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98 matches for
Mägi R,
showing the first 20.
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
Soranzo N,
Sanna S,
Wheeler E,
Gieger C,
Radke D,
Dupuis J,
Bouatia-Naji N,
Langenberg C,
Prokopenko I,
Stolerman E,
Sandhu MS,
Heeney MM
and 165 more — show all
Devaney JM,
Reilly MP,
Ricketts SL,
Stewart AF,
Voight BF,
Willenborg C,
Wright B,
Altshuler D,
Arking D,
Balkau B,
Barnes D,
Boerwinkle E,
Böhm B,
Bonnefond A,
Bonnycastle LL,
Boomsma DI,
Bornstein SR,
Böttcher Y,
Bumpstead S,
Burnett-Miller MS,
Campbell H,
Cao A,
Chambers J,
Clark R,
Collins FS,
Coresh J,
de Geus EJ,
Dei M,
Deloukas P,
Döring A,
Egan JM,
Elosua R,
Ferrucci L,
Forouhi N,
Fox CS,
Franklin C,
Franzosi MG,
Gallina S,
Goel A,
Graessler J,
Grallert H,
Greinacher A,
Hadley D,
Hall A,
Hamsten A,
Hayward C,
Heath S,
Herder C,
Homuth G,
Hottenga JJ,
Hunter-Merrill R,
Illig T,
Jackson AU,
Jula A,
Kleber M,
Knouff CW,
Kong A,
Kooner J,
Köttgen A,
Kovacs P,
Krohn K,
Kühnel B,
Kuusisto J,
Laakso M,
Lathrop M,
Lecoeur C,
Li M,
Li M,
Loos RJ,
Luan J,
Lyssenko V,
Mägi R,
Magnusson PK,
Mälarstig A,
Mangino M,
Martínez-Larrad MT,
März W,
McArdle WL,
McPherson R,
Meisinger C,
Meitinger T,
Melander O,
Mohlke KL,
Mooser VE,
Morken MA,
Narisu N,
Nathan DM,
Nauck M,
O'Donnell C,
Oexle K,
Olla N,
Pankow JS,
Payne F,
Peden JF,
Pedersen NL,
Peltonen L,
Perola M,
Polasek O,
Porcu E,
Rader DJ,
Rathmann W,
Ripatti S,
Rocheleau G,
Roden M,
Rudan I,
Salomaa V,
Saxena R,
Schlessinger D,
Schunkert H,
Schwarz P,
Seedorf U,
Selvin E,
Serrano-Ríos M,
Shrader P,
Silveira A,
Siscovick D,
Song K,
Spector TD,
Stefansson K,
Steinthorsdottir V,
Strachan DP,
Strawbridge R,
Stumvoll M,
Surakka I,
Swift AJ,
Tanaka T,
Teumer A,
Thorleifsson G,
Thorsteinsdottir U,
Tönjes A,
Usala G,
Vitart V,
Völzke H,
Wallaschofski H,
Waterworth DM,
Watkins H,
Wichmann HE,
Wild SH,
Willemsen G,
Williams GH,
Wilson JF,
Winkelmann J,
Wright AF,
Zabena C,
Zhao JH,
Epstein SE,
Erdmann J,
Hakonarson HH,
Kathiresan S,
Khaw KT,
Roberts R,
Samani NJ,
Fleming MD,
Sladek R,
Abecasis G,
Boehnke M,
Froguel P,
Groop L,
McCarthy MI,
Kao WH,
Florez JC,
Uda M,
Wareham NJ,
Barroso I,
Meigs JB
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure
Rämö JT,
Kiiskinen T,
Seist R,
Krebs K,
Kanai M,
Karjalainen J,
Kurki M,
Hämäläinen E,
Häppölä P,
Havulinna AS,
Hautakangas H,
Mägi R
and 11 more — show all
Palta P,
Esko T,
Metspalu A,
Pirinen M,
Karczewski KJ,
Ripatti S,
Milani L,
Stankovic KM,
Mäkitie A,
Daly MJ,
Palotie A
FinnGen
Nature communications · 2023 · PMID 36653343 · open access
5 pages
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Brito Nunes C,
Rukins V,
Cisse AH,
White F,
McBride N,
Kuang A,
Allard C,
Ronkainen J,
Hughes A,
Elliott A,
Thorleifsson G,
Vaudel M
and 67 more — show all
Laisk T,
Gu Y,
Lamri A,
Chen L,
Tuhkanen J,
Lahti J,
Calas L,
Muntaner M,
Karhunen V,
Choi J,
Heiskala A,
Hatem G,
Fragoso-Bargas N,
Rifas-Shiman SL,
Paz-Lopez G,
Stinson SE,
Bhowmik B,
Ahlqvist E,
Deleuze JF,
Eriksson JG,
Park J,
Teo K,
Räikkönen K,
Stefansson K,
Molina-Vega M,
Subbarao P,
Beaumont RN,
Johansson S,
Tuomi T,
Hansen T,
Engelbrechtsen L,
Morcillo S,
Oken E,
Quigstad E,
Birkeland KI,
Vääräsmäki M,
Hattersley AT,
Sebert S,
Hitman GA,
Kwak SH,
Järvelin MR,
Prasad RB,
Heude B,
Meirhaeghe A,
Bouchard L,
Jacques PÉ,
Laivuori H,
Tan KH,
Anand SS,
van Heel DA,
Liu S,
Njølstad PR,
Steinthorsdottir V,
Widén E,
Keikkala E,
Scholtens DM,
Lowe WL,
Finer S,
Morris AP,
Mägi R,
Zöllner J,
Borges MC,
Lawlor DA,
Hivert MF,
Freathy RM,
Evans DM,
Moen GH
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2026 · PMID 42225636 · open access
5 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
New loci associated with kidney function and chronic kidney disease
Köttgen A,
Pattaro C,
Böger CA,
Fuchsberger C,
Olden M,
Glazer NL,
Parsa A,
Gao X,
Yang Q,
Smith AV,
O'Connell JR,
Li M
and 120 more — show all
Schmidt H,
Tanaka T,
Isaacs A,
Ketkar S,
Hwang SJ,
Johnson AD,
Dehghan A,
Teumer A,
Paré G,
Atkinson EJ,
Zeller T,
Lohman K,
Cornelis MC,
Probst-Hensch NM,
Kronenberg F,
Tönjes A,
Hayward C,
Aspelund T,
Eiriksdottir G,
Launer LJ,
Harris TB,
Rampersaud E,
Mitchell BD,
Arking DE,
Boerwinkle E,
Struchalin M,
Cavalieri M,
Singleton A,
Giallauria F,
Metter J,
de Boer IH,
Haritunians T,
Lumley T,
Siscovick D,
Psaty BM,
Zillikens MC,
Oostra BA,
Feitosa M,
Province M,
de Andrade M,
Turner ST,
Schillert A,
Ziegler A,
Wild PS,
Schnabel RB,
Wilde S,
Munzel TF,
Leak TS,
Illig T,
Klopp N,
Meisinger C,
Wichmann HE,
Koenig W,
Zgaga L,
Zemunik T,
Kolcic I,
Minelli C,
Hu FB,
Johansson A,
Igl W,
Zaboli G,
Wild SH,
Wright AF,
Campbell H,
Ellinghaus D,
Schreiber S,
Aulchenko YS,
Felix JF,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
Imboden M,
Nitsch D,
Brandstätter A,
Kollerits B,
Kedenko L,
Mägi R,
Stumvoll M,
Kovacs P,
Boban M,
Campbell S,
Endlich K,
Völzke H,
Kroemer HK,
Nauck M,
Völker U,
Polasek O,
Vitart V,
Badola S,
Parker AN,
Ridker PM,
Kardia SL,
Blankenberg S,
Liu Y,
Curhan GC,
Franke A,
Rochat T,
Paulweber B,
Prokopenko I,
Wang W,
Gudnason V,
Shuldiner AR,
Coresh J,
Schmidt R,
Ferrucci L,
Shlipak MG,
van Duijn CM,
Borecki I,
Krämer BK,
Rudan I,
Gyllensten U,
Wilson JF,
Witteman JC,
Pramstaller PP,
Rettig R,
Hastie N,
Chasman DI,
Kao WH,
Heid IM,
Fox CS
Nature genetics · 2010 · PMID 20383146
4 pages
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies
Tamm R,
Mägi R,
Tremmel R,
Winter S,
Mihailov E,
Smid A,
Möricke A,
Klein K,
Schrappe M,
Stanulla M,
Houlston R,
Weinshilboum R
and 5 more — show all
Clinical pharmacology and therapeutics · 2017 · PMID 27770449
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
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
de las Fuentes L,
Sung YJ,
Noordam R,
Winkler T,
Feitosa MF,
Schwander K,
Bentley AR,
Brown MR,
Guo X,
Manning A,
Chasman DI,
Aschard H
and 211 more — show all
Bartz TM,
Bielak LF,
Campbell A,
Cheng CY,
Dorajoo R,
Hartwig FP,
Horimoto ARVR,
Li C,
Li-Gao R,
Liu Y,
Marten J,
Musani SK,
Ntalla I,
Rankinen T,
Richard M,
Sim X,
Smith AV,
Tajuddin SM,
Tayo BO,
Vojinovic D,
Warren HR,
Xuan D,
Alver M,
Boissel M,
Chai JF,
Chen X,
Christensen K,
Divers J,
Evangelou E,
Gao C,
Girotto G,
Harris SE,
He M,
Hsu FC,
Kühnel B,
Laguzzi F,
Li X,
Lyytikäinen LP,
Nolte IM,
Poveda A,
Rauramaa R,
Riaz M,
Rueedi R,
Shu XO,
Snieder H,
Sofer T,
Takeuchi F,
Verweij N,
Ware EB,
Weiss S,
Yanek LR,
Amin N,
Arking DE,
Arnett DK,
Bergmann S,
Boerwinkle E,
Brody JA,
Broeckel U,
Brumat M,
Burke G,
Cabrera CP,
Canouil M,
Chee ML,
Chen YI,
Cocca M,
Connell J,
de Silva HJ,
de Vries PS,
Eiriksdottir G,
Faul JD,
Fisher V,
Forrester T,
Fox EF,
Friedlander Y,
Gao H,
Gigante B,
Giulianini F,
Gu CC,
Gu D,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hunt S,
Ikram MA,
Irvin MR,
Kähönen M,
Kavousi M,
Khor CC,
Kilpeläinen TO,
Koh WP,
Komulainen P,
Kraja AT,
Krieger JE,
Langefeld CD,
Li Y,
Liang J,
Liewald DCM,
Liu CT,
Liu J,
Lohman KK,
Mägi R,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mook-Kanamori DO,
Nalls MA,
Nelson CP,
Norris JM,
O'Connell J,
Ogunniyi A,
Padmanabhan S,
Palmer ND,
Pedersen NL,
Perls T,
Peters A,
Petersmann A,
Peyser PA,
Polasek O,
Porteous DJ,
Raffel LJ,
Rice TK,
Rotter JI,
Rudan I,
Rueda-Ochoa OL,
Sabanayagam C,
Salako BL,
Schreiner PJ,
Shikany JM,
Sidney SS,
Sims M,
Sitlani CM,
Smith JA,
Starr JM,
Strauch K,
Swertz MA,
Teumer A,
Tham YC,
Uitterlinden AG,
Vaidya D,
van der Ende MY,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Weir DR,
Wen W,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zhao W,
Zonderman AB,
Becker DM,
Bowden DW,
Deary IJ,
Dörr M,
Esko T,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Jonas JB,
Kammerer CM,
Kato N,
Lakka TA,
Leander K,
Lehtimäki T,
Magnusson PKE,
Marques-Vidal P,
Penninx BWJH,
Samani NJ,
van der Harst P,
Wagenknecht LE,
Wu T,
Zheng W,
Zhu X,
Bouchard C,
Cooper RS,
Correa A,
Evans MK,
Gudnason V,
Hayward C,
Horta BL,
Kelly TN,
Kritchevsky SB,
Levy D,
Palmas WR,
Pereira AC,
Province MM,
Psaty BM,
Ridker PM,
Rotimi CN,
Tai ES,
van Dam RM,
van Duijn CM,
Wong TY,
Rice K,
Gauderman WJ,
Morrison AC,
North KE,
Kardia SLR,
Caulfield MJ,
Elliott P,
Munroe PB,
Franks PW,
Rao DC,
Fornage M
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer
Koel M,
Võsa U,
Jõeloo M,
Läll K,
Gualdo NP,
Laivuori H,
Lemmelä S,
Daly M,
Palta P,
Mägi R,
Laisk T
Estonian Biobank Research Team; FinnGen
Human molecular genetics · 2023 · PMID 36929174 · 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
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
and 290 more — show all
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
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
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Joshi PK,
Pirastu N,
Kentistou KA,
Fischer K,
Hofer E,
Schraut KE,
Clark DW,
Nutile T,
Barnes CLK,
Timmers PRHJ,
Shen X,
Gandin I
and 101 more — show all
McDaid AF,
Hansen TF,
Gordon SD,
Giulianini F,
Boutin TS,
Abdellaoui A,
Zhao W,
Medina-Gomez C,
Bartz TM,
Trompet S,
Lange LA,
Raffield L,
van der Spek A,
Galesloot TE,
Proitsi P,
Yanek LR,
Bielak LF,
Payton A,
Murgia F,
Concas MP,
Biino G,
Tajuddin SM,
Seppälä I,
Amin N,
Boerwinkle E,
Børglum AD,
Campbell A,
Demerath EW,
Demuth I,
Faul JD,
Ford I,
Gialluisi A,
Gögele M,
Graff M,
Hingorani A,
Hottenga JJ,
Hougaard DM,
Hurme MA,
Ikram MA,
Jylhä M,
Kuh D,
Ligthart L,
Lill CM,
Lindenberger U,
Lumley T,
Mägi R,
Marques-Vidal P,
Medland SE,
Milani L,
Nagy R,
Ollier WER,
Peyser PA,
Pramstaller PP,
Ridker PM,
Rivadeneira F,
Ruggiero D,
Saba Y,
Schmidt R,
Schmidt H,
Slagboom PE,
Smith BH,
Smith JA,
Sotoodehnia N,
Steinhagen-Thiessen E,
van Rooij FJA,
Verbeek AL,
Vermeulen SH,
Vollenweider P,
Wang Y,
Werge T,
Whitfield JB,
Zonderman AB,
Lehtimäki T,
Evans MK,
Pirastu M,
Fuchsberger C,
Bertram L,
Pendleton N,
Kardia SLR,
Ciullo M,
Becker DM,
Wong A,
Psaty BM,
van Duijn CM,
Wilson JG,
Jukema JW,
Kiemeney L,
Uitterlinden AG,
Franceschini N,
North KE,
Weir DR,
Metspalu A,
Boomsma DI,
Hayward C,
Chasman D,
Martin NG,
Sattar N,
Campbell H,
Esko T,
Kutalik Z,
Wilson JF
Nature communications · 2017 · PMID 29030599 · open access
3 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
Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis
Sliz E,
Huilaja L,
Pasanen A,
Laisk T,
Reimann E,
Mägi R,
Hannula-Jouppi K,
Peltonen S,
Salmi T,
Koulu L,
Tasanen K,
Kettunen J
FinnGen · Estonian Biobank Research Team
The Journal of allergy and clinical immunology · 2022 · PMID 34454985
3 pages
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Noordam R,
Wang W,
Nagarajan P,
Wang H,
Brown MR,
Bentley AR,
Hui Q,
Kraja AT,
Morrison JL,
O'Connel JR,
Lee S,
Schwander K
and 137 more — show all
Bartz TM,
de Las Fuentes L,
Feitosa MF,
Guo X,
Hanfei X,
Harris SE,
Huang Z,
Kals M,
Lefevre C,
Mangino M,
Milaneschi Y,
van der Most PJ,
Pacheco NL,
Palmer ND,
Rao V,
Rauramaa R,
Sun Q,
Tabara Y,
Vojinovic D,
Wang Y,
Weiss S,
Yang Q,
Zhao W,
Zhu W,
Ansari MAY,
Aschard H,
Anugu P,
Assimes TL,
Attia J,
Baker LD,
Ballantyne C,
Bazzano L,
Boerwinkle E,
Cade B,
Chen HH,
Chen W,
Ida Chen YD,
Chen Z,
Cho K,
De Anda-Duran I,
Dimitrov L,
Do A,
Edwards T,
Faquih T,
Hingorani A,
Fisher-Hoch SP,
Gaziano JM,
Gharib SA,
Giri A,
Ghanbari M,
Grabe HJ,
Graff M,
Charles Gu C,
He J,
Heikkinen S,
Hixson J,
Ho YL,
Hood MM,
Houghton SC,
Karvonen-Gutierrez CA,
Kawaguchi T,
Kilpeläinen TO,
Komulainen P,
Lin HJ,
Linchangco GV Jr,
Luik AI,
Ma J,
Meigs JB,
McCormick JB,
Menni C,
Nolte IM,
Norris JM,
Petty LE,
Polikowsky HG,
Raffield LM,
Rich SS,
Riha RL,
Russ TC,
Ruiz-Narvaez EA,
Sitlani CM,
Smith JA,
Snieder H,
Sofer T,
Shen B,
Tang J,
Taylor KD,
Teder-Laving M,
Triatin R,
Tsai MY,
Völzke H,
Westerman KE,
Xia R,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Zhu X,
Below JE,
Cox SR,
Evans M,
Fornage M,
Fox ER,
Franceschini N,
Harlow SD,
Holliday E,
Ikram MA,
Kelly T,
Lakka TA,
Lawlor DA,
Li C,
Liu CT,
Mägi R,
Manning AK,
Matsuda F,
Morrison AC,
Nauck M,
North KE,
Penninx BW,
Province MA,
Psaty BM,
Rotter JI,
Spector TD,
Wagenknecht LE,
van Dijk KW,
Jaquish CE,
Wilson PW,
Peyser PA,
Munroe PB,
de Vries PS,
Gauderman WJ,
Sun YV,
Chen H,
Miller CL,
Winkler TW,
Rao DC,
Redline S,
van Heemst D
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
A central role for GRB10 in regulation of islet function in man
Prokopenko I,
Poon W,
Mägi R,
Prasad B R,
Salehi SA,
Almgren P,
Osmark P,
Bouatia-Naji N,
Wierup N,
Fall T,
Stančáková A,
Barker A
and 53 more — show all
Lagou V,
Osmond C,
Xie W,
Lahti J,
Jackson AU,
Cheng YC,
Liu J,
O'Connell JR,
Blomstedt PA,
Fadista J,
Fadista J,
Alkayyali S,
Dayeh T,
Ahlqvist E,
Taneera J,
Lecoeur C,
Kumar A,
Hansson O,
Hansson K,
Voight BF,
Kang HM,
Levy-Marchal C,
Vatin V,
Palotie A,
Syvänen AC,
Mari A,
Weedon MN,
Loos RJ,
Ong KK,
Nilsson P,
Isomaa B,
Tuomi T,
Wareham NJ,
Stumvoll M,
Widen E,
Lakka TA,
Langenberg C,
Tönjes A,
Rauramaa R,
Kuusisto J,
Frayling TM,
Froguel P,
Walker M,
Eriksson JG,
Ling C,
Kovacs P,
Ingelsson E,
McCarthy MI,
Shuldiner AR,
Silver KD,
Laakso M,
Groop L,
Lyssenko V
PLoS genetics · 2014 · PMID 24699409 · 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.