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73 matches for
Sulem P,
showing the first 20.
Deciphering the genetics and mechanisms of predisposition to multiple myeloma
Went M,
Duran-Lozano L,
Halldorsson GH,
Gunnell A,
Ugidos-Damboriena N,
Law P,
Ekdahl L,
Sud A,
Thorleifsson G,
Thodberg M,
Olafsdottir T,
Lamarca-Arrizabalaga A
and 38 more — show all
Cafaro C,
Niroula A,
Ajore R,
Lopez de Lapuente Portilla A,
Ali Z,
Pertesi M,
Goldschmidt H,
Stefansdottir L,
Kristinsson SY,
Stacey SN,
Love TJ,
Rognvaldsson S,
Hajek R,
Vodicka P,
Pettersson-Kymmer U,
Späth F,
Schinke C,
Van Rhee F,
Sulem P,
Ferkingstad E,
Hjorleifsson Eldjarn G,
Mellqvist UH,
Jonsdottir I,
Morgan G,
Sonneveld P,
Waage A,
Weinhold N,
Thomsen H,
Försti A,
Hansson M,
Juul-Vangsted A,
Thorsteinsdottir U,
Hemminki K,
Kaiser M,
Rafnar T,
Stefansson K,
Houlston R,
Nilsson B
Nature communications · 2024 · PMID 39103364 · open access
9 pages
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
Stolk L,
Perry JR,
Chasman DI,
He C,
Mangino M,
Sulem P,
Barbalic M,
Broer L,
Byrne EM,
Ernst F,
Esko T,
Franceschini N
and 167 more — show all
Gudbjartsson DF,
Hottenga JJ,
Kraft P,
McArdle PF,
Porcu E,
Shin SY,
Smith AV,
van Wingerden S,
Zhai G,
Zhuang WV,
Albrecht E,
Alizadeh BZ,
Aspelund T,
Bandinelli S,
Lauc LB,
Beckmann JS,
Boban M,
Boerwinkle E,
Broekmans FJ,
Burri A,
Campbell H,
Chanock SJ,
Chen C,
Cornelis MC,
Corre T,
Coviello AD,
d'Adamo P,
Davies G,
de Faire U,
de Geus EJ,
Deary IJ,
Dedoussis GV,
Deloukas P,
Ebrahim S,
Eiriksdottir G,
Emilsson V,
Eriksson JG,
Fauser BC,
Ferreli L,
Ferrucci L,
Fischer K,
Folsom AR,
Garcia ME,
Gasparini P,
Gieger C,
Glazer N,
Grobbee DE,
Hall P,
Haller T,
Hankinson SE,
Hass M,
Hayward C,
Heath AC,
Hofman A,
Ingelsson E,
Janssens AC,
Johnson AD,
Karasik D,
Kardia SL,
Keyzer J,
Kiel DP,
Kolcic I,
Kutalik Z,
Lahti J,
Lai S,
Laisk T,
Laven JS,
Lawlor DA,
Liu J,
Lopez LM,
Louwers YV,
Magnusson PK,
Marongiu M,
Martin NG,
Klaric IM,
Masciullo C,
McKnight B,
Medland SE,
Melzer D,
Mooser V,
Navarro P,
Newman AB,
Nyholt DR,
Onland-Moret NC,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peeters PH,
Pistis G,
Plump AS,
Polasek O,
Pop VJ,
Psaty BM,
Räikkönen K,
Rehnberg E,
Rotter JI,
Rudan I,
Sala C,
Salumets A,
Scuteri A,
Singleton A,
Smith JA,
Snieder H,
Soranzo N,
Stacey SN,
Starr JM,
Stathopoulou MG,
Stirrups K,
Stolk RP,
Styrkarsdottir U,
Sun YV,
Tenesa A,
Thorand B,
Toniolo D,
Tryggvadottir L,
Tsui K,
Ulivi S,
van Dam RM,
van der Schouw YT,
van Gils CH,
van Nierop P,
Vink JM,
Visscher PM,
Voorhuis M,
Waeber G,
Wallaschofski H,
Wichmann HE,
Widen E,
Wijnands-van Gent CJ,
Willemsen G,
Wilson JF,
Wolffenbuttel BH,
Wright AF,
Yerges-Armstrong LM,
Zemunik T,
Zgaga L,
Zillikens MC,
Zygmunt M,
Arnold AM,
Boomsma DI,
Buring JE,
Crisponi L,
Demerath EW,
Gudnason V,
Harris TB,
Hu FB,
Hunter DJ,
Launer LJ,
Metspalu A,
Montgomery GW,
Oostra BA,
Ridker PM,
Sanna S,
Schlessinger D,
Spector TD,
Stefansson K,
Streeten EA,
Thorsteinsdottir U,
Uda M,
Uitterlinden AG,
van Duijn CM,
Völzke H,
Murray A,
Murabito JM,
Visser JA,
Lunetta KL
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
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
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
Tyrmi JS,
Karjalainen J,
Venkatesh SS,
Benoit-Pilven C,
Lemmelä SM,
Brunak S,
Aagaard B,
Bruun MT,
Erikstrup C,
Ullum H,
Pedersen OB,
Banasik K
and 19 more — show all
Sørensen E,
Mikkelsen C,
Schwinn M,
Sturluson A,
Ostrowski SR,
Kettunen J,
Nielsen HS,
Nyegaard M,
Westergaard D,
Rafnar T,
Sulem P,
Stefansson K,
Palta P,
Laisk T,
Tukiainen T,
Lindgren CM,
Daly M,
Havulinna AS,
Laivuori HM
FinnGen · Estonian Biobank research team and 1 more consortia
Nature communications · 2026 · PMID 42178310 · open access
8 pages
New basal cell carcinoma susceptibility loci
Stacey SN,
Helgason H,
Gudjonsson SA,
Thorleifsson G,
Zink F,
Sigurdsson A,
Kehr B,
Gudmundsson J,
Sulem P,
Sigurgeirsson B,
Benediktsdottir KR,
Thorisdottir K
and 31 more — show all
Ragnarsson R,
Fuentelsaz V,
Corredera C,
Gilaberte Y,
Grasa M,
Planelles D,
Sanmartin O,
Rudnai P,
Gurzau E,
Koppova K,
Nexø BA,
Tjønneland A,
Overvad K,
Jonasson JG,
Tryggvadottir L,
Johannsdottir H,
Kristinsdottir AM,
Stefansson H,
Masson G,
Magnusson OT,
Halldorsson BV,
Kong A,
Rafnar T,
Thorsteinsdottir U,
Vogel U,
Kumar R,
Nagore E,
Mayordomo JI,
Gudbjartsson DF,
Olafsson JH,
Stefansson K
Nature communications · 2015 · PMID 25855136 · open access
7 pages
Sequence variants associating with urinary biomarkers
Benonisdottir S,
Kristjansson RP,
Oddsson A,
Steinthorsdottir V,
Mikaelsdottir E,
Kehr B,
Jensson BO,
Arnadottir GA,
Sulem G,
Sveinbjornsson G,
Kristmundsdottir S,
Ivarsdottir EV
and 26 more — show all
Tragante V,
Gunnarsson B,
Runolfsdottir HL,
Arthur JG,
Deaton AM,
Eyjolfsson GI,
Davidsson OB,
Asselbergs FW,
Hreidarsson AB,
Rafnar T,
Thorleifsson G,
Edvardsson V,
Sigurdsson G,
Helgadottir A,
Halldorsson BV,
Masson G,
Holm H,
Onundarson PT,
Indridason OS,
Benediktsson R,
Palsson R,
Gudbjartsson DF,
Olafsson I,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Human molecular genetics · 2019 · PMID 30476138 · open access
7 pages
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
Styrkarsdottir U,
Stefansson OA,
Gunnarsdottir K,
Thorleifsson G,
Lund SH,
Stefansdottir L,
Juliusson K,
Agustsdottir AB,
Zink F,
Halldorsson GH,
Ivarsdottir EV,
Benonisdottir S
and 40 more — show all
Jonsson H,
Gylfason A,
Norland K,
Trajanoska K,
Boer CG,
Southam L,
Leung JCS,
Tang NLS,
Kwok TCY,
Lee JSW,
Ho SC,
Byrjalsen I,
Center JR,
Lee SH,
Koh JM,
Lohmander LS,
Ho-Pham LT,
Nguyen TV,
Eisman JA,
Woo J,
Leung PC,
Loughlin J,
Zeggini E,
Christiansen C,
Rivadeneira F,
van Meurs J,
Uitterlinden AG,
Mogensen B,
Jonsson H,
Ingvarsson T,
Sigurdsson G,
Benediktsson R,
Sulem P,
Jonsdottir I,
Masson G,
Holm H,
Norddahl GL,
Thorsteinsdottir U,
Gudbjartsson DF,
Stefansson K
Nature communications · 2019 · PMID 31053729 · open access
7 pages
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Ivarsdottir EV,
Holm H,
Benonisdottir S,
Olafsdottir T,
Sveinbjornsson G,
Thorleifsson G,
Eggertsson HP,
Halldorsson GH,
Hjorleifsson KE,
Melsted P,
Gylfason A,
Arnadottir GA
and 16 more — show all
Oddsson A,
Jensson BO,
Jonasdottir A,
Jonasdottir A,
Juliusdottir T,
Stefansdottir L,
Tragante V,
Halldorsson BV,
Petersen H,
Thorgeirsson G,
Thorsteinsdottir U,
Sulem P,
Hinriksdottir I,
Jonsdottir I,
Gudbjartsson DF,
Stefansson K
Communications biology · 2021 · PMID 34108613 · open access
7 pages
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Skuladottir AT,
Stefansdottir L,
Halldorsson GH,
Stefansson OA,
Bjornsdottir A,
Jonsson P,
Palmadottir V,
Thorgeirsson TE,
Walters GB,
Gisladottir RS,
Bjornsdottir G,
Jonsdottir GA
and 20 more — show all
Sulem P,
Gudbjartsson DF,
Knowlton KU,
Jones DA,
Ottas A,
Pedersen OB,
Didriksen M,
Brunak S,
Banasik K,
Hansen TF,
Erikstrup C,
Haavik J,
Andreassen OA,
Rye D,
Igland J,
Ostrowski SR,
Milani LA,
Nadauld LD,
Stefansson H,
Stefansson K
Estonian Biobank · DBDS Genomic Consortium
Communications biology · 2024 · PMID 38671141 · open access
7 pages
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
Grarup N,
Sulem P,
Sandholt CH,
Thorleifsson G,
Ahluwalia TS,
Steinthorsdottir V,
Bjarnason H,
Gudbjartsson DF,
Magnusson OT,
Sparsø T,
Albrechtsen A,
Kong A
and 19 more — show all
Masson G,
Tian G,
Cao H,
Nie C,
Kristiansen K,
Husemoen LL,
Thuesen B,
Li Y,
Nielsen R,
Linneberg A,
Olafsson I,
Eyjolfsson GI,
Jørgensen T,
Wang J,
Wang J,
Hansen T,
Thorsteinsdottir U,
Stefánsson K,
Pedersen O
PLoS genetics · 2013 · PMID 23754956 · open access
6 pages
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
Kristjansson RP,
Oddsson A,
Helgason H,
Sveinbjornsson G,
Arnadottir GA,
Jensson BO,
Jonasdottir A,
Jonasdottir A,
Bragi Walters G,
Sulem G,
Oskarsdottir A,
Benonisdottir S
and 12 more — show all
Davidsson OB,
Masson G,
Magnusson OT,
Holm H,
Sigurdardottir O,
Jonsdottir I,
Eyjolfsson GI,
Olafsson I,
Gudbjartsson DF,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Nature communications · 2016 · PMID 26838040 · open access
6 pages
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Fehringer G,
Kraft P,
Pharoah PD,
Eeles RA,
Chatterjee N,
Schumacher FR,
Schildkraut JM,
Lindström S,
Brennan P,
Bickeböller H,
Houlston RS,
Landi MT
and 121 more — show all
Caporaso N,
Risch A,
Amin Al Olama A,
Berndt SI,
Giovannucci EL,
Grönberg H,
Kote-Jarai Z,
Ma J,
Muir K,
Stampfer MJ,
Stevens VL,
Wiklund F,
Willett WC,
Goode EL,
Permuth JB,
Risch HA,
Reid BM,
Bezieau S,
Brenner H,
Chan AT,
Chang-Claude J,
Hudson TJ,
Kocarnik JK,
Newcomb PA,
Schoen RE,
Slattery ML,
White E,
Adank MA,
Ahsan H,
Aittomäki K,
Baglietto L,
Blomquist C,
Canzian F,
Czene K,
Dos-Santos-Silva I,
Eliassen AH,
Figueroa JD,
Flesch-Janys D,
Fletcher O,
Garcia-Closas M,
Gaudet MM,
Johnson N,
Hall P,
Hazra A,
Hein R,
Hofman A,
Hopper JL,
Irwanto A,
Johansson M,
Kaaks R,
Kibriya MG,
Lichtner P,
Liu J,
Lund E,
Makalic E,
Meindl A,
Müller-Myhsok B,
Muranen TA,
Nevanlinna H,
Peeters PH,
Peto J,
Prentice RL,
Rahman N,
Sanchez MJ,
Schmidt DF,
Schmutzler RK,
Southey MC,
Tamimi R,
Travis RC,
Turnbull C,
Uitterlinden AG,
Wang Z,
Whittemore AS,
Yang XR,
Zheng W,
Zheng W,
Buchanan DD,
Casey G,
Conti DV,
Edlund CK,
Gallinger S,
Haile RW,
Jenkins M,
Le Marchand L,
Li L,
Lindor NM,
Schmit SL,
Thibodeau SN,
Woods MO,
Rafnar T,
Gudmundsson J,
Stacey SN,
Stefansson K,
Sulem P,
Chen YA,
Tyrer JP,
Christiani DC,
Wei Y,
Shen H,
Hu Z,
Shu XO,
Shiraishi K,
Takahashi A,
Bossé Y,
Obeidat M,
Nickle D,
Timens W,
Freedman ML,
Li Q,
Seminara D,
Chanock SJ,
Gong J,
Peters U,
Gruber SB,
Amos CI,
Sellers TA,
Easton DF,
Hunter DJ,
Haiman CA,
Henderson BE,
Hung RJ
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Olafsdottir TA,
Theodors F,
Bjarnadottir K,
Bjornsdottir US,
Agustsdottir AB,
Stefansson OA,
Ivarsdottir EV,
Sigurdsson JK,
Benonisdottir S,
Eyjolfsson GI,
Gislason D,
Gislason T
and 23 more — show all
Guðmundsdóttir S,
Gylfason A,
Halldorsson BV,
Halldorsson GH,
Juliusdottir T,
Kristinsdottir AM,
Ludviksdottir D,
Ludviksson BR,
Masson G,
Norland K,
Onundarson PT,
Olafsson I,
Sigurdardottir O,
Stefansdottir L,
Sveinbjornsson G,
Tragante V,
Gudbjartsson DF,
Thorleifsson G,
Sulem P,
Thorsteinsdottir U,
Norddahl GL,
Jonsdottir I,
Stefansson K
Nature communications · 2020 · PMID 31959851 · open access
6 pages
Identification of sequence variants influencing immunoglobulin levels
Jonsson S,
Sveinbjornsson G,
de Lapuente Portilla AL,
Swaminathan B,
Plomp R,
Dekkers G,
Ajore R,
Ali M,
Bentlage AEH,
Elmér E,
Eyjolfsson GI,
Gudjonsson SA
and 26 more — show all
Gullberg U,
Gylfason A,
Halldorsson BV,
Hansson M,
Holm H,
Johansson Å,
Johnsson E,
Jonasdottir A,
Ludviksson BR,
Oddsson A,
Olafsson I,
Olafsson S,
Sigurdardottir O,
Sigurdsson A,
Stefansdottir L,
Masson G,
Sulem P,
Wuhrer M,
Wihlborg AK,
Thorleifsson G,
Gudbjartsson DF,
Thorsteinsdottir U,
Vidarsson G,
Jonsdottir I,
Nilsson B,
Stefansson K
Nature genetics · 2017 · PMID 28628107
5 pages
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
Styrkarsdottir U,
Lund SH,
Thorleifsson G,
Zink F,
Stefansson OA,
Sigurdsson JK,
Juliusson K,
Bjarnadottir K,
Sigurbjornsdottir S,
Jonsson S,
Norland K,
Stefansdottir L
and 17 more — show all
Sigurdsson A,
Sveinbjornsson G,
Oddsson A,
Bjornsdottir G,
Gudmundsson RL,
Halldorsson GH,
Rafnar T,
Jonsdottir I,
Steingrimsson E,
Norddahl GL,
Masson G,
Sulem P,
Jonsson H,
Ingvarsson T,
Gudbjartsson DF,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2018 · PMID 30374069
5 pages
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Kristjansson RP,
Benonisdottir S,
Davidsson OB,
Oddsson A,
Tragante V,
Sigurdsson JK,
Stefansdottir L,
Jonsson S,
Jensson BO,
Arthur JG,
Arnadottir GA,
Sulem G
and 28 more — show all
Halldorsson BV,
Gunnarsson B,
Halldorsson GH,
Stefansson OA,
Oskarsson GR,
Deaton AM,
Olafsson I,
Eyjolfsson GI,
Sigurdardottir O,
Onundarson PT,
Gislason D,
Gislason T,
Ludviksson BR,
Ludviksdottir D,
Olafsdottir TA,
Rafnar T,
Masson G,
Zink F,
Bjornsdottir G,
Magnusson OT,
Bjornsdottir US,
Thorleifsson G,
Norddahl GL,
Gudbjartsson DF,
Thorsteinsdottir U,
Jonsdottir I,
Sulem P,
Stefansson K
Nature genetics · 2019 · PMID 30643255
5 pages
Genetic insight into sick sinus syndrome
Thorolfsdottir RB,
Sveinbjornsson G,
Aegisdottir HM,
Benonisdottir S,
Stefansdottir L,
Ivarsdottir EV,
Halldorsson GH,
Sigurdsson JK,
Torp-Pedersen C,
Weeke PE,
Brunak S,
Westergaard D
and 32 more — show all
Pedersen OB,
Sorensen E,
Nielsen KR,
Burgdorf KS,
Banasik K,
Brumpton B,
Zhou W,
Oddsson A,
Tragante V,
Hjorleifsson KE,
Davidsson OB,
Rajamani S,
Jonsson S,
Torfason B,
Valgardsson AS,
Thorgeirsson G,
Frigge ML,
Thorleifsson G,
Norddahl GL,
Helgadottir A,
Gretarsdottir S,
Sulem P,
Jonsdottir I,
Willer CJ,
Hveem K,
Bundgaard H,
Ullum H,
Arnar DO,
Thorsteinsdottir U,
Gudbjartsson DF,
Holm H,
Stefansson K
DBDS Genomic Consortium
European heart journal · 2021 · PMID 33580673 · open access
5 pages
Genetic correction of PSA values using sequence variants associated with PSA levels
Gudmundsson J,
Besenbacher S,
Sulem P,
Gudbjartsson DF,
Olafsson I,
Arinbjarnarson S,
Agnarsson BA,
Benediktsdottir KR,
Isaksson HJ,
Kostic JP,
Gudjonsson SA,
Stacey SN
and 37 more — show all
Gylfason A,
Sigurdsson A,
Holm H,
Bjornsdottir US,
Eyjolfsson GI,
Navarrete S,
Fuertes F,
Garcia-Prats MD,
Polo E,
Checherita IA,
Jinga M,
Badea P,
Aben KK,
Schalken JA,
van Oort IM,
Sweep FC,
Helfand BT,
Davis M,
Donovan JL,
Hamdy FC,
Kristjansson K,
Gulcher JR,
Masson G,
Kong A,
Catalona WJ,
Mayordomo JI,
Geirsson G,
Einarsson GV,
Barkardottir RB,
Jonsson E,
Jinga V,
Mates D,
Kiemeney LA,
Neal DE,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Science translational medicine · 2010 · PMID 21160077
4 pages
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Stacey SN,
Zink F,
Halldorsson GH,
Stefansdottir L,
Gudjonsson SA,
Einarsson G,
Hjörleifsson G,
Eiriksdottir T,
Helgadottir A,
Björnsdottir G,
Thorgeirsson TE,
Olafsdottir TA
and 19 more — show all
Jonsdottir I,
Gretarsdottir S,
Tragante V,
Magnusson MK,
Jonsson H,
Gudmundsson J,
Olafsson S,
Holm H,
Gudbjartsson DF,
Sulem P,
Helgason A,
Thorsteinsdottir U,
Tryggvadottir L,
Rafnar T,
Melsted P,
Ulfarsson MÖ,
Vidarsson B,
Thorleifsson G,
Stefansson K
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
The genetic architecture of fibromyalgia across 2.5 million individuals
Kerrebijn I,
Bjornsdottir G,
Arbabi K,
Urpa L,
Haapaniemi H,
Thorleifsson G,
Stefansdottir L,
Frangakis S,
Valliere J,
Kunorozva L,
Abner E,
Ji C
and 41 more — show all
Kangur M,
Aagaard B,
Bliddal H,
Brunak S,
Bruun MT,
Didriksen M,
Erikstrup C,
Finer S,
Geirsson AJ,
Gudbjartsson DF,
Hansen TF,
van Heel D,
Jonsdottir I,
Knight S,
Knowlton KU,
Mikkelsen C,
Nadauld LD,
Olafsdottir TA,
Ostrowski SR,
Pedersen OBV,
Saevarsdottir S,
Skuladottir AT,
Sørensen E,
Stefansson H,
Sulem P,
Sveinsson OA,
Thorlacius GE,
Thorsteinsdottir U,
Ullum H,
Vikingsson A,
Werge TM,
Saxena R,
Stefansson K,
Brummett CM,
Glintborg B,
Clauw DJ,
Thorgeirsson TE,
Williams FMK,
Sinnott-Armstrong N,
Ollila HM,
Wainberg M
Chronic Pain Genomics Consortium · FinnGen and 3 more consortia
Nature medicine · 2026 · PMID 42521817 · open access
4 pages
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