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226 matches for
Uitterlinden AG,
showing the first 20.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
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
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Bradfield JP,
Vogelezang S,
Felix JF,
Chesi A,
Helgeland Ø,
Horikoshi M,
Karhunen V,
Lowry E,
Cousminer DL,
Ahluwalia TS,
Thiering E,
Boh ET
and 87 more — show all
Zafarmand MH,
Vilor-Tejedor N,
Wang CA,
Joro R,
Chen Z,
Gauderman WJ,
Pitkänen N,
Parra EJ,
Fernandez-Rhodes L,
Alyass A,
Monnereau C,
Curtin JA,
Have CT,
McCormack SE,
Hollensted M,
Frithioff-Bøjsøe C,
Valladares-Salgado A,
Peralta-Romero J,
Teo YY,
Standl M,
Leinonen JT,
Holm JC,
Peters T,
Vioque J,
Vrijheid M,
Simpson A,
Custovic A,
Vaudel M,
Canouil M,
Lindi V,
Atalay M,
Kähönen M,
Raitakari OT,
van Schaik BDC,
Berkowitz RI,
Cole SA,
Voruganti VS,
Wang Y,
Highland HM,
Comuzzie AG,
Butte NF,
Justice AE,
Gahagan S,
Blanco E,
Lehtimäki T,
Lakka TA,
Hebebrand J,
Bonnefond A,
Grarup N,
Froguel P,
Lyytikäinen LP,
Cruz M,
Kobes S,
Hanson RL,
Zemel BS,
Hinney A,
Teo KK,
Meyre D,
North KE,
Gilliland FD,
Bisgaard H,
Bustamante M,
Bonnelykke K,
Pennell CE,
Rivadeneira F,
Uitterlinden AG,
Baier LJ,
Vrijkotte TGM,
Heinrich J,
Sørensen TIA,
Saw SM,
Pedersen O,
Hansen T,
Eriksson J,
Widén E,
McCarthy MI,
Njølstad PR,
Power C,
Hyppönen E,
Sebert S,
Brown CD,
Järvelin MR,
Timpson NJ,
Johansson S,
Hakonarson H,
Jaddoe VWV,
Grant SFA
Early Growth Genetics Consortium
Human molecular genetics · 2019 · PMID 31504550
5 pages
Novel genetic loci affecting facial shape variation in humans
Xiong Z,
Dankova G,
Howe LJ,
Lee MK,
Hysi PG,
de Jong MA,
Zhu G,
Adhikari K,
Li D,
Li Y,
Pan B,
Feingold E
and 37 more — show all
Marazita ML,
Shaffer JR,
McAloney K,
Xu SH,
Jin L,
Wang S,
de Vrij FM,
Lendemeijer B,
Richmond S,
Zhurov A,
Lewis S,
Sharp GC,
Paternoster L,
Thompson H,
Gonzalez-Jose R,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
Poletti G,
Bedoya G,
Rothhammer F,
Uitterlinden AG,
Ikram MA,
Wolvius E,
Kushner SA,
Nijsten TE,
Palstra RT,
Boehringer S,
Medland SE,
Tang K,
Ruiz-Linares A,
Martin NG,
Spector TD,
Stergiakouli E,
Weinberg SM,
Liu F,
Kayser M
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
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
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Simcoe M,
Valdes A,
Liu F,
Furlotte NA,
Evans DM,
Hemani G,
Ring SM,
Smith GD,
Duffy DL,
Zhu G,
Gordon SD,
Medland SE
and 32 more — show all
Vuckovic D,
Girotto G,
Sala C,
Catamo E,
Concas MP,
Brumat M,
Gasparini P,
Toniolo D,
Cocca M,
Robino A,
Yazar S,
Hewitt A,
Wu W,
Kraft P,
Hammond CJ,
Shi Y,
Chen Y,
Zeng C,
Klaver CCW,
Uitterlinden AG,
Ikram MA,
Hamer MA,
van Duijn CM,
Nijsten T,
Han J,
Mackey DA,
Martin NG,
Cheng CY,
Hinds DA,
Spector TD,
Kayser M,
Hysi PG
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
Combining genome-wide association studies highlight novel loci involved in human facial variation
Xiong Z,
Gao X,
Chen Y,
Feng Z,
Pan S,
Lu H,
Uitterlinden AG,
Nijsten T,
Ikram A,
Rivadeneira F,
Ghanbari M,
Wang Y
and 2 more — show all
Nature communications · 2022 · PMID 36539420 · open access
5 pages
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Aulchenko YS,
Ripatti S,
Lindqvist I,
Boomsma D,
Heid IM,
Pramstaller PP,
Penninx BW,
Janssens AC,
Wilson JF,
Spector T,
Martin NG,
Pedersen NL
and 45 more — show all
Kyvik KO,
Kaprio J,
Hofman A,
Freimer NB,
Jarvelin MR,
Gyllensten U,
Campbell H,
Rudan I,
Johansson A,
Marroni F,
Hayward C,
Vitart V,
Jonasson I,
Pattaro C,
Wright A,
Hastie N,
Pichler I,
Hicks AA,
Falchi M,
Willemsen G,
Hottenga JJ,
de Geus EJ,
Montgomery GW,
Whitfield J,
Magnusson P,
Saharinen J,
Perola M,
Silander K,
Isaacs A,
Sijbrands EJ,
Uitterlinden AG,
Witteman JC,
Oostra BA,
Elliott P,
Ruokonen A,
Sabatti C,
Gieger C,
Meitinger T,
Kronenberg F,
Döring A,
Wichmann HE,
Smit JH,
McCarthy MI,
van Duijn CM,
Peltonen L
ENGAGE Consortium
Nature genetics · 2009 · PMID 19060911
4 pages
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Rivadeneira F,
Styrkársdottir U,
Estrada K,
Halldórsson BV,
Hsu YH,
Richards JB,
Zillikens MC,
Kavvoura FK,
Amin N,
Aulchenko YS,
Cupples LA,
Deloukas P
and 23 more — show all
Demissie S,
Grundberg E,
Hofman A,
Kong A,
Karasik D,
van Meurs JB,
Oostra B,
Pastinen T,
Pols HA,
Sigurdsson G,
Soranzo N,
Thorleifsson G,
Thorsteinsdottir U,
Williams FM,
Wilson SG,
Zhou Y,
Ralston SH,
van Duijn CM,
Spector T,
Kiel DP,
Stefansson K,
Ioannidis JP,
Uitterlinden AG
Genetic Factors for Osteoporosis (GEFOS) Consortium
Nature genetics · 2009 · PMID 19801982 · open access
4 pages
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Dupuis J,
Langenberg C,
Prokopenko I,
Saxena R,
Soranzo N,
Jackson AU,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Gloyn AL,
Lindgren CM,
Mägi R
and 292 more — show all
Morris AP,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Thorleifsson G,
Steinthorsdottir V,
Henneman P,
Grallert H,
Dehghan A,
Hottenga JJ,
Franklin CS,
Navarro P,
Song K,
Goel A,
Perry JR,
Egan JM,
Lajunen T,
Grarup N,
Sparsø T,
Doney A,
Voight BF,
Stringham HM,
Li M,
Kanoni S,
Shrader P,
Cavalcanti-Proença C,
Kumari M,
Qi L,
Timpson NJ,
Gieger C,
Zabena C,
Rocheleau G,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Payne F,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ardlie K,
Ariyurek Y,
Balkau B,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Benediktsson R,
Bennett AJ,
Bergmann S,
Bochud M,
Boerwinkle E,
Bonnefond A,
Bonnycastle LL,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Charpentier G,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Cornelis M,
Crawford G,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Dina C,
Erdos MR,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Fox CS,
Frants R,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Groves CJ,
Grundy S,
Gwilliam R,
Gyllensten U,
Hadjadj S,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hassanali N,
Hayward C,
Heath SC,
Hercberg S,
Herder C,
Hicks AA,
Hillman DR,
Hingorani AD,
Hofman A,
Hui J,
Hung J,
Isomaa B,
Johnson PR,
Jørgensen T,
Jula A,
Kaakinen M,
Kaprio J,
Kesaniemi YA,
Kivimaki M,
Knight B,
Koskinen S,
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Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
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.