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showing the first 7.
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
Scott LJ,
Mägi R,
Marullo L,
Gaulton KJ,
Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
Eicher JD,
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,
Mӓnnistö S,
Peltonen L,
Tikkanen E,
Charpentier G,
Eury E,
Lobbens S,
Gigante B,
Leander K,
McLeod O,
Bottinger EP,
Gottesman O,
Ruderfer D,
Blüher M,
Kovacs P,
Tonjes A,
Maruthur NM,
Scapoli C,
Erbel R,
Jöckel KH,
Moebus S,
de Faire U,
Hamsten A,
Stumvoll M,
Deloukas P,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Ripatti S,
Salomaa V,
Pedersen NL,
Boehm BO,
Bergman RN,
Collins FS,
Mohlke KL,
Tuomilehto J,
Hansen T,
Pedersen O,
Barroso I,
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,
Groop LC,
Langenberg C,
Wareham NJ,
Sijbrands E,
van Duijn CM,
Florez JC,
Meigs JB,
Boerwinkle E,
Gieger C,
Strauch K,
Metspalu A,
Morris AD,
Palmer CNA,
Hu FB,
Thorsteinsdottir U,
Stefansson K,
Dupuis J,
Morris AP,
Boehnke M,
McCarthy MI,
Prokopenko I
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Beaumont RN,
Warrington NM,
Cavadino A,
Tyrrell J,
Nodzenski M,
Horikoshi M,
Geller F,
Myhre R,
Richmond RC,
Paternoster L,
Bradfield JP,
Kreiner-Møller E
and 74 more — show all
Huikari V,
Metrustry S,
Lunetta KL,
Painter JN,
Hottenga JJ,
Allard C,
Barton SJ,
Espinosa A,
Marsh JA,
Potter C,
Zhang G,
Ang W,
Berry DJ,
Bouchard L,
Das S,
Hakonarson H,
Heikkinen J,
Helgeland Ø,
Hocher B,
Hofman A,
Inskip HM,
Jones SE,
Kogevinas M,
Lind PA,
Marullo L,
Medland SE,
Murray A,
Murray JC,
Njølstad PR,
Nohr EA,
Reichetzeder C,
Ring SM,
Ruth KS,
Santa-Marina L,
Scholtens DM,
Sebert S,
Sengpiel V,
Tuke MA,
Vaudel M,
Weedon MN,
Willemsen G,
Wood AR,
Yaghootkar H,
Muglia LJ,
Bartels M,
Relton CL,
Pennell CE,
Chatzi L,
Estivill X,
Holloway JW,
Boomsma DI,
Montgomery GW,
Murabito JM,
Spector TD,
Power C,
Järvelin MR,
Bisgaard H,
Grant SFA,
Sørensen TIA,
Jaddoe VW,
Jacobsson B,
Melbye M,
McCarthy MI,
Hattersley AT,
Hayes MG,
Frayling TM,
Hivert MF,
Felix JF,
Hyppönen E,
Lowe WL Jr,
Evans DM,
Lawlor DA,
Feenstra B,
Freathy RM
Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
1 page
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
and 290 more — show all
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Cooper RS,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
Kooner JS,
Laakso M,
Laurie CC,
Lee IT,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
Rauramaa R,
Redline S,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang JS,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Franceschini N,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Rice K,
Munroe PB,
Morrison AC,
Rao DC,
Rotimi CN,
Cupples LA
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Deelen J,
Evans DS,
Arking DE,
Tesi N,
Nygaard M,
Liu X,
Wojczynski MK,
Biggs ML,
van der Spek A,
Atzmon G,
Ware EB,
Sarnowski C
and 72 more — show all
Smith AV,
Seppälä I,
Cordell HJ,
Dose J,
Amin N,
Arnold AM,
Ayers KL,
Barzilai N,
Becker EJ,
Beekman M,
Blanché H,
Christensen K,
Christiansen L,
Collerton JC,
Cubaynes S,
Cummings SR,
Davies K,
Debrabant B,
Deleuze JF,
Duncan R,
Faul JD,
Franceschi C,
Galan P,
Gudnason V,
Harris TB,
Huisman M,
Hurme MA,
Jagger C,
Jansen I,
Jylhä M,
Kähönen M,
Karasik D,
Kardia SLR,
Kingston A,
Kirkwood TBL,
Launer LJ,
Lehtimäki T,
Lieb W,
Lyytikäinen LP,
Martin-Ruiz C,
Min J,
Nebel A,
Newman AB,
Nie C,
Nohr EA,
Orwoll ES,
Perls TT,
Province MA,
Psaty BM,
Raitakari OT,
Reinders MJT,
Robine JM,
Rotter JI,
Sebastiani P,
Smith J,
Sørensen TIA,
Taylor KD,
Uitterlinden AG,
van der Flier W,
van der Lee SJ,
van Duijn CM,
van Heemst D,
Vaupel JW,
Weir D,
Ye K,
Zeng Y,
Zheng W,
Holstege H,
Kiel DP,
Lunetta KL,
Slagboom PE,
Murabito JM
Nature communications · 2019 · PMID 31413261 · open access
1 page
Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
Sarnowski C,
Chen H,
Biggs ML,
Wassertheil-Smoller S,
Bressler J,
Irvin MR,
Ryan KA,
Karasik D,
Arnett DK,
Cupples LA,
Fardo DW,
Gogarten SM
and 16 more — show all
Heavner BD,
Jain D,
Kang HM,
Kooperberg C,
Mainous AG,
Mitchell BD,
Morrison AC,
O'Connell JR,
Psaty BM,
Rice K,
Smith AV,
Vasan RS,
Windham BG,
Kiel DP,
Murabito JM,
Lunetta KL
TOPMed Longevity and Healthy Aging Working Group · from the NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
PloS one · 2021 · PMID 34214102 · open access
1 page
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
Williamson A,
Norris DM,
Yin X,
Broadaway KA,
Moxley AH,
Vadlamudi S,
Wilson EP,
Jackson AU,
Ahuja V,
Andersen MK,
Arzumanyan Z,
Bonnycastle LL
and 103 more — show all
Bornstein SR,
Bretschneider MP,
Buchanan TA,
Chang YC,
Chuang LM,
Chung RH,
Clausen TD,
Damm P,
Delgado GE,
de Mello VD,
Dupuis J,
Dwivedi OP,
Erdos MR,
Fernandes Silva L,
Frayling TM,
Gieger C,
Goodarzi MO,
Guo X,
Gustafsson S,
Hakaste L,
Hammar U,
Hatem G,
Herrmann S,
Højlund K,
Horn K,
Hsueh WA,
Hung YJ,
Hwu CM,
Jonsson A,
Kårhus LL,
Kleber ME,
Kovacs P,
Lakka TA,
Lauzon M,
Lee IT,
Lindgren CM,
Lindström J,
Linneberg A,
Liu CT,
Luan J,
Aly DM,
Mathiesen E,
Moissl AP,
Morris AP,
Narisu N,
Perakakis N,
Peters A,
Prasad RB,
Rodionov RN,
Roll K,
Rundsten CF,
Sarnowski C,
Savonen K,
Scholz M,
Sharma S,
Stinson SE,
Suleman S,
Tan J,
Taylor KD,
Uusitupa M,
Vistisen D,
Witte DR,
Walther R,
Wu P,
Xiang AH,
Zethelius B,
Ahlqvist E,
Bergman RN,
Chen YI,
Collins FS,
Fall T,
Florez JC,
Fritsche A,
Grallert H,
Groop L,
Hansen T,
Koistinen HA,
Komulainen P,
Laakso M,
Lind L,
Loeffler M,
März W,
Meigs JB,
Raffel LJ,
Rauramaa R,
Rotter JI,
Schwarz PEH,
Stumvoll M,
Sundström J,
Tönjes A,
Tuomi T,
Tuomilehto J,
Wagner R,
Barroso I,
Walker M,
Grarup N,
Boehnke M,
Wareham NJ,
Mohlke KL,
Wheeler E,
O'Rahilly S,
Fazakerley DJ,
Langenberg C
Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37291194 · open access
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
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.