For researchers
Is your paper here?
2,662 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
13 matches for
Kiess W.
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Warrington NM,
Beaumont RN,
Horikoshi M,
Day FR,
Helgeland Ø,
Laurin C,
Bacelis J,
Peng S,
Hao K,
Feenstra B,
Wood AR,
Mahajan A
and 196 more — show all
Tyrrell J,
Robertson NR,
Rayner NW,
Qiao Z,
Moen GH,
Vaudel M,
Marsit CJ,
Chen J,
Nodzenski M,
Schnurr TM,
Zafarmand MH,
Bradfield JP,
Grarup N,
Kooijman MN,
Li-Gao R,
Geller F,
Ahluwalia TS,
Paternoster L,
Rueedi R,
Huikari V,
Hottenga JJ,
Lyytikäinen LP,
Cavadino A,
Metrustry S,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Vilor-Tejedor N,
Joshi PK,
Painter JN,
Ntalla I,
Myhre R,
Pitkänen N,
van Leeuwen EM,
Joro R,
Lagou V,
Richmond RC,
Espinosa A,
Barton SJ,
Inskip HM,
Holloway JW,
Santa-Marina L,
Estivill X,
Ang W,
Marsh JA,
Reichetzeder C,
Marullo L,
Hocher B,
Lunetta KL,
Murabito JM,
Relton CL,
Kogevinas M,
Chatzi L,
Allard C,
Bouchard L,
Hivert MF,
Zhang G,
Muglia LJ,
Heikkinen J,
Morgen CS,
van Kampen AHC,
van Schaik BDC,
Mentch FD,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Hemani G,
Ring SM,
Bennett AJ,
Gaulton KJ,
Fernandez-Tajes J,
van Zuydam NR,
Medina-Gomez C,
de Haan HG,
Rosendaal FR,
Kutalik Z,
Marques-Vidal P,
Das S,
Willemsen G,
Mbarek H,
Müller-Nurasyid M,
Standl M,
Appel EVR,
Fonvig CE,
Trier C,
van Beijsterveldt CEM,
Murcia M,
Bustamante M,
Bonas-Guarch S,
Hougaard DM,
Mercader JM,
Linneberg A,
Schraut KE,
Lind PA,
Medland SE,
Shields BM,
Knight BA,
Chai JF,
Panoutsopoulou K,
Bartels M,
Sánchez F,
Stokholm J,
Torrents D,
Vinding RK,
Willems SM,
Atalay M,
Chawes BL,
Kovacs P,
Prokopenko I,
Tuke MA,
Yaghootkar H,
Ruth KS,
Jones SE,
Loh PR,
Murray A,
Weedon MN,
Tönjes A,
Stumvoll M,
Michaelsen KF,
Eloranta AM,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Niinikoski H,
Pahkala K,
Raitakari OT,
Jacobsson B,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Montgomery GW,
Campbell H,
Wilson JF,
Vrijkotte TGM,
Vrijheid M,
de Geus EJCN,
Hayes MG,
Kadarmideen HN,
Holm JC,
Beilin LJ,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Hattersley AT,
Spector TD,
Kähönen M,
Viikari JS,
Lehtimäki T,
Boomsma DI,
Sebert S,
Vollenweider P,
Sørensen TIA,
Bisgaard H,
Bønnelykke K,
Murray JC,
Melbye M,
Nohr EA,
Mook-Kanamori DO,
Rivadeneira F,
Hofman A,
Felix JF,
Jaddoe VWV,
Hansen T,
Pisinger C,
Vaag AA,
Pedersen O,
Uitterlinden AG,
Järvelin MR,
Power C,
Hyppönen E,
Scholtens DM,
Lowe WL Jr,
Davey Smith G,
Timpson NJ,
Morris AP,
Wareham NJ,
Hakonarson H,
Grant SFA,
Frayling TM,
Lawlor DA,
Njølstad PR,
Johansson S,
Ong KK,
McCarthy MI,
Perry JRB,
Evans DM,
Freathy RM
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Wuttke M,
Li Y,
Li M,
Sieber KB,
Feitosa MF,
Gorski M,
Tin A,
Wang L,
Chu AY,
Hoppmann A,
Kirsten H,
Giri A
and 315 more — show all
Chai JF,
Sveinbjornsson G,
Tayo BO,
Nutile T,
Fuchsberger C,
Marten J,
Cocca M,
Ghasemi S,
Xu Y,
Horn K,
Noce D,
van der Most PJ,
Sedaghat S,
Yu Z,
Akiyama M,
Afaq S,
Ahluwalia TS,
Almgren P,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boehnke M,
Boerwinkle E,
Boissel M,
Bottinger EP,
Boutin TS,
Brenner H,
Brumat M,
Burkhardt R,
Butterworth AS,
Campana E,
Campbell A,
Campbell H,
Canouil M,
Carroll RJ,
Catamo E,
Chambers JC,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cheng Y,
Christensen K,
Cifkova R,
Ciullo M,
Concas MP,
Cook JP,
Coresh J,
Corre T,
Sala CF,
Cusi D,
Danesh J,
Daw EW,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Delgado G,
Demirkan A,
Di Angelantonio E,
Dittrich K,
Divers J,
Dorajoo R,
Eckardt KU,
Ehret G,
Elliott P,
Endlich K,
Evans MK,
Felix JF,
Foo VHX,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Friedlander Y,
Froguel P,
Gansevoort RT,
Gao H,
Gasparini P,
Gaziano JM,
Giedraitis V,
Gieger C,
Girotto G,
Giulianini F,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hartman CA,
Hayward C,
Hellwege JN,
Heng CK,
Hicks AA,
Hofer E,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Indridason OS,
Ingelsson E,
Ising M,
Jaddoe VWV,
Jakobsdottir J,
Jonas JB,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kammerer CM,
Kanai M,
Kastarinen M,
Kerr SM,
Khor CC,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Kraja AT,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
Kuokkanen M,
Kuusisto J,
La Bianca M,
Laakso M,
Lange LA,
Langefeld CD,
Lee JJ,
Lehne B,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Liu J,
Loeffler M,
Loos RJF,
Lucae S,
Lukas MA,
Lyytikäinen LP,
Mägi R,
Magnusson PKE,
Mahajan A,
Martin NG,
Martins J,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Melander O,
Metspalu A,
Mikaelsdottir EK,
Milaneschi Y,
Miliku K,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell J,
O'Donoghue ML,
Olafsson I,
Oldehinkel AJ,
Orho-Melander M,
Ouwehand WH,
Padmanabhan S,
Palmer ND,
Palsson R,
Penninx BWJH,
Perls T,
Perola M,
Pirastu M,
Pirastu N,
Pistis G,
Podgornaia AI,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Pramstaller PP,
Preuss MH,
Prins BP,
Province MA,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Ridker PM,
Rivadeneira F,
Rizzi F,
Roberts DJ,
Robino A,
Rossing P,
Rudan I,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Sabanayagam C,
Salomaa V,
Salvi E,
Saum KU,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Schupf N,
Shaffer CM,
Shi Y,
Smith AV,
Smith BH,
Soranzo N,
Spracklen CN,
Strauch K,
Stringham HM,
Stumvoll M,
Svensson PO,
Szymczak S,
Tai ES,
Tajuddin SM,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorleifsson G,
Toniolo D,
Tönjes A,
Tremblay J,
Tzoulaki I,
Uitterlinden AG,
Vaccargiu S,
van Dam RM,
van der Harst P,
van Duijn CM,
Velez Edward DR,
Verweij N,
Vogelezang S,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Wallentin L,
Wang YX,
Wang C,
Waterworth DM,
Bin Wei W,
White H,
Whitfield JB,
Wild SH,
Wilson JF,
Wojczynski MK,
Wong C,
Wong TY,
Xu L,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang W,
Zonderman AB,
Rotter JI,
Bochud M,
Psaty BM,
Vitart V,
Wilson JG,
Dehghan A,
Parsa A,
Chasman DI,
Ho K,
Morris AP,
Devuyst O,
Akilesh S,
Pendergrass SA,
Sim X,
Böger CA,
Okada Y,
Edwards TL,
Snieder H,
Stefansson K,
Hung AM,
Heid IM,
Scholz M,
Teumer A,
Köttgen A,
Pattaro C
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer A,
Li Y,
Ghasemi S,
Prins BP,
Wuttke M,
Hermle T,
Giri A,
Sieber KB,
Qiu C,
Kirsten H,
Tin A,
Chu AY
and 174 more — show all
Bansal N,
Feitosa MF,
Wang L,
Chai JF,
Cocca M,
Fuchsberger C,
Gorski M,
Hoppmann A,
Horn K,
Li M,
Marten J,
Noce D,
Nutile T,
Sedaghat S,
Sveinbjornsson G,
Tayo BO,
van der Most PJ,
Xu Y,
Yu Z,
Gerstner L,
Ärnlöv J,
Bakker SJL,
Baptista D,
Biggs ML,
Boerwinkle E,
Brenner H,
Burkhardt R,
Carroll RJ,
Chee ML,
Chee ML,
Chen M,
Cheng CY,
Cook JP,
Coresh J,
Corre T,
Danesh J,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Dittrich K,
Divers J,
Eckardt KU,
Ehret G,
Endlich K,
Felix JF,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Gansevoort RT,
Giedraitis V,
Gögele M,
Grundner-Culemann F,
Gudbjartsson DF,
Gudnason V,
Hamet P,
Harris TB,
Hicks AA,
Holm H,
Foo VHX,
Hwang SJ,
Ikram MA,
Ingelsson E,
Jaddoe VWV,
Jakobsdottir J,
Josyula NS,
Jung B,
Kähönen M,
Khor CC,
Kiess W,
Koenig W,
Körner A,
Kovacs P,
Kramer H,
Krämer BK,
Kronenberg F,
Lange LA,
Langefeld CD,
Lee JJ,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Mahajan A,
Maranville JC,
Mascalzoni D,
McMullen B,
Meisinger C,
Meitinger T,
Miliku K,
Mook-Kanamori DO,
Müller-Nurasyid M,
Mychaleckyj JC,
Nauck M,
Nikus K,
Ning B,
Noordam R,
Connell JO,
Olafsson I,
Palmer ND,
Peters A,
Podgornaia AI,
Ponte B,
Poulain T,
Pramstaller PP,
Rabelink TJ,
Raffield LM,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Rivadeneira F,
Runz H,
Ryan KA,
Sabanayagam C,
Saum KU,
Schöttker B,
Shaffer CM,
Shi Y,
Smith AV,
Strauch K,
Stumvoll M,
Sun BB,
Szymczak S,
Tai ES,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorsteinsdottir U,
Tönjes A,
Tremblay J,
Uitterlinden AG,
van der Harst P,
Verweij N,
Vogelezang S,
Völker U,
Waldenberger M,
Wang C,
Wilson OD,
Wong C,
Wong TY,
Yang Q,
Yasuda M,
Akilesh S,
Bochud M,
Böger CA,
Devuyst O,
Edwards TL,
Ho K,
Morris AP,
Parsa A,
Pendergrass SA,
Psaty BM,
Rotter JI,
Stefansson K,
Wilson JG,
Susztak K,
Snieder H,
Heid IM,
Scholz M,
Butterworth AS,
Hung AM,
Pattaro C,
Köttgen A
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
and 213 more — show all
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
Okada Y,
Edwards TL,
Stefansson K,
Susztak K,
Scholz M,
Heid IM,
Hung AM,
Teumer A,
Pattaro C,
Woodward OM,
Vitart V,
Köttgen A
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
The trans-ancestral genomic architecture of glycemic traits
Chen J,
Spracklen CN,
Marenne G,
Varshney A,
Corbin LJ,
Luan J,
Willems SM,
Wu Y,
Zhang X,
Horikoshi M,
Boutin TS,
Mägi R
and 393 more — show all
Waage J,
Li-Gao R,
Chan KHK,
Yao J,
Anasanti MD,
Chu AY,
Claringbould A,
Heikkinen J,
Hong J,
Hottenga JJ,
Huo S,
Kaakinen MA,
Louie T,
März W,
Moreno-Macias H,
Ndungu A,
Nelson SC,
Nolte IM,
North KE,
Raulerson CK,
Ray D,
Rohde R,
Rybin D,
Schurmann C,
Sim X,
Southam L,
Stewart ID,
Wang CA,
Wang Y,
Wu P,
Zhang W,
Ahluwalia TS,
Appel EVR,
Bielak LF,
Brody JA,
Burtt NP,
Cabrera CP,
Cade BE,
Chai JF,
Chai X,
Chang LC,
Chen CH,
Chen BH,
Chitrala KN,
Chiu YF,
de Haan HG,
Delgado GE,
Demirkan A,
Duan Q,
Engmann J,
Fatumo SA,
Gayán J,
Giulianini F,
Gong JH,
Gustafsson S,
Hai Y,
Hartwig FP,
He J,
Heianza Y,
Huang T,
Huerta-Chagoya A,
Hwang MY,
Jensen RA,
Kawaguchi T,
Kentistou KA,
Kim YJ,
Kleber ME,
Kooner IK,
Lai S,
Lange LA,
Langefeld CD,
Lauzon M,
Li M,
Ligthart S,
Liu J,
Loh M,
Long J,
Lyssenko V,
Mangino M,
Marzi C,
Montasser ME,
Nag A,
Nakatochi M,
Noce D,
Noordam R,
Pistis G,
Preuss M,
Raffield L,
Rasmussen-Torvik LJ,
Rich SS,
Robertson NR,
Rueedi R,
Ryan K,
Sanna S,
Saxena R,
Schraut KE,
Sennblad B,
Setoh K,
Smith AV,
Sparsø T,
Strawbridge RJ,
Takeuchi F,
Tan J,
Trompet S,
van den Akker E,
van der Most PJ,
Verweij N,
Vogel M,
Wang H,
Wang C,
Wang N,
Warren HR,
Wen W,
Wilsgaard T,
Wong A,
Wood AR,
Xie T,
Zafarmand MH,
Zhao JH,
Zhao W,
Amin N,
Arzumanyan Z,
Astrup A,
Bakker SJL,
Baldassarre D,
Beekman M,
Bergman RN,
Bertoni A,
Blüher M,
Bonnycastle LL,
Bornstein SR,
Bowden DW,
Cai Q,
Campbell A,
Campbell H,
Chang YC,
de Geus EJC,
Dehghan A,
Du S,
Eiriksdottir G,
Farmaki AE,
Frånberg M,
Fuchsberger C,
Gao Y,
Gjesing AP,
Goel A,
Han S,
Hartman CA,
Herder C,
Hicks AA,
Hsieh CH,
Hsueh WA,
Ichihara S,
Igase M,
Ikram MA,
Johnson WC,
Jørgensen ME,
Joshi PK,
Kalyani RR,
Kandeel FR,
Katsuya T,
Khor CC,
Kiess W,
Kolcic I,
Kuulasmaa T,
Kuusisto J,
Läll K,
Lam K,
Lawlor DA,
Lee NR,
Lemaitre RN,
Li H,
Lin SY,
Lindström J,
Linneberg A,
Liu J,
Lorenzo C,
Matsubara T,
Matsuda F,
Mingrone G,
Mooijaart S,
Moon S,
Nabika T,
Nadkarni GN,
Nadler JL,
Nelis M,
Neville MJ,
Norris JM,
Ohyagi Y,
Peters A,
Peyser PA,
Polasek O,
Qi Q,
Raven D,
Reilly DF,
Reiner A,
Rivideneira F,
Roll K,
Rudan I,
Sabanayagam C,
Sandow K,
Sattar N,
Schürmann A,
Shi J,
Stringham HM,
Taylor KD,
Teslovich TM,
Thuesen B,
Timmers PRHJ,
Tremoli E,
Tsai MY,
Uitterlinden A,
van Dam RM,
van Heemst D,
van Hylckama Vlieg A,
van Vliet-Ostaptchouk JV,
Vangipurapu J,
Vestergaard H,
Wang T,
Willems van Dijk K,
Zemunik T,
Abecasis GR,
Adair LS,
Aguilar-Salinas CA,
Alarcón-Riquelme ME,
An P,
Aviles-Santa L,
Becker DM,
Beilin LJ,
Bergmann S,
Bisgaard H,
Black C,
Boehnke M,
Boerwinkle E,
Böhm BO,
Bønnelykke K,
Boomsma DI,
Bottinger EP,
Buchanan TA,
Canouil M,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YI,
Cheng CY,
Collins FS,
Correa A,
Cucca F,
de Silva HJ,
Dedoussis G,
Elmståhl S,
Evans MK,
Ferrannini E,
Ferrucci L,
Florez JC,
Franks PW,
Frayling TM,
Froguel P,
Gigante B,
Goodarzi MO,
Gordon-Larsen P,
Grallert H,
Grarup N,
Grimsgaard S,
Groop L,
Gudnason V,
Guo X,
Hamsten A,
Hansen T,
Hayward C,
Heckbert SR,
Horta BL,
Huang W,
Ingelsson E,
James PS,
Jarvelin MR,
Jonas JB,
Jukema JW,
Kaleebu P,
Kaplan R,
Kardia SLR,
Kato N,
Keinanen-Kiukaanniemi SM,
Kim BJ,
Kivimaki M,
Koistinen HA,
Kooner JS,
Körner A,
Kovacs P,
Kuh D,
Kumari M,
Kutalik Z,
Laakso M,
Lakka TA,
Launer LJ,
Leander K,
Li H,
Lin X,
Lind L,
Lindgren C,
Liu S,
Loos RJF,
Magnusson PKE,
Mahajan A,
Metspalu A,
Mook-Kanamori DO,
Mori TA,
Munroe PB,
Njølstad I,
O'Connell JR,
Oldehinkel AJ,
Ong KK,
Padmanabhan S,
Palmer CNA,
Palmer ND,
Pedersen O,
Pennell CE,
Porteous DJ,
Pramstaller PP,
Province MA,
Psaty BM,
Qi L,
Raffel LJ,
Rauramaa R,
Redline S,
Ridker PM,
Rosendaal FR,
Saaristo TE,
Sandhu M,
Saramies J,
Schneiderman N,
Schwarz P,
Scott LJ,
Selvin E,
Sever P,
Shu XO,
Slagboom PE,
Small KS,
Smith BH,
Snieder H,
Sofer T,
Sørensen TIA,
Spector TD,
Stanton A,
Steves CJ,
Stumvoll M,
Sun L,
Tabara Y,
Tai ES,
Timpson NJ,
Tönjes A,
Tuomilehto J,
Tusie T,
Uusitupa M,
van der Harst P,
van Duijn C,
Vitart V,
Vollenweider P,
Vrijkotte TGM,
Wagenknecht LE,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Wei WB,
Wickremasinghe AR,
Willemsen G,
Wilson JF,
Wong TY,
Wu JY,
Xiang AH,
Yanek LR,
Yengo L,
Yokota M,
Zeggini E,
Zheng W,
Zonderman AB,
Rotter JI,
Gloyn AL,
McCarthy MI,
Dupuis J,
Meigs JB,
Scott RA,
Prokopenko I,
Leong A,
Liu CT,
Parker SCJ,
Mohlke KL,
Langenberg C,
Wheeler E,
Morris AP,
Barroso I
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
Wheeler E,
Leong A,
Liu CT,
Hivert MF,
Strawbridge RJ,
Podmore C,
Li M,
Yao J,
Sim X,
Hong J,
Chu AY,
Zhang W
and 203 more — show all
Wang X,
Chen P,
Maruthur NM,
Porneala BC,
Sharp SJ,
Jia Y,
Kabagambe EK,
Chang LC,
Chen WM,
Elks CE,
Evans DS,
Fan Q,
Giulianini F,
Go MJ,
Hottenga JJ,
Hu Y,
Jackson AU,
Kanoni S,
Kim YJ,
Kleber ME,
Ladenvall C,
Lecoeur C,
Lim SH,
Lu Y,
Mahajan A,
Marzi C,
Nalls MA,
Navarro P,
Nolte IM,
Rose LM,
Rybin DV,
Sanna S,
Shi Y,
Stram DO,
Takeuchi F,
Tan SP,
van der Most PJ,
Van Vliet-Ostaptchouk JV,
Wong A,
Yengo L,
Zhao W,
Goel A,
Martinez Larrad MT,
Radke D,
Salo P,
Tanaka T,
van Iperen EPA,
Abecasis G,
Afaq S,
Alizadeh BZ,
Bertoni AG,
Bonnefond A,
Böttcher Y,
Bottinger EP,
Campbell H,
Carlson OD,
Chen CH,
Cho YS,
Garvey WT,
Gieger C,
Goodarzi MO,
Grallert H,
Hamsten A,
Hartman CA,
Herder C,
Hsiung CA,
Huang J,
Igase M,
Isono M,
Katsuya T,
Khor CC,
Kiess W,
Kohara K,
Kovacs P,
Lee J,
Lee WJ,
Lehne B,
Li H,
Liu J,
Lobbens S,
Luan J,
Lyssenko V,
Meitinger T,
Miki T,
Miljkovic I,
Moon S,
Mulas A,
Müller G,
Müller-Nurasyid M,
Nagaraja R,
Nauck M,
Pankow JS,
Polasek O,
Prokopenko I,
Ramos PS,
Rasmussen-Torvik L,
Rathmann W,
Rich SS,
Robertson NR,
Roden M,
Roussel R,
Rudan I,
Scott RA,
Scott WR,
Sennblad B,
Siscovick DS,
Strauch K,
Sun L,
Swertz M,
Tajuddin SM,
Taylor KD,
Teo YY,
Tham YC,
Tönjes A,
Wareham NJ,
Willemsen G,
Wilsgaard T,
Hingorani AD,
Egan J,
Ferrucci L,
Hovingh GK,
Jula A,
Kivimaki M,
Kumari M,
Njølstad I,
Palmer CNA,
Serrano Ríos M,
Stumvoll M,
Watkins H,
Aung T,
Blüher M,
Boehnke M,
Boomsma DI,
Bornstein SR,
Chambers JC,
Chasman DI,
Chen YI,
Chen YT,
Cheng CY,
Cucca F,
de Geus EJC,
Deloukas P,
Evans MK,
Fornage M,
Friedlander Y,
Froguel P,
Groop L,
Gross MD,
Harris TB,
Hayward C,
Heng CK,
Ingelsson E,
Kato N,
Kim BJ,
Koh WP,
Kooner JS,
Körner A,
Kuh D,
Kuusisto J,
Laakso M,
Lin X,
Liu Y,
Loos RJF,
Magnusson PKE,
März W,
McCarthy MI,
Oldehinkel AJ,
Ong KK,
Pedersen NL,
Pereira MA,
Peters A,
Ridker PM,
Sabanayagam C,
Sale M,
Saleheen D,
Saltevo J,
Schwarz PE,
Sheu WHH,
Snieder H,
Spector TD,
Tabara Y,
Tuomilehto J,
van Dam RM,
Wilson JG,
Wilson JF,
Wolffenbuttel BHR,
Wong TY,
Wu JY,
Yuan JM,
Zonderman AB,
Soranzo N,
Guo X,
Roberts DJ,
Florez JC,
Sladek R,
Dupuis J,
Morris AP,
Tai ES,
Selvin E,
Rotter JI,
Langenberg C,
Barroso I,
Meigs JB
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Felix JF,
Bradfield JP,
Monnereau C,
van der Valk RJ,
Stergiakouli E,
Chesi A,
Gaillard R,
Feenstra B,
Thiering E,
Kreiner-Møller E,
Mahajan A,
Pitkänen N
and 99 more — show all
Joro R,
Cavadino A,
Huikari V,
Franks S,
Groen-Blokhuis MM,
Cousminer DL,
Marsh JA,
Lehtimäki T,
Curtin JA,
Vioque J,
Ahluwalia TS,
Myhre R,
Price TS,
Vilor-Tejedor N,
Yengo L,
Grarup N,
Ntalla I,
Ang W,
Atalay M,
Bisgaard H,
Blakemore AI,
Bonnefond A,
Carstensen L,
Eriksson J,
Flexeder C,
Franke L,
Geller F,
Geserick M,
Hartikainen AL,
Haworth CM,
Hirschhorn JN,
Hofman A,
Holm JC,
Horikoshi M,
Hottenga JJ,
Huang J,
Kadarmideen HN,
Kähönen M,
Kiess W,
Lakka HM,
Lakka TA,
Lewin AM,
Liang L,
Lyytikäinen LP,
Ma B,
Magnus P,
McCormack SE,
McMahon G,
Mentch FD,
Middeldorp CM,
Murray CS,
Pahkala K,
Pers TH,
Pfäffle R,
Postma DS,
Power C,
Simpson A,
Sengpiel V,
Tiesler CM,
Torrent M,
Uitterlinden AG,
van Meurs JB,
Vinding R,
Waage J,
Wardle J,
Zeggini E,
Zemel BS,
Dedoussis GV,
Pedersen O,
Froguel P,
Sunyer J,
Plomin R,
Jacobsson B,
Hansen T,
Gonzalez JR,
Custovic A,
Raitakari OT,
Pennell CE,
Widén E,
Boomsma DI,
Koppelman GH,
Sebert S,
Järvelin MR,
Hyppönen E,
McCarthy MI,
Lindi V,
Harri N,
Körner A,
Bønnelykke K,
Heinrich J,
Melbye M,
Rivadeneira F,
Hakonarson H,
Ring SM,
Smith GD,
Sørensen TI,
Timpson NJ,
Grant SF,
Jaddoe VW
Bone Mineral Density in Childhood Study (BMDCS) · Early Genetics and Lifecourse Epidemiology (EAGLE) consortium and 2 more consortia
Human molecular genetics · 2016 · PMID 26604143
8 pages
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Scholz M,
Horn K,
Pott J,
Wuttke M,
Kühnapfel A,
Nasr MK,
Kirsten H,
Li Y,
Hoppmann A,
Gorski M,
Ghasemi S,
Li M
and 147 more — show all
Tin A,
Chai JF,
Cocca M,
Wang J,
Nutile T,
Akiyama M,
Åsvold BO,
Bansal N,
Biggs ML,
Boutin T,
Brenner H,
Brumpton B,
Burkhardt R,
Cai J,
Campbell A,
Campbell H,
Chalmers J,
Chasman DI,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cifkova R,
Daviglus M,
Delgado G,
Dittrich K,
Edwards TL,
Endlich K,
Michael Gaziano J,
Giri A,
Giulianini F,
Gordon SD,
Gudbjartsson DF,
Hallan S,
Hamet P,
Hartman CA,
Hayward C,
Heid IM,
Hellwege JN,
Holleczek B,
Holm H,
Hutri-Kähönen N,
Hveem K,
Isermann B,
Jonas JB,
Joshi PK,
Kamatani Y,
Kanai M,
Kastarinen M,
Khor CC,
Kiess W,
Kleber ME,
Körner A,
Kovacs P,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kuokkanen M,
Kähönen M,
Lange LA,
Lash JP,
Lehtimäki T,
Li H,
Lin BM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Magnusson PKE,
Martin NG,
Matsuda K,
Milaneschi Y,
Mishra PP,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
März W,
Nauck M,
Nikus K,
Nolte IM,
Noordam R,
Okada Y,
Olafsson I,
Oldehinkel AJ,
Penninx BWJH,
Perola M,
Pirastu N,
Polasek O,
Porteous DJ,
Poulain T,
Psaty BM,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rasheed H,
Reilly DF,
Rice KM,
Richmond A,
Ridker PM,
Rotter JI,
Rudan I,
Sabanayagam C,
Salomaa V,
Schneiderman N,
Schöttker B,
Sims M,
Snieder H,
Stark KJ,
Stefansson K,
Stocker H,
Stumvoll M,
Sulem P,
Sveinbjornsson G,
Svensson PO,
Tai ES,
Taylor KD,
Tayo BO,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomas LF,
Tremblay J,
Tönjes A,
van der Most PJ,
Vitart V,
Völker U,
Wang YX,
Wang C,
Wei WB,
Whitfield JB,
Wild SH,
Wilson JF,
Winkler TW,
Wong TY,
Woodward M,
Sim X,
Chu AY,
Feitosa MF,
Thorsteinsdottir U,
Hung AM,
Teumer A,
Franceschini N,
Parsa A,
Köttgen A,
Schlosser P,
Pattaro C
Nature communications · 2024 · PMID 38233393 · open access
8 pages
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
Willems SM,
Ng NHJ,
Fernandez J,
Fine RS,
Wheeler E,
Wessel J,
Kitajima H,
Marenne G,
Sim X,
Yaghootkar H,
Wang S,
Chen S
and 228 more — show all
Chen Y,
Chen YI,
Grarup N,
Li-Gao R,
Varga TV,
Asimit JL,
Feng S,
Strawbridge RJ,
Kleinbrink EL,
Ahluwalia TS,
An P,
Appel EV,
Arking DE,
Auvinen J,
Bielak LF,
Bihlmeyer NA,
Bork-Jensen J,
Brody JA,
Campbell A,
Chu AY,
Davies G,
Demirkan A,
Floyd JS,
Giulianini F,
Guo X,
Gustafsson S,
Jackson AU,
Jakobsdottir J,
Järvelin MR,
Jensen RA,
Kanoni S,
Keinanen-Kiukaanniemi S,
Li M,
Lu Y,
Luan J,
Manning AK,
Marten J,
Meidtner K,
Mook-Kanamori DO,
Muka T,
Pistis G,
Prins B,
Rice KM,
Sanna S,
Smith AV,
Smith JA,
Southam L,
Stringham HM,
Tragante V,
van der Laan SW,
Warren HR,
Yao J,
Yiorkas AM,
Zhang W,
Zhao W,
Graff M,
Highland HM,
Justice AE,
Marouli E,
Medina-Gomez C,
Afaq S,
Alhejily WA,
Amin N,
Asselbergs FW,
Bonnycastle LL,
Bots ML,
Brandslund I,
Chen J,
Danesh J,
de Mutsert R,
Dehghan A,
Ebeling T,
Elliott P,
Farmaki AE,
Faul JD,
Franks PW,
Franks S,
Fritsche A,
Gjesing AP,
Goodarzi MO,
Gudnason V,
Hallmans G,
Harris TB,
Herzig KH,
Hivert MF,
Jørgensen T,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Karaleftheri M,
Kardia SLR,
Kinnunen L,
Koistinen HA,
Komulainen P,
Kovacs P,
Kuusisto J,
Laakso M,
Lange LA,
Launer LJ,
Leong A,
Lindström J,
Manning Fox JE,
Männistö S,
Maruthur NM,
Moilanen L,
Mulas A,
Nalls MA,
Neville M,
Pankow JS,
Pattie A,
Petersen ERB,
Puolijoki H,
Rasheed A,
Redmond P,
Renström F,
Roden M,
Saleheen D,
Saltevo J,
Savonen K,
Sebert S,
Skaaby T,
Small KS,
Stančáková A,
Stokholm J,
Strauch K,
Tai ES,
Taylor KD,
Thuesen BH,
Tönjes A,
Tsafantakis E,
Tuomi T,
Tuomilehto J,
Uusitupa M,
Vääräsmäki M,
Vaartjes I,
Zoledziewska M,
Abecasis G,
Balkau B,
Bisgaard H,
Blakemore AI,
Blüher M,
Boeing H,
Boerwinkle E,
Bønnelykke K,
Bottinger EP,
Caulfield MJ,
Chambers JC,
Chasman DI,
Cheng CY,
Collins FS,
Coresh J,
Cucca F,
de Borst GJ,
Deary IJ,
Dedoussis G,
Deloukas P,
den Ruijter HM,
Dupuis J,
Evans MK,
Ferrannini E,
Franco OH,
Grallert H,
Hansen T,
Hattersley AT,
Hayward C,
Hirschhorn JN,
Ikram A,
Ingelsson E,
Karpe F,
Kaw KT,
Kiess W,
Kooner JS,
Körner A,
Lakka T,
Langenberg C,
Lind L,
Lindgren CM,
Linneberg A,
Lipovich L,
Liu CT,
Liu J,
Liu Y,
Loos RJF,
MacDonald PE,
Mohlke KL,
Morris AD,
Munroe PB,
Murray A,
Padmanabhan S,
Palmer CNA,
Pasterkamp G,
Pedersen O,
Peyser PA,
Polasek O,
Porteous D,
Province MA,
Psaty BM,
Rauramaa R,
Ridker PM,
Rolandsson O,
Rorsman P,
Rosendaal FR,
Rudan I,
Salomaa V,
Schulze MB,
Sladek R,
Smith BH,
Spector TD,
Starr JM,
Stumvoll M,
van Duijn CM,
Walker M,
Wareham NJ,
Weir DR,
Wilson JG,
Wong TY,
Zeggini E,
Zonderman AB,
Rotter JI,
Morris AP,
Boehnke M,
Florez JC,
McCarthy MI,
Meigs JB,
Mahajan A,
Scott RA,
Gloyn AL,
Barroso I
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
5 pages
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou V,
Mägi R,
Hottenga JJ,
Grallert H,
Perry JRB,
Bouatia-Naji N,
Marullo L,
Rybin D,
Jansen R,
Min JL,
Dimas AS,
Ulrich A
and 192 more — show all
Zudina L,
Gådin JR,
Jiang L,
Faggian A,
Bonnefond A,
Fadista J,
Stathopoulou MG,
Isaacs A,
Willems SM,
Navarro P,
Tanaka T,
Jackson AU,
Montasser ME,
O'Connell JR,
Bielak LF,
Webster RJ,
Saxena R,
Stafford JM,
Pourcain BS,
Timpson NJ,
Salo P,
Shin SY,
Amin N,
Smith AV,
Li G,
Verweij N,
Goel A,
Ford I,
Johnson PCD,
Johnson T,
Kapur K,
Thorleifsson G,
Strawbridge RJ,
Rasmussen-Torvik LJ,
Esko T,
Mihailov E,
Fall T,
Fraser RM,
Mahajan A,
Kanoni S,
Giedraitis V,
Kleber ME,
Silbernagel G,
Meyer J,
Müller-Nurasyid M,
Ganna A,
Sarin AP,
Yengo L,
Shungin D,
Luan J,
Horikoshi M,
An P,
Sanna S,
Boettcher Y,
Rayner NW,
Nolte IM,
Zemunik T,
Iperen EV,
Kovacs P,
Hastie ND,
Wild SH,
McLachlan S,
Campbell S,
Polasek O,
Carlson O,
Egan J,
Kiess W,
Willemsen G,
Kuusisto J,
Laakso M,
Dimitriou M,
Hicks AA,
Rauramaa R,
Bandinelli S,
Thorand B,
Liu Y,
Miljkovic I,
Lind L,
Doney A,
Perola M,
Hingorani A,
Kivimaki M,
Kumari M,
Bennett AJ,
Groves CJ,
Herder C,
Koistinen HA,
Kinnunen L,
Faire U,
Bakker SJL,
Uusitupa M,
Palmer CNA,
Jukema JW,
Sattar N,
Pouta A,
Snieder H,
Boerwinkle E,
Pankow JS,
Magnusson PK,
Krus U,
Scapoli C,
de Geus EJCN,
Blüher M,
Wolffenbuttel BHR,
Province MA,
Abecasis GR,
Meigs JB,
Hovingh GK,
Lindström J,
Wilson JF,
Wright AF,
Dedoussis GV,
Bornstein SR,
Schwarz PEH,
Tönjes A,
Winkelmann BR,
Boehm BO,
März W,
Metspalu A,
Price JF,
Deloukas P,
Körner A,
Lakka TA,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Bergman RN,
Tuomilehto J,
Wareham NJ,
Langenberg C,
Männistö S,
Franks PW,
Hayward C,
Vitart V,
Kaprio J,
Visvikis-Siest S,
Balkau B,
Altshuler D,
Rudan I,
Stumvoll M,
Campbell H,
van Duijn CM,
Gieger C,
Illig T,
Ferrucci L,
Pedersen NL,
Pramstaller PP,
Boehnke M,
Frayling TM,
Shuldiner AR,
Peyser PA,
Kardia SLR,
Palmer LJ,
Penninx BW,
Meneton P,
Harris TB,
Navis G,
Harst PV,
Smith GD,
Forouhi NG,
Loos RJF,
Salomaa V,
Soranzo N,
Boomsma DI,
Groop L,
Tuomi T,
Hofman A,
Munroe PB,
Gudnason V,
Siscovick DS,
Watkins H,
Lecoeur C,
Vollenweider P,
Franco-Cereceda A,
Eriksson P,
Jarvelin MR,
Stefansson K,
Hamsten A,
Nicholson G,
Karpe F,
Dermitzakis ET,
Lindgren CM,
McCarthy MI,
Froguel P,
Kaakinen MA,
Lyssenko V,
Watanabe RM,
Ingelsson E,
Florez JC,
Dupuis J,
Barroso I,
Morris AP,
Prokopenko I
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups
Scherag A,
Dina C,
Hinney A,
Vatin V,
Scherag S,
Vogel CI,
Müller TD,
Grallert H,
Wichmann HE,
Balkau B,
Heude B,
Jarvelin MR
and 38 more — show all
Hartikainen AL,
Levy-Marchal C,
Weill J,
Delplanque J,
Körner A,
Kiess W,
Kovacs P,
Rayner NW,
Prokopenko I,
McCarthy MI,
Schäfer H,
Jarick I,
Boeing H,
Fisher E,
Reinehr T,
Heinrich J,
Rzehak P,
Berdel D,
Borte M,
Biebermann H,
Krude H,
Rosskopf D,
Rimmbach C,
Rief W,
Fromme T,
Klingenspor M,
Schürmann A,
Schulz N,
Nöthen MM,
Mühleisen TW,
Erbel R,
Jöckel KH,
Moebus S,
Boes T,
Illig T,
Froguel P,
Hebebrand J,
Meyre D
PLoS genetics · 2010 · PMID 20421936 · open access
2 pages
A novel common variant in DCST2 is associated with length in early life and height in adulthood
van der Valk RJ,
Kreiner-Møller E,
Kooijman MN,
Guxens M,
Stergiakouli E,
Sääf A,
Bradfield JP,
Geller F,
Hayes MG,
Cousminer DL,
Körner A,
Thiering E
and 105 more — show all
Curtin JA,
Myhre R,
Huikari V,
Joro R,
Kerkhof M,
Warrington NM,
Pitkänen N,
Ntalla I,
Horikoshi M,
Veijola R,
Freathy RM,
Teo YY,
Barton SJ,
Evans DM,
Kemp JP,
St Pourcain B,
Ring SM,
Davey Smith G,
Bergström A,
Kull I,
Hakonarson H,
Mentch FD,
Bisgaard H,
Chawes B,
Stokholm J,
Waage J,
Eriksen P,
Sevelsted A,
Melbye M,
van Duijn CM,
Medina-Gomez C,
Hofman A,
de Jongste JC,
Taal HR,
Uitterlinden AG,
Armstrong LL,
Eriksson J,
Palotie A,
Bustamante M,
Estivill X,
Gonzalez JR,
Llop S,
Kiess W,
Mahajan A,
Flexeder C,
Tiesler CM,
Murray CS,
Simpson A,
Magnus P,
Sengpiel V,
Hartikainen AL,
Keinanen-Kiukaanniemi S,
Lewin A,
Da Silva Couto Alves A,
Blakemore AI,
Buxton JL,
Kaakinen M,
Rodriguez A,
Sebert S,
Vaarasmaki M,
Lakka T,
Lindi V,
Gehring U,
Postma DS,
Ang W,
Newnham JP,
Lyytikäinen LP,
Pahkala K,
Raitakari OT,
Panoutsopoulou K,
Zeggini E,
Boomsma DI,
Groen-Blokhuis M,
Ilonen J,
Franke L,
Hirschhorn JN,
Pers TH,
Liang L,
Huang J,
Hocher B,
Knip M,
Saw SM,
Holloway JW,
Melén E,
Grant SF,
Feenstra B,
Lowe WL,
Widén E,
Sergeyev E,
Grallert H,
Custovic A,
Jacobsson B,
Jarvelin MR,
Atalay M,
Koppelman GH,
Pennell CE,
Niinikoski H,
Dedoussis GV,
Mccarthy MI,
Frayling TM,
Sunyer J,
Timpson NJ,
Rivadeneira F,
Bønnelykke K,
Jaddoe VW
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
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.