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75 matches for
Jarvelin MR,
showing the first 20.
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Grosche S,
Marenholz I,
Esparza-Gordillo J,
Arnau-Soler A,
Pairo-Castineira E,
Rüschendorf F,
Ahluwalia TS,
Almqvist C,
Arnold A,
Baurecht H,
Bisgaard H,
Bønnelykke K
and 50 more — show all
Brown SJ,
Bustamante M,
Curtin JA,
Custovic A,
Dharmage SC,
Esplugues A,
Falchi M,
Fernandez-Orth D,
Ferreira MAR,
Franke A,
Gerdes S,
Gieger C,
Hakonarson H,
Holt PG,
Homuth G,
Hubner N,
Hysi PG,
Jarvelin MR,
Karlsson R,
Koppelman GH,
Lau S,
Lutz M,
Magnusson PKE,
Marks GB,
Müller-Nurasyid M,
Nöthen MM,
Paternoster L,
Pennell CE,
Peters A,
Rawlik K,
Robertson CF,
Rodriguez E,
Sebert S,
Simpson A,
Sleiman PMA,
Standl M,
Stölzl D,
Strauch K,
Szwajda A,
Tenesa A,
Thompson PJ,
Ullemar V,
Visconti A,
Vonk JM,
Wang CA,
Weidinger S,
Wielscher M,
Worth CL,
Xu CJ,
Lee YA
Australian Asthma Genetics Consortium (AAGC)
Nature communications · 2021 · PMID 34785669 · open access
6 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
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C,
Johnson T,
Gateva V,
Tobin MD,
Bochud M,
Coin L,
Najjar SS,
Zhao JH,
Heath SC,
Eyheramendy S,
Papadakis K,
Voight BF
and 147 more — show all
Scott LJ,
Zhang F,
Farrall M,
Tanaka T,
Wallace C,
Chambers JC,
Khaw KT,
Nilsson P,
van der Harst P,
Polidoro S,
Grobbee DE,
Onland-Moret NC,
Bots ML,
Wain LV,
Elliott KS,
Teumer A,
Luan J,
Lucas G,
Kuusisto J,
Burton PR,
Hadley D,
McArdle WL,
Brown M,
Dominiczak A,
Newhouse SJ,
Samani NJ,
Webster J,
Zeggini E,
Beckmann JS,
Bergmann S,
Lim N,
Song K,
Vollenweider P,
Waeber G,
Waterworth DM,
Yuan X,
Groop L,
Orho-Melander M,
Allione A,
Di Gregorio A,
Guarrera S,
Panico S,
Ricceri F,
Romanazzi V,
Sacerdote C,
Vineis P,
Barroso I,
Sandhu MS,
Luben RN,
Crawford GJ,
Jousilahti P,
Perola M,
Boehnke M,
Bonnycastle LL,
Collins FS,
Jackson AU,
Mohlke KL,
Stringham HM,
Valle TT,
Willer CJ,
Bergman RN,
Morken MA,
Döring A,
Gieger C,
Illig T,
Meitinger T,
Org E,
Org E,
Pfeufer A,
Wichmann HE,
Kathiresan S,
Marrugat J,
O'Donnell CJ,
Schwartz SM,
Siscovick DS,
Subirana I,
Freimer NB,
Hartikainen AL,
McCarthy MI,
O'Reilly PF,
Peltonen L,
Pouta A,
de Jong PE,
Snieder H,
van Gilst WH,
Clarke R,
Goel A,
Hamsten A,
Peden JF,
Seedorf U,
Syvänen AC,
Tognoni G,
Lakatta EG,
Sanna S,
Scheet P,
Schlessinger D,
Scuteri A,
Dörr M,
Ernst F,
Felix SB,
Homuth G,
Lorbeer R,
Reffelmann T,
Rettig R,
Völker U,
Galan P,
Gut IG,
Hercberg S,
Lathrop GM,
Zelenika D,
Deloukas P,
Soranzo N,
Williams FM,
Zhai G,
Salomaa V,
Laakso M,
Elosua R,
Forouhi NG,
Völzke H,
Uiterwaal CS,
van der Schouw YT,
Numans ME,
Matullo G,
Navis G,
Berglund G,
Bingham SA,
Kooner JS,
Connell JM,
Bandinelli S,
Ferrucci L,
Watkins H,
Spector TD,
Tuomilehto J,
Altshuler D,
Strachan DP,
Laan M,
Meneton P,
Wareham NJ,
Uda M,
Jarvelin MR,
Mooser V,
Melander O,
Loos RJ,
Elliott P,
Abecasis GR,
Caulfield M,
Munroe PB
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · 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,
Kovacs P,
Kyvik KO,
Lathrop GM,
Lawlor DA,
Le Bacquer O,
Lecoeur C,
Li Y,
Lyssenko V,
Mahley R,
Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McCulloch LJ,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Morken MA,
Mukherjee S,
Naitza S,
Narisu N,
Neville MJ,
Oostra BA,
Orrù M,
Pakyz R,
Palmer CN,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
Pedersen NL,
Perola M,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Psaty BM,
Rathmann W,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Roden M,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Scott LJ,
Seedorf U,
Sharp SJ,
Shields B,
Sigurethsson G,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tanaka T,
Thorand B,
Tichet J,
Tönjes A,
Tuomi T,
Uitterlinden AG,
van Dijk KW,
van Hoek M,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Walters GB,
Ward KL,
Watkins H,
Weedon MN,
Wild SH,
Willemsen G,
Willemsen G,
Witteman JC,
Yarnell JW,
Zeggini E,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Loos RJ,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Hattersley AT,
Silander K,
Salomaa V,
Smith GD,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Dedoussis GV,
Serrano-Ríos M,
Morris AD,
Lind L,
Palmer LJ,
Hu FB,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pankow JS,
Sampson MJ,
Kuusisto J,
Laakso M,
Hansen T,
Pedersen O,
Pramstaller PP,
Wichmann HE,
Illig T,
Rudan I,
Wright AF,
Stumvoll M,
Campbell H,
Wilson JF,
Bergman RN,
Buchanan TA,
Collins FS,
Mohlke KL,
Tuomilehto J,
Valle TT,
Altshuler D,
Rotter JI,
Siscovick DS,
Penninx BW,
Boomsma DI,
Deloukas P,
Spector TD,
Frayling TM,
Ferrucci L,
Kong A,
Thorsteinsdottir U,
Stefansson K,
van Duijn CM,
Aulchenko YS,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Waterworth DM,
Vollenweider P,
Peltonen L,
Mooser V,
Abecasis GR,
Wareham NJ,
Sladek R,
Froguel P,
Watanabe RM,
Meigs JB,
Groop L,
Boehnke M,
McCarthy MI,
Florez JC,
Barroso I
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Nature genetics · 2010 · PMID 20081858 · 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
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Day F,
Karaderi T,
Jones MR,
Meun C,
He C,
Drong A,
Kraft P,
Lin N,
Huang H,
Broer L,
Magi R,
Saxena R
and 37 more — show all
Laisk T,
Urbanek M,
Hayes MG,
Thorleifsson G,
Fernandez-Tajes J,
Mahajan A,
Mullin BH,
Stuckey BGA,
Spector TD,
Wilson SG,
Goodarzi MO,
Davis L,
Obermayer-Pietsch B,
Uitterlinden AG,
Anttila V,
Neale BM,
Jarvelin MR,
Fauser B,
Kowalska I,
Visser JA,
Andersen M,
Ong K,
Stener-Victorin E,
Ehrmann D,
Legro RS,
Salumets A,
McCarthy MI,
Morin-Papunen L,
Thorsteinsdottir U,
Stefansson K,
Styrkarsdottir U,
Perry JRB,
Dunaif A,
Laven J,
Franks S,
Lindgren CM,
Welt CK
23andMe Research Team
PLoS genetics · 2018 · PMID 30566500 · open access
4 pages
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Li C,
Stoma S,
Lotta LA,
Warner S,
Albrecht E,
Allione A,
Arp PP,
Broer L,
Buxton JL,
Da Silva Couto Alves A,
Deelen J,
Fedko IO
and 84 more — show all
Gordon SD,
Jiang T,
Karlsson R,
Kerrison N,
Loe TK,
Mangino M,
Milaneschi Y,
Miraglio B,
Pervjakova N,
Russo A,
Surakka I,
van der Spek A,
Verhoeven JE,
Amin N,
Beekman M,
Blakemore AI,
Canzian F,
Hamby SE,
Hottenga JJ,
Jones PD,
Jousilahti P,
Mägi R,
Medland SE,
Montgomery GW,
Nyholt DR,
Perola M,
Pietiläinen KH,
Salomaa V,
Sillanpää E,
Suchiman HE,
van Heemst D,
Willemsen G,
Agudo A,
Boeing H,
Boomsma DI,
Chirlaque MD,
Fagherazzi G,
Ferrari P,
Franks P,
Gieger C,
Eriksson JG,
Gunter M,
Hägg S,
Hovatta I,
Imaz L,
Kaprio J,
Kaaks R,
Key T,
Krogh V,
Martin NG,
Melander O,
Metspalu A,
Moreno C,
Onland-Moret NC,
Nilsson P,
Ong KK,
Overvad K,
Palli D,
Panico S,
Pedersen NL,
Penninx BWJH,
Quirós JR,
Jarvelin MR,
Rodríguez-Barranco M,
Scott RA,
Severi G,
Slagboom PE,
Spector TD,
Tjonneland A,
Trichopoulou A,
Tumino R,
Uitterlinden AG,
van der Schouw YT,
van Duijn CM,
Weiderpass E,
Denchi EL,
Matullo G,
Butterworth AS,
Danesh J,
Samani NJ,
Wareham NJ,
Nelson CP,
Langenberg C,
Codd V
American journal of human genetics · 2020 · PMID 32109421 · open access
4 pages
Genetic effects on the timing of parturition and links to fetal birth weight
Solé-Navais P,
Flatley C,
Steinthorsdottir V,
Vaudel M,
Juodakis J,
Chen J,
Laisk T,
LaBella AL,
Westergaard D,
Bacelis J,
Brumpton B,
Skotte L
and 73 more — show all
Borges MC,
Helgeland Ø,
Mahajan A,
Wielscher M,
Lin F,
Briggs C,
Wang CA,
Moen GH,
Beaumont RN,
Bradfield JP,
Abraham A,
Thorleifsson G,
Gabrielsen ME,
Ostrowski SR,
Modzelewska D,
Nohr EA,
Hypponen E,
Srivastava A,
Talbot O,
Allard C,
Williams SM,
Menon R,
Shields BM,
Sveinbjornsson G,
Xu H,
Melbye M,
Lowe W Jr,
Bouchard L,
Oken E,
Pedersen OB,
Gudbjartsson DF,
Erikstrup C,
Sørensen E,
Lie RT,
Teramo K,
Hallman M,
Juliusdottir T,
Hakonarson H,
Ullum H,
Hattersley AT,
Sletner L,
Merialdi M,
Rifas-Shiman SL,
Steingrimsdottir T,
Scholtens D,
Power C,
West J,
Nyegaard M,
Capra JA,
Skogholt AH,
Magnus P,
Andreassen OA,
Thorsteinsdottir U,
Grant SFA,
Qvigstad E,
Pennell CE,
Hivert MF,
Hayes GM,
Jarvelin MR,
McCarthy MI,
Lawlor DA,
Nielsen HS,
Mägi R,
Rokas A,
Hveem K,
Stefansson K,
Feenstra B,
Njolstad P,
Muglia LJ,
Freathy RM,
Johansson S,
Zhang G,
Jacobsson B
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Lindgren CM,
Heid IM,
Randall JC,
Lamina C,
Steinthorsdottir V,
Qi L,
Speliotes EK,
Thorleifsson G,
Willer CJ,
Herrera BM,
Jackson AU,
Lim N
and 131 more — show all
Scheet P,
Soranzo N,
Amin N,
Aulchenko YS,
Chambers JC,
Drong A,
Luan J,
Lyon HN,
Rivadeneira F,
Sanna S,
Timpson NJ,
Zillikens MC,
Zhao JH,
Almgren P,
Bandinelli S,
Bennett AJ,
Bergman RN,
Bonnycastle LL,
Bumpstead SJ,
Chanock SJ,
Cherkas L,
Chines P,
Coin L,
Cooper C,
Crawford G,
Doering A,
Dominiczak A,
Doney AS,
Ebrahim S,
Elliott P,
Erdos MR,
Estrada K,
Ferrucci L,
Fischer G,
Forouhi NG,
Gieger C,
Grallert H,
Groves CJ,
Grundy S,
Guiducci C,
Hadley D,
Hamsten A,
Havulinna AS,
Hofman A,
Holle R,
Holloway JW,
Illig T,
Isomaa B,
Jacobs LC,
Jameson K,
Jousilahti P,
Karpe F,
Kuusisto J,
Laitinen J,
Lathrop GM,
Lawlor DA,
Mangino M,
McArdle WL,
Meitinger T,
Morken MA,
Morris AP,
Munroe P,
Narisu N,
Nordström A,
Nordström P,
Oostra BA,
Palmer CN,
Payne F,
Peden JF,
Prokopenko I,
Renström F,
Ruokonen A,
Salomaa V,
Sandhu MS,
Scott LJ,
Scuteri A,
Silander K,
Song K,
Yuan X,
Stringham HM,
Swift AJ,
Tuomi T,
Uda M,
Vollenweider P,
Waeber G,
Wallace C,
Walters GB,
Weedon MN,
Witteman JC,
Zhang C,
Zhang W,
Caulfield MJ,
Collins FS,
Davey Smith G,
Day IN,
Franks PW,
Hattersley AT,
Hu FB,
Jarvelin MR,
Kong A,
Kooner JS,
Laakso M,
Lakatta E,
Mooser V,
Morris AD,
Peltonen L,
Samani NJ,
Spector TD,
Strachan DP,
Tanaka T,
Tuomilehto J,
Uitterlinden AG,
van Duijn CM,
Wareham NJ,
Hugh Watkins,
Waterworth DM,
Boehnke M,
Deloukas P,
Groop L,
Hunter DJ,
Thorsteinsdottir U,
Schlessinger D,
Wichmann HE,
Frayling TM,
Abecasis GR,
Hirschhorn JN,
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Wareham N,
Eriksson J,
Jousilahti P,
Laitinen T,
Pekkanen J,
Raitakari OT,
O'Connor GT,
Salomaa V,
Jarvelin MR,
Hirschhorn JN
Australian Asthma Genetics Consortium Collaborators
PloS one · 2012 · PMID 23028483 · open access
2 pages
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
Hancock DB,
Soler Artigas M,
Gharib SA,
Henry A,
Manichaikul A,
Ramasamy A,
Loth DW,
Imboden M,
Koch B,
McArdle WL,
Smith AV,
Smolonska J
and 78 more — show all
Sood A,
Tang W,
Wilk JB,
Zhai G,
Zhao JH,
Aschard H,
Burkart KM,
Curjuric I,
Eijgelsheim M,
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Gu X,
Harris TB,
Janson C,
Homuth G,
Hysi PG,
Liu JZ,
Loehr LR,
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Loos RJ,
Manning AK,
Marciante KD,
Obeidat M,
Postma DS,
Aldrich MC,
Brusselle GG,
Chen TH,
Eiriksdottir G,
Franceschini N,
Heinrich J,
Rotter JI,
Wijmenga C,
Williams OD,
Bentley AR,
Hofman A,
Laurie CC,
Lumley T,
Morrison AC,
Joubert BR,
Rivadeneira F,
Couper DJ,
Kritchevsky SB,
Liu Y,
Wjst M,
Wain LV,
Vonk JM,
Uitterlinden AG,
Rochat T,
Rich SS,
Psaty BM,
O'Connor GT,
North KE,
Mirel DB,
Meibohm B,
Launer LJ,
Khaw KT,
Hartikainen AL,
Hammond CJ,
Gläser S,
Marchini J,
Kraft P,
Wareham NJ,
Völzke H,
Stricker BH,
Spector TD,
Probst-Hensch NM,
Jarvis D,
Jarvelin MR,
Heckbert SR,
Gudnason V,
Boezen HM,
Barr RG,
Cassano PA,
Strachan DP,
Fornage M,
Hall IP,
Dupuis J,
Tobin MD,
London SJ
PLoS genetics · 2012 · PMID 23284291 · open access
2 pages
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
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.