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25 matches for
Goodarzi MO,
showing the first 5.
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3
Kaplan RC,
Petersen AK,
Chen MH,
Teumer A,
Glazer NL,
Döring A,
Lam CS,
Friedrich N,
Newman A,
Müller M,
Yang Q,
Homuth G
and 25 more — show all
Cappola A,
Klopp N,
Smith H,
Ernst F,
Psaty BM,
Wichmann HE,
Sawyer DB,
Biffar R,
Rotter JI,
Gieger C,
Sullivan LS,
Völzke H,
Rice K,
Spyroglou A,
Kroemer HK,
Ida Chen YD,
Manolopoulou J,
Nauck M,
Strickler HD,
Goodarzi MO,
Reincke M,
Pollak MN,
Bidlingmaier M,
Vasan RS,
Wallaschofski H
Human molecular genetics · 2011 · PMID 21216879
1 page
A genome-wide association search for type 2 diabetes genes in African Americans
Palmer ND,
McDonough CW,
Hicks PJ,
Roh BH,
Wing MR,
An SS,
Hester JM,
Cooke JN,
Bostrom MA,
Rudock ME,
Talbert ME,
Lewis JP
and 379 more — show all
Ferrara A,
Lu L,
Ziegler JT,
Sale MM,
Divers J,
Shriner D,
Adeyemo A,
Rotimi CN,
Ng MC,
Langefeld CD,
Freedman BI,
Bowden DW,
Voight BF,
Scott LJ,
Steinthorsdottir V,
Morris AP,
Dina C,
Welch RP,
Zeggini E,
Huth C,
Aulchenko YS,
Thorleifsson G,
McCulloch LJ,
Ferreira T,
Grallert H,
Amin N,
Wu G,
Willer CJ,
Raychaudhuri S,
McCarroll SA,
Langenberg C,
Hofmann OM,
Dupuis J,
Qi L,
Segrè AV,
van Hoek M,
Navarro P,
Ardlie K,
Balkau B,
Benediktsson R,
Bennett AJ,
Blagieva R,
Boerwinkle E,
Bonnycastle LL,
Boström KB,
Bravenboer B,
Bumpstead S,
Burtt NP,
Charpentier G,
Chines PS,
Cornelis M,
Couper DJ,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
Gieger C,
Grarup N,
Green T,
Griffin S,
Groves CJ,
Guiducci C,
Hadjadj S,
Hassanali N,
Herder C,
Isomaa B,
Jackson AU,
Johnson PR,
Jørgensen T,
Kao WH,
Klopp N,
Kong A,
Kraft P,
Kuusisto J,
Lauritzen T,
Li M,
Lieverse A,
Lindgren CM,
Lyssenko V,
Marre M,
Meitinger T,
Midthjell K,
Morken MA,
Narisu N,
Nilsson P,
Owen KR,
Payne F,
Perry JR,
Petersen AK,
Platou C,
Proença C,
Prokopenko I,
Rathmann W,
Rayner NW,
Robertson NR,
Rocheleau G,
Roden M,
Sampson MJ,
Saxena R,
Shields BM,
Shrader P,
Sigurdsson G,
Sparsø T,
Strassburger K,
Stringham HM,
Sun Q,
Swift AJ,
Thorand B,
Tichet J,
Tuomi T,
van Dam RM,
van Haeften TW,
van Herpt T,
van Vliet-Ostaptchouk JV,
Walters GB,
Weedon MN,
Wijmenga C,
Witteman J,
Bergman RN,
Cauchi S,
Collins FS,
Gloyn AL,
Gyllensten U,
Hansen T,
Hide WA,
Hitman GA,
Hofman A,
Hunter DJ,
Hveem K,
Laakso M,
Mohlke KL,
Morris AD,
Palmer CN,
Pramstaller PP,
Rudan I,
Sijbrands E,
Stein LD,
Tuomilehto J,
Uitterlinden A,
Walker M,
Wareham NJ,
Watanabe RM,
Abecasis GR,
Boehm BO,
Campbell H,
Daly MJ,
Hattersley AT,
Hu FB,
Meigs JB,
Pankow JS,
Pedersen O,
Wichmann HE,
Barroso I,
Florez JC,
Frayling TM,
Groop L,
Sladek R,
Thorsteinsdottir U,
Wilson JF,
Illig T,
Froguel P,
van Duijn CM,
Stefansson K,
Altshuler D,
Boehnke M,
McCarthy MI,
Soranzo N,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Mägi R,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Henneman P,
Dehghan A,
Hottenga JJ,
Song K,
Goel A,
Egan JM,
Lajunen T,
Doney A,
Kanoni S,
Cavalcanti-Proença C,
Kumari M,
Timpson NJ,
Zabena C,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ariyurek Y,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Bergmann S,
Bochud M,
Bonnefond A,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Frants R,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Grundy S,
Gwilliam R,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hayward C,
Heath SC,
Hercberg S,
Hicks AA,
Hillman DR,
Hingorani AD,
Hui J,
Hung J,
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,
Mahley R,
Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Mukherjee S,
Naitza S,
Neville MJ,
Oostra BA,
Orrù M,
Pakyz R,
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,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Seedorf U,
Sharp SJ,
Shields B,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tanaka T,
Tönjes A,
Uitterlinden AG,
van Dijk KW,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Ward KL,
Watkins H,
Wild SH,
Willemsen G,
Willemsen G,
Witteman JC,
Yarnell JW,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Loos RJ,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Silander K,
Salomaa V,
Smith GD,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Dedoussis GV,
Serrano-Ríos M,
Lind L,
Palmer LJ,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pramstaller PP,
Wright AF,
Stumvoll M,
Hamsten A,
Buchanan TA,
Valle TT,
Rotter JI,
Siscovick DS,
Penninx BW,
Boomsma DI,
Deloukas P,
Spector TD,
Ferrucci L,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Waterworth DM,
Vollenweider P,
Peltonen L,
Mooser V,
Sladek R
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations
Hayes MG,
Urbanek M,
Ehrmann DA,
Armstrong LL,
Lee JY,
Sisk R,
Karaderi T,
Barber TM,
McCarthy MI,
Franks S,
Lindgren CM,
Welt CK
and 11 more — show all
Diamanti-Kandarakis E,
Panidis D,
Goodarzi MO,
Azziz R,
Zhang Y,
James RG,
Olivier M,
Kissebah AH,
Stener-Victorin E,
Legro RS,
Dunaif A
Reproductive Medicine Network
Nature communications · 2015 · PMID 26284813 · 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
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Burns K,
Mullin BH,
Moolhuijsen LME,
Laisk T,
Tyrmi JS,
Cui J,
Actkins KV,
Louwers YV,
Davis LK,
Dudbridge F,
Azziz R,
Goodarzi MO
and 7 more — show all
Estonian Biobank Research Team · FinnGen and 1 more consortia
BMC genomics · 2024 · PMID 38408933 · open access
1 page
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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.