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9 matches for
Lannfelt L.
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay M,
Goel A,
Won HH,
Hall LM,
Willenborg C,
Kanoni S,
Saleheen D,
Kyriakou T,
Nelson CP,
Hopewell JC,
Webb TR,
Zeng L
and 139 more — show all
Dehghan A,
Alver M,
Armasu SM,
Auro K,
Bjonnes A,
Chasman DI,
Chen S,
Ford I,
Franceschini N,
Gieger C,
Grace C,
Gustafsson S,
Huang J,
Hwang SJ,
Kim YK,
Kleber ME,
Lau KW,
Lu X,
Lu Y,
Lyytikäinen LP,
Mihailov E,
Morrison AC,
Pervjakova N,
Qu L,
Rose LM,
Salfati E,
Saxena R,
Scholz M,
Smith AV,
Tikkanen E,
Uitterlinden A,
Yang X,
Zhang W,
Zhao W,
de Andrade M,
de Vries PS,
van Zuydam NR,
Anand SS,
Bertram L,
Beutner F,
Dedoussis G,
Frossard P,
Gauguier D,
Goodall AH,
Gottesman O,
Haber M,
Han BG,
Huang J,
Jalilzadeh S,
Kessler T,
König IR,
Lannfelt L,
Lieb W,
Lind L,
Lindgren CM,
Lokki ML,
Magnusson PK,
Mallick NH,
Mehra N,
Meitinger T,
Memon FU,
Morris AP,
Nieminen MS,
Pedersen NL,
Peters A,
Rallidis LS,
Rasheed A,
Samuel M,
Shah SH,
Sinisalo J,
Stirrups KE,
Trompet S,
Wang L,
Zaman KS,
Ardissino D,
Boerwinkle E,
Borecki IB,
Bottinger EP,
Buring JE,
Chambers JC,
Collins R,
Cupples LA,
Danesh J,
Demuth I,
Elosua R,
Epstein SE,
Esko T,
Feitosa MF,
Franco OH,
Franzosi MG,
Granger CB,
Gu D,
Gudnason V,
Hall AS,
Hamsten A,
Harris TB,
Hazen SL,
Hengstenberg C,
Hofman A,
Ingelsson E,
Iribarren C,
Jukema JW,
Karhunen PJ,
Kim BJ,
Kooner JS,
Kullo IJ,
Lehtimäki T,
Loos RJF,
Melander O,
Metspalu A,
März W,
Palmer CN,
Perola M,
Quertermous T,
Rader DJ,
Ridker PM,
Ripatti S,
Roberts R,
Salomaa V,
Sanghera DK,
Schwartz SM,
Seedorf U,
Stewart AF,
Stott DJ,
Thiery J,
Zalloua PA,
O'Donnell CJ,
Reilly MP,
Assimes TL,
Thompson JR,
Erdmann J,
Clarke R,
Watkins H,
Kathiresan S,
McPherson R,
Deloukas P,
Schunkert H,
Samani NJ,
Farrall M
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
Winkler TW,
Justice AE,
Graff M,
Barata L,
Feitosa MF,
Chu S,
Czajkowski J,
Esko T,
Fall T,
Kilpeläinen TO,
Lu Y,
Mägi R
and 427 more — show all
Mihailov E,
Pers TH,
Rüeger S,
Teumer A,
Ehret GB,
Ferreira T,
Heard-Costa NL,
Karjalainen J,
Lagou V,
Mahajan A,
Neinast MD,
Prokopenko I,
Simino J,
Teslovich TM,
Jansen R,
Westra HJ,
White CC,
Absher D,
Ahluwalia TS,
Ahmad S,
Albrecht E,
Alves AC,
Bragg-Gresham JL,
de Craen AJ,
Bis JC,
Bonnefond A,
Boucher G,
Cadby G,
Cheng YC,
Chiang CW,
Delgado G,
Demirkan A,
Dueker N,
Eklund N,
Eiriksdottir G,
Eriksson J,
Feenstra B,
Fischer K,
Frau F,
Galesloot TE,
Geller F,
Goel A,
Gorski M,
Grammer TB,
Gustafsson S,
Haitjema S,
Hottenga JJ,
Huffman JE,
Jackson AU,
Jacobs KB,
Johansson Å,
Kaakinen M,
Kleber ME,
Lahti J,
Mateo Leach I,
Lehne B,
Liu Y,
Lo KS,
Lorentzon M,
Luan J,
Madden PA,
Mangino M,
McKnight B,
Medina-Gomez C,
Monda KL,
Montasser ME,
Müller G,
Müller-Nurasyid M,
Nolte IM,
Panoutsopoulou K,
Pascoe L,
Paternoster L,
Rayner NW,
Renström F,
Rizzi F,
Rose LM,
Ryan KA,
Salo P,
Sanna S,
Scharnagl H,
Shi J,
Smith AV,
Southam L,
Stančáková A,
Steinthorsdottir V,
Strawbridge RJ,
Sung YJ,
Tachmazidou I,
Tanaka T,
Thorleifsson G,
Trompet S,
Pervjakova N,
Tyrer JP,
Vandenput L,
van der Laan SW,
van der Velde N,
van Setten J,
van Vliet-Ostaptchouk JV,
Verweij N,
Vlachopoulou E,
Waite LL,
Wang SR,
Wang Z,
Wild SH,
Willenborg C,
Wilson JF,
Wong A,
Yang J,
Yengo L,
Yerges-Armstrong LM,
Yu L,
Zhang W,
Zhao JH,
Andersson EA,
Bakker SJ,
Baldassarre D,
Banasik K,
Barcella M,
Barlassina C,
Bellis C,
Benaglio P,
Blangero J,
Blüher M,
Bonnet F,
Bonnycastle LL,
Boyd HA,
Bruinenberg M,
Buchman AS,
Campbell H,
Chen YD,
Chines PS,
Claudi-Boehm S,
Cole J,
Collins FS,
de Geus EJ,
de Groot LC,
Dimitriou M,
Duan J,
Enroth S,
Eury E,
Farmaki AE,
Forouhi NG,
Friedrich N,
Gejman PV,
Gigante B,
Glorioso N,
Go AS,
Gottesman O,
Gräßler J,
Grallert H,
Grarup N,
Gu YM,
Broer L,
Ham AC,
Hansen T,
Harris TB,
Hartman CA,
Hassinen M,
Hastie N,
Hattersley AT,
Heath AC,
Henders AK,
Hernandez D,
Hillege H,
Holmen O,
Hovingh KG,
Hui J,
Husemoen LL,
Hutri-Kähönen N,
Hysi PG,
Illig T,
De Jager PL,
Jalilzadeh S,
Jørgensen T,
Jukema JW,
Juonala M,
Kanoni S,
Karaleftheri M,
Khaw KT,
Kinnunen L,
Kittner SJ,
Koenig W,
Kolcic I,
Kovacs P,
Krarup NT,
Kratzer W,
Krüger J,
Kuh D,
Kumari M,
Kyriakou T,
Langenberg C,
Lannfelt L,
Lanzani C,
Lotay V,
Launer LJ,
Leander K,
Lindström J,
Linneberg A,
Liu YP,
Lobbens S,
Luben R,
Lyssenko V,
Männistö S,
Magnusson PK,
McArdle WL,
Menni C,
Merger S,
Milani L,
Montgomery GW,
Morris AP,
Narisu N,
Nelis M,
Ong KK,
Palotie A,
Pérusse L,
Pichler I,
Pilia MG,
Pouta A,
Rheinberger M,
Ribel-Madsen R,
Richards M,
Rice KM,
Rice TK,
Rivolta C,
Salomaa V,
Sanders AR,
Sarzynski MA,
Scholtens S,
Scott RA,
Scott WR,
Sebert S,
Sengupta S,
Sennblad B,
Seufferlein T,
Silveira A,
Slagboom PE,
Smit JH,
Sparsø TH,
Stirrups K,
Stolk RP,
Stringham HM,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Thorand B,
Tönjes A,
Tremblay A,
Tsafantakis E,
van der Most PJ,
Völker U,
Vohl MC,
Vonk JM,
Waldenberger M,
Walker RW,
Wennauer R,
Widén E,
Willemsen G,
Wilsgaard T,
Wright AF,
Zillikens MC,
van Dijk SC,
van Schoor NM,
Asselbergs FW,
de Bakker PI,
Beckmann JS,
Beilby J,
Bennett DA,
Bergman RN,
Bergmann S,
Böger CA,
Boehm BO,
Boerwinkle E,
Boomsma DI,
Bornstein SR,
Bottinger EP,
Bouchard C,
Chambers JC,
Chanock SJ,
Chasman DI,
Cucca F,
Cusi D,
Dedoussis G,
Erdmann J,
Eriksson JG,
Evans DA,
de Faire U,
Farrall M,
Ferrucci L,
Ford I,
Franke L,
Franks PW,
Froguel P,
Gansevoort RT,
Gieger C,
Grönberg H,
Gudnason V,
Gyllensten U,
Hall P,
Hamsten A,
van der Harst P,
Hayward C,
Heliövaara M,
Hengstenberg C,
Hicks AA,
Hingorani A,
Hofman A,
Hu F,
Huikuri HV,
Hveem K,
James AL,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Kathiresan S,
Kiemeney LA,
Kivimaki M,
Knekt PB,
Koistinen HA,
Kooner JS,
Koskinen S,
Kuusisto J,
Maerz W,
Martin NG,
Laakso M,
Lakka TA,
Lehtimäki T,
Lettre G,
Levinson DF,
Lind L,
Lokki ML,
Mäntyselkä P,
Melbye M,
Metspalu A,
Mitchell BD,
Moll FL,
Murray JC,
Musk AW,
Nieminen MS,
Njølstad I,
Ohlsson C,
Oldehinkel AJ,
Oostra BA,
Palmer LJ,
Pankow JS,
Pasterkamp G,
Pedersen NL,
Pedersen O,
Penninx BW,
Perola M,
Peters A,
Polašek O,
Pramstaller PP,
Psaty BM,
Qi L,
Quertermous T,
Raitakari OT,
Rankinen T,
Rauramaa R,
Ridker PM,
Rioux JD,
Rivadeneira F,
Rotter JI,
Rudan I,
den Ruijter HM,
Saltevo J,
Sattar N,
Schunkert H,
Schwarz PE,
Shuldiner AR,
Sinisalo J,
Snieder H,
Sørensen TI,
Spector TD,
Staessen JA,
Stefania B,
Thorsteinsdottir U,
Stumvoll M,
Tardif JC,
Tremoli E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
Verbeek AL,
Vermeulen SH,
Viikari JS,
Vitart V,
Völzke H,
Vollenweider P,
Waeber G,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Zeggini E,
Chakravarti A,
Clegg DJ,
Cupples LA,
Gordon-Larsen P,
Jaquish CE,
Rao DC,
Abecasis GR,
Assimes TL,
Barroso I,
Berndt SI,
Boehnke M,
Deloukas P,
Fox CS,
Groop LC,
Hunter DJ,
Ingelsson E,
Kaplan RC,
McCarthy MI,
Mohlke KL,
O'Connell JR,
Schlessinger D,
Strachan DP,
Stefansson K,
van Duijn CM,
Hirschhorn JN,
Lindgren CM,
Heid IM,
North KE,
Borecki IB,
Kutalik Z,
Loos RJ
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
and 150 more — show all
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
and 269 more — show all
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
and 198 more — show all
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
Liu C,
Kraja AT,
Fallgaard Nielsen S,
Rasheed A,
Samuel M,
Zhao W,
Bonnycastle LL,
Jackson AU,
Narisu N,
Swift AJ,
Southam L,
Marten J,
Huyghe JR,
Stančáková A,
Fava C,
Ohlsson T,
Matchan A,
Stirrups KE,
Bork-Jensen J,
Gjesing AP,
Kontto J,
Perola M,
Shaw-Hawkins S,
Havulinna AS,
Zhang H,
Donnelly LA,
Groves CJ,
Rayner NW,
Neville MJ,
Robertson NR,
Yiorkas AM,
Herzig KH,
Kajantie E,
Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
Evangelou E,
Moayyeri A,
Vergnaud AC,
Nelson CP,
Poveda A,
Varga TV,
Caslake M,
de Craen AJ,
Trompet S,
Luan J,
Scott RA,
Harris SE,
Liewald DC,
Marioni R,
Menni C,
Farmaki AE,
Hallmans G,
Renström F,
Huffman JE,
Hassinen M,
Burgess S,
Vasan RS,
Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
Vogt T,
Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
Justice AE,
Marouli E,
Lindström J,
Uusitupa M,
Komulainen P,
Lakka TA,
Rauramaa R,
Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
Dedoussis G,
Spector TD,
Jousilahti P,
Männistö S,
Deary IJ,
Starr JM,
Langenberg C,
Wareham NJ,
Brown MJ,
Dominiczak AF,
Connell JM,
Jukema JW,
Sattar N,
Ford I,
Packard CJ,
Esko T,
Mägi R,
Metspalu A,
de Boer RA,
van der Meer P,
van der Harst P,
Gambaro G,
Ingelsson E,
Lind L,
de Bakker PI,
Numans ME,
Brandslund I,
Christensen C,
Petersen ER,
Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
Husemoen LL,
Linneberg A,
Skaaby T,
Thuesen B,
Karpe F,
Tuomilehto J,
Doney AS,
Morris AD,
Palmer CN,
Holmen OL,
Hveem K,
Willer CJ,
Tuomi T,
Groop L,
Käräjämäki A,
Palotie A,
Ripatti S,
Salomaa V,
Alam DS,
Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
Poulter N,
Stanton AV,
Sever P,
Amouyel P,
Arveiler D,
Blankenberg S,
Ferrières J,
Kee F,
Kuulasmaa K,
Müller-Nurasyid M,
Veronesi G,
Virtamo J,
Deloukas P,
Elliott P,
Zeggini E,
Kathiresan S,
Melander O,
Kuusisto J,
Laakso M,
Padmanabhan S,
Porteous D,
Hayward C,
Scotland G,
Collins FS,
Mohlke KL,
Hansen T,
Pedersen O,
Boehnke M,
Stringham HM,
Frossard P,
Newton-Cheh C,
Tobin MD,
Nordestgaard BG,
Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
Samani NJ,
Saleheen D,
Asselbergs FW,
Lindgren CM,
Danesh J,
Wain LV,
Butterworth AS,
Howson JM,
Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
Manning AK,
Hivert MF,
Scott RA,
Grimsby JL,
Bouatia-Naji N,
Chen H,
Rybin D,
Liu CT,
Bielak LF,
Prokopenko I,
Amin N,
Barnes D
and 204 more — show all
Cadby G,
Hottenga JJ,
Ingelsson E,
Jackson AU,
Johnson T,
Kanoni S,
Ladenvall C,
Lagou V,
Lahti J,
Lecoeur C,
Liu Y,
Martinez-Larrad MT,
Montasser ME,
Navarro P,
Perry JR,
Rasmussen-Torvik LJ,
Salo P,
Sattar N,
Shungin D,
Strawbridge RJ,
Tanaka T,
van Duijn CM,
An P,
de Andrade M,
Andrews JS,
Aspelund T,
Atalay M,
Aulchenko Y,
Balkau B,
Bandinelli S,
Beckmann JS,
Beilby JP,
Bellis C,
Bergman RN,
Blangero J,
Boban M,
Boehnke M,
Boerwinkle E,
Bonnycastle LL,
Boomsma DI,
Borecki IB,
Böttcher Y,
Bouchard C,
Brunner E,
Budimir D,
Campbell H,
Carlson O,
Chines PS,
Clarke R,
Collins FS,
Corbatón-Anchuelo A,
Couper D,
de Faire U,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Egan JM,
Eiriksdottir G,
Erdos MR,
Eriksson JG,
Eury E,
Ferrucci L,
Ford I,
Forouhi NG,
Fox CS,
Franzosi MG,
Franks PW,
Frayling TM,
Froguel P,
Galan P,
de Geus E,
Gigante B,
Glazer NL,
Goel A,
Groop L,
Gudnason V,
Hallmans G,
Hamsten A,
Hansson O,
Harris TB,
Hayward C,
Heath S,
Hercberg S,
Hicks AA,
Hingorani A,
Hofman A,
Hui J,
Hung J,
Jarvelin MR,
Jhun MA,
Johnson PC,
Jukema JW,
Jula A,
Kao WH,
Kaprio J,
Kardia SL,
Keinanen-Kiukaanniemi S,
Kivimaki M,
Kolcic I,
Kovacs P,
Kumari M,
Kuusisto J,
Kyvik KO,
Laakso M,
Lakka T,
Lannfelt L,
Lathrop GM,
Launer LJ,
Leander K,
Li G,
Lind L,
Lindstrom J,
Lobbens S,
Loos RJ,
Luan J,
Lyssenko V,
Mägi R,
Magnusson PK,
Marmot M,
Meneton P,
Mohlke KL,
Mooser V,
Morken MA,
Miljkovic I,
Narisu N,
O'Connell J,
Ong KK,
Oostra BA,
Palmer LJ,
Palotie A,
Pankow JS,
Peden JF,
Pedersen NL,
Pehlic M,
Peltonen L,
Penninx B,
Pericic M,
Perola M,
Perusse L,
Peyser PA,
Polasek O,
Pramstaller PP,
Province MA,
Räikkönen K,
Rauramaa R,
Rehnberg E,
Rice K,
Rotter JI,
Rudan I,
Ruokonen A,
Saaristo T,
Sabater-Lleal M,
Salomaa V,
Savage DB,
Saxena R,
Schwarz P,
Seedorf U,
Sennblad B,
Serrano-Rios M,
Shuldiner AR,
Sijbrands EJ,
Siscovick DS,
Smit JH,
Small KS,
Smith NL,
Smith AV,
Stančáková A,
Stirrups K,
Stumvoll M,
Sun YV,
Swift AJ,
Tönjes A,
Tuomilehto J,
Trompet S,
Uitterlinden AG,
Uusitupa M,
Vikström M,
Vitart V,
Vohl MC,
Voight BF,
Vollenweider P,
Waeber G,
Waterworth DM,
Watkins H,
Wheeler E,
Widen E,
Wild SH,
Willems SM,
Willemsen G,
Wilson JF,
Witteman JC,
Wright AF,
Yaghootkar H,
Zelenika D,
Zemunik T,
Zgaga L,
Wareham NJ,
McCarthy MI,
Barroso I,
Watanabe RM,
Florez JC,
Dupuis J,
Meigs JB,
Langenberg C
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
Wild PS,
Felix JF,
Schillert A,
Teumer A,
Chen MH,
Leening MJG,
Völker U,
Großmann V,
Brody JA,
Irvin MR,
Shah SJ,
Pramana S
and 112 more — show all
Lieb W,
Schmidt R,
Stanton AV,
Malzahn D,
Smith AV,
Sundström J,
Minelli C,
Ruggiero D,
Lyytikäinen LP,
Tiller D,
Smith JG,
Monnereau C,
Di Tullio MR,
Musani SK,
Morrison AC,
Pers TH,
Morley M,
Kleber ME,
Aragam J,
Benjamin EJ,
Bis JC,
Bisping E,
Broeckel U,
Cheng S,
Deckers JW,
Del Greco M F,
Edelmann F,
Fornage M,
Franke L,
Friedrich N,
Harris TB,
Hofer E,
Hofman A,
Huang J,
Hughes AD,
Kähönen M,
Investigators K,
Kruppa J,
Lackner KJ,
Lannfelt L,
Laskowski R,
Launer LJ,
Leosdottir M,
Lin H,
Lindgren CM,
Loley C,
MacRae CA,
Mascalzoni D,
Mayet J,
Medenwald D,
Morris AP,
Müller C,
Müller-Nurasyid M,
Nappo S,
Nilsson PM,
Nuding S,
Nutile T,
Peters A,
Pfeufer A,
Pietzner D,
Pramstaller PP,
Raitakari OT,
Rice KM,
Rivadeneira F,
Rotter JI,
Ruohonen ST,
Sacco RL,
Samdarshi TE,
Schmidt H,
Sharp ASP,
Shields DC,
Sorice R,
Sotoodehnia N,
Stricker BH,
Surendran P,
Thom S,
Töglhofer AM,
Uitterlinden AG,
Wachter R,
Völzke H,
Ziegler A,
Münzel T,
März W,
Cappola TP,
Hirschhorn JN,
Mitchell GF,
Smith NL,
Fox ER,
Dueker ND,
Jaddoe VWV,
Melander O,
Russ M,
Lehtimäki T,
Ciullo M,
Hicks AA,
Lind L,
Gudnason V,
Pieske B,
Barron AJ,
Zweiker R,
Schunkert H,
Ingelsson E,
Liu K,
Arnett DK,
Psaty BM,
Blankenberg S,
Larson MG,
Felix SB,
Franco OH,
Zeller T,
Vasan RS,
Dörr M
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
Scott LJ,
Mägi R,
Marullo L,
Gaulton KJ,
Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
Eicher JD,
Jackson AU,
Ferreira T
and 163 more — show all
Lee Y,
Ma C,
Steinthorsdottir V,
Thorleifsson G,
Qi L,
Van Zuydam NR,
Mahajan A,
Chen H,
Almgren P,
Voight BF,
Grallert H,
Müller-Nurasyid M,
Ried JS,
Rayner NW,
Robertson N,
Karssen LC,
van Leeuwen EM,
Willems SM,
Fuchsberger C,
Kwan P,
Teslovich TM,
Chanda P,
Li M,
Lu Y,
Dina C,
Thuillier D,
Yengo L,
Jiang L,
Sparso T,
Kestler HA,
Chheda H,
Eisele L,
Gustafsson S,
Frånberg M,
Strawbridge RJ,
Benediktsson R,
Hreidarsson AB,
Kong A,
Sigurðsson G,
Kerrison ND,
Luan J,
Liang L,
Meitinger T,
Roden M,
Thorand B,
Esko T,
Mihailov E,
Fox C,
Liu CT,
Rybin D,
Isomaa B,
Lyssenko V,
Tuomi T,
Couper DJ,
Pankow JS,
Grarup N,
Have CT,
Jørgensen ME,
Jørgensen T,
Linneberg A,
Cornelis MC,
van Dam RM,
Hunter DJ,
Kraft P,
Sun Q,
Edkins S,
Owen KR,
Perry JRB,
Wood AR,
Zeggini E,
Tajes-Fernandes J,
Abecasis GR,
Bonnycastle LL,
Chines PS,
Stringham HM,
Koistinen HA,
Kinnunen L,
Sennblad B,
Mühleisen TW,
Nöthen MM,
Pechlivanis S,
Baldassarre D,
Gertow K,
Humphries SE,
Tremoli E,
Klopp N,
Meyer J,
Steinbach G,
Wennauer R,
Eriksson JG,
Mӓnnistö S,
Peltonen L,
Tikkanen E,
Charpentier G,
Eury E,
Lobbens S,
Gigante B,
Leander K,
McLeod O,
Bottinger EP,
Gottesman O,
Ruderfer D,
Blüher M,
Kovacs P,
Tonjes A,
Maruthur NM,
Scapoli C,
Erbel R,
Jöckel KH,
Moebus S,
de Faire U,
Hamsten A,
Stumvoll M,
Deloukas P,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Ripatti S,
Salomaa V,
Pedersen NL,
Boehm BO,
Bergman RN,
Collins FS,
Mohlke KL,
Tuomilehto J,
Hansen T,
Pedersen O,
Barroso I,
Lannfelt L,
Ingelsson E,
Lind L,
Lindgren CM,
Cauchi S,
Froguel P,
Loos RJF,
Balkau B,
Boeing H,
Franks PW,
Barricarte Gurrea A,
Palli D,
van der Schouw YT,
Altshuler D,
Groop LC,
Langenberg C,
Wareham NJ,
Sijbrands E,
van Duijn CM,
Florez JC,
Meigs JB,
Boerwinkle E,
Gieger C,
Strauch K,
Metspalu A,
Morris AD,
Palmer CNA,
Hu FB,
Thorsteinsdottir U,
Stefansson K,
Dupuis J,
Morris AP,
Boehnke M,
McCarthy MI,
Prokopenko I
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Sims R,
van der Lee SJ,
Naj AC,
Bellenguez C,
Badarinarayan N,
Jakobsdottir J,
Kunkle BW,
Boland A,
Raybould R,
Bis JC,
Martin ER,
Grenier-Boley B
and 437 more — show all
Heilmann-Heimbach S,
Chouraki V,
Kuzma AB,
Sleegers K,
Vronskaya M,
Ruiz A,
Graham RR,
Olaso R,
Hoffmann P,
Grove ML,
Vardarajan BN,
Hiltunen M,
Nöthen MM,
White CC,
Hamilton-Nelson KL,
Epelbaum J,
Maier W,
Choi SH,
Beecham GW,
Dulary C,
Herms S,
Smith AV,
Funk CC,
Derbois C,
Forstner AJ,
Ahmad S,
Li H,
Bacq D,
Harold D,
Satizabal CL,
Valladares O,
Squassina A,
Thomas R,
Brody JA,
Qu L,
Sánchez-Juan P,
Morgan T,
Wolters FJ,
Zhao Y,
Garcia FS,
Denning N,
Fornage M,
Malamon J,
Naranjo MCD,
Majounie E,
Mosley TH,
Dombroski B,
Wallon D,
Lupton MK,
Dupuis J,
Whitehead P,
Fratiglioni L,
Medway C,
Jian X,
Mukherjee S,
Keller L,
Brown K,
Lin H,
Cantwell LB,
Panza F,
McGuinness B,
Moreno-Grau S,
Burgess JD,
Solfrizzi V,
Proitsi P,
Adams HH,
Allen M,
Seripa D,
Pastor P,
Cupples LA,
Price ND,
Hannequin D,
Frank-García A,
Levy D,
Chakrabarty P,
Caffarra P,
Giegling I,
Beiser AS,
Giedraitis V,
Hampel H,
Garcia ME,
Wang X,
Lannfelt L,
Mecocci P,
Eiriksdottir G,
Crane PK,
Pasquier F,
Boccardi V,
Henández I,
Barber RC,
Scherer M,
Tarraga L,
Adams PM,
Leber M,
Chen Y,
Albert MS,
Riedel-Heller S,
Emilsson V,
Beekly D,
Braae A,
Schmidt R,
Blacker D,
Masullo C,
Schmidt H,
Doody RS,
Spalletta G,
Longstreth WT Jr,
Fairchild TJ,
Bossù P,
Lopez OL,
Frosch MP,
Sacchinelli E,
Ghetti B,
Yang Q,
Huebinger RM,
Jessen F,
Li S,
Kamboh MI,
Morris J,
Sotolongo-Grau O,
Katz MJ,
Corcoran C,
Dunstan M,
Braddel A,
Thomas C,
Meggy A,
Marshall R,
Gerrish A,
Chapman J,
Aguilar M,
Taylor S,
Hill M,
Fairén MD,
Hodges A,
Vellas B,
Soininen H,
Kloszewska I,
Daniilidou M,
Uphill J,
Patel Y,
Hughes JT,
Lord J,
Turton J,
Hartmann AM,
Cecchetti R,
Fenoglio C,
Serpente M,
Arcaro M,
Caltagirone C,
Orfei MD,
Ciaramella A,
Pichler S,
Mayhaus M,
Gu W,
Lleó A,
Fortea J,
Blesa R,
Barber IS,
Brookes K,
Cupidi C,
Maletta RG,
Carrell D,
Sorbi S,
Moebus S,
Urbano M,
Pilotto A,
Kornhuber J,
Bosco P,
Todd S,
Craig D,
Johnston J,
Gill M,
Lawlor B,
Lynch A,
Fox NC,
Hardy J,
Albin RL,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Baldwin CT,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Bigio EH,
Bird TD,
Boeve BF,
Bowen JD,
Boxer A,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Carroll SL,
Diaz CC,
Chui HC,
Clark DG,
Cribbs DH,
Crocco EA,
DeCarli C,
Dick M,
Duara R,
Evans DA,
Faber KM,
Fallon KB,
Fardo DW,
Farlow MR,
Ferris S,
Foroud TM,
Galasko DR,
Gearing M,
Geschwind DH,
Gilbert JR,
Graff-Radford NR,
Green RC,
Growdon JH,
Hamilton RL,
Harrell LE,
Honig LS,
Huentelman MJ,
Hulette CM,
Hyman BT,
Jarvik GP,
Abner E,
Jin LW,
Jun G,
Karydas A,
Kaye JA,
Kim R,
Kowall NW,
Kramer JH,
LaFerla FM,
Lah JJ,
Leverenz JB,
Levey AI,
Li G,
Lieberman AP,
Lunetta KL,
Lyketsos CG,
Marson DC,
Martiniuk F,
Mash DC,
Masliah E,
McCormick WC,
McCurry SM,
McDavid AN,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Morris JC,
Murrell JR,
Myers AJ,
O'Bryant S,
Olichney JM,
Pankratz VS,
Parisi JE,
Paulson HL,
Perry W,
Peskind E,
Pierce A,
Poon WW,
Potter H,
Quinn JF,
Raj A,
Raskind M,
Reisberg B,
Reitz C,
Ringman JM,
Roberson ED,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Sager MA,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Smith AG,
Sonnen JA,
Spina S,
Stern RA,
Swerdlow RH,
Tanzi RE,
Thornton-Wells TA,
Trojanowski JQ,
Troncoso JC,
Van Deerlin VM,
Van Eldik LJ,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Wilhelmsen KC,
Williamson J,
Wingo TS,
Woltjer RL,
Wright CB,
Yu CE,
Yu L,
Garzia F,
Golamaully F,
Septier G,
Engelborghs S,
Vandenberghe R,
De Deyn PP,
Fernadez CM,
Benito YA,
Thonberg H,
Forsell C,
Lilius L,
Kinhult-Stählbom A,
Kilander L,
Brundin R,
Concari L,
Helisalmi S,
Koivisto AM,
Haapasalo A,
Dermecourt V,
Fievet N,
Hanon O,
Dufouil C,
Brice A,
Ritchie K,
Dubois B,
Himali JJ,
Keene CD,
Tschanz J,
Fitzpatrick AL,
Kukull WA,
Norton M,
Aspelund T,
Larson EB,
Munger R,
Rotter JI,
Lipton RB,
Bullido MJ,
Hofman A,
Montine TJ,
Coto E,
Boerwinkle E,
Petersen RC,
Alvarez V,
Rivadeneira F,
Reiman EM,
Gallo M,
O'Donnell CJ,
Reisch JS,
Bruni AC,
Royall DR,
Dichgans M,
Sano M,
Galimberti D,
St George-Hyslop P,
Scarpini E,
Tsuang DW,
Mancuso M,
Bonuccelli U,
Winslow AR,
Daniele A,
Wu CK,
Peters O,
Nacmias B,
Riemenschneider M,
Heun R,
Brayne C,
Rubinsztein DC,
Bras J,
Guerreiro R,
Al-Chalabi A,
Shaw CE,
Collinge J,
Mann D,
Tsolaki M,
Clarimón J,
Sussams R,
Lovestone S,
O'Donovan MC,
Owen MJ,
Behrens TW,
Mead S,
Goate AM,
Uitterlinden AG,
Holmes C,
Cruchaga C,
Ingelsson M,
Bennett DA,
Powell J,
Golde TE,
Graff C,
De Jager PL,
Morgan K,
Ertekin-Taner N,
Combarros O,
Psaty BM,
Passmore P,
Younkin SG,
Berr C,
Gudnason V,
Rujescu D,
Dickson DW,
Dartigues JF,
DeStefano AL,
Ortega-Cubero S,
Hakonarson H,
Campion D,
Boada M,
Kauwe JK,
Farrer LA,
Van Broeckhoven C,
Ikram MA,
Jones L,
Haines JL,
Tzourio C,
Launer LJ,
Escott-Price V,
Mayeux R,
Deleuze JF,
Amin N,
Holmans PA,
Pericak-Vance MA,
Amouyel P,
van Duijn CM,
Ramirez A,
Wang LS,
Lambert JC,
Seshadri S,
Williams J,
Schellenberg GD
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
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