Hafdís Helgadóttir

Article: FRONTIERS IN NEUROLOGY. 2023;14:1170005

Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders

Ek M; Nilsson D; Engvall M; Malmgren H; Thonberg H; Pettersson M; Anderlid B-M; Hammarsjo A; Helgadottir HT; Arnardottir S; Naess K; Nennesmo I; Paucar M; Hjartarson HT; Press R; Solders G; Sejersen T; Lindstrand A; Kvarnung M

Article: GENETICS IN MEDICINE. 2022;24(11):2296-2307

Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability

Lindstrand A; Ek M; Kvarnung M; Anderlid B-M; Bjoerck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjoe A; Helgadottir HT; Hellstroem-Pigg M; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-A; Lieden A; Lindeloef H; Malmgren H; Nilsson D; Svensson E; Paucar M; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Soller MJ; Pettersson M; Nordgren A

Article: HEREDITARY CANCER IN CLINICAL PRACTICE. 2022;20(1):28

Unravelling genetic variants of a swedish family with high risk of prostate cancer

Barilla S; Lindblom A; Helgadottir HT

Article: BIOMEDICINES. 2022;10(5):1004

Whole-Exome Sequencing of Germline Variants in Non-BRCA Families with Hereditary Breast Cancer

Liu Y; Helgadottir HT; Kharaziha P; Choi J; Lopez-Giraldez F; Mane SM; Hoiom V; Juhlin CC; Larsson C; Bajalica-Lagercrantz S

Article: MOLECULAR CARCINOGENESIS. 2022;61(3):288-300

Colorectal cancer risk susceptibility loci in a Swedish population

Liu W; Mahdessian H; Helgadottir H; Zhou X; Thutkawkorapin J; Jiao X; Wolk A; Lindblom A

Article: CANCERS. 2022;14(5):1206

A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16

Barnekow E; Liu W; Helgadottir HT; Michailidou K; Dennis J; Bryant P; Thutkawkorapin J; Wendt C; Czene K; Hall P; Margolin S; Lindblom A

Article: INTERNATIONAL JOURNAL OF CANCER. 2021;149(3):627-634

Identification of known and novel familial cancer genes in Swedish colorectal cancer families

Helgadottir HT; Thutkawkorapin J; Rohlin A; Nordling M; Lagerstedt-Robinson K; Lindblom A

Article: SCIENTIFIC REPORTS. 2021;11(1):14737

Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genes

Helgadottir HT; Thutkawkorapin J; Lagerstedt-Robinson K; Lindblom A

Article: GENOME BIOLOGY. 2019;20(1):285

Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type

Franco I; Helgadottir HT; Moggio A; Larsson M; Vrtacnik P; Johansson A; Norgren N; Lundin P; Mas-Ponte D; Nordstrom J; Lundgren T; Stenvinkel P; Wennberg L; Supek F; Eriksson M

Article: JOURNAL OF INVESTIGATIVE DERMATOLOGY. 2019;139(11):2272-2280.e12

Accumulation of Progerin Affects the Symmetry of Cell Division and Is Associated with Impaired Wnt Signaling and the Mislocalization of Nuclear Envelope Proteins

Sola-Carvajal A; Revechon G; Helgadottir HT; Whisenant D; Hagblom R; Dohla J; Katajisto P; Brodin D; Fagerstrom-Billai F; Viceconte N; Eriksson M

Article: HUMAN MOLECULAR GENETICS. 2019;28(16):2675-2685

Somatic mutation that affects transcription factor binding upstream of CD55 in the temporal cortex of a late-onset Alzheimer disease patient

Helgadottir H; Lundin P; Arzt EW; Lindstrom A-K; Graff C; Eriksson M

Article: NATURE COMMUNICATIONS. 2018;9(1):800

Somatic mutagenesis in satellite cells associates with human skeletal muscle aging

Franco I; Johansson A; Olsson K; Vrtacnik P; Lundin P; Helgadottir HT; Larsson M; Revechon G; Bosia C; Pagnani A; Provero P; Gustafsson T; Fischer H; Eriksson M

Article: EUROPEAN HEART JOURNAL. 2017;38(1):27-34

A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation

Gudbjartsson DF; Holm H; Sulem P; Masson G; Oddsson A; Magnusson OT; Saemundsdottir J; Helgadottir HT; Helgason H; Johannsdottir H; Gretarsdottir S; Gudjonsson SA; Njolstad I; Lochen M-L; Baum L; Ma RCW; Sigfusson G; Kong A; Thorgeirsson G; Sverrisson JT; Thorsteinsdottir U; Stefansson K; Arnar DO

Article: MOLECULAR PSYCHIATRY. 2016;21(5):594-600

A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

Thorgeirsson TE; Steinberg S; Reginsson GW; Bjornsdottir G; Rafnar T; Jonsdottir I; Helgadottir A; Gretarsdottir S; Helgadottir H; Jonsson S; Matthiasson SE; Gislason T; Tyrfingsson T; Gudbjartsson T; Isaksson HJ; Hardardottir H; Sigvaldason A; Kiemeney LA; Haugen A; Zienolddiny S; Wolf HJ; Franklin WA; Panadero A; Mayordomo JI; Hall IP; Ronmark E; Lundback B; Dirksen A; Ashraf H; Pedersen JH; Masson G; Sulem P; Thorsteinsdottir U; Gudbjartsson DF; Stefansson K

Article: NATURE GENETICS. 2016;48(3):318-322

HLA class II sequence variants influence tuberculosis risk in populations of European ancestry

Sveinbjornsson G; Gudbjartsson DF; Halldorsson BV; Kristinsson KG; Gottfredsson M; Barrett JC; Gudmundsson LJ; Blondal K; Gylfason A; Gudjonsson SA; Helgadottir HT; Jonasdottir A; Jonasdottir A; Karason A; Kardum LB; Knezevic J; Kristjansson H; Kristjansson M; Love A; Luo Y; Magnusson OT; Sulem P; Kong A; Masson G; Thorsteinsdottir U; Dembic Z; Nejentsev S; Blondal T; Jonsdottir I; Stefansson K

Article: HUMAN MOLECULAR GENETICS. 2015;24(19):5637-5643

Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease

Huttenlocher J; Stefansson H; Steinberg S; Helgadottir HT; Sveinbjornsdottir S; Riess O; Bauer P; Stefansson K

Article: NATURE GENETICS. 2015;47(5):435-444

Large-scale whole-genome sequencing of the Icelandic population

Gudbjartsson DF; Helgason H; Gudjonsson SA; Zink F; Oddson A; Gylfason A; Besenbacher S; Magnusson G; Halldorsson BV; Hjartarson E; Sigurdsson GT; Stacey SN; Frigge ML; Holm H; Saemundsdottir J; Helgadottir HT; Johannsdottir H; Sigfusson G; Thorgeirsson G; Sverrisson JT; Gretarsdottir S; Walters GB; Rafnar T; Thjodleifsson B; Bjornsson ES; Olafsson S; Thorarinsdottir H; Steingrimsdottir T; Gudmundsdottir TS; Theodors A; Jonasson JG; Sigurdsson A; Bjornsdottir G; Jonsson JJ; Thorarensen O; Ludvigsson P; Gudbjartsson H; Eyjolfsson GI; Sigurdardottir O; Olafsson I; Arnar DO; Magnusson OT; Kong A; Masson G; Thorsteinsdottir U; Helgason A; Sulem P; Stefansson K

Article: ANNALS OF THE RHEUMATIC DISEASES. 2014;73(12):2130-2136

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

Evangelou E; Kerkhof HJ; Styrkarsdottir U; Ntzani EE; Bos SD; Esko T; Evans DS; Metrustry S; Panoutsopoulou K; Ramos YFM; Thorleifsson G; Tsilidis KK; Arden N; Aslam N; Bellamy N; Birrell F; Blanco FJ; Carr A; Chapman K; Day-Williams AG; Deloukas P; Doherty M; Engstrom G; Helgadottir HT; Hofman A; Ingvarsson T; Jonsson H; Keis A; Keurentjes JC; Kloppenburg M; Lind PA; McCaskie A; Martin NG; Milani L; Montgomery GW; Nelissen RGHH; Nevitt MC; Nilsson PM; Ollier WER; Parimi N; Rai A; Ralston SH; Reed MR; Riancho JA; Rivadeneira F; Rodriguez-Fontenla C; Southam L; Thorsteinsdottir U; Tsezou A; AWallis G; Wilkinson JM; Gonzalez A; Lane NE; Lohmander LS; Loughlin J; Metspalu A; Uitterlinden AG; Jonsdottir I; Stefansson K; Slagboom PE; Zeggini E; Meulenbelt I; Ioannidis JPA; Spector TD; van Meurs JBJ; Valdes AM

Article: HUMAN MOLECULAR GENETICS. 2014;23(11):3045-3053

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma

Stacey SN; Sulem P; Gudbjartsson DF; Jonasdottir A; Thorleifsson G; Gudjonsson SA; Masson G; Gudmundsson J; Sigurgeirsson B; Benediktsdottir KR; Thorisdottir K; Ragnarsson R; Fuentelsaz V; Corredera C; Grasa M; Planelles D; Sanmartin O; Rudnai P; Gurzau E; Koppova K; Hemminki K; Nexo BA; Tjonneland A; Overvad K; Johannsdottir H; Helgadottir HT; Thorsteinsdottir U; Kong A; Vogel U; Kumar R; Nagore E; Mayordomo JI; Rafnar T; Olafsson JH; Stefansson K

Article: NATURE GENETICS. 2014;46(5):498-502

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31

Styrkarsdottir U; Thorleifsson G; Helgadottir HT; Bomer N; Metrustry S; Bierma-Zeinstra S; Strijbosch AM; Evangelou E; Hart D; Beekman M; Jonasdottir A; Sigurdsson A; Eiriksson FF; Thorsteinsdottir M; Frigge ML; Kong A; Gudjonsson SA; Magnusson OT; Masson G; Hofman A; Arden NK; Ingvarsson T; Lohmander S; Kloppenburg M; Rivadeneira F; Nelissen RGHH; Spector T; Uitterlinden A; Slagboom PE; Thorsteinsdottir U; Jonsdottir I; Valdes AM; Meulenbelt I; van Meurs J; Jonsson H; Stefansson K

Article: ARTHRITIS & RHEUMATOLOGY. 2014;66(4):940-949

Assessment of Osteoarthritis Candidate Genes in a Meta-Analysis of Nine Genome-Wide Association Studies

Rodriguez-Fontenla C; Calaza M; Evangelou E; Valdes AM; Arden N; Blanco FJ; Carr A; Chapman K; Deloukas P; Doherty M; Esko T; Garces Aleta CM; Gomez-Reino Carnota JJ; Helgadottir H; Hofman A; Jonsdottir I; Kerkhof HJM; Kloppenburg M; McCaskie A; Ntzani EE; Ollier WER; Oreiro N; Panoutsopoulou K; Ralston SH; Ramos YF; Riancho JA; Rivadeneira F; Eline Slagboom P; Styrkarsdottir U; Thorsteinsdottir U; Thorleifsson G; Tsezou A; Uitterlinden AG; Wallis GA; Wilkinson JM; Zhai G; Zhu Y; Felson DT; Ioannidis JPA; Loughlin J; Metspalu A; Meulenbelt I; Stefansson K; van Meurs JB; Zeggini E; Spector TD; Gonzalez A

Article: NATURE GENETICS. 2014;46(3):294-298

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

Steinthorsdottir V; Thorleifsson G; Sulem P; Helgason H; Grarup N; Sigurdsson A; Helgadottir HT; Johannsdottir H; Magnusson OT; Gudjonsson SA; Justesen JM; Harder MN; Jorgensen ME; Christensen C; Brandslund I; Sandbaek A; Lauritzen T; Vestergaard H; Linneberg A; Jorgensen T; Hansen T; Daneshpour MS; Fallah M-S; Hreidarsson AB; Sigurdsson G; Azizi F; Benediktsson R; Masson G; Helgason A; Kong A; Gudbjartsson DF; Pedersen O; Thorsteinsdottir U; Stefansson K

Article: NATURE. 2013;497(7450):517-520

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

Styrkarsdottir U; Thorleifsson G; Sulem P; Gudbjartsson DF; Sigurdsson A; Jonasdottir A; Jonasdottir A; Oddsson A; Helgason A; Magnusson OT; BragiWalters G; Frigge ML; Helgadottir HT; Johannsdottir H; Bergsteinsdottir K; Ogmundsdottir MH; Center JR; Nguyen TV; Eisman JA; Christiansen C; Steingrimsson E; Jonasson JG; Tryggvadottir L; Eyjolfsson GI; Theodors A; Jonsson T; Ingvarsson T; Olafsson I; Rafnar T; Kong A; Sigurdsson G; Masson G; Thorsteinsdottir U; Stefansson K

Article: NATURE COMMUNICATIONS. 2013;4:2776

A common variant at 8q24.21 is associated with renal cell cancer

Gudmundsson J; Sulem P; Gudbjartsson DF; Masson G; Petursdottir V; Hardarson S; Gudjonsson SA; Johannsdottir H; Helgadottir HT; Stacey SN; Magnusson OT; Helgason H; Panadero A; van der Zanden LF; Aben KKH; Vermeulen SH; Oosterwijk E; Kong A; Mayordomo JI; Sverrisdottir A; Jonsson E; Gudbjartsson T; Einarsson GV; Kiemeney LA; Thorsteinsdottir U; Rafnar T; Stefansson K

Article: NATURE GENETICS. 2012;44(12):1326-1329

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

Gudmundsson J; Sulem P; Gudbjartsson DF; Masson G; Agnarsson BA; Benediktsdottir KR; Sigurdsson A; Magnusson OT; Gudjonsson SA; Magnusdottir DN; Johannsdottir H; Helgadottir HT; Stacey SN; Jonasdottir A; Olafsdottir SB; Thorleifsson G; Jonasson JG; Tryggvadottir L; Navarrete S; Fuertes F; Helfand BT; Hu Q; Csiki IE; Mates IN; Jinga V; Aben KKH; van Oort IM; Vermeulen SH; Donovan JL; Hamdy FC; Ng C-F; Chiu PKF; Lau K-M; Ng MCY; Gulcher JR; Kong A; Catalona WJ; Mayordomo JI; Einarsson GV; Barkardottir RB; Jonsson E; Mates D; Neal DE; Kiemeney LA; Thorsteinsdottir U; Rafnar T; Stefansson K

Article: NATURE GENETICS. 2012;44(3):319-322

Discovery of common variants associated with low TSH levels and thyroid cancer risk

Gudmundsson J; Sulem P; Gudbjartsson DF; Jonasson JG; Masson G; He H; Jonasdottir A; Sigurdsson A; Stacey SN; Johannsdottir H; Helgadottir HT; Li W; Nagy R; Ringel MD; Kloos RT; de Visser MCH; Plantinga TS; den Heijer M; Aguillo E; Panadero A; Prats E; Garcia-Castano A; De Juan A; Rivera F; Walters GB; Bjarnason H; Tryggvadottir L; Eyjolfsson GI; Bjornsdottir US; Holm H; Olafsson I; Kristjansson K; Kristvinsson H; Magnusson OT; Thorleifsson G; Gulcher JR; Kong A; Kiemeney LALM; Jonsson T; Hjartarson H; Mayordomo JI; Netea-Maier RT; de la Chapelle A; Hrafnkelsson J; Thorsteinsdottir U; Rafnar T; Stefansson K

Article: HUMAN MOLECULAR GENETICS. 2011;20(21):4268-4281

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene

Rafnar T; Vermeulen SH; Sulem P; Thorleifsson G; Aben KK; Witjes JA; Grotenhuis AJ; Verhaegh GW; Hulsbergen-van de Kaa CA; Besenbacher S; Gudbjartsson D; Stacey SN; Gudmundsson J; Johannsdottir H; Bjarnason H; Zanon C; Helgadottir H; Jonasson JG; Tryggvadottir L; Jonsson E; Geirsson G; Nikulasson S; Petursdottir V; Bishop DT; Chung-Sak S; Choudhury A; Elliott F; Barrett JH; Knowles MA; de Verdier PJ; Ryk C; Lindblom A; Rudnai P; Gurzau E; Koppova K; Vineis P; Polidoro S; Guarrera S; Sacerdote C; Panadero A; Sanz-Velez JI; Sanchez M; Valdivia G; Garcia-Prats MD; Hengstler JG; Selinski S; Gerullis H; Ovsiannikov D; Khezri A; Aminsharifi A; Malekzadeh M; van den Berg LH; Ophoff RA; Veldink JH; Zeegers MP; Kellen E; Fostinelli J; Andreoli D; Arici C; Porru S; Buntinx F; Ghaderi A; Golka K; Mayordomo JI; Matullo G; Kumar R; Steineck G; Kiltie AE; Kong A; Thorsteinsdottir U; Stefansson K; Kiemeney LA

Article: NATURE GENETICS. 2011;43(11):1127-1130

Identification of low-frequency variants associated with gout and serum uric acid levels

Sulem P; Gudbjartsson DF; Walters GB; Helgadottir HT; Helgason A; Gudjonsson SA; Zanon C; Besenbacher S; Bjornsdottir G; Magnusson OT; Magnusson G; Hjartarson E; Saemundsdottir J; Gylfason A; Jonasdottir A; Holm H; Karason A; Rafnar T; Stefansson H; Andreassen OA; Pedersen JH; Pack AI; de Visser MCH; Kiemeney LA; Geirsson AJ; Eyjolfsson GI; Olafsson I; Kong A; Masson G; Jonsson H; Thorsteinsdottir U; Jonsdottir I; Stefansson K

Article: NATURE GENETICS. 2011;43(11):1104-1107

Mutations in BRIP1 confer high risk of ovarian cancer

Rafnar T; Gudbjartsson DF; Sulem P; Jonasdottir A; Sigurdsson A; Jonasdottir A; Besenbacher S; Lundin P; Stacey SN; Gudmundsson J; Magnusson OT; le Roux L; Orlygsdottir G; Helgadottir HT; Johannsdottir H; Gylfason A; Tryggvadottir L; Jonasson JG; de Juan A; Ortega E; Ramon-Cajal JM; Garcia-Prats MD; Mayordomo C; Panadero A; Rivera F; Aben KKH; van Altena AM; Massuger LFAG; Aavikko M; Kujala PM; Staff S; Aaltonen LA; Olafsdottir K; Bjornsson J; Kong A; Salvarsdottir A; Saemundsson H; Olafsson K; Benediktsdottir KR; Gulcher J; Masson G; Kiemeney LA; Mayordomo JI; Thorsteinsdottir U; Stefansson K

Article: NATURE GENETICS. 2011;43(11):1098-1103

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

Stacey SN; Sulem P; Jonasdottir A; Masson G; Gudmundsson J; Gudbjartsson DF; Magnusson OT; Gudjonsson SA; Sigurgeirsson B; Thorisdottir K; Ragnarsson R; Benediktsdottir KR; Nexo BA; Tjonneland A; Overvad K; Rudnai P; Gurzau E; Koppova K; Hemminki K; Corredera C; Fuentelsaz V; Grasa P; Navarrete S; Fuertes F; Garcia-Prats MD; Sanambrosio E; Panadero A; De Juan A; Garcia A; Rivera F; Planelles D; Soriano V; Requena C; Aben KK; van Rossum MM; Cremers RGHM; van Oort IM; van Spronsen D-J; Schalken JA; Peters WHM; Helfand BT; Donovan JL; Hamdy FC; Badescu D; Codreanu O; Jinga M; Csiki IE; Constantinescu V; Badea P; Mates IN; Dinu DE; Constantin A; Mates D; Kristjansdottir S; Agnarsson BA; Jonsson E; Barkardottir RB; Einarsson GV; Sigurdsson F; Moller PH; Stefansson T; Valdimarsson T; Johannsson OT; Sigurdsson H; Jonsson T; Jonasson JG; Tryggvadottir L; Rice T; Hansen HM; Xiao Y; Lachance DH; Neill BPO; Kosel ML; Decker PA; Thorleifsson G; Johannsdottir H; Helgadottir HT; Sigurdsson A; Steinthorsdottir V; Lindblom A; Sandler RS; Keku TO; Banasik K; Jorgensen T; Witte DR; Hansen T; Pedersen O; Jinga V; Neal DE; Catalona WJ; Wrensch M; Wiencke J; Jenkins RB; Nagore E; Vogel U; Kiemeney LA; Kumar R; Mayordomo JI; Olafsson JH; Kong A; Thorsteinsdottir U; Rafnar T; Stefansson K

Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2011;89(3):446-450

A Variant in MCF2L Is Associated with Osteoarthritis

Day-Williams AG; Southam L; Panoutsopoulou K; Rayner NW; Esko T; Estrada K; Helgadottir HT; Hofman A; Ingvarsson T; Jonsson H; Keis A; Kerkhof HJM; Thorleifsson G; Arden NK; Carr A; Chapman K; Deloukas P; Loughlin J; McCaskie A; Ollier WER; Ralston SH; Spector TD; Wallis GA; Wilkinson JM; Aslam N; Birell F; Carluke I; Joseph J; Rai A; Reed M; Walker K; Doherty SA; Jonsdottir I; Maciewicz RA; Muir KR; Metspalu A; Rivadeneira F; Stefansson K; Styrkarsdottir U; Uitterlinden AG; van Meurs JBJ; Zhang W; Valdes AM; Doherty M; Zeggini E

Article: NATURE GENETICS. 2011;43(4):316-320

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

Holm H; Gudbjartsson DF; Sulem P; Masson G; Helgadottir HT; Zanon C; Magnusson OT; Helgason A; Saemundsdottir J; Gylfason A; Stefansdottir H; Gretarsdottir S; Matthiasson SE; Thorgeirsson G; Jonasdottir A; Sigurdsson A; Stefansson H; Werge T; Rafnar T; Kiemeney LA; Parvez B; Muhammad R; Roden DM; Darbar D; Thorleifsson G; Walters GB; Kong A; Thorsteinsdottir U; Arnar DO; Stefansson K

Article: ANNALS OF THE RHEUMATIC DISEASES. 2011;70(2):349-355

Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22

Evangelou E; Valdes AM; Kerkhof HJM; Styrkarsdottir U; Zhu Y; Meulenbelt I; Lories RJ; Karassa FB; Tylzanowski P; Bos SD; Akune T; Arden NK; Carr A; Chapman K; Cupples LA; Dai J; Deloukas P; Doherty M; Doherty S; Engstrom G; Gonzalez A; Halldorsson BV; Hammond CL; Hart DJ; Helgadottir H; Hofman A; Ikegawa S; Ingvarsson T; Jiang Q; Jonsson H; Kaprio J; Kawaguchi H; Kisand K; Kloppenburg M; Kujala UM; Lohmander LS; Loughlin J; Luyten FP; Mabuchi A; McCaskie A; Nakajima M; Nilsson PM; Nishida N; Ollier WER; Panoutsopoulou K; van de Putte T; Ralston SH; Rivadeneira F; Saarela J; Schulte-Merker S; Shi D; Slagboom PE; Sudo A; Tamm A; Tamm A; Thorleifsson G; Thorsteinsdottir U; Tsezou A; Wallis GA; Wilkinson JM; Yoshimura N; Zeggini E; Zhai G; Zhang F; Jonsdottir I; Uitterlinden AG; Felson DT; van Meurs JB; Stefansson K; Ioannidis JPA; Spector TD

Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2010;18(8):902-908

A sequence variant on 17q21 is associated with age at onset and severity of asthma

Halapi E; Gudbjartsson DF; Jonsdottir GM; Bjornsdottir US; Thorleifsson G; Helgadottir H; Williams C; Koppelman GH; Heinzmann A; Boezen HM; Jonasdottir A; Blondal T; Gudjonsson SA; Jonasdottir A; Thorlacius T; Henry AP; Altmueller J; Krueger M; Shin HD; Uh S-T; Cheong HS; Jonsdottir B; Ludviksson BR; Ludviksdottir D; Gislason D; Park C-S; Deichmann K; Thompson PJ; Wjst M; Hall IP; Postma DS; Gislason T; Kong A; Jonsdottir I; Thorsteinsdottir U; Stefansson K

Article: NATURE GENETICS. 2009;41(4):460-464

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; 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

Article: NATURE GENETICS. 2009;41(3):342-347

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; Beilby J; Warrington NM; James A; Palmer LJ; Koppelman GH; Heinzmann A; Krueger M; Boezen HM; Wheatley A; Altmuller J; Shin HD; Uh S-T; Cheong HS; Jonsdottir B; Gislason D; Park C-S; Rasmussen LM; Porsbjerg C; Hansen JW; Backer V; Werge T; Janson C; Joensson U-B; Ng MCY; Chan J; So WY; Ma R; Shah SH; Granger CB; Quyyumi AA; Levey AI; Vaccarino V; Reilly MP; Rader DJ; Williams MJA; 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

Article: NATURE GENETICS. 2009;41(2):221-227

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

Rafnar T; Sulem P; Stacey SN; Geller F; Gudmundsson J; Sigurdsson A; Jakobsdottir M; Helgadottir H; Thorlacius S; Aben KKH; Bloendal T; Thorgeirsson TE; Thorleifsson G; Kristjansson K; Thorisdottir K; Ragnarsson R; Sigurgeirsson B; Skuladottir H; Gudbjartsson T; Isaksson HJ; Einarsson GV; Benediktsdottir KR; Agnarsson BA; Olafsson K; Salvarsdottir A; Bjarnason H; Asgeirsdottir M; Kristinsson KT; Matthiasdottir S; Sveinsdottir SG; Polidoro S; Hoeiom V; Botella-Estrada R; Hemminki K; Rudnai P; Bishop DT; Campagna M; Kellen E; Zeegers MP; de Verdier P; Ferrer A; Isla D; Vidal MJ; Andres R; Saez B; Juberias P; Banzo J; Navarrete S; Tres A; Kan D; Lindblom A; Gurzau E; Koppova K; de Vegt F; Schalken JA; van der Heijden HFM; Smit HJ; Termeer RA; Oosterwijk E; van Hooij O; Nagore E; Porru S; Steineck G; Hansson J; Buntinx F; Catalona WJ; Matullo G; Vineis P; Kiltie AE; Mayordomo JI; Kumar R; Kiemeney LA; Frigge ML; Jonsson T; Saemundsson H; Barkardottir RB; Jonsson E; Jonsson S; Olafsson JH; Gulcher JR; Masson G; Gudbjartsson DF; Kong A; Thorsteinsdottir U; Stefansson K

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