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92 matches for
Fornage M,
showing the first 20.
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium
Guan W,
Steffen BT,
Lemaitre RN,
Wu JHY,
Tanaka T,
Manichaikul A,
Foy M,
Rich SS,
Wang L,
Nettleton JA,
Tang W,
Gu X
and 12 more — show all
Bandinelli S,
King IB,
McKnight B,
Psaty BM,
Siscovick D,
Djousse L,
Chen YI,
Ferrucci L,
Fornage M,
Mozafarrian D,
Tsai MY,
Steffen LM
Circulation. Cardiovascular genetics · 2014 · PMID 24823311
5 pages
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
van Rooij FJA,
Qayyum R,
Smith AV,
Zhou Y,
Trompet S,
Tanaka T,
Keller MF,
Chang LC,
Schmidt H,
Yang ML,
Chen MH,
Hayes J
and 88 more — show all
Johnson AD,
Yanek LR,
Mueller C,
Lange L,
Floyd JS,
Ghanbari M,
Zonderman AB,
Jukema JW,
Hofman A,
van Duijn CM,
Desch KC,
Saba Y,
Ozel AB,
Snively BM,
Wu JY,
Schmidt R,
Fornage M,
Klein RJ,
Fox CS,
Matsuda K,
Kamatani N,
Wild PS,
Stott DJ,
Ford I,
Slagboom PE,
Yang J,
Chu AY,
Lambert AJ,
Uitterlinden AG,
Franco OH,
Hofer E,
Ginsburg D,
Hu B,
Keating B,
Schick UM,
Brody JA,
Li JZ,
Chen Z,
Zeller T,
Guralnik JM,
Chasman DI,
Peters LL,
Kubo M,
Becker DM,
Li J,
Eiriksdottir G,
Rotter JI,
Levy D,
Grossmann V,
Patel KV,
Chen CH,
Ridker PM,
Tang H,
Launer LJ,
Rice KM,
Li-Gao R,
Ferrucci L,
Evans MK,
Choudhuri A,
Trompouki E,
Abraham BJ,
Yang S,
Takahashi A,
Kamatani Y,
Kooperberg C,
Harris TB,
Jee SH,
Coresh J,
Tsai FJ,
Longo DL,
Chen YT,
Felix JF,
Yang Q,
Psaty BM,
Boerwinkle E,
Becker LC,
Mook-Kanamori DO,
Wilson JG,
Gudnason V,
O'Donnell CJ,
Dehghan A,
Cupples LA,
Nalls MA,
Morris AP,
Okada Y,
Reiner AP,
Zon LI,
Ganesh SK
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 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
Large-scale association analyses identify host factors influencing human gut microbiome composition
Kurilshikov A,
Medina-Gomez C,
Bacigalupe R,
Radjabzadeh D,
Wang J,
Demirkan A,
Le Roy CI,
Raygoza Garay JA,
Finnicum CT,
Liu X,
Zhernakova DV,
Bonder MJ
and 92 more — show all
Hansen TH,
Frost F,
Rühlemann MC,
Turpin W,
Moon JY,
Kim HN,
Lüll K,
Barkan E,
Shah SA,
Fornage M,
Szopinska-Tokov J,
Wallen ZD,
Borisevich D,
Agreus L,
Andreasson A,
Bang C,
Bedrani L,
Bell JT,
Bisgaard H,
Boehnke M,
Boomsma DI,
Burk RD,
Claringbould A,
Croitoru K,
Davies GE,
van Duijn CM,
Duijts L,
Falony G,
Fu J,
van der Graaf A,
Hansen T,
Homuth G,
Hughes DA,
Ijzerman RG,
Jackson MA,
Jaddoe VWV,
Joossens M,
Jørgensen T,
Keszthelyi D,
Knight R,
Laakso M,
Laudes M,
Launer LJ,
Lieb W,
Lusis AJ,
Masclee AAM,
Moll HA,
Mujagic Z,
Qibin Q,
Rothschild D,
Shin H,
Sørensen SJ,
Steves CJ,
Thorsen J,
Timpson NJ,
Tito RY,
Vieira-Silva S,
Völker U,
Völzke H,
Võsa U,
Wade KH,
Walter S,
Watanabe K,
Weiss S,
Weiss FU,
Weissbrod O,
Westra HJ,
Willemsen G,
Payami H,
Jonkers DMAE,
Arias Vasquez A,
de Geus EJC,
Meyer KA,
Stokholm J,
Segal E,
Org E,
Wijmenga C,
Kim HL,
Kaplan RC,
Spector TD,
Uitterlinden AG,
Rivadeneira F,
Franke A,
Lerch MM,
Franke L,
Sanna S,
D'Amato M,
Pedersen O,
Paterson AD,
Kraaij R,
Raes J,
Zhernakova A
Nature genetics · 2021 · PMID 33462485
5 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
Soler Artigas M,
Loth DW,
Wain LV,
Gharib SA,
Obeidat M,
Tang W,
Zhai G,
Zhao JH,
Smith AV,
Huffman JE,
Albrecht E,
Jackson CM
and 158 more — show all
Evans DM,
Cadby G,
Fornage M,
Manichaikul A,
Lopez LM,
Johnson T,
Aldrich MC,
Aspelund T,
Barroso I,
Campbell H,
Cassano PA,
Couper DJ,
Eiriksdottir G,
Franceschini N,
Garcia M,
Gieger C,
Gislason GK,
Grkovic I,
Hammond CJ,
Hancock DB,
Harris TB,
Ramasamy A,
Heckbert SR,
Heliövaara M,
Homuth G,
Hysi PG,
James AL,
James AL,
Jankovic S,
Joubert BR,
Karrasch S,
Klopp N,
Koch B,
Kritchevsky SB,
Launer LJ,
Liu Y,
Loehr LR,
Lohman K,
Loos RJ,
Lumley T,
Al Balushi KA,
Ang WQ,
Barr RG,
Beilby J,
Blakey JD,
Boban M,
Boraska V,
Brisman J,
Britton JR,
Brusselle GG,
Cooper C,
Curjuric I,
Dahgam S,
Deary IJ,
Ebrahim S,
Eijgelsheim M,
Francks C,
Gaysina D,
Granell R,
Gu X,
Hankinson JL,
Hardy R,
Harris SE,
Henderson J,
Henry A,
Hingorani AD,
Hofman A,
Holt PG,
Hui J,
Hunter ML,
Imboden M,
Jameson KA,
Kerr SM,
Kolcic I,
Kronenberg F,
Liu JZ,
Marchini J,
McKeever T,
Morris AD,
Olin AC,
Porteous DJ,
Postma DS,
Rich SS,
Ring SM,
Rivadeneira F,
Rochat T,
Sayer AA,
Sayers I,
Sly PD,
Smith GD,
Sood A,
Starr JM,
Uitterlinden AG,
Vonk JM,
Wannamethee SG,
Whincup PH,
Wijmenga C,
Williams OD,
Wong A,
Mangino M,
Marciante KD,
McArdle WL,
Meibohm B,
Morrison AC,
North KE,
Omenaas E,
Palmer LJ,
Pietiläinen KH,
Pin I,
Pola Sbreve Ek O,
Pouta A,
Psaty BM,
Hartikainen AL,
Rantanen T,
Ripatti S,
Rotter JI,
Rudan I,
Rudnicka AR,
Schulz H,
Shin SY,
Spector TD,
Surakka I,
Vitart V,
Völzke H,
Wareham NJ,
Warrington NM,
Wichmann HE,
Wild SH,
Wilk JB,
Wjst M,
Wright AF,
Zgaga L,
Zemunik T,
Pennell CE,
Nyberg F,
Kuh D,
Holloway JW,
Boezen HM,
Lawlor DA,
Morris RW,
Probst-Hensch N,
Kaprio J,
Wilson JF,
Hayward C,
Kähönen M,
Heinrich J,
Musk AW,
Jarvis DL,
Gläser S,
Järvelin MR,
Ch Stricker BH,
Elliott P,
O'Connor GT,
Strachan DP,
London SJ,
Hall IP,
Gudnason V,
Tobin MD
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
and 70 more — show all
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Loth DW,
Soler Artigas M,
Gharib SA,
Wain LV,
Franceschini N,
Koch B,
Pottinger TD,
Smith AV,
Duan Q,
Oldmeadow C,
Lee MK,
Strachan DP
and 148 more — show all
James AL,
Huffman JE,
Vitart V,
Ramasamy A,
Wareham NJ,
Kaprio J,
Wang XQ,
Trochet H,
Kähönen M,
Flexeder C,
Albrecht E,
Lopez LM,
de Jong K,
Thyagarajan B,
Alves AC,
Enroth S,
Omenaas E,
Joshi PK,
Fall T,
Viñuela A,
Launer LJ,
Loehr LR,
Fornage M,
Li G,
Wilk JB,
Tang W,
Manichaikul A,
Lahousse L,
Harris TB,
North KE,
Rudnicka AR,
Hui J,
Gu X,
Lumley T,
Wright AF,
Hastie ND,
Campbell S,
Kumar R,
Pin I,
Scott RA,
Pietiläinen KH,
Surakka I,
Liu Y,
Holliday EG,
Schulz H,
Heinrich J,
Davies G,
Vonk JM,
Wojczynski M,
Pouta A,
Johansson A,
Wild SH,
Ingelsson E,
Rivadeneira F,
Völzke H,
Hysi PG,
Eiriksdottir G,
Morrison AC,
Rotter JI,
Gao W,
Postma DS,
White WB,
Rich SS,
Hofman A,
Aspelund T,
Couper D,
Smith LJ,
Psaty BM,
Lohman K,
Burchard EG,
Uitterlinden AG,
Garcia M,
Joubert BR,
McArdle WL,
Musk AB,
Hansel N,
Heckbert SR,
Zgaga L,
van Meurs JB,
Navarro P,
Rudan I,
Oh YM,
Redline S,
Jarvis DL,
Zhao JH,
Rantanen T,
O'Connor GT,
Ripatti S,
Scott RJ,
Karrasch S,
Grallert H,
Gaddis NC,
Starr JM,
Wijmenga C,
Minster RL,
Lederer DJ,
Pekkanen J,
Gyllensten U,
Campbell H,
Morris AP,
Gläser S,
Hammond CJ,
Burkart KM,
Beilby J,
Kritchevsky SB,
Gudnason V,
Hancock DB,
Williams OD,
Polasek O,
Zemunik T,
Kolcic I,
Petrini MF,
Wjst M,
Kim WJ,
Porteous DJ,
Scotland G,
Smith BH,
Viljanen A,
Heliövaara M,
Attia JR,
Sayers I,
Hampel R,
Gieger C,
Deary IJ,
Boezen HM,
Newman A,
Jarvelin MR,
Wilson JF,
Lind L,
Stricker BH,
Teumer A,
Spector TD,
Melén E,
Peters MJ,
Lange LA,
Barr RG,
Bracke KR,
Verhamme FM,
Sung J,
Hiemstra PS,
Cassano PA,
Sood A,
Hayward C,
Dupuis J,
Hall IP,
Brusselle GG,
Tobin MD,
London SJ
Nature genetics · 2014 · PMID 24929828
4 pages
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Verhaaren BF,
Debette S,
Bis JC,
Smith JA,
Ikram MK,
Adams HH,
Beecham AH,
Rajan KB,
Lopez LM,
Barral S,
van Buchem MA,
van der Grond J
and 90 more — show all
Smith AV,
Hegenscheid K,
Aggarwal NT,
de Andrade M,
Atkinson EJ,
Beekman M,
Beiser AS,
Blanton SH,
Boerwinkle E,
Brickman AM,
Bryan RN,
Chauhan G,
Chen CP,
Chouraki V,
de Craen AJ,
Crivello F,
Deary IJ,
Deelen J,
De Jager PL,
Dufouil C,
Elkind MS,
Evans DA,
Freudenberger P,
Gottesman RF,
Guðnason V,
Habes M,
Heckbert SR,
Heiss G,
Hilal S,
Hofer E,
Hofman A,
Ibrahim-Verbaas CA,
Knopman DS,
Lewis CE,
Liao J,
Liewald DC,
Luciano M,
van der Lugt A,
Martinez OO,
Mayeux R,
Mazoyer B,
Nalls M,
Nauck M,
Niessen WJ,
Oostra BA,
Psaty BM,
Rice KM,
Rotter JI,
von Sarnowski B,
Schmidt H,
Schreiner PJ,
Schuur M,
Sidney SS,
Sigurdsson S,
Slagboom PE,
Stott DJ,
van Swieten JC,
Teumer A,
Töglhofer AM,
Traylor M,
Trompet S,
Turner ST,
Tzourio C,
Uh HW,
Uitterlinden AG,
Vernooij MW,
Wang JJ,
Wong TY,
Wardlaw JM,
Windham BG,
Wittfeld K,
Wolf C,
Wright CB,
Yang Q,
Zhao W,
Zijdenbos A,
Jukema JW,
Sacco RL,
Kardia SL,
Amouyel P,
Mosley TH,
Longstreth WT Jr,
DeCarli CC,
van Duijn CM,
Schmidt R,
Launer LJ,
Grabe HJ,
Seshadri SS,
Ikram MA,
Fornage M
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
de las Fuentes L,
Sung YJ,
Noordam R,
Winkler T,
Feitosa MF,
Schwander K,
Bentley AR,
Brown MR,
Guo X,
Manning A,
Chasman DI,
Aschard H
and 211 more — show all
Bartz TM,
Bielak LF,
Campbell A,
Cheng CY,
Dorajoo R,
Hartwig FP,
Horimoto ARVR,
Li C,
Li-Gao R,
Liu Y,
Marten J,
Musani SK,
Ntalla I,
Rankinen T,
Richard M,
Sim X,
Smith AV,
Tajuddin SM,
Tayo BO,
Vojinovic D,
Warren HR,
Xuan D,
Alver M,
Boissel M,
Chai JF,
Chen X,
Christensen K,
Divers J,
Evangelou E,
Gao C,
Girotto G,
Harris SE,
He M,
Hsu FC,
Kühnel B,
Laguzzi F,
Li X,
Lyytikäinen LP,
Nolte IM,
Poveda A,
Rauramaa R,
Riaz M,
Rueedi R,
Shu XO,
Snieder H,
Sofer T,
Takeuchi F,
Verweij N,
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2 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
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.