
Perry JR,
Chasman DI,
He C,
Mangino M,
Sulem P,
Barbalic M,
Broer L,
Byrne EM,
Ernst F,
Esko T,
Franceschini N
and 167 more — show all
Gudbjartsson DF,
Hottenga JJ,
Kraft P,
McArdle PF,
Porcu E,
Shin SY,
Smith AV,
van Wingerden S,
Zhai G,
Zhuang WV,
Albrecht E,
Alizadeh BZ,
Aspelund T,
Bandinelli S,
Lauc LB,
Beckmann JS,
Boban M,
Boerwinkle E,
Broekmans FJ,
Burri A,
Campbell H,
Chanock SJ,
Chen C,
Cornelis MC,
Corre T,
Coviello AD,
d'Adamo P,
Davies G,
de Faire U,
de Geus EJ,
Deary IJ,
Dedoussis GV,
Deloukas P,
Ebrahim S,
Eiriksdottir G,
Emilsson V,
Eriksson JG,
Fauser BC,
Ferreli L,
Ferrucci L,
Fischer K,
Folsom AR,
Garcia ME,
Gasparini P,
Gieger C,
Glazer N,
Grobbee DE,
Hall P,
Haller T,
Hankinson SE,
Hass M,
Hayward C,
Heath AC,
Hofman A,
Ingelsson E,
Janssens AC,
Johnson AD,
Karasik D,
Kardia SL,
Keyzer J,
Kiel DP,
Kolcic I,
Kutalik Z,
Lahti J,
Lai S,
Laisk T,
Laven JS,
Lawlor DA,
Liu J,
Lopez LM,
Louwers YV,
Magnusson PK,
Marongiu M,
Martin NG,
Klaric IM,
Masciullo C,
McKnight B,
Medland SE,
Melzer D,
Mooser V,
Navarro P,
Newman AB,
Nyholt DR,
Onland-Moret NC,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peeters PH,
Pistis G,
Plump AS,
Polasek O,
Pop VJ,
Psaty BM,
Räikkönen K,
Rehnberg E,
Rotter JI,
Rudan I,
Sala C,
Salumets A,
Scuteri A,
Singleton A,
Smith JA,
Snieder H,
Soranzo N,
Stacey SN,
Starr JM,
Stathopoulou MG,
Stirrups K,
Stolk RP,
Styrkarsdottir U,
Sun YV,
Tenesa A,
Thorand B,
Toniolo D,
Tryggvadottir L,
Tsui K,
Ulivi S,
van Dam RM,
van der Schouw YT,
van Gils CH,
van Nierop P,
Vink JM,
Visscher PM,
Voorhuis M,
Waeber G,
Wallaschofski H,
Wichmann HE,
Widen E,
Wijnands-van Gent CJ,
Willemsen G,
Wilson JF,
Wolffenbuttel BH,
Wright AF,
Yerges-Armstrong LM,
Zemunik T,
Zgaga L,
Zillikens MC,
Zygmunt M,
Arnold AM,
Boomsma DI,
Buring JE,
Crisponi L,
Demerath EW,
Gudnason V,
Harris TB,
Hu FB,
Hunter DJ,
Launer LJ,
Metspalu A,
Montgomery GW,
Oostra BA,
Ridker PM,
Sanna S,
Schlessinger D,
Spector TD,
Stefansson K,
Streeten EA,
Thorsteinsdottir U,
Uda M,
Uitterlinden AG,
van Duijn CM,
Völzke H,
Murray A,
Murabito JM,
Visser JA,
Lunetta KL
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
den Hoed M,
Eijgelsheim M,
Esko T,
Brundel BJ,
Peal DS,
Evans DM,
Nolte IM,
Segrè AV,
Holm H,
Handsaker RE,
Westra HJ,
Johnson T
and 256 more — show all
Isaacs A,
Yang J,
Lundby A,
Zhao JH,
Kim YJ,
Go MJ,
Almgren P,
Bochud M,
Boucher G,
Cornelis MC,
Gudbjartsson D,
Hadley D,
van der Harst P,
Hayward C,
den Heijer M,
Igl W,
Jackson AU,
Kutalik Z,
Luan J,
Kemp JP,
Kristiansson K,
Ladenvall C,
Lorentzon M,
Montasser ME,
Njajou OT,
O'Reilly PF,
Padmanabhan S,
St Pourcain B,
Rankinen T,
Salo P,
Tanaka T,
Timpson NJ,
Vitart V,
Waite L,
Wheeler W,
Zhang W,
Draisma HH,
Feitosa MF,
Kerr KF,
Lind PA,
Mihailov E,
Onland-Moret NC,
Song C,
Weedon MN,
Xie W,
Yengo L,
Absher D,
Albert CM,
Alonso A,
Arking DE,
de Bakker PI,
Balkau B,
Barlassina C,
Benaglio P,
Bis JC,
Bouatia-Naji N,
Brage S,
Chanock SJ,
Chines PS,
Chung M,
Darbar D,
Dina C,
Dörr M,
Elliott P,
Felix SB,
Fischer K,
Fuchsberger C,
de Geus EJ,
Goyette P,
Gudnason V,
Harris TB,
Hartikainen AL,
Havulinna AS,
Heckbert SR,
Hicks AA,
Hofman A,
Holewijn S,
Hoogstra-Berends F,
Hottenga JJ,
Jensen MK,
Johansson A,
Junttila J,
Kääb S,
Kanon B,
Ketkar S,
Khaw KT,
Knowles JW,
Kooner AS,
Kors JA,
Kumari M,
Milani L,
Laiho P,
Lakatta EG,
Langenberg C,
Leusink M,
Liu Y,
Luben RN,
Lunetta KL,
Lynch SN,
Markus MR,
Marques-Vidal P,
Mateo Leach I,
McArdle WL,
McCarroll SA,
Medland SE,
Miller KA,
Montgomery GW,
Morrison AC,
Müller-Nurasyid M,
Navarro P,
Nelis M,
O'Connell JR,
O'Donnell CJ,
Ong KK,
Newman AB,
Peters A,
Polasek O,
Pouta A,
Pramstaller PP,
Psaty BM,
Rao DC,
Ring SM,
Rossin EJ,
Rudan D,
Sanna S,
Scott RA,
Sehmi JS,
Sharp S,
Shin JT,
Singleton AB,
Smith AV,
Soranzo N,
Spector TD,
Stewart C,
Stringham HM,
Tarasov KV,
Uitterlinden AG,
Vandenput L,
Hwang SJ,
Whitfield JB,
Wijmenga C,
Wild SH,
Willemsen G,
Wilson JF,
Witteman JC,
Wong A,
Wong Q,
Jamshidi Y,
Zitting P,
Boer JM,
Boomsma DI,
Borecki IB,
van Duijn CM,
Ekelund U,
Forouhi NG,
Froguel P,
Hingorani A,
Ingelsson E,
Kivimaki M,
Kronmal RA,
Kuh D,
Lind L,
Martin NG,
Oostra BA,
Pedersen NL,
Quertermous T,
Rotter JI,
van der Schouw YT,
Verschuren WM,
Walker M,
Albanes D,
Arnar DO,
Assimes TL,
Bandinelli S,
Boehnke M,
de Boer RA,
Bouchard C,
Caulfield WL,
Chambers JC,
Curhan G,
Cusi D,
Eriksson J,
Ferrucci L,
van Gilst WH,
Glorioso N,
de Graaf J,
Groop L,
Gyllensten U,
Hsueh WC,
Hu FB,
Huikuri HV,
Hunter DJ,
Iribarren C,
Isomaa B,
Jarvelin MR,
Jula A,
Kähönen M,
Kiemeney LA,
van der Klauw MM,
Kooner JS,
Kraft P,
Iacoviello L,
Lehtimäki T,
Lokki ML,
Mitchell BD,
Navis G,
Nieminen MS,
Ohlsson C,
Poulter NR,
Qi L,
Raitakari OT,
Rimm EB,
Rioux JD,
Rizzi F,
Rudan I,
Salomaa V,
Sever PS,
Shields DC,
Shuldiner AR,
Sinisalo J,
Stanton AV,
Stolk RP,
Strachan DP,
Tardif JC,
Thorsteinsdottir U,
Tuomilehto J,
van Veldhuisen DJ,
Virtamo J,
Viikari J,
Vollenweider P,
Waeber G,
Widen E,
Cho YS,
Olsen JV,
Visscher PM,
Willer C,
Franke L,
Erdmann J,
Thompson JR,
Pfeufer A,
Sotoodehnia N,
Newton-Cheh C,
Ellinor PT,
Stricker BH,
Metspalu A,
Perola M,
Beckmann JS,
Smith GD,
Stefansson K,
Wareham NJ,
Munroe PB,
Sibon OC,
Milan DJ,
Snieder H,
Samani NJ,
Loos RJ
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
Ferreira MA,
Matheson MC,
Tang CS,
Granell R,
Ang W,
Hui J,
Kiefer AK,
Duffy DL,
Baltic S,
Danoy P,
Bui M,
Price L
and 22 more — show all
Sly PD,
Eriksson N,
Madden PA,
Abramson MJ,
Holt PG,
Heath AC,
Hunter M,
Musk B,
Robertson CF,
Le Souëf P,
Montgomery GW,
Henderson AJ,
Tung JY,
Dharmage SC,
Brown MA,
James A,
Thompson PJ,
Pennell C,
Martin NG,
Evans DM,
Hinds DA,
Hopper JL
Australian Asthma Genetics Consortium Collaborators
The Journal of allergy and clinical immunology · 2014 · PMID 24388013
8 pages
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
Mahajan A,
Rodan AR,
Le TH,
Gaulton KJ,
Haessler J,
Stilp AM,
Kamatani Y,
Zhu G,
Sofer T,
Puri S,
Schellinger JN,
Chu PL
and 26 more — show all
Cechova S,
van Zuydam N,
Arnlov J,
Flessner MF,
Giedraitis V,
Heath AC,
Kubo M,
Larsson A,
Lindgren CM,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
Reiner AP,
Sundström J,
Thornton TA,
Lind L,
Ingelsson E,
Cai J,
Martin NG,
Kooperberg C,
Matsuda K,
Whitfield JB,
Okada Y,
Laurie CC,
Morris AP,
Franceschini N
SUMMIT Consortium · BioBank Japan Project
American journal of human genetics · 2016 · PMID 27588450 · open access
8 pages
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Demontis D,
Walters RK,
Martin J,
Mattheisen M,
Als TD,
Agerbo E,
Baldursson G,
Belliveau R,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Cerrato F,
Chambert K
and 69 more — show all
Churchhouse C,
Dumont A,
Eriksson N,
Gandal M,
Goldstein JI,
Grasby KL,
Grove J,
Gudmundsson OO,
Hansen CS,
Hauberg ME,
Hollegaard MV,
Howrigan DP,
Huang H,
Maller JB,
Martin AR,
Martin NG,
Moran J,
Pallesen J,
Palmer DS,
Pedersen CB,
Pedersen MG,
Poterba T,
Poulsen JB,
Ripke S,
Robinson EB,
Satterstrom FK,
Stefansson H,
Stevens C,
Turley P,
Walters GB,
Won H,
Wright MJ,
Andreassen OA,
Asherson P,
Burton CL,
Boomsma DI,
Cormand B,
Dalsgaard S,
Franke B,
Gelernter J,
Geschwind D,
Hakonarson H,
Haavik J,
Kranzler HR,
Kuntsi J,
Langley K,
Lesch KP,
Middeldorp C,
Reif A,
Rohde LA,
Roussos P,
Schachar R,
Sklar P,
Sonuga-Barke EJS,
Sullivan PF,
Thapar A,
Tung JY,
Waldman ID,
Medland SE,
Stefansson K,
Nordentoft M,
Hougaard DM,
Werge T,
Mors O,
Mortensen PB,
Daly MJ,
Faraone SV,
Børglum AD,
Neale BM
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 1 more consortia
Nature genetics · 2019 · PMID 30478444
8 pages
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
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Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
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23andMe Research Team · International Visible Trait Genetics Consortium
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