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113 matches for
Evans D,
showing the first 20.
Genome-wide association study identifies five loci associated with lung function
Repapi E,
Sayers I,
Wain LV,
Burton PR,
Johnson T,
Obeidat M,
Zhao JH,
Ramasamy A,
Zhai G,
Vitart V,
Huffman JE,
Igl W
and 83 more — show all
Albrecht E,
Deloukas P,
Henderson J,
Granell R,
McArdle WL,
Rudnicka AR,
Barroso I,
Loos RJ,
Wareham NJ,
Mustelin L,
Rantanen T,
Surakka I,
Imboden M,
Wichmann HE,
Grkovic I,
Jankovic S,
Zgaga L,
Hartikainen AL,
Peltonen L,
Gyllensten U,
Johansson A,
Zaboli G,
Campbell H,
Wild SH,
Wilson JF,
Gläser S,
Homuth G,
Völzke H,
Mangino M,
Soranzo N,
Spector TD,
Polasek O,
Rudan I,
Wright AF,
Heliövaara M,
Ripatti S,
Pouta A,
Naluai AT,
Olin AC,
Torén K,
Cooper MN,
James AL,
James AL,
Palmer LJ,
Hingorani AD,
Wannamethee SG,
Whincup PH,
Smith GD,
Ebrahim S,
McKeever TM,
Pavord ID,
MacLeod AK,
Morris AD,
Porteous DJ,
Cooper C,
Dennison E,
Shaheen S,
Karrasch S,
Schnabel E,
Schulz H,
Grallert H,
Bouatia-Naji N,
Delplanque J,
Froguel P,
Blakey JD,
Britton JR,
Morris RW,
Holloway JW,
Lawlor DA,
Hui J,
Nyberg F,
Jarvelin MR,
Jackson C,
Kähönen M,
Kaprio J,
Probst-Hensch NM,
Koch B,
Hayward C,
Evans DM,
Elliott P,
Strachan DP,
Hall IP,
Tobin MD
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
3 pages
Genome-wide association study identifies five new breast cancer susceptibility loci
Turnbull C,
Ahmed S,
Morrison J,
Pernet D,
Renwick A,
Maranian M,
Seal S,
Ghoussaini M,
Hines S,
Healey CS,
Hughes D,
Warren-Perry M
and 14 more — show all
Tapper W,
Eccles D,
Evans DG,
Hooning M,
Schutte M,
van den Ouweland A,
Houlston R,
Ross G,
Langford C,
Pharoah PD,
Stratton MR,
Dunning AM,
Rahman N,
Easton DF
Breast Cancer Susceptibility Collaboration (UK)
Nature genetics · 2010 · PMID 20453838
3 pages
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Naj AC,
Jun G,
Beecham GW,
Wang LS,
Vardarajan BN,
Buros J,
Gallins PJ,
Buxbaum JD,
Jarvik GP,
Crane PK,
Larson EB,
Bird TD
and 143 more — show all
Boeve BF,
Graff-Radford NR,
De Jager PL,
Evans D,
Schneider JA,
Carrasquillo MM,
Ertekin-Taner N,
Younkin SG,
Cruchaga C,
Kauwe JS,
Nowotny P,
Kramer P,
Hardy J,
Huentelman MJ,
Myers AJ,
Barmada MM,
Demirci FY,
Baldwin CT,
Green RC,
Rogaeva E,
St George-Hyslop P,
Arnold SE,
Barber R,
Beach T,
Bigio EH,
Bowen JD,
Boxer A,
Burke JR,
Cairns NJ,
Carlson CS,
Carney RM,
Carroll SL,
Chui HC,
Clark DG,
Corneveaux J,
Cotman CW,
Cummings JL,
DeCarli C,
DeKosky ST,
Diaz-Arrastia R,
Dick M,
Dickson DW,
Ellis WG,
Faber KM,
Fallon KB,
Farlow MR,
Ferris S,
Frosch MP,
Galasko DR,
Ganguli M,
Gearing M,
Geschwind DH,
Ghetti B,
Gilbert JR,
Gilman S,
Giordani B,
Glass JD,
Growdon JH,
Hamilton RL,
Harrell LE,
Head E,
Honig LS,
Hulette CM,
Hyman BT,
Jicha GA,
Jin LW,
Johnson N,
Karlawish J,
Karydas A,
Kaye JA,
Kim R,
Koo EH,
Kowall NW,
Lah JJ,
Levey AI,
Lieberman AP,
Lopez OL,
Mack WJ,
Marson DC,
Martiniuk F,
Mash DC,
Masliah E,
McCormick WC,
McCurry SM,
McDavid AN,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Parisi JE,
Perl DP,
Peskind E,
Petersen RC,
Poon WW,
Quinn JF,
Rajbhandary RA,
Raskind M,
Reisberg B,
Ringman JM,
Roberson ED,
Rosenberg RN,
Sano M,
Schneider LS,
Seeley W,
Shelanski ML,
Slifer MA,
Smith CD,
Sonnen JA,
Spina S,
Stern RA,
Tanzi RE,
Trojanowski JQ,
Troncoso JC,
Van Deerlin VM,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Williamson J,
Woltjer RL,
Cantwell LB,
Dombroski BA,
Beekly D,
Lunetta KL,
Martin ER,
Kamboh MI,
Saykin AJ,
Reiman EM,
Bennett DA,
Morris JC,
Montine TJ,
Goate AM,
Blacker D,
Tsuang DW,
Hakonarson H,
Kukull WA,
Foroud TM,
Haines JL,
Mayeux R,
Pericak-Vance MA,
Farrer LA,
Schellenberg GD
Nature genetics · 2011 · PMID 21460841 · open access
3 pages
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Evans DM,
Spencer CC,
Pointon JJ,
Su Z,
Harvey D,
Kochan G,
Oppermann U,
Dilthey A,
Pirinen M,
Stone MA,
Appleton L,
Moutsianas L
and 81 more — show all
Leslie S,
Wordsworth T,
Kenna TJ,
Karaderi T,
Thomas GP,
Ward MM,
Weisman MH,
Farrar C,
Bradbury LA,
Danoy P,
Inman RD,
Maksymowych W,
Gladman D,
Rahman P,
Morgan A,
Marzo-Ortega H,
Bowness P,
Gaffney K,
Gaston JS,
Smith M,
Bruges-Armas J,
Couto AR,
Sorrentino R,
Paladini F,
Ferreira MA,
Xu H,
Liu Y,
Jiang L,
Lopez-Larrea C,
Díaz-Peña R,
López-Vázquez A,
Zayats T,
Band G,
Bellenguez C,
Blackburn H,
Blackwell JM,
Bramon E,
Bumpstead SJ,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Freeman C,
Gillman M,
Gray E,
Gwilliam R,
Hammond N,
Hunt SE,
Jankowski J,
Jayakumar A,
Langford C,
Liddle J,
Markus HS,
Mathew CG,
McCann OT,
McCarthy MI,
Palmer CN,
Peltonen L,
Plomin R,
Potter SC,
Rautanen A,
Ravindrarajah R,
Ricketts M,
Samani N,
Sawcer SJ,
Strange A,
Trembath RC,
Viswanathan AC,
Waller M,
Weston P,
Whittaker P,
Widaa S,
Wood NW,
McVean G,
Reveille JD,
Wordsworth BP,
Brown MA,
Donnelly P
Spondyloarthritis Research Consortium of Canada (SPARCC) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 1 more consortia
Nature genetics · 2011 · PMID 21743469
3 pages
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Anttila V,
Winsvold BS,
Gormley P,
Kurth T,
Bettella F,
McMahon G,
Kallela M,
Malik R,
de Vries B,
Terwindt G,
Medland SE,
Todt U
and 85 more — show all
McArdle WL,
Quaye L,
Koiranen M,
Ikram MA,
Lehtimäki T,
Stam AH,
Ligthart L,
Wedenoja J,
Dunham I,
Neale BM,
Palta P,
Hamalainen E,
Schürks M,
Rose LM,
Buring JE,
Ridker PM,
Steinberg S,
Stefansson H,
Jakobsson F,
Lawlor DA,
Evans DM,
Ring SM,
Färkkilä M,
Artto V,
Kaunisto MA,
Freilinger T,
Schoenen J,
Frants RR,
Pelzer N,
Weller CM,
Zielman R,
Heath AC,
Madden PAF,
Montgomery GW,
Martin NG,
Borck G,
Göbel H,
Heinze A,
Heinze-Kuhn K,
Williams FMK,
Hartikainen AL,
Pouta A,
van den Ende J,
Uitterlinden AG,
Hofman A,
Amin N,
Hottenga JJ,
Vink JM,
Heikkilä K,
Alexander M,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Wichmann HE,
Aromaa A,
Eriksson JG,
Traynor B,
Trabzuni D,
Rossin E,
Lage K,
Jacobs SBR,
Jacobs SBR,
Gibbs JR,
Birney E,
Kaprio J,
Penninx BW,
Boomsma DI,
van Duijn C,
van Duijn C,
Raitakari O,
Jarvelin MR,
Zwart JA,
Cherkas L,
Strachan DP,
Kubisch C,
Ferrari MD,
van den Maagdenberg AMJM,
Dichgans M,
Wessman M,
Smith GD,
Stefansson K,
Daly MJ,
Nyholt DR,
Chasman D,
Palotie A
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
Evangelou E,
Kerkhof HJ,
Styrkarsdottir U,
Ntzani EE,
Bos SD,
Esko T,
Evans DS,
Metrustry S,
Panoutsopoulou K,
Ramos YF,
Thorleifsson G,
Tsilidis KK
and 54 more — show all
Arden N,
Aslam N,
Bellamy N,
Birrell F,
Blanco FJ,
Carr A,
Chapman K,
Day-Williams AG,
Deloukas P,
Doherty M,
Engström G,
Helgadottir HT,
Hofman A,
Ingvarsson T,
Jonsson H,
Keis A,
Keurentjes JC,
Kloppenburg M,
Lind PA,
McCaskie A,
Martin NG,
Milani L,
Montgomery GW,
Nelissen RG,
Nevitt MC,
Nilsson PM,
Ollier WE,
Parimi N,
Rai A,
Ralston SH,
Reed MR,
Riancho JA,
Rivadeneira F,
Rodriguez-Fontenla C,
Southam L,
Thorsteinsdottir U,
Tsezou A,
Wallis GA,
Wilkinson JM,
Gonzalez A,
Lane NE,
Lohmander LS,
Loughlin J,
Metspalu A,
Uitterlinden AG,
Jonsdottir I,
Stefansson K,
Slagboom PE,
Zeggini E,
Meulenbelt I,
Ioannidis JP,
Spector TD,
van Meurs JB,
Valdes AM
arcOGEN Consortium
Annals of the rheumatic diseases · 2014 · PMID 23989986 · open access
3 pages
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants
van der Valk RJ,
Duijts L,
Timpson NJ,
Salam MT,
Standl M,
Curtin JA,
Genuneit J,
Kerhof M,
Kreiner-Møller E,
Cáceres A,
Gref A,
Liang LL
and 46 more — show all
Taal HR,
Bouzigon E,
Demenais F,
Nadif R,
Ober C,
Thompson EE,
Estrada K,
Hofman A,
Uitterlinden AG,
van Duijn C,
Rivadeneira F,
Li X,
Eckel SP,
Berhane K,
Gauderman WJ,
Granell R,
Evans DM,
St Pourcain B,
McArdle W,
Kemp JP,
Smith GD,
Tiesler CM,
Flexeder C,
Simpson A,
Murray CS,
Fuchs O,
Postma DS,
Bønnelykke K,
Torrent M,
Andersson M,
Sleiman P,
Hakonarson H,
Cookson WO,
Moffatt MF,
Paternoster L,
Melén E,
Sunyer J,
Bisgaard H,
Koppelman GH,
Ege M,
Custovic A,
Heinrich J,
Gilliland FD,
Henderson AJ,
Jaddoe VW,
de Jongste JC
EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium
The Journal of allergy and clinical immunology · 2014 · PMID 24315451
3 pages
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
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways
Bustamante M,
Standl M,
Bassat Q,
Vilor-Tejedor N,
Medina-Gomez C,
Bonilla C,
Ahluwalia TS,
Bacelis J,
Bradfield JP,
Tiesler CM,
Rivadeneira F,
Ring S
and 27 more — show all
Vissing NH,
Fink NR,
Jugessur A,
Mentch FD,
Ballester F,
Kriebel J,
Kiefte-de Jong JC,
Wolsk HM,
Llop S,
Thiering E,
Beth SA,
Timpson NJ,
Andersen J,
Schulz H,
Jaddoe VW,
Evans DM,
Waage J,
Hakonarson H,
Grant SF,
Jacobsson B,
Bønnelykke K,
Bisgaard H,
Davey Smith G,
Moll HA,
Heinrich J,
Estivill X,
Sunyer J
Human molecular genetics · 2016 · PMID 27559109
3 pages
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
Richards JB,
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Hivert MF,
Loos RJ,
Perry JR,
Tanaka T,
Timpson NJ,
Semple RK,
Soranzo N,
Song K,
Rocha N
and 54 more — show all
Grundberg E,
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Sladek R,
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Spector TD
GIANT Consortium
PLoS genetics · 2009 · PMID 20011104 · open access
2 pages
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals
Heid IM,
Henneman P,
Hicks A,
Coassin S,
Winkler T,
Aulchenko YS,
Fuchsberger C,
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Richards JB
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Perry JR,
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van Duijn CM
Atherosclerosis · 2010 · PMID 20018283
2 pages
Genome-wide association study reveals multiple loci associated with primary tooth development during infancy
Pillas D,
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Sipilä K,
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Millwood IY,
Kaakinen M,
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Pouta A,
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PLoS genetics · 2010 · PMID 20195514 · open access
2 pages
Genome-wide association studies of the PR interval in African Americans
Smith JG,
Magnani JW,
Palmer C,
Meng YA,
Soliman EZ,
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Kerr KF,
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Sotoodehnia N,
Redline S,
Pfeufer A
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Müller M,
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Liu Y,
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Newton-Cheh C,
Benjamin EJ,
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Heckbert SR,
Fox ER
Candidate-gene Association Resource (CARe) Consortium
PLoS genetics · 2011 · PMID 21347284 · open access
2 pages
Genome-wide association study identifies four loci associated with eruption of permanent teeth
Geller F,
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Zhang H,
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Hansen T,
Esserlind AL,
Boyd HA,
Nohr EA,
Timpson NJ,
Fatemifar G,
Paternoster L,
Evans DM
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PLoS genetics · 2011 · PMID 21931568 · open access
2 pages
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
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Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
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Bailey-Wilson JE
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St Pourcain B,
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Stambolian D,
Mackey DA,
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Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies
Knipe DW,
Evans DM,
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Eeles R,
Easton DF,
Kote-Jarai Z,
Al Olama AA,
Benlloch S,
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Hamdy FC,
Neal DE,
Smith GD
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Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2014 · PMID 24753544
2 pages
A novel common variant in DCST2 is associated with length in early life and height in adulthood
van der Valk RJ,
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Stergiakouli E,
Sääf A,
Bradfield JP,
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Thiering E
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Curtin JA,
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Franke L,
Hirschhorn JN,
Pers TH,
Liang L,
Huang J,
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Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
2 pages
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Matteini AM,
Tanaka T,
Karasik D,
Atzmon G,
Chou WC,
Eicher JD,
Johnson AD,
Arnold AM,
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Davies G,
Evans DS,
Holtfreter B
and 55 more — show all
Lohman K,
Lunetta KL,
Mangino M,
Smith AV,
Smith JA,
Teumer A,
Yu L,
Arking DE,
Buchman AS,
Chibinik LB,
De Jager PL,
Evans DA,
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Gillham-Nasenya I,
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Hofman A,
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Liu Y,
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Zhao W,
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Aging cell · 2016 · PMID 27325353 · open access
2 pages
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
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Trompet S,
Arsenault BJ,
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Smit RA,
Smith AV,
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Barnes MR,
Barratt BJ,
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Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
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Post W,
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Rice K,
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Rivadeneira F,
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Wei WQ,
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Gudnason V,
Hitman G,
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Stein CM,
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Caulfield MJ,
Jukema JW,
Rotter JI,
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Journal of medical genetics · 2016 · PMID 27587472
2 pages
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