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37 matches for
Singleton A,
showing the first 20.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Ganesh SK,
Zakai NA,
van Rooij FJ,
Soranzo N,
Smith AV,
Nalls MA,
Chen MH,
Kottgen A,
Glazer NL,
Dehghan A,
Kuhnel B,
Aspelund T
and 50 more — show all
Yang Q,
Tanaka T,
Jaffe A,
Bis JC,
Verwoert GC,
Teumer A,
Fox CS,
Guralnik JM,
Ehret GB,
Rice K,
Felix JF,
Rendon A,
Eiriksdottir G,
Levy D,
Patel KV,
Boerwinkle E,
Rotter JI,
Hofman A,
Sambrook JG,
Hernandez DG,
Zheng G,
Bandinelli S,
Singleton AB,
Coresh J,
Lumley T,
Uitterlinden AG,
Vangils JM,
Launer LJ,
Cupples LA,
Oostra BA,
Zwaginga JJ,
Ouwehand WH,
Thein SL,
Meisinger C,
Deloukas P,
Nauck M,
Spector TD,
Gieger C,
Gudnason V,
van Duijn CM,
Psaty BM,
Ferrucci L,
Chakravarti A,
Greinacher A,
O'Donnell CJ,
Witteman JC,
Furth S,
Cushman M,
Harris TB,
Lin JP
Nature genetics · 2009 · PMID 19862010 · open access
12 pages+
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls MA,
Pankratz N,
Lill CM,
Do CB,
Hernandez DG,
Saad M,
DeStefano AL,
Kara E,
Bras J,
Sharma M,
Schulte C,
Keller MF
and 35 more — show all
Arepalli S,
Letson C,
Edsall C,
Stefansson H,
Liu X,
Pliner H,
Lee JH,
Cheng R,
Ikram MA,
Ioannidis JP,
Hadjigeorgiou GM,
Bis JC,
Martinez M,
Perlmutter JS,
Goate A,
Marder K,
Fiske B,
Sutherland M,
Xiromerisiou G,
Myers RH,
Clark LN,
Stefansson K,
Hardy JA,
Heutink P,
Chen H,
Wood NW,
Houlden H,
Payami H,
Brice A,
Scott WK,
Gasser T,
Bertram L,
Eriksson N,
Foroud T,
Singleton AB
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and 10 more consortia
Nature genetics · 2014 · PMID 25064009 · open access
12 pages+
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
Kia DA,
Noyce AJ,
Xue A,
Bras J,
Young E
and 39 more — show all
von Coelln R,
Simón-Sánchez J,
Schulte C,
Sharma M,
Krohn L,
Pihlstrøm L,
Siitonen A,
Iwaki H,
Leonard H,
Faghri F,
Gibbs JR,
Hernandez DG,
Scholz SW,
Botia JA,
Martinez M,
Corvol JC,
Lesage S,
Jankovic J,
Shulman LM,
Sutherland M,
Tienari P,
Majamaa K,
Toft M,
Andreassen OA,
Bangale T,
Brice A,
Yang J,
Gan-Or Z,
Gasser T,
Heutink P,
Shulman JM,
Wood NW,
Hinds DA,
Hardy JA,
Morris HR,
Gratten J,
Visscher PM,
Graham RR,
Singleton AB
23andMe Research Team · System Genomics of Parkinson's Disease Consortium and 1 more consortia
The Lancet. Neurology · 2019 · PMID 31701892
12 pages+
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
Graff M,
Justice AE,
Young KL,
Marouli E,
Zhang X,
Fine RS,
Lim E,
Buchanan V,
Rand K,
Feitosa MF,
Wojczynski MK,
Yanek LR
and 213 more — show all
Shao Y,
Rohde R,
Adeyemo AA,
Aldrich MC,
Allison MA,
Ambrosone CB,
Ambs S,
Amos C,
Arnett DK,
Atwood L,
Bandera EV,
Bartz T,
Becker DM,
Berndt SI,
Bernstein L,
Bielak LF,
Blot WJ,
Bottinger EP,
Bowden DW,
Bradfield JP,
Brody JA,
Broeckel U,
Burke G,
Cade BE,
Cai Q,
Caporaso N,
Carlson C,
Carpten J,
Casey G,
Chanock SJ,
Chen G,
Chen M,
Chen YI,
Chen WM,
Chesi A,
Chiang CWK,
Chu L,
Coetzee GA,
Conti DV,
Cooper RS,
Cushman M,
Demerath E,
Deming SL,
Dimitrov L,
Ding J,
Diver WR,
Duan Q,
Evans MK,
Falusi AG,
Faul JD,
Fornage M,
Fox C,
Freedman BI,
Garcia M,
Gillanders EM,
Goodman P,
Gottesman O,
Grant SFA,
Guo X,
Hakonarson H,
Haritunians T,
Harris TB,
Harris CC,
Henderson BE,
Hennis A,
Hernandez DG,
Hirschhorn JN,
McNeill LH,
Howard TD,
Howard B,
Hsing AW,
Hsu YH,
Hu JJ,
Huff CD,
Huo D,
Ingles SA,
Irvin MR,
John EM,
Johnson KC,
Jordan JM,
Kabagambe EK,
Kang SJ,
Kardia SL,
Keating BJ,
Kittles RA,
Klein EA,
Kolb S,
Kolonel LN,
Kooperberg C,
Kuller L,
Kutlar A,
Lange L,
Langefeld CD,
Le Marchand L,
Leonard H,
Lettre G,
Levin AM,
Li Y,
Li J,
Liu Y,
Liu Y,
Liu S,
Lohman K,
Lotay V,
Lu Y,
Maixner W,
Manson JE,
McKnight B,
Meng Y,
Monda KL,
Monroe K,
Moore JH,
Mosley TH,
Mudgal P,
Murphy AB,
Nadukuru R,
Nalls MA,
Nathanson KL,
Nayak U,
N'Diaye A,
Nemesure B,
Neslund-Dudas C,
Neuhouser ML,
Nyante S,
Ochs-Balcom H,
Ogundiran TO,
Ogunniyi A,
Ojengbede O,
Okut H,
Olopade OI,
Olshan A,
Padhukasahasram B,
Palmer J,
Palmer CD,
Palmer ND,
Papanicolaou G,
Patel SR,
Pettaway CA,
Peyser PA,
Press MF,
Rao DC,
Rasmussen-Torvik LJ,
Redline S,
Reiner AP,
Rhie SK,
Rodriguez-Gil JL,
Rotimi CN,
Rotter JI,
Ruiz-Narvaez EA,
Rybicki BA,
Salako B,
Sale MM,
Sanderson M,
Schadt E,
Schreiner PJ,
Schurmann C,
Schwartz AG,
Shriner DA,
Signorello LB,
Singleton AB,
Siscovick DS,
Smith JA,
Smith S,
Speliotes E,
Spitz M,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Sucheston L,
Sun YV,
Tajuddin SM,
Taylor H,
Taylor K,
Tayo BO,
Thun MJ,
Tucker MA,
Vaidya D,
Van Den Berg DJ,
Vedantam S,
Vitolins M,
Wang Z,
Ware EB,
Wassertheil-Smoller S,
Weir DR,
Wiencke JK,
Williams SM,
Williams LK,
Wilson JG,
Witte JS,
Wrensch M,
Wu X,
Yao J,
Zakai N,
Zanetti K,
Zemel BS,
Zhao W,
Zhao JH,
Zheng W,
Zhi D,
Zhou J,
Zhu X,
Ziegler RG,
Zmuda J,
Zonderman AB,
Psaty BM,
Borecki IB,
Cupples LA,
Liu CT,
Haiman CA,
Loos R,
Ng MCY,
North KE
American journal of human genetics · 2021 · PMID 33713608
12 pages+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
and 610 more — show all
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
Rüeger S,
Sim X,
Vrieze S,
Ahluwalia TS,
Akiyama M,
Allison MA,
Alvarez M,
Andersen MK,
Ani A,
Appadurai V,
Arbeeva L,
Bhaskar S,
Bielak LF,
Bollepalli S,
Bonnycastle LL,
Bork-Jensen J,
Bradfield JP,
Bradford Y,
Braund PS,
Brody JA,
Burgdorf KS,
Cade BE,
Cai H,
Cai Q,
Campbell A,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
Cocca M,
Concas MP,
Couture C,
Cuellar-Partida G,
Danning R,
Daw EW,
Degenhard F,
Delgado GE,
Delitala A,
Demirkan A,
Deng X,
Devineni P,
Dietl A,
Dimitriou M,
Dimitrov L,
Dorajoo R,
Ekici AB,
Engmann JE,
Fairhurst-Hunter Z,
Farmaki AE,
Faul JD,
Fernandez-Lopez JC,
Forer L,
Francescatto M,
Freitag-Wolf S,
Fuchsberger C,
Galesloot TE,
Gao Y,
Gao Z,
Geller F,
Giannakopoulou O,
Giulianini F,
Gjesing AP,
Goel A,
Gordon SD,
Gorski M,
Grove J,
Guo X,
Gustafsson S,
Haessler J,
Hansen TF,
Havulinna AS,
Haworth SJ,
He J,
Heard-Costa N,
Hebbar P,
Hindy G,
Ho YA,
Hofer E,
Holliday E,
Horn K,
Hornsby WE,
Hottenga JJ,
Huang H,
Huang J,
Huerta-Chagoya A,
Huffman JE,
Hung YJ,
Huo S,
Hwang MY,
Iha H,
Ikeda DD,
Isono M,
Jackson AU,
Jäger S,
Jansen IE,
Johansson I,
Jonas JB,
Jonsson A,
Jørgensen T,
Kalafati IP,
Kanai M,
Kanoni S,
Kårhus LL,
Kasturiratne A,
Katsuya T,
Kawaguchi T,
Kember RL,
Kentistou KA,
Kim HN,
Kim YJ,
Kleber ME,
Knol MJ,
Kurbasic A,
Lauzon M,
Le P,
Lea R,
Lee JY,
Leonard HL,
Li SA,
Li X,
Li X,
Liang J,
Lin H,
Lin SY,
Liu J,
Liu X,
Lo KS,
Long J,
Lores-Motta L,
Luan J,
Lyssenko V,
Lyytikäinen LP,
Mahajan A,
Mamakou V,
Mangino M,
Manichaikul A,
Marten J,
Mattheisen M,
Mavarani L,
McDaid AF,
Meidtner K,
Melendez TL,
Mercader JM,
Milaneschi Y,
Miller JE,
Millwood IY,
Mishra PP,
Mitchell RE,
Møllehave LT,
Morgan A,
Mucha S,
Munz M,
Nakatochi M,
Nelson CP,
Nethander M,
Nho CW,
Nielsen AA,
Nolte IM,
Nongmaithem SS,
Noordam R,
Ntalla I,
Nutile T,
Pandit A,
Christofidou P,
Pärna K,
Pauper M,
Petersen ERB,
Petersen LV,
Pitkänen N,
Polašek O,
Poveda A,
Preuss MH,
Pyarajan S,
Raffield LM,
Rakugi H,
Ramirez J,
Rasheed A,
Raven D,
Rayner NW,
Riveros C,
Rohde R,
Ruggiero D,
Ruotsalainen SE,
Ryan KA,
Sabater-Lleal M,
Saxena R,
Scholz M,
Sendamarai A,
Shen B,
Shi J,
Shin JH,
Sidore C,
Sitlani CM,
Slieker RC,
Smit RAJ,
Smith AV,
Smith JA,
Smyth LJ,
Southam L,
Steinthorsdottir V,
Sun L,
Takeuchi F,
Tallapragada DSP,
Taylor KD,
Tayo BO,
Tcheandjieu C,
Terzikhan N,
Tesolin P,
Teumer A,
Theusch E,
Thompson DJ,
Thorleifsson G,
Timmers PRHJ,
Trompet S,
Turman C,
Vaccargiu S,
van der Laan SW,
van der Most PJ,
van Klinken JB,
van Setten J,
Verma SS,
Verweij N,
Veturi Y,
Wang CA,
Wang C,
Wang L,
Wang Z,
Warren HR,
Bin Wei W,
Wickremasinghe AR,
Wielscher M,
Wiggins KL,
Winsvold BS,
Wong A,
Wu Y,
Wuttke M,
Xia R,
Xie T,
Yamamoto K,
Yang J,
Yao J,
Young H,
Yousri NA,
Yu L,
Zeng L,
Zhang W,
Zhang X,
Zhao JH,
Zhao W,
Zhou W,
Zimmermann ME,
Zoledziewska M,
Adair LS,
Adams HHH,
Aguilar-Salinas CA,
Al-Mulla F,
Arnett DK,
Asselbergs FW,
Åsvold BO,
Attia J,
Banas B,
Bandinelli S,
Bennett DA,
Bergler T,
Bharadwaj D,
Biino G,
Bisgaard H,
Boerwinkle E,
Böger CA,
Bønnelykke K,
Boomsma DI,
Børglum AD,
Borja JB,
Bouchard C,
Bowden DW,
Brandslund I,
Brumpton B,
Buring JE,
Caulfield MJ,
Chambers JC,
Chandak GR,
Chanock SJ,
Chaturvedi N,
Chen YI,
Chen Z,
Cheng CY,
Christophersen IE,
Ciullo M,
Cole JW,
Collins FS,
Cooper RS,
Cruz M,
Cucca F,
Cupples LA,
Cutler MJ,
Damrauer SM,
Dantoft TM,
de Borst GJ,
de Groot LCPGM,
De Jager PL,
de Kleijn DPV,
Janaka de Silva H,
Dedoussis GV,
den Hollander AI,
Du S,
Easton DF,
Elders PJM,
Eliassen AH,
Ellinor PT,
Elmståhl S,
Erdmann J,
Evans MK,
Fatkin D,
Feenstra B,
Feitosa MF,
Ferrucci L,
Ford I,
Fornage M,
Franke A,
Franks PW,
Freedman BI,
Gasparini P,
Gieger C,
Girotto G,
Goddard ME,
Golightly YM,
Gonzalez-Villalpando C,
Gordon-Larsen P,
Grallert H,
Grant SFA,
Grarup N,
Griffiths L,
Gudnason V,
Haiman C,
Hakonarson H,
Hansen T,
Hartman CA,
Hattersley AT,
Hayward C,
Heckbert SR,
Heng CK,
Hengstenberg C,
Hewitt AW,
Hishigaki H,
Hoyng CB,
Huang PL,
Huang W,
Hunt SC,
Hveem K,
Hyppönen E,
Iacono WG,
Ichihara S,
Ikram MA,
Isasi CR,
Jackson RD,
Jarvelin MR,
Jin ZB,
Jöckel KH,
Joshi PK,
Jousilahti P,
Jukema JW,
Kähönen M,
Kamatani Y,
Kang KD,
Kaprio J,
Kardia SLR,
Karpe F,
Kato N,
Kee F,
Kessler T,
Khera AV,
Khor CC,
Kiemeney LALM,
Kim BJ,
Kim EK,
Kim HL,
Kirchhof P,
Kivimaki M,
Koh WP,
Koistinen HA,
Kolovou GD,
Kooner JS,
Kooperberg C,
Köttgen A,
Kovacs P,
Kraaijeveld A,
Kraft P,
Krauss RM,
Kumari M,
Kutalik Z,
Laakso M,
Lange LA,
Langenberg C,
Launer LJ,
Le Marchand L,
Lee H,
Lee NR,
Lehtimäki T,
Li H,
Li L,
Lieb W,
Lin X,
Lind L,
Linneberg A,
Liu CT,
Liu J,
Loeffler M,
London B,
Lubitz SA,
Lye SJ,
Mackey DA,
Mägi R,
Magnusson PKE,
Marcus GM,
Vidal PM,
Martin NG,
März W,
Matsuda F,
McGarrah RW,
McGue M,
McKnight AJ,
Medland SE,
Mellström D,
Metspalu A,
Mitchell BD,
Mitchell P,
Mook-Kanamori DO,
Morris AD,
Mucci LA,
Munroe PB,
Nalls MA,
Nazarian S,
Nelson AE,
Neville MJ,
Newton-Cheh C,
Nielsen CS,
Nöthen MM,
Ohlsson C,
Oldehinkel AJ,
Orozco L,
Pahkala K,
Pajukanta P,
Palmer CNA,
Parra EJ,
Pattaro C,
Pedersen O,
Pennell CE,
Penninx BWJH,
Perusse L,
Peters A,
Peyser PA,
Porteous DJ,
Posthuma D,
Power C,
Pramstaller PP,
Province MA,
Qi Q,
Qu J,
Rader DJ,
Raitakari OT,
Ralhan S,
Rallidis LS,
Rao DC,
Redline S,
Reilly DF,
Reiner AP,
Rhee SY,
Ridker PM,
Rienstra M,
Ripatti S,
Ritchie MD,
Roden DM,
Rosendaal FR,
Rotter JI,
Rudan I,
Rutters F,
Sabanayagam C,
Saleheen D,
Salomaa V,
Samani NJ,
Sanghera DK,
Sattar N,
Schmidt B,
Schmidt H,
Schmidt R,
Schulze MB,
Schunkert H,
Scott LJ,
Scott RJ,
Sever P,
Shiroma EJ,
Shoemaker MB,
Shu XO,
Simonsick EM,
Sims M,
Singh JR,
Singleton AB,
Sinner MF,
Smith JG,
Snieder H,
Spector TD,
Stampfer MJ,
Stark KJ,
Strachan DP,
't Hart LM,
Tabara Y,
Tang H,
Tardif JC,
Thanaraj TA,
Timpson NJ,
Tönjes A,
Tremblay A,
Tuomi T,
Tuomilehto J,
Tusié-Luna MT,
Uitterlinden AG,
van Dam RM,
van der Harst P,
Van der Velde N,
van Duijn CM,
van Schoor NM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wacher-Rodarte NH,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Weir DR,
Werge TM,
Widen E,
Wilkens LR,
Willemsen G,
Willett WC,
Wilson JF,
Wong TY,
Woo JT,
Wright AF,
Wu JY,
Xu H,
Yajnik CS,
Yokota M,
Yuan JM,
Zeggini E,
Zemel BS,
Zheng W,
Zhu X,
Zmuda JM,
Zonderman AB,
Zwart JA,
Chasman DI,
Cho YS,
Heid IM,
McCarthy MI,
Ng MCY,
O'Donnell CJ,
Rivadeneira F,
Thorsteinsdottir U,
Sun YV,
Tai ES,
Boehnke M,
Deloukas P,
Justice AE,
Lindgren CM,
Loos RJF,
Mohlke KL,
North KE,
Stefansson K,
Walters RG,
Winkler TW,
Young KL,
Loh PR,
Yang J,
Esko T,
Assimes TL,
Auton A,
Abecasis GR,
Willer CJ,
Locke AE,
Berndt SI,
Lettre G,
Frayling TM,
Okada Y,
Wood AR,
Visscher PM,
Hirschhorn JN
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
Kim JJ,
Vitale D,
Otani DV,
Lian MM,
Heilbron K,
Iwaki H,
Lake J,
Solsberg CW,
Leonard H,
Makarious MB,
Tan EK,
Singleton AB
and 6 more — show all
23andMe Research Team · Global Parkinson’s Genetics Program (GP2)
Nature genetics · 2024 · PMID 38155330 · open access
12 pages+
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Evans DS,
Avery CL,
Nalls MA,
Li G,
Barnard J,
Smith EN,
Tanaka T,
Butler AM,
Buxbaum SG,
Alonso A,
Arking DE,
Berenson GS
and 49 more — show all
Bis JC,
Buyske S,
Carty CL,
Chen W,
Chung MK,
Cummings SR,
Deo R,
Eaton CB,
Fox ER,
Heckbert SR,
Heiss G,
Hindorff LA,
Hsueh WC,
Isaacs A,
Jamshidi Y,
Kerr KF,
Liu F,
Liu Y,
Lohman KK,
Magnani JW,
Maher JF,
Mehra R,
Meng YA,
Musani SK,
Newton-Cheh C,
North KE,
Psaty BM,
Redline S,
Rotter JI,
Schnabel RB,
Schork NJ,
Shohet RV,
Singleton AB,
Smith JD,
Soliman EZ,
Srinivasan SR,
Taylor HA Jr,
Van Wagoner DR,
Wilson JG,
Young T,
Zhang ZM,
Zonderman AB,
Evans MK,
Ferrucci L,
Murray SS,
Tranah GJ,
Whitsel EA,
Reiner AP,
Sotoodehnia N
CHARGE QRS Consortium
Human molecular genetics · 2016 · PMID 27577874
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,
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LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
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BioBank Japan Project · CHARGE Consortium
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Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
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
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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
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How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
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