For researchers
Is your paper here?
2,675 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.
145 matches for
Thorsteinsdottir U,
showing the first 20.
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Jones GT,
Tromp G,
Kuivaniemi H,
Gretarsdottir S,
Baas AF,
Giusti B,
Strauss E,
Van't Hof FN,
Webb TR,
Erdman R,
Ritchie MD,
Elmore JR
and 105 more — show all
Verma A,
Pendergrass S,
Kullo IJ,
Ye Z,
Peissig PL,
Gottesman O,
Verma SS,
Malinowski J,
Rasmussen-Torvik LJ,
Borthwick KM,
Smelser DT,
Crosslin DR,
de Andrade M,
Ryer EJ,
McCarty CA,
Böttinger EP,
Pacheco JA,
Crawford DC,
Carrell DS,
Gerhard GS,
Franklin DP,
Carey DJ,
Phillips VL,
Williams MJ,
Wei W,
Blair R,
Hill AA,
Vasudevan TM,
Lewis DR,
Thomson IA,
Krysa J,
Hill GB,
Roake J,
Merriman TR,
Oszkinis G,
Galora S,
Saracini C,
Abbate R,
Pulli R,
Pratesi C,
Saratzis A,
Verissimo AR,
Bumpstead S,
Badger SA,
Clough RE,
Cockerill G,
Hafez H,
Scott DJ,
Futers TS,
Romaine SP,
Bridge K,
Griffin KJ,
Bailey MA,
Smith A,
Thompson MM,
van Bockxmeer FM,
Matthiasson SE,
Thorleifsson G,
Thorsteinsdottir U,
Blankensteijn JD,
Teijink JA,
Wijmenga C,
de Graaf J,
Kiemeney LA,
Lindholt JS,
Hughes A,
Bradley DT,
Stirrups K,
Golledge J,
Norman PE,
Powell JT,
Humphries SE,
Hamby SE,
Goodall AH,
Nelson CP,
Sakalihasan N,
Courtois A,
Ferrell RE,
Eriksson P,
Folkersen L,
Franco-Cereceda A,
Eicher JD,
Johnson AD,
Betsholtz C,
Ruusalepp A,
Franzén O,
Schadt EE,
Björkegren JL,
Lipovich L,
Drolet AM,
Verhoeven EL,
Zeebregts CJ,
Geelkerken RH,
van Sambeek MR,
van Sterkenburg SM,
de Vries JP,
Stefansson K,
Thompson JR,
de Bakker PI,
Deloukas P,
Sayers RD,
Harrison SC,
van Rij AM,
Samani NJ,
Bown MJ
Circulation research · 2017 · PMID 27899403 · open access
3 pages
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming
Gisladottir RS,
Ivarsdottir EV,
Helgason A,
Jonsson L,
Hannesdottir NK,
Rutsdottir G,
Arnadottir GA,
Skuladottir A,
Jonsson BA,
Norddahl GL,
Ulfarsson MO,
Helgason H
and 16 more — show all
Halldorsson BV,
Nawaz MS,
Tragante V,
Sveinbjornsson G,
Thorgeirsson T,
Oddsson A,
Kristjansson RP,
Bjornsdottir G,
Thorgeirsson G,
Jonsdottir I,
Holm H,
Gudbjartsson DF,
Thorsteinsdottir U,
Stefansson H,
Sulem P,
Stefansson K
Current biology : CB · 2020 · PMID 33035477
3 pages
Variants conferring risk of atrial fibrillation on chromosome 4q25
Gudbjartsson DF,
Arnar DO,
Helgadottir A,
Gretarsdottir S,
Holm H,
Sigurdsson A,
Jonasdottir A,
Baker A,
Thorleifsson G,
Kristjansson K,
Palsson A,
Blondal T
and 28 more — show all
Sulem P,
Backman VM,
Hardarson GA,
Palsdottir E,
Helgason A,
Sigurjonsdottir R,
Sverrisson JT,
Kostulas K,
Ng MC,
Baum L,
So WY,
Wong KS,
Chan JC,
Furie KL,
Greenberg SM,
Sale M,
Kelly P,
MacRae CA,
Smith EE,
Rosand J,
Hillert J,
Ma RC,
Ellinor PT,
Thorgeirsson G,
Gulcher JR,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature · 2007 · PMID 17603472
2 pages
Multiple genetic loci for bone mineral density and fractures
Styrkarsdottir U,
Halldorsson BV,
Gretarsdottir S,
Gudbjartsson DF,
Walters GB,
Ingvarsson T,
Jonsdottir T,
Saemundsdottir J,
Center JR,
Nguyen TV,
Bagger Y,
Gulcher JR
and 6 more — show all
The New England journal of medicine · 2008 · PMID 18445777
2 pages
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Thorleifsson G,
Walters GB,
Gudbjartsson DF,
Steinthorsdottir V,
Sulem P,
Helgadottir A,
Styrkarsdottir U,
Gretarsdottir S,
Thorlacius S,
Jonsdottir I,
Jonsdottir T,
Olafsdottir EJ
and 23 more — show all
Olafsdottir GH,
Jonsson T,
Jonsson F,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Lauritzen T,
Aben KK,
Verbeek AL,
Roeleveld N,
Kampman E,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Becker DM,
Gulcher J,
Kiemeney LA,
Pedersen O,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19079260
2 pages
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Gudbjartsson DF,
Bjornsdottir US,
Halapi E,
Helgadottir A,
Sulem P,
Jonsdottir GM,
Thorleifsson G,
Helgadottir H,
Steinthorsdottir V,
Stefansson H,
Williams C,
Hui J
and 61 more — show all
Beilby J,
Warrington NM,
James A,
Palmer LJ,
Koppelman GH,
Heinzmann A,
Krueger M,
Boezen HM,
Wheatley A,
Altmuller J,
Shin HD,
Uh ST,
Cheong HS,
Jonsdottir B,
Gislason D,
Park CS,
Rasmussen LM,
Porsbjerg C,
Hansen JW,
Backer V,
Werge T,
Janson C,
Jönsson UB,
Ng MC,
Chan J,
So WY,
Ma R,
Shah SH,
Granger CB,
Quyyumi AA,
Levey AI,
Vaccarino V,
Reilly MP,
Rader DJ,
Williams MJ,
van Rij AM,
Jones GT,
Trabetti E,
Malerba G,
Pignatti PF,
Boner A,
Pescollderungg L,
Girelli D,
Olivieri O,
Martinelli N,
Ludviksson BR,
Ludviksdottir D,
Eyjolfsson GI,
Arnar D,
Thorgeirsson G,
Deichmann K,
Thompson PJ,
Wjst M,
Hall IP,
Postma DS,
Gislason T,
Gulcher J,
Kong A,
Jonsdottir I,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19198610
2 pages
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Jonasson JG,
Sigurdsson A,
Bergthorsson JT,
He H,
Blondal T,
Geller F,
Jakobsdottir M,
Magnusdottir DN,
Matthiasdottir S
and 26 more — show all
Stacey SN,
Skarphedinsson OB,
Helgadottir H,
Li W,
Nagy R,
Aguillo E,
Faure E,
Prats E,
Saez B,
Martinez M,
Eyjolfsson GI,
Bjornsdottir US,
Holm H,
Kristjansson K,
Frigge ML,
Kristvinsson H,
Gulcher JR,
Jonsson T,
Rafnar T,
Hjartarsson H,
Mayordomo JI,
de la Chapelle A,
Hrafnkelsson J,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature genetics · 2009 · PMID 19198613
2 pages
Common variants conferring risk of schizophrenia
Stefansson H,
Ophoff RA,
Steinberg S,
Andreassen OA,
Cichon S,
Rujescu D,
Werge T,
Pietiläinen OP,
Mors O,
Mortensen PB,
Sigurdsson E,
Gustafsson O
and 75 more — show all
Nyegaard M,
Tuulio-Henriksson A,
Ingason A,
Hansen T,
Suvisaari J,
Lonnqvist J,
Paunio T,
Børglum AD,
Hartmann A,
Fink-Jensen A,
Nordentoft M,
Hougaard D,
Norgaard-Pedersen B,
Böttcher Y,
Olesen J,
Breuer R,
Möller HJ,
Giegling I,
Rasmussen HB,
Timm S,
Mattheisen M,
Bitter I,
Réthelyi JM,
Magnusdottir BB,
Sigmundsson T,
Olason P,
Masson G,
Gulcher JR,
Haraldsson M,
Fossdal R,
Thorgeirsson TE,
Thorsteinsdottir U,
Ruggeri M,
Tosato S,
Franke B,
Strengman E,
Kiemeney LA,
Melle I,
Djurovic S,
Abramova L,
Kaleda V,
Sanjuan J,
de Frutos R,
Bramon E,
Vassos E,
Fraser G,
Ettinger U,
Picchioni M,
Walker N,
Toulopoulou T,
Need AC,
Ge D,
Yoon JL,
Shianna KV,
Freimer NB,
Cantor RM,
Murray R,
Kong A,
Golimbet V,
Carracedo A,
Arango C,
Costas J,
Jönsson EG,
Terenius L,
Agartz I,
Petursson H,
Nöthen MM,
Rietschel M,
Matthews PM,
Muglia P,
Peltonen L,
St Clair D,
Goldstein DB,
Stefansson K,
Collier DA
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Wu X,
Ye Y,
Kiemeney LA,
Sulem P,
Rafnar T,
Matullo G,
Seminara D,
Yoshida T,
Saeki N,
Andrew AS,
Dinney CP,
Czerniak B
and 36 more — show all
Zhang ZF,
Kiltie AE,
Bishop DT,
Vineis P,
Porru S,
Buntinx F,
Kellen E,
Zeegers MP,
Kumar R,
Rudnai P,
Gurzau E,
Koppova K,
Mayordomo JI,
Sanchez M,
Saez B,
Lindblom A,
de Verdier P,
Steineck G,
Mills GB,
Schned A,
Guarrera S,
Polidoro S,
Chang SC,
Lin J,
Chang DW,
Hale KS,
Majewski T,
Grossman HB,
Thorlacius S,
Thorsteinsdottir U,
Aben KK,
Witjes JA,
Stefansson K,
Amos CI,
Karagas MR,
Gu J
Nature genetics · 2009 · PMID 19648920
2 pages
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Gretarsdottir S,
Baas AF,
Thorleifsson G,
Holm H,
den Heijer M,
de Vries JP,
Kranendonk SE,
Zeebregts CJ,
van Sterkenburg SM,
Geelkerken RH,
van Rij AM,
Williams MJ
and 90 more — show all
Boll AP,
Kostic JP,
Jonasdottir A,
Jonasdottir A,
Walters GB,
Masson G,
Sulem P,
Saemundsdottir J,
Mouy M,
Magnusson KP,
Tromp G,
Elmore JR,
Sakalihasan N,
Limet R,
Defraigne JO,
Ferrell RE,
Ronkainen A,
Ruigrok YM,
Wijmenga C,
Grobbee DE,
Shah SH,
Granger CB,
Quyyumi AA,
Vaccarino V,
Patel RS,
Zafari AM,
Levey AI,
Austin H,
Girelli D,
Pignatti PF,
Olivieri O,
Martinelli N,
Malerba G,
Trabetti E,
Becker LC,
Becker DM,
Reilly MP,
Rader DJ,
Mueller T,
Dieplinger B,
Haltmayer M,
Urbonavicius S,
Lindblad B,
Gottsäter A,
Gaetani E,
Pola R,
Wells P,
Rodger M,
Forgie M,
Langlois N,
Corral J,
Vicente V,
Fontcuberta J,
España F,
Grarup N,
Jørgensen T,
Witte DR,
Hansen T,
Pedersen O,
Aben KK,
de Graaf J,
Holewijn S,
Folkersen L,
Franco-Cereceda A,
Eriksson P,
Collier DA,
Stefansson H,
Steinthorsdottir V,
Rafnar T,
Valdimarsson EM,
Magnadottir HB,
Sveinbjornsdottir S,
Olafsson I,
Magnusson MK,
Palmason R,
Haraldsdottir V,
Andersen K,
Onundarson PT,
Thorgeirsson G,
Kiemeney LA,
Powell JT,
Carey DJ,
Kuivaniemi H,
Lindholt JS,
Jones GT,
Kong A,
Blankensteijn JD,
Matthiasson SE,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20622881
2 pages
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Schumann G,
Coin LJ,
Lourdusamy A,
Charoen P,
Berger KH,
Stacey D,
Desrivières S,
Aliev FA,
Khan AA,
Amin N,
Aulchenko YS,
Bakalkin G
and 104 more — show all
Bakker SJ,
Balkau B,
Beulens JW,
Bilbao A,
de Boer RA,
Beury D,
Bots ML,
Breetvelt EJ,
Cauchi S,
Cavalcanti-Proença C,
Chambers JC,
Clarke TK,
Dahmen N,
de Geus EJ,
Dick D,
Ducci F,
Easton A,
Edenberg HJ,
Esko T,
Fernández-Medarde A,
Foroud T,
Freimer NB,
Girault JA,
Grobbee DE,
Guarrera S,
Gudbjartsson DF,
Hartikainen AL,
Heath AC,
Hesselbrock V,
Hofman A,
Hottenga JJ,
Isohanni MK,
Kaprio J,
Khaw KT,
Kuehnel B,
Laitinen J,
Lobbens S,
Luan J,
Mangino M,
Maroteaux M,
Matullo G,
McCarthy MI,
Mueller C,
Navis G,
Numans ME,
Núñez A,
Nyholt DR,
Onland-Moret CN,
Oostra BA,
O'Reilly PF,
Palkovits M,
Penninx BW,
Polidoro S,
Pouta A,
Prokopenko I,
Ricceri F,
Santos E,
Smit JH,
Soranzo N,
Song K,
Sovio U,
Stumvoll M,
Surakk I,
Thorgeirsson TE,
Thorsteinsdottir U,
Troakes C,
Tyrfingsson T,
Tönjes A,
Uiterwaal CS,
Uitterlinden AG,
van der Harst P,
van der Schouw YT,
Staehlin O,
Vogelzangs N,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Whitfield JB,
Wichmann EH,
Willemsen G,
Witteman JC,
Yuan X,
Zhai G,
Zhao JH,
Zhang W,
Martin NG,
Metspalu A,
Doering A,
Scott J,
Spector TD,
Loos RJ,
Boomsma DI,
Mooser V,
Peltonen L,
Stefansson K,
van Duijn CM,
Vineis P,
Sommer WH,
Kooner JS,
Spanagel R,
Heberlein UA,
Jarvelin MR,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
2 pages
A genome-wide association study of early menopause and the combined impact of identified variants
Perry JR,
Corre T,
Esko T,
Chasman DI,
Fischer K,
Franceschini N,
He C,
Kutalik Z,
Mangino M,
Rose LM,
Vernon Smith A,
Stolk L
and 54 more — show all
Sulem P,
Weedon MN,
Zhuang WV,
Arnold A,
Ashworth A,
Bergmann S,
Buring JE,
Burri A,
Chen C,
Cornelis MC,
Couper DJ,
Goodarzi MO,
Gudnason V,
Harris T,
Hofman A,
Jones M,
Kraft P,
Launer L,
Laven JS,
Li G,
McKnight B,
Masciullo C,
Milani L,
Orr N,
Psaty BM,
Ridker PM,
Rivadeneira F,
Sala C,
Salumets A,
Schoemaker M,
Traglia M,
Waeber G,
Chanock SJ,
Demerath EW,
Garcia M,
Hankinson SE,
Hu FB,
Hunter DJ,
Lunetta KL,
Metspalu A,
Montgomery GW,
Murabito JM,
Newman AB,
Ong KK,
Spector TD,
Stefansson K,
Swerdlow AJ,
Thorsteinsdottir U,
Van Dam RM,
Uitterlinden AG,
Visser JA,
Vollenweider P,
Toniolo D,
Murray A
ReproGen Consortium
Human molecular genetics · 2013 · PMID 23307926 · open access
2 pages
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
and 66 more — show all
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
Spector TD,
Mirshahi A,
Saw SM,
Vingerling JR,
Teo YY,
Haines JL,
Wolfs RC,
Lemij HG,
Tai ES,
Jansonius NM,
Jonas JB,
Cheng CY,
Aung T,
Viswanathan AC,
Klaver CC,
Craig JE,
Macgregor S,
Mackey DA,
Lotery AJ,
Stefansson K,
Bergen AA,
Young TL,
Wiggs JL,
Pfeiffer N,
Wong TY,
Pasquale LR,
Hewitt AW,
van Duijn CM,
Hammond CJ
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
2 pages
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
Yang J,
Croteau-Chonka DC,
Esko T
and 470 more — show all
Fall T,
Ferreira T,
Gustafsson S,
Kutalik Z,
Luan J,
Mägi R,
Randall JC,
Winkler TW,
Wood AR,
Workalemahu T,
Faul JD,
Smith JA,
Zhao JH,
Zhao W,
Chen J,
Fehrmann R,
Hedman ÅK,
Karjalainen J,
Schmidt EM,
Absher D,
Amin N,
Anderson D,
Beekman M,
Bolton JL,
Bragg-Gresham JL,
Buyske S,
Demirkan A,
Deng G,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Goel A,
Gong J,
Jackson AU,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Mangino M,
Leach IM,
Medina-Gomez C,
Medland SE,
Nalls MA,
Palmer CD,
Pasko D,
Pechlivanis S,
Peters MJ,
Prokopenko I,
Shungin D,
Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Isaacs A,
Albrecht E,
Ärnlöv J,
Arscott GM,
Attwood AP,
Bandinelli S,
Barrett A,
Bas IN,
Bellis C,
Bennett AJ,
Berne C,
Blagieva R,
Blüher M,
Böhringer S,
Bonnycastle LL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Caspersen IH,
Chen YI,
Clarke R,
Daw EW,
de Craen AJM,
Delgado G,
Dimitriou M,
Doney ASF,
Eklund N,
Estrada K,
Eury E,
Folkersen L,
Fraser RM,
Garcia ME,
Geller F,
Giedraitis V,
Gigante B,
Go AS,
Golay A,
Goodall AH,
Gordon SD,
Gorski M,
Grabe HJ,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
Groves CJ,
Gusto G,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hengstenberg C,
Holmen O,
Hottenga JJ,
James AL,
Jeff JM,
Johansson Å,
Jolley J,
Juliusdottir T,
Kinnunen L,
Koenig W,
Koskenvuo M,
Kratzer W,
Laitinen J,
Lamina C,
Leander K,
Lee NR,
Lichtner P,
Lind L,
Lindström J,
Lo KS,
Lobbens S,
Lorbeer R,
Lu Y,
Mach F,
Magnusson PKE,
Mahajan A,
McArdle WL,
McLachlan S,
Menni C,
Merger S,
Mihailov E,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Mulas A,
Müller G,
Müller-Nurasyid M,
Musk AW,
Nagaraja R,
Nöthen MM,
Nolte IM,
Pilz S,
Rayner NW,
Renstrom F,
Rettig R,
Ried JS,
Ripke S,
Robertson NR,
Rose LM,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Scott WR,
Seufferlein T,
Shi J,
Smith AV,
Smolonska J,
Stanton AV,
Steinthorsdottir V,
Stirrups K,
Stringham HM,
Sundström J,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Tayo BO,
Thorand B,
Thorleifsson G,
Tyrer JP,
Uh HW,
Vandenput L,
Verhulst FC,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Warren HR,
Waterworth D,
Weedon MN,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Brennan EP,
Choi M,
Dastani Z,
Drong AW,
Eriksson P,
Franco-Cereceda A,
Gådin JR,
Gharavi AG,
Goddard ME,
Handsaker RE,
Huang J,
Karpe F,
Kathiresan S,
Keildson S,
Kiryluk K,
Kubo M,
Lee JY,
Liang L,
Lifton RP,
Ma B,
McCarroll SA,
McKnight AJ,
Min JL,
Moffatt MF,
Montgomery GW,
Murabito JM,
Nicholson G,
Nyholt DR,
Okada Y,
Perry JRB,
Dorajoo R,
Reinmaa E,
Salem RM,
Sandholm N,
Scott RA,
Stolk L,
Takahashi A,
Tanaka T,
van 't Hooft FM,
Vinkhuyzen AAE,
Westra HJ,
Zheng W,
Zondervan KT,
Heath AC,
Arveiler D,
Bakker SJL,
Beilby J,
Bergman RN,
Blangero J,
Bovet P,
Campbell H,
Caulfield MJ,
Cesana G,
Chakravarti A,
Chasman DI,
Chines PS,
Collins FS,
Crawford DC,
Cupples LA,
Cusi D,
Danesh J,
de Faire U,
den Ruijter HM,
Dominiczak AF,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Felix SB,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Franco OH,
Gansevoort RT,
Gejman PV,
Gieger C,
Gottesman O,
Gudnason V,
Gyllensten U,
Hall AS,
Harris TB,
Hattersley AT,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Homuth G,
Hovingh GK,
Humphries SE,
Hunt SC,
Hyppönen E,
Illig T,
Jacobs KB,
Jarvelin MR,
Jöckel KH,
Johansen B,
Jousilahti P,
Jukema JW,
Jula AM,
Kaprio J,
Kastelein JJP,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Knekt P,
Kooner JS,
Kooperberg C,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Marchand LL,
Lehtimäki T,
Lyssenko V,
Männistö S,
Marette A,
Matise TC,
McKenzie CA,
McKnight B,
Moll FL,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Madden PAF,
Pasterkamp G,
Peden JF,
Peters A,
Postma DS,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ridker PM,
Rioux JD,
Ritchie MD,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schunkert H,
Schwarz PEH,
Sever P,
Shuldiner AR,
Sinisalo J,
Stolk RP,
Strauch K,
Tönjes A,
Trégouët DA,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Völker U,
Waeber G,
Willemsen G,
Witteman JC,
Zillikens MC,
Adair LS,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bornstein SR,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PIW,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hui J,
Hunter DJ,
Hveem K,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Metspalu A,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CNA,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Power C,
Quertermous T,
Rauramaa R,
Rivadeneira F,
Saaristo TE,
Saleheen D,
Sattar N,
Schadt EE,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Thorsteinsdottir U,
Stumvoll M,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Weir DR,
Wichmann HE,
Wilson JF,
Zanen P,
Borecki IB,
Deloukas P,
Fox CS,
Heid IM,
O'Connell JR,
Strachan DP,
Stefansson K,
van Duijn CM,
Abecasis GR,
Franke L,
Frayling TM,
McCarthy MI,
Visscher PM,
Scherag A,
Willer CJ,
Boehnke M,
Mohlke KL,
Lindgren CM,
Beckmann JS,
Barroso I,
North KE,
Ingelsson E,
Hirschhorn JN,
Loos RJF,
Speliotes EK
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
Common and rare variants associated with kidney stones and biochemical traits
Oddsson A,
Sulem P,
Helgason H,
Edvardsson VO,
Thorleifsson G,
Sveinbjörnsson G,
Haraldsdottir E,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Masson G,
Holm H
and 5 more — show all
Nature communications · 2015 · PMID 26272126 · open access
2 pages
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
Day FR,
Hinds DA,
Tung JY,
Stolk L,
Styrkarsdottir U,
Saxena R,
Bjonnes A,
Broer L,
Dunger DB,
Halldorsson BV,
Lawlor DA,
Laval G
and 15 more — show all
Mathieson I,
McCardle WL,
Louwers Y,
Meun C,
Ring S,
Scott RA,
Sulem P,
Uitterlinden AG,
Wareham NJ,
Thorsteinsdottir U,
Welt C,
Stefansson K,
Laven JSE,
Ong KK,
Perry JRB
Nature communications · 2015 · PMID 26416764 · open access
2 pages
Genome-wide analysis yields new loci associating with aortic valve stenosis
Helgadottir A,
Thorleifsson G,
Gretarsdottir S,
Stefansson OA,
Tragante V,
Thorolfsdottir RB,
Jonsdottir I,
Bjornsson T,
Steinthorsdottir V,
Verweij N,
Nielsen JB,
Zhou W
and 34 more — show all
Folkersen L,
Martinsson A,
Heydarpour M,
Prakash S,
Oskarsson G,
Gudbjartsson T,
Geirsson A,
Olafsson I,
Sigurdsson EL,
Almgren P,
Melander O,
Franco-Cereceda A,
Hamsten A,
Fritsche L,
Lin M,
Yang B,
Hornsby W,
Guo D,
Brummett CM,
Abecasis G,
Mathis M,
Milewicz D,
Body SC,
Eriksson P,
Willer CJ,
Hveem K,
Newton-Cheh C,
Smith JG,
Danielsen R,
Thorgeirsson G,
Thorsteinsdottir U,
Gudbjartsson DF,
Holm H,
Stefansson K
Nature communications · 2018 · PMID 29511194 · open access
2 pages
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci
Ghouse J,
Tragante V,
Muhammad A,
Ahlberg G,
Skov MW,
Roden DM,
Jonsdottir I,
Andreasen L,
Lundegaard PR,
Trudsø LC,
Banasik K,
Brunak S
and 15 more — show all
Ostrowski SR,
Torp-Pedersen C,
Pedersen OV,
Sørensen E,
Køber L,
Iversen K,
Thorsteinsdottir U,
Thorgeirsson G,
Ullum H,
Gudbjartsson DF,
Mosley JD,
Holm H,
Stefansson K,
Bundgaard H,
Olesen MS
eMERGE consortium
European heart journal · 2022 · PMID 35751511
2 pages
Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect
Styrkarsdottir U,
Stefansdottir L,
Thorleifsson G,
Stefansson OA,
Saevarsdottir S,
Lund SH,
Rafnar T,
Hoshijima K,
Novak K,
Oreiro N,
Rego-Perez I,
Hansen C
and 10 more — show all
Annals of the rheumatic diseases · 2023 · PMID 36931692 · open access
2 pages
Genome-wide association study in 21,271 individuals identifies 9 novel loci associated with circulating CD34<sup>+</sup> hematopoietic stem and progenitor cell levels
Xie Y,
Lamarca A,
Cafaro C,
Thorleifsson G,
Ekdahl L,
Torres Di Bello D,
Ali Z,
La Y,
Stefansdottir L,
Antill A,
Pertesi M,
Mahecha Escobar ML
and 9 more — show all
HemaSphere · 2026 · PMID 42388415 · 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.