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30 matches for
Hernandez D,
showing the first 10.
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
and 247 more — show all
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
3 pages
Genetic variation associated with circulating monocyte count in the eMERGE Network
Crosslin DR,
McDavid A,
Weston N,
Zheng X,
Hart E,
de Andrade M,
Kullo IJ,
McCarty CA,
Doheny KF,
Pugh E,
Kho A,
Hayes MG
and 52 more — show all
Ritchie MD,
Saip A,
Crawford DC,
Crane PK,
Newton K,
Carrell DS,
Gallego CJ,
Nalls MA,
Li R,
Mirel DB,
Crenshaw A,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Zakai NA,
Yango Q,
Garcia M,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Felix JF,
Dehghan A,
Wilson JG,
Bis JC,
Fox CS,
Glazer NL,
Cupples LA,
Coresh J,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Larson EB,
Carlson CS,
Jarvik GP
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
2 pages
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Monda KL,
Chen GK,
Taylor KC,
Palmer C,
Edwards TL,
Lange LA,
Ng MC,
Adeyemo AA,
Allison MA,
Bielak LF,
Chen G,
Graff M
and 196 more — show all
Irvin MR,
Rhie SK,
Li G,
Liu Y,
Liu Y,
Lu Y,
Nalls MA,
Sun YV,
Wojczynski MK,
Yanek LR,
Aldrich MC,
Ademola A,
Amos CI,
Bandera EV,
Bock CH,
Britton A,
Broeckel U,
Cai Q,
Caporaso NE,
Carlson CS,
Carpten J,
Casey G,
Chen WM,
Chen F,
Chen YD,
Chiang CW,
Coetzee GA,
Demerath E,
Deming-Halverson SL,
Driver RW,
Dubbert P,
Feitosa MF,
Feng Y,
Freedman BI,
Gillanders EM,
Gottesman O,
Guo X,
Haritunians T,
Harris T,
Harris CC,
Hennis AJ,
Hernandez DG,
McNeill LH,
Howard TD,
Howard BV,
Howard VJ,
Johnson KC,
Kang SJ,
Keating BJ,
Kolb S,
Kuller LH,
Kutlar A,
Langefeld CD,
Lettre G,
Lohman K,
Lotay V,
Lyon H,
Manson JE,
Maixner W,
Meng YA,
Monroe KR,
Morhason-Bello I,
Murphy AB,
Mychaleckyj JC,
Nadukuru R,
Nathanson KL,
Nayak U,
N'diaye A,
Nemesure B,
Wu SY,
Leske MC,
Neslund-Dudas C,
Neuhouser M,
Nyante S,
Ochs-Balcom H,
Ogunniyi A,
Ogundiran TO,
Ojengbede O,
Olopade OI,
Palmer JR,
Ruiz-Narvaez EA,
Palmer ND,
Press MF,
Rampersaud E,
Rasmussen-Torvik LJ,
Rodriguez-Gil JL,
Salako B,
Schadt EE,
Schwartz AG,
Shriner DA,
Siscovick D,
Smith SB,
Wassertheil-Smoller S,
Speliotes EK,
Spitz MR,
Sucheston L,
Taylor H,
Tayo BO,
Tucker MA,
Van Den Berg DJ,
Edwards DR,
Wang Z,
Wiencke JK,
Winkler TW,
Witte JS,
Wrensch M,
Wu X,
Yang JJ,
Levin AM,
Young TR,
Zakai NA,
Cushman M,
Zanetti KA,
Zhao JH,
Zhao W,
Zheng Y,
Zhou J,
Ziegler RG,
Zmuda JM,
Fernandes JK,
Gilkeson GS,
Kamen DL,
Hunt KJ,
Spruill IJ,
Ambrosone CB,
Ambs S,
Arnett DK,
Atwood L,
Becker DM,
Berndt SI,
Bernstein L,
Blot WJ,
Borecki IB,
Bottinger EP,
Bowden DW,
Burke G,
Chanock SJ,
Cooper RS,
Ding J,
Duggan D,
Evans MK,
Fox C,
Garvey WT,
Bradfield JP,
Hakonarson H,
Grant SF,
Hsing A,
Chu L,
Hu JJ,
Huo D,
Ingles SA,
John EM,
Jordan JM,
Kabagambe EK,
Kardia SL,
Kittles RA,
Goodman PJ,
Klein EA,
Kolonel LN,
Le Marchand L,
Liu S,
McKnight B,
Millikan RC,
Mosley TH,
Padhukasahasram B,
Williams LK,
Patel SR,
Peters U,
Pettaway CA,
Peyser PA,
Psaty BM,
Redline S,
Rotimi CN,
Rybicki BA,
Sale MM,
Schreiner PJ,
Signorello LB,
Singleton AB,
Stanford JL,
Strom SS,
Thun MJ,
Vitolins M,
Zheng W,
Moore JH,
Williams SM,
Ketkar S,
Zhu X,
Zonderman AB,
Kooperberg C,
Papanicolaou GJ,
Henderson BE,
Reiner AP,
Hirschhorn JN,
Loos RJ,
North KE,
Haiman CA
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations
O'Seaghdha CM,
Wu H,
Yang Q,
Kapur K,
Guessous I,
Zuber AM,
Köttgen A,
Stoudmann C,
Teumer A,
Kutalik Z,
Mangino M,
Dehghan A
and 97 more — show all
Zhang W,
Eiriksdottir G,
Li G,
Tanaka T,
Portas L,
Lopez LM,
Hayward C,
Lohman K,
Matsuda K,
Padmanabhan S,
Firsov D,
Sorice R,
Ulivi S,
Brockhaus AC,
Kleber ME,
Mahajan A,
Ernst FD,
Gudnason V,
Launer LJ,
Mace A,
Boerwinckle E,
Arking DE,
Tanikawa C,
Nakamura Y,
Brown MJ,
Gaspoz JM,
Theler JM,
Siscovick DS,
Psaty BM,
Bergmann S,
Vollenweider P,
Vitart V,
Wright AF,
Zemunik T,
Boban M,
Kolcic I,
Navarro P,
Brown EM,
Estrada K,
Ding J,
Harris TB,
Bandinelli S,
Hernandez D,
Singleton AB,
Girotto G,
Ruggiero D,
d'Adamo AP,
Robino A,
Meitinger T,
Meisinger C,
Davies G,
Starr JM,
Chambers JC,
Boehm BO,
Winkelmann BR,
Huang J,
Murgia F,
Wild SH,
Campbell H,
Morris AP,
Franco OH,
Hofman A,
Uitterlinden AG,
Rivadeneira F,
Völker U,
Hannemann A,
Biffar R,
Hoffmann W,
Shin SY,
Lescuyer P,
Henry H,
Schurmann C,
Munroe PB,
Gasparini P,
Pirastu N,
Ciullo M,
Gieger C,
März W,
Lind L,
Spector TD,
Smith AV,
Rudan I,
Wilson JF,
Polasek O,
Deary IJ,
Pirastu M,
Ferrucci L,
Liu Y,
Kestenbaum B,
Kooner JS,
Witteman JC,
Nauck M,
Kao WH,
Wallaschofski H,
Bonny O,
Fox CS,
Bochud M
SUNLIGHT Consortium · GEFOS Consortium
PLoS genetics · 2013 · PMID 24068962 · open access
2 pages
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Simón-Sánchez J,
Schulte C,
Bras JM,
Sharma M,
Gibbs JR,
Berg D,
Paisan-Ruiz C,
Lichtner P,
Scholz SW,
Hernandez DG,
Krüger R,
Federoff M
and 35 more — show all
Klein C,
Goate A,
Perlmutter J,
Bonin M,
Nalls MA,
Illig T,
Gieger C,
Houlden H,
Steffens M,
Okun MS,
Racette BA,
Cookson MR,
Foote KD,
Fernandez HH,
Traynor BJ,
Schreiber S,
Arepalli S,
Zonozi R,
Gwinn K,
van der Brug M,
Lopez G,
Chanock SJ,
Schatzkin A,
Park Y,
Hollenbeck A,
Gao J,
Huang X,
Wood NW,
Lorenz D,
Deuschl G,
Chen H,
Riess O,
Hardy JA,
Singleton AB,
Gasser T
Nature genetics · 2009 · PMID 19915575 · open access
1 page
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
Laaksovirta H,
Peuralinna T,
Schymick JC,
Scholz SW,
Lai SL,
Myllykangas L,
Sulkava R,
Jansson L,
Hernandez DG,
Gibbs JR,
Nalls MA,
Heckerman D
and 2 more — show all
The Lancet. Neurology · 2010 · PMID 20801718
1 page
CUBN is a gene locus for albuminuria
Böger CA,
Chen MH,
Tin A,
Olden M,
Köttgen A,
de Boer IH,
Fuchsberger C,
O'Seaghdha CM,
Pattaro C,
Teumer A,
Liu CT,
Glazer NL
and 103 more — show all
Li M,
O'Connell JR,
Tanaka T,
Peralta CA,
Kutalik Z,
Luan J,
Zhao JH,
Hwang SJ,
Akylbekova E,
Kramer H,
van der Harst P,
Smith AV,
Lohman K,
de Andrade M,
Hayward C,
Kollerits B,
Tönjes A,
Aspelund T,
Ingelsson E,
Eiriksdottir G,
Launer LJ,
Harris TB,
Shuldiner AR,
Mitchell BD,
Arking DE,
Franceschini N,
Boerwinkle E,
Egan J,
Hernandez D,
Reilly M,
Townsend RR,
Lumley T,
Siscovick DS,
Psaty BM,
Kestenbaum B,
Haritunians T,
Bergmann S,
Vollenweider P,
Waeber G,
Mooser V,
Waterworth D,
Johnson AD,
Florez JC,
Meigs JB,
Lu X,
Turner ST,
Atkinson EJ,
Leak TS,
Aasarød K,
Skorpen F,
Syvänen AC,
Illig T,
Baumert J,
Koenig W,
Krämer BK,
Devuyst O,
Mychaleckyj JC,
Minelli C,
Bakker SJ,
Kedenko L,
Paulweber B,
Coassin S,
Endlich K,
Kroemer HK,
Biffar R,
Stracke S,
Völzke H,
Stumvoll M,
Mägi R,
Campbell H,
Vitart V,
Hastie ND,
Gudnason V,
Kardia SL,
Liu Y,
Polasek O,
Curhan G,
Kronenberg F,
Prokopenko I,
Rudan I,
Arnlöv J,
Hallan S,
Navis G,
Parsa A,
Ferrucci L,
Coresh J,
Shlipak MG,
Bull SB,
Paterson NJ,
Wichmann HE,
Wareham NJ,
Loos RJ,
Rotter JI,
Pramstaller PP,
Cupples LA,
Beckmann JS,
Yang Q,
Heid IM,
Rettig R,
Dreisbach AW,
Bochud M,
Fox CS,
Kao WH
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Genome-wide meta-analyses of smoking behaviors in African Americans
David SP,
Hamidovic A,
Chen GK,
Bergen AW,
Wessel J,
Kasberger JL,
Brown WM,
Petruzella S,
Thacker EL,
Kim Y,
Nalls MA,
Tranah GJ
and 68 more — show all
Sung YJ,
Ambrosone CB,
Arnett D,
Bandera EV,
Becker DM,
Becker L,
Berndt SI,
Bernstein L,
Blot WJ,
Broeckel U,
Buxbaum SG,
Caporaso N,
Casey G,
Chanock SJ,
Deming SL,
Diver WR,
Eaton CB,
Evans DS,
Evans MK,
Fornage M,
Franceschini N,
Harris TB,
Henderson BE,
Hernandez DG,
Hitsman B,
Hu JJ,
Hunt SC,
Ingles SA,
John EM,
Kittles R,
Kolb S,
Kolonel LN,
Le Marchand L,
Liu Y,
Lohman KK,
McKnight B,
Millikan RC,
Murphy A,
Neslund-Dudas C,
Nyante S,
Press M,
Psaty BM,
Rao DC,
Redline S,
Rodriguez-Gil JL,
Rybicki BA,
Signorello LB,
Singleton AB,
Smoller J,
Snively B,
Spring B,
Stanford JL,
Strom SS,
Swan GE,
Taylor KD,
Thun MJ,
Wilson AF,
Witte JS,
Yamamura Y,
Yanek LR,
Yu K,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman AB,
Jorgenson E,
Haiman CA,
Furberg H
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Gottlieb DJ,
Hek K,
Chen TH,
Watson NF,
Eiriksdottir G,
Byrne EM,
Cornelis M,
Warby SC,
Bandinelli S,
Cherkas L,
Evans DS,
Grabe HJ
and 74 more — show all
Lahti J,
Li M,
Lehtimäki T,
Lumley T,
Marciante KD,
Pérusse L,
Psaty BM,
Robbins J,
Tranah GJ,
Vink JM,
Wilk JB,
Stafford JM,
Bellis C,
Biffar R,
Bouchard C,
Cade B,
Curhan GC,
Eriksson JG,
Ewert R,
Ferrucci L,
Fülöp T,
Gehrman PR,
Goodloe R,
Harris TB,
Heath AC,
Hernandez D,
Hofman A,
Hottenga JJ,
Hunter DJ,
Jensen MK,
Johnson AD,
Kähönen M,
Kao L,
Kraft P,
Larkin EK,
Lauderdale DS,
Luik AI,
Medici M,
Montgomery GW,
Palotie A,
Patel SR,
Pistis G,
Porcu E,
Quaye L,
Raitakari O,
Redline S,
Rimm EB,
Rotter JI,
Smith AV,
Spector TD,
Teumer A,
Uitterlinden AG,
Vohl MC,
Widen E,
Willemsen G,
Young T,
Zhang X,
Liu Y,
Blangero J,
Boomsma DI,
Gudnason V,
Hu F,
Mangino M,
Martin NG,
O'Connor GT,
Stone KL,
Tanaka T,
Viikari J,
Gharib SA,
Punjabi NM,
Räikkönen K,
Völzke H,
Mignot E,
Tiemeier H
Molecular psychiatry · 2015 · PMID 25469926 · open access
1 page
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Bandres-Ciga S,
Ahmed S,
Sabir MS,
Blauwendraat C,
Adarmes-Gómez AD,
Bernal-Bernal I,
Bonilla-Toribio M,
Buiza-Rueda D,
Carrillo F,
Carrión-Claro M,
Gómez-Garre P,
Jesús S
and 83 more — show all
Labrador-Espinosa MA,
Macias D,
Méndez-Del-Barrio C,
Periñán-Tocino T,
Tejera-Parrado C,
Vargas-González L,
Diez-Fairen M,
Alvarez I,
Tartari JP,
Buongiorno M,
Aguilar M,
Gorostidi A,
Bergareche JA,
Mondragon E,
Vinagre-Aragon A,
Croitoru I,
Ruiz-Martínez J,
Dols-Icardo O,
Kulisevsky J,
Marín-Lahoz J,
Pagonabarraga J,
Pascual-Sedano B,
Ezquerra M,
Cámara A,
Compta Y,
Fernández M,
Fernández-Santiago R,
Muñoz E,
Tolosa E,
Valldeoriola F,
Gonzalez-Aramburu I,
Sanchez Rodriguez A,
Sierra M,
Menéndez-González M,
Blazquez M,
Garcia C,
Suarez-San Martin E,
García-Ruiz P,
Martínez-Castrillo JC,
Vela-Desojo L,
Ruz C,
Barrero FJ,
Escamilla-Sevilla F,
Mínguez-Castellanos A,
Cerdan D,
Tabernero C,
Gomez Heredia MJ,
Perez Errazquin F,
Romero-Acebal M,
Feliz C,
Lopez-Sendon JL,
Mata M,
Martínez Torres I,
Kim JJ,
Dalgard CL,
Brooks J,
Saez-Atienzar S,
Gibbs JR,
Jorda R,
Botia JA,
Bonet-Ponce L,
Morrison KE,
Clarke C,
Tan M,
Morris H,
Edsall C,
Hernandez D,
Simon-Sanchez J,
Nalls MA,
Scholz SW,
Jimenez-Escrig A,
Duarte J,
Vives F,
Duran R,
Hoenicka J,
Alvarez V,
Infante J,
Marti MJ,
Clarimón J,
López de Munain A,
Pastor P,
Mir P,
Singleton A
American Genome Center · International Parkinson Disease Genomics Consortium
Movement disorders : official journal of the Movement Disorder Society · 2019 · PMID 31660654
1 page
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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.