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16 matches for
Edkins S.
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Tsoi LC,
Spain SL,
Knight J,
Ellinghaus E,
Stuart PE,
Capon F,
Ding J,
Li Y,
Tejasvi T,
Gudjonsson JE,
Kang HM,
Allen MH
and 53 more — show all
McManus R,
Novelli G,
Samuelsson L,
Schalkwijk J,
Ståhle M,
Burden AD,
Smith CH,
Cork MJ,
Estivill X,
Bowcock AM,
Krueger GG,
Weger W,
Worthington J,
Tazi-Ahnini R,
Nestle FO,
Hayday A,
Hoffmann P,
Winkelmann J,
Wijmenga C,
Langford C,
Edkins S,
Andrews R,
Blackburn H,
Strange A,
Band G,
Pearson RD,
Vukcevic D,
Spencer CC,
Deloukas P,
Mrowietz U,
Schreiber S,
Weidinger S,
Koks S,
Kingo K,
Esko T,
Metspalu A,
Lim HW,
Voorhees JJ,
Weichenthal M,
Wichmann HE,
Chandran V,
Rosen CF,
Rahman P,
Gladman DD,
Griffiths CE,
Reis A,
Kere J,
Nair RP,
Franke A,
Barker JN,
Abecasis GR,
Elder JT,
Trembath RC
Collaborative Association Study of Psoriasis (CASP) · Genetic Analysis of Psoriasis Consortium and 2 more consortia
Nature genetics · 2012 · PMID 23143594 · open access
12 pages+
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Berndt SI,
Gustafsson S,
Mägi R,
Ganna A,
Wheeler E,
Feitosa MF,
Justice AE,
Monda KL,
Croteau-Chonka DC,
Day FR,
Esko T,
Fall T
and 310 more — show all
Ferreira T,
Gentilini D,
Jackson AU,
Luan J,
Randall JC,
Vedantam S,
Willer CJ,
Winkler TW,
Wood AR,
Workalemahu T,
Hu YJ,
Lee SH,
Liang L,
Lin DY,
Min JL,
Neale BM,
Thorleifsson G,
Yang J,
Albrecht E,
Amin N,
Bragg-Gresham JL,
Cadby G,
den Heijer M,
Eklund N,
Fischer K,
Goel A,
Hottenga JJ,
Huffman JE,
Jarick I,
Johansson Å,
Johnson T,
Kanoni S,
Kleber ME,
König IR,
Kristiansson K,
Kutalik Z,
Lamina C,
Lecoeur C,
Li G,
Mangino M,
McArdle WL,
Medina-Gomez C,
Müller-Nurasyid M,
Ngwa JS,
Nolte IM,
Paternoster L,
Pechlivanis S,
Perola M,
Peters MJ,
Preuss M,
Rose LM,
Shi J,
Shungin D,
Smith AV,
Strawbridge RJ,
Surakka I,
Teumer A,
Trip MD,
Tyrer J,
Van Vliet-Ostaptchouk JV,
Vandenput L,
Waite LL,
Zhao JH,
Absher D,
Asselbergs FW,
Atalay M,
Attwood AP,
Balmforth AJ,
Basart H,
Beilby J,
Bonnycastle LL,
Brambilla P,
Bruinenberg M,
Campbell H,
Chasman DI,
Chines PS,
Collins FS,
Connell JM,
Cookson WO,
de Faire U,
de Vegt F,
Dei M,
Dimitriou M,
Edkins S,
Estrada K,
Evans DM,
Farrall M,
Ferrario MM,
Ferrières J,
Franke L,
Frau F,
Gejman PV,
Grallert H,
Grönberg H,
Gudnason V,
Hall AS,
Hall P,
Hartikainen AL,
Hayward C,
Heard-Costa NL,
Heath AC,
Hebebrand J,
Homuth G,
Hu FB,
Hunt SE,
Hyppönen E,
Iribarren C,
Jacobs KB,
Jansson JO,
Jula A,
Kähönen M,
Kathiresan S,
Kee F,
Khaw KT,
Kivimäki M,
Koenig W,
Kraja AT,
Kumari M,
Kuulasmaa K,
Kuusisto J,
Laitinen JH,
Lakka TA,
Langenberg C,
Launer LJ,
Lind L,
Lindström J,
Liu J,
Liuzzi A,
Lokki ML,
Lorentzon M,
Madden PA,
Magnusson PK,
Manunta P,
Marek D,
März W,
Mateo Leach I,
McKnight B,
Medland SE,
Mihailov E,
Milani L,
Montgomery GW,
Mooser V,
Mühleisen TW,
Munroe PB,
Musk AW,
Narisu N,
Navis G,
Nicholson G,
Nohr EA,
Ong KK,
Oostra BA,
Palmer CN,
Palotie A,
Peden JF,
Pedersen N,
Peters A,
Polasek O,
Pouta A,
Pramstaller PP,
Prokopenko I,
Pütter C,
Radhakrishnan A,
Raitakari O,
Rendon A,
Rivadeneira F,
Rudan I,
Saaristo TE,
Sambrook JG,
Sanders AR,
Sanna S,
Saramies J,
Schipf S,
Schreiber S,
Schunkert H,
Shin SY,
Signorini S,
Sinisalo J,
Skrobek B,
Soranzo N,
Stančáková A,
Stark K,
Stephens JC,
Stirrups K,
Stolk RP,
Stumvoll M,
Swift AJ,
Theodoraki EV,
Thorand B,
Tregouet DA,
Tremoli E,
Van der Klauw MM,
van Meurs JB,
Vermeulen SH,
Viikari J,
Virtamo J,
Vitart V,
Waeber G,
Wang Z,
Widén E,
Wild SH,
Willemsen G,
Winkelmann BR,
Witteman JC,
Wolffenbuttel BH,
Wong A,
Wright AF,
Zillikens MC,
Amouyel P,
Boehm BO,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Chanock SJ,
Cupples LA,
Cusi D,
Dedoussis GV,
Erdmann J,
Eriksson JG,
Franks PW,
Froguel P,
Gieger C,
Gyllensten U,
Hamsten A,
Harris TB,
Hengstenberg C,
Hicks AA,
Hingorani A,
Hinney A,
Hofman A,
Hovingh KG,
Hveem K,
Illig T,
Jarvelin MR,
Jöckel KH,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Kuh D,
Laakso M,
Lehtimäki T,
Levinson DF,
Martin NG,
Metspalu A,
Morris AD,
Nieminen MS,
Njølstad I,
Ohlsson C,
Oldehinkel AJ,
Ouwehand WH,
Palmer LJ,
Penninx B,
Power C,
Province MA,
Psaty BM,
Qi L,
Rauramaa R,
Ridker PM,
Ripatti S,
Salomaa V,
Samani NJ,
Snieder H,
Sørensen TI,
Spector TD,
Stefansson K,
Tönjes A,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Vollenweider P,
Wallaschofski H,
Wareham NJ,
Watkins H,
Wichmann HE,
Wilson JF,
Abecasis GR,
Assimes TL,
Barroso I,
Boehnke M,
Borecki IB,
Deloukas P,
Fox CS,
Frayling T,
Groop LC,
Haritunian T,
Heid IM,
Hunter D,
Kaplan RC,
Karpe F,
Moffatt MF,
Mohlke KL,
O'Connell JR,
Pawitan Y,
Schadt EE,
Schlessinger D,
Steinthorsdottir V,
Strachan DP,
Thorsteinsdottir U,
van Duijn CM,
Visscher PM,
Di Blasio AM,
Hirschhorn JN,
Lindgren CM,
Morris AP,
Meyre D,
Scherag A,
McCarthy MI,
Speliotes EK,
North KE,
Loos RJ,
Ingelsson E
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Beecham AH,
Patsopoulos NA,
Xifara DK,
Davis MF,
Kemppinen A,
Cotsapas C,
Shah TS,
Spencer C,
Booth D,
Goris A,
Oturai A,
Saarela J
and 181 more — show all
Fontaine B,
Hemmer B,
Martin C,
Zipp F,
D'Alfonso S,
Martinelli-Boneschi F,
Taylor B,
Harbo HF,
Kockum I,
Hillert J,
Olsson T,
Ban M,
Oksenberg JR,
Hintzen R,
Barcellos LF,
Agliardi C,
Alfredsson L,
Alizadeh M,
Anderson C,
Andrews R,
Søndergaard HB,
Baker A,
Band G,
Baranzini SE,
Barizzone N,
Barrett J,
Bellenguez C,
Bergamaschi L,
Bernardinelli L,
Berthele A,
Biberacher V,
Binder TM,
Blackburn H,
Bomfim IL,
Brambilla P,
Broadley S,
Brochet B,
Brundin L,
Buck D,
Butzkueven H,
Caillier SJ,
Camu W,
Carpentier W,
Cavalla P,
Celius EG,
Coman I,
Comi G,
Corrado L,
Cosemans L,
Cournu-Rebeix I,
Cree BA,
Cusi D,
Damotte V,
Defer G,
Delgado SR,
Deloukas P,
di Sapio A,
Dilthey AT,
Donnelly P,
Dubois B,
Duddy M,
Edkins S,
Elovaara I,
Esposito F,
Evangelou N,
Fiddes B,
Field J,
Franke A,
Freeman C,
Frohlich IY,
Galimberti D,
Gieger C,
Gourraud PA,
Graetz C,
Graham A,
Grummel V,
Guaschino C,
Hadjixenofontos A,
Hakonarson H,
Halfpenny C,
Hall G,
Hall P,
Hamsten A,
Harley J,
Harrower T,
Hawkins C,
Hellenthal G,
Hillier C,
Hobart J,
Hoshi M,
Hunt SE,
Jagodic M,
Jelčić I,
Jochim A,
Kendall B,
Kermode A,
Kilpatrick T,
Koivisto K,
Konidari I,
Korn T,
Kronsbein H,
Langford C,
Larsson M,
Lathrop M,
Lebrun-Frenay C,
Lechner-Scott J,
Lee MH,
Leone MA,
Leppä V,
Liberatore G,
Lie BA,
Lill CM,
Lindén M,
Link J,
Luessi F,
Lycke J,
Macciardi F,
Männistö S,
Manrique CP,
Martin R,
Martinelli V,
Mason D,
Mazibrada G,
McCabe C,
Mero IL,
Mescheriakova J,
Moutsianas L,
Myhr KM,
Nagels G,
Nicholas R,
Nilsson P,
Piehl F,
Pirinen M,
Price SE,
Quach H,
Reunanen M,
Robberecht W,
Robertson NP,
Rodegher M,
Rog D,
Salvetti M,
Schnetz-Boutaud NC,
Sellebjerg F,
Selter RC,
Schaefer C,
Shaunak S,
Shen L,
Shields S,
Siffrin V,
Slee M,
Sorensen PS,
Sorosina M,
Sospedra M,
Spurkland A,
Strange A,
Sundqvist E,
Thijs V,
Thorpe J,
Ticca A,
Tienari P,
van Duijn C,
Visser EM,
Vucic S,
Westerlind H,
Wiley JS,
Wilkins A,
Wilson JF,
Winkelmann J,
Zajicek J,
Zindler E,
Haines JL,
Pericak-Vance MA,
Ivinson AJ,
Stewart G,
Hafler D,
Hauser SL,
Compston A,
McVean G,
De Jager P,
Sawcer SJ,
McCauley JL
International Multiple Sclerosis Genetics Consortium (IMSGC) · Wellcome Trust Case Control Consortium 2 (WTCCC2) and 1 more consortia
Nature genetics · 2013 · PMID 24076602 · open access
12 pages+
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Ehret GB,
Ferreira T,
Chasman DI,
Jackson AU,
Schmidt EM,
Johnson T,
Thorleifsson G,
Luan J,
Donnelly LA,
Kanoni S,
Petersen AK,
Pihur V
and 301 more — show all
Strawbridge RJ,
Shungin D,
Hughes MF,
Meirelles O,
Kaakinen M,
Bouatia-Naji N,
Kristiansson K,
Shah S,
Kleber ME,
Guo X,
Lyytikäinen LP,
Fava C,
Eriksson N,
Nolte IM,
Magnusson PK,
Salfati EL,
Rallidis LS,
Theusch E,
Smith AJP,
Folkersen L,
Witkowska K,
Pers TH,
Joehanes R,
Kim SK,
Lataniotis L,
Jansen R,
Johnson AD,
Warren H,
Kim YJ,
Zhao W,
Wu Y,
Tayo BO,
Bochud M,
Absher D,
Adair LS,
Amin N,
Arking DE,
Axelsson T,
Baldassarre D,
Balkau B,
Bandinelli S,
Barnes MR,
Barroso I,
Bevan S,
Bis JC,
Bjornsdottir G,
Boehnke M,
Boerwinkle E,
Bonnycastle LL,
Boomsma DI,
Bornstein SR,
Brown MJ,
Burnier M,
Cabrera CP,
Chambers JC,
Chang IS,
Cheng CY,
Chines PS,
Chung RH,
Collins FS,
Connell JM,
Döring A,
Dallongeville J,
Danesh J,
de Faire U,
Delgado G,
Dominiczak AF,
Doney ASF,
Drenos F,
Edkins S,
Eicher JD,
Elosua R,
Enroth S,
Erdmann J,
Eriksson P,
Esko T,
Evangelou E,
Evans A,
Fall T,
Farrall M,
Felix JF,
Ferrières J,
Ferrucci L,
Fornage M,
Forrester T,
Franceschini N,
Duran OHF,
Franco-Cereceda A,
Fraser RM,
Ganesh SK,
Gao H,
Gertow K,
Gianfagna F,
Gigante B,
Giulianini F,
Goel A,
Goodall AH,
Goodarzi MO,
Gorski M,
Gräßler J,
Groves C,
Gudnason V,
Gyllensten U,
Hallmans G,
Hartikainen AL,
Hassinen M,
Havulinna AS,
Hayward C,
Hercberg S,
Herzig KH,
Hicks AA,
Hingorani AD,
Hirschhorn JN,
Hofman A,
Holmen J,
Holmen OL,
Hottenga JJ,
Howard P,
Hsiung CA,
Hunt SC,
Ikram MA,
Illig T,
Iribarren C,
Jensen RA,
Kähönen M,
Kang H,
Kathiresan S,
Keating BJ,
Khaw KT,
Kim YK,
Kim E,
Kivimaki M,
Klopp N,
Kolovou G,
Komulainen P,
Kooner JS,
Kosova G,
Krauss RM,
Kuh D,
Kutalik Z,
Kuusisto J,
Kvaløy K,
Lakka TA,
Lee NR,
Lee IT,
Lee WJ,
Levy D,
Li X,
Liang KW,
Lin H,
Lin L,
Lindström J,
Lobbens S,
Männistö S,
Müller G,
Müller-Nurasyid M,
Mach F,
Markus HS,
Marouli E,
McCarthy MI,
McKenzie CA,
Meneton P,
Menni C,
Metspalu A,
Mijatovic V,
Moilanen L,
Montasser ME,
Morris AD,
Morrison AC,
Mulas A,
Nagaraja R,
Narisu N,
Nikus K,
O'Donnell CJ,
O'Reilly PF,
Ong KK,
Paccaud F,
Palmer CD,
Parsa A,
Pedersen NL,
Penninx BW,
Perola M,
Peters A,
Poulter N,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rao DC,
Rasheed A,
Rayner NWNWR,
Renström F,
Rettig R,
Rice KM,
Roberts R,
Rose LM,
Rossouw J,
Samani NJ,
Sanna S,
Saramies J,
Schunkert H,
Sebert S,
Sheu WH,
Shin YA,
Sim X,
Smit JH,
Smith AV,
Sosa MX,
Spector TD,
Stančáková A,
Stanton A,
Stirrups KE,
Stringham HM,
Sundstrom J,
Swift AJ,
Syvänen AC,
Tai ES,
Tanaka T,
Tarasov KV,
Teumer A,
Thorsteinsdottir U,
Tobin MD,
Tremoli E,
Uitterlinden AG,
Uusitupa M,
Vaez A,
Vaidya D,
van Duijn CM,
van Iperen EPA,
Vasan RS,
Verwoert GC,
Virtamo J,
Vitart V,
Voight BF,
Vollenweider P,
Wagner A,
Wain LV,
Wareham NJ,
Watkins H,
Weder AB,
Westra HJ,
Wilks R,
Wilsgaard T,
Wilson JF,
Wong TY,
Yang TP,
Yao J,
Yengo L,
Zhang W,
Zhao JH,
Zhu X,
Bovet P,
Cooper RS,
Mohlke KL,
Saleheen D,
Lee JY,
Elliott P,
Gierman HJ,
Willer CJ,
Franke L,
Hovingh GK,
Taylor KD,
Dedoussis G,
Sever P,
Wong A,
Lind L,
Assimes TL,
Njølstad I,
Schwarz PE,
Langenberg C,
Snieder H,
Caulfield MJ,
Melander O,
Laakso M,
Saltevo J,
Rauramaa R,
Tuomilehto J,
Ingelsson E,
Lehtimäki T,
Hveem K,
Palmas W,
März W,
Kumari M,
Salomaa V,
Chen YI,
Rotter JI,
Froguel P,
Jarvelin MR,
Lakatta EG,
Kuulasmaa K,
Franks PW,
Hamsten A,
Wichmann HE,
Palmer CNA,
Stefansson K,
Ridker PM,
Loos RJF,
Chakravarti A,
Deloukas P,
Morris AP,
Newton-Cheh C,
Munroe PB
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Sawcer S,
Hellenthal G,
Pirinen M,
Spencer CC,
Patsopoulos NA,
Moutsianas L,
Dilthey A,
Su Z,
Freeman C,
Hunt SE,
Edkins S,
Gray E
and 230 more — show all
Booth DR,
Potter SC,
Goris A,
Band G,
Oturai AB,
Strange A,
Saarela J,
Bellenguez C,
Fontaine B,
Gillman M,
Hemmer B,
Gwilliam R,
Zipp F,
Jayakumar A,
Martin R,
Leslie S,
Hawkins S,
Giannoulatou E,
D'alfonso S,
Blackburn H,
Martinelli Boneschi F,
Liddle J,
Harbo HF,
Perez ML,
Spurkland A,
Waller MJ,
Mycko MP,
Ricketts M,
Comabella M,
Hammond N,
Kockum I,
McCann OT,
Ban M,
Whittaker P,
Kemppinen A,
Weston P,
Hawkins C,
Widaa S,
Zajicek J,
Dronov S,
Robertson N,
Bumpstead SJ,
Barcellos LF,
Ravindrarajah R,
Abraham R,
Alfredsson L,
Ardlie K,
Aubin C,
Baker A,
Baker K,
Baranzini SE,
Bergamaschi L,
Bergamaschi R,
Bernstein A,
Berthele A,
Boggild M,
Bradfield JP,
Brassat D,
Broadley SA,
Buck D,
Butzkueven H,
Capra R,
Carroll WM,
Cavalla P,
Celius EG,
Cepok S,
Chiavacci R,
Clerget-Darpoux F,
Clysters K,
Comi G,
Cossburn M,
Cournu-Rebeix I,
Cox MB,
Cozen W,
Cree BA,
Cross AH,
Cusi D,
Daly MJ,
Davis E,
de Bakker PI,
Debouverie M,
D'hooghe MB,
Dixon K,
Dobosi R,
Dubois B,
Ellinghaus D,
Elovaara I,
Esposito F,
Fontenille C,
Foote S,
Franke A,
Galimberti D,
Ghezzi A,
Glessner J,
Gomez R,
Gout O,
Graham C,
Grant SF,
Guerini FR,
Hakonarson H,
Hall P,
Hamsten A,
Hartung HP,
Heard RN,
Heath S,
Hobart J,
Hoshi M,
Infante-Duarte C,
Ingram G,
Ingram W,
Islam T,
Jagodic M,
Kabesch M,
Kermode AG,
Kilpatrick TJ,
Kim C,
Klopp N,
Koivisto K,
Larsson M,
Lathrop M,
Lechner-Scott JS,
Leone MA,
Leppä V,
Liljedahl U,
Bomfim IL,
Lincoln RR,
Link J,
Liu J,
Lorentzen AR,
Lupoli S,
Macciardi F,
Mack T,
Marriott M,
Martinelli V,
Mason D,
McCauley JL,
Mentch F,
Mero IL,
Mihalova T,
Montalban X,
Mottershead J,
Myhr KM,
Naldi P,
Ollier W,
Page A,
Palotie A,
Pelletier J,
Piccio L,
Pickersgill T,
Piehl F,
Pobywajlo S,
Quach HL,
Ramsay PP,
Reunanen M,
Reynolds R,
Rioux JD,
Rodegher M,
Roesner S,
Rubio JP,
Rückert IM,
Salvetti M,
Salvi E,
Santaniello A,
Schaefer CA,
Schreiber S,
Schulze C,
Scott RJ,
Sellebjerg F,
Selmaj KW,
Sexton D,
Shen L,
Simms-Acuna B,
Skidmore S,
Sleiman PM,
Smestad C,
Sørensen PS,
Søndergaard HB,
Stankovich J,
Strange RC,
Sulonen AM,
Sundqvist E,
Syvänen AC,
Taddeo F,
Taylor B,
Blackwell JM,
Tienari P,
Bramon E,
Tourbah A,
Brown MA,
Tronczynska E,
Casas JP,
Tubridy N,
Corvin A,
Vickery J,
Jankowski J,
Villoslada P,
Markus HS,
Wang K,
Mathew CG,
Wason J,
Palmer CN,
Wichmann HE,
Plomin R,
Willoughby E,
Rautanen A,
Winkelmann J,
Wittig M,
Trembath RC,
Yaouanq J,
Viswanathan AC,
Zhang H,
Wood NW,
Zuvich R,
Deloukas P,
Langford C,
Duncanson A,
Oksenberg JR,
Pericak-Vance MA,
Haines JL,
Olsson T,
Hillert J,
Ivinson AJ,
De Jager PL,
Peltonen L,
Stewart GJ,
Hafler DA,
Hauser SL,
McVean G,
Donnelly P,
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International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
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Spencer CC,
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Donnelly P
LeishGEN Consortium · Wellcome Trust Case Control Consortium 2
Nature genetics · 2013 · PMID 23291585 · open access
1 page
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
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Marullo L,
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Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
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Jackson AU,
Ferreira T
and 163 more — show all
Lee Y,
Ma C,
Steinthorsdottir V,
Thorleifsson G,
Qi L,
Van Zuydam NR,
Mahajan A,
Chen H,
Almgren P,
Voight BF,
Grallert H,
Müller-Nurasyid M,
Ried JS,
Rayner NW,
Robertson N,
Karssen LC,
van Leeuwen EM,
Willems SM,
Fuchsberger C,
Kwan P,
Teslovich TM,
Chanda P,
Li M,
Lu Y,
Dina C,
Thuillier D,
Yengo L,
Jiang L,
Sparso T,
Kestler HA,
Chheda H,
Eisele L,
Gustafsson S,
Frånberg M,
Strawbridge RJ,
Benediktsson R,
Hreidarsson AB,
Kong A,
Sigurðsson G,
Kerrison ND,
Luan J,
Liang L,
Meitinger T,
Roden M,
Thorand B,
Esko T,
Mihailov E,
Fox C,
Liu CT,
Rybin D,
Isomaa B,
Lyssenko V,
Tuomi T,
Couper DJ,
Pankow JS,
Grarup N,
Have CT,
Jørgensen ME,
Jørgensen T,
Linneberg A,
Cornelis MC,
van Dam RM,
Hunter DJ,
Kraft P,
Sun Q,
Edkins S,
Owen KR,
Perry JRB,
Wood AR,
Zeggini E,
Tajes-Fernandes J,
Abecasis GR,
Bonnycastle LL,
Chines PS,
Stringham HM,
Koistinen HA,
Kinnunen L,
Sennblad B,
Mühleisen TW,
Nöthen MM,
Pechlivanis S,
Baldassarre D,
Gertow K,
Humphries SE,
Tremoli E,
Klopp N,
Meyer J,
Steinbach G,
Wennauer R,
Eriksson JG,
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Collins FS,
Mohlke KL,
Tuomilehto J,
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Lannfelt L,
Ingelsson E,
Lind L,
Lindgren CM,
Cauchi S,
Froguel P,
Loos RJF,
Balkau B,
Boeing H,
Franks PW,
Barricarte Gurrea A,
Palli D,
van der Schouw YT,
Altshuler D,
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Morris AD,
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Prokopenko I
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
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
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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
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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
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to it, not because it was assessed and turned down.
Which pages rest on a paper?
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