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Suggested authors matching "AUTH:Thorgeirsson T" with an ORCID

Thorgeir Thorgeirsson
Decode genetics / Amgen
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Genome-wide association study of borderline personality disorder identifies six loci and highlights shared risk with mental and somatic disorders
Streit F, Awasthi S, Hall AS, Niarchou M, Marouli E, Babajide O, Braun A, Frank J, Zillich L, Callies C, Avetyan D, Zillich E, Naamanka J, Aherrahrou Z, Ahmad Z, Ask H, Batzler A, Benros ME, Brand-de Wilde OM, [...] Witt SH
medRxiv, 13 Nov 2024
Cited by: 0 articles | PPR: PPR939284
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Sequence variants associated with BMI affect disease risk through BMI itself.
Einarsson G, Thorleifsson G, Steinthorsdottir V, Zink F, Helgason H, Olafsdottir T, Rognvaldsson S, Tragante V, Ulfarsson MO, Sveinbjornsson G, Snaebjarnarson AS, Einarsson H, Aegisdottir HM, Jonsdottir GA, Helgadottir A, Gretarsdottir S, Styrkarsdottir U, Arnason HK, Bjarnason R, [...] Stefansson K
Nat Commun, 15(1):9335, 12 Nov 2024
Cited by: 0 articles | PMID: 39532837 | PMCID: PMC11557886
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Trigeminal neuralgia and its comorbidities: a nationwide disease trajectory study.
Worm J, Worm J, Jørgensen IF, Davídsson ÓB, Hjalgrim H, Röder T, Ostrowski SR, Pedersen OB, Erikstrup C, Bruun MT, Jensen BA, Sørensen E, Ullum H, Björnsdóttir G, Thorgeirsson T, Stefánsson H, Sveinsson ÓÁ, Stefánsson K, Schytz HW, [...] DBDS Genomic Consortium
Pain, 01 Oct 2024
Cited by: 0 articles | PMID: 39365662
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Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.
Skuladottir AT, Tragante V, Sveinbjornsson G, Helgason H, Sturluson A, Bjornsdottir A, Jonsson P, Palmadottir V, Sveinsson OA, Jensson BO, Gudjonsson SA, Ivarsdottir EV, Gisladottir RS, Gunnarsson AF, Walters GB, Jonsdottir GA, Thorgeirsson TE, Bjornsdottir G, Holm H, [...] Stefansson K
NPJ Parkinsons Dis, 10(1):140, 15 Aug 2024
Cited by: 0 articles | PMID: 39147844 | PMCID: PMC11327306
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Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs
Koch E, Jurgenson T, Einarsson G, Mitchell B, Harder A, Garcia-Marin LM, Krebs K, Lin Y, Xiong Y, Research Team EB, Lu Y, Hagg S, Renteria ME, Medland SE, Wray NR, Martin NG, Huebel C, Breen G, Thorgeirsson T, [...] O'Connell KS
medRxiv, 15 Jul 2024
Cited by: 0 articles | PPR: PPR881602
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HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study.
Qu K, Li MX, Yu P, International Headache Genetics Consortium, Wu BH, Shi M, Dong M
Sci Rep, 14(1):12094, 27 May 2024
Cited by: 2 articles | PMID: 38802400 | PMCID: PMC11130224
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Homozygosity for R47H in TREM2 and the Risk of Alzheimer's Disease.
Stefansson H, Walters GB, Sveinbjornsson G, Tragante V, Einarsson G, Helgason H, Sigurðsson A, Beyter D, Snaebjarnarson AS, Ivarsdottir EV, Thorleifsson G, Halldorsson BV, Norddahl G, Styrkarsdottir U, Sturluson A, Holm H, Helgason A, Moore K, Eggertsson HP, [...] DemGen Study Group and DBDS Genomic Consortium
N Engl J Med, 390(23):2217-2219, 01 Jun 2024
Cited by: 1 article | PMID: 38899702
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Genetic causal relationship between immune diseases and migraine: a Mendelian randomization study.
Li G, Duan S, International Headache Genetics Consortium (IHGC), Zheng T, Zhu T, Qu B, Liu L, Liu Z
Front Immunol, 15:1376698, 08 Apr 2024
Cited by: 0 articles | PMID: 38650934 | PMCID: PMC11033421
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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, Sulem P, Gudbjartsson DF, Knowlton KU, Jones DA, Ottas A, Estonian Biobank, Pedersen OB, [...] Stefansson K
Commun Biol, 7(1):504, 26 Apr 2024
Cited by: 0 articles | PMID: 38671141 | PMCID: PMC11053069
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Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.
Bjornsdottir G, Chalmer MA, Stefansdottir L, Skuladottir AT, Einarsson G, Andresdottir M, Beyter D, Ferkingstad E, Gretarsdottir S, Halldorsson BV, Halldorsson GH, Helgadottir A, Helgason H, Hjorleifsson Eldjarn G, Jonasdottir A, Jonasdottir A, Jonsdottir I, Knowlton KU, Nadauld LD, [...] Stefansson K
Nat Genet, 55(11):1843-1853, 26 Oct 2023
Cited by: 7 articles | PMID: 37884687 | PMCID: PMC10632135
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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, Jonsdottir I, Gretarsdottir S, Tragante V, Magnusson MK, Jonsson H, Gudmundsson J, Olafsson S, [...] Stefansson K
Nat Genet, 55(12):2149-2159, 06 Nov 2023
Cited by: 12 articles | PMID: 37932435 | PMCID: PMC10703693
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Genomics yields biological and phenotypic insights into bipolar disorder
O’Connell KS, Koromina M, van der Veen T, Boltz T, David FS, Kay Yang JM, Lin K, Wang X, Coleman JRI, Coleman JRI, Coleman JRI, Mitchell BL, McGrouther CC, Rangan AV, Lind PA, Koch E, Harder A, Parker N, Bendl J, [...] Jones I
medRxiv, 07 Oct 2023
Cited by: 0 articles | PPR: PPR738044
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Complex effects of sequence variants on lipid levels and coronary artery disease.
Snaebjarnarson AS, Helgadottir A, Arnadottir GA, Ivarsdottir EV, Thorleifsson G, Ferkingstad E, Einarsson G, Sveinbjornsson G, Thorgeirsson TE, Ulfarsson MO, Halldorsson BV, Olafsson I, Erikstrup C, Pedersen OB, Nyegaard M, Bruun MT, Ullum H, Brunak S, Iversen KK, [...] Gudbjartsson DF
Cell, 186(19):4085-4099.e15, 01 Sep 2023
Cited by: 4 articles | PMID: 37714134
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Polygenic risk prediction: why and when out-of-sample prediction R² can exceed SNP-based heritability.
Wang X, Walker A, Revez JA, Ni G, Adams MJ, McIntosh AM, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Visscher PM, Wray NR
Am J Hum Genet, 110(7):1207-1215, 27 Jun 2023
Cited by: 4 articles | PMID: 37379836 | PMCID: PMC10357496
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Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.
Winsvold BS, Harder AVE, Ran C, Chalmer MA, Dalmasso MC, Ferkingstad E, Tripathi KP, Bacchelli E, Børte S, Fourier C, Petersen AS, Vijfhuizen LS, Magnusson SH, O'Connor E, Bjornsdottir G, Häppölä P, Wang YF, Callesen I, Kelderman T, [...] International Consortium for Cluster Headache Genetics
Ann Neurol, 94(4):713-726, 07 Aug 2023
Cited by: 8 articles | PMID: 37486023 | PMCID: PMC10952302
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Migraine, chronic kidney disease and kidney function: observational and genetic analyses.
Zhang W, Zhang L, Yang L, Xiao C, Wu X, Yan P, Cui H, Yang C, Zhu J, Wu X, Tang M, Wang Y, Chen L, Liu Y, Zou Y, Zhang L, Yang C, Yao Y, Li J, [...] International Headache Genetics Consortium
Hum Genet, 142(8):1185-1200, 12 Jun 2023
Cited by: 4 articles | PMID: 37306871 | PMCID: PMC10449948
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Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.
Als TD, Kurki MI, Grove J, Voloudakis G, Therrien K, Tasanko E, Nielsen TT, Naamanka J, Veerapen K, Levey DF, Bendl J, Bybjerg-Grauholm J, Zeng B, Demontis D, Rosengren A, Athanasiadis G, Bækved-Hansen M, Qvist P, Bragi Walters G, [...] Børglum AD
Nat Med, 29(7):1832-1844, 18 Jul 2023
Cited by: 49 articles | PMID: 37464041 | PMCID: PMC10839245
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A causal effects of gut microbiota in the development of migraine.
He Q, Wang W, Xiong Y, Tao C, Ma L, Ma J, You C, International Headache Genetics Consortium
J Headache Pain, 24(1):90, 17 Jul 2023
Cited by: 12 articles | PMID: 37460956 | PMCID: PMC10353251
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A New Digital Health Program for Patients With Inflammatory Bowel Disease: Preliminary Program Evaluation.
Oddsson SJ, Gunnarsdottir T, Johannsdottir LG, Amundadottir ML, Frimannsdottir A, Molander P, Ylanne AK, Islind AS, Oskarsdottir M, Thorgeirsson T
JMIR Form Res, 7:e39331, 28 Apr 2023
Cited by: 3 articles | PMID: 37115598 | PMCID: PMC10182451
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Genetic variants associated with syncope implicate neural and autonomic processes.
Aegisdottir HM, Thorolfsdottir RB, Sveinbjornsson G, Stefansson OA, Gunnarsson B, Tragante V, Thorleifsson G, Stefansdottir L, Thorgeirsson TE, Ferkingstad E, Sulem P, Norddahl G, Rutsdottir G, Banasik K, Christensen AH, Mikkelsen C, Pedersen OB, Brunak S, Bruun MT, [...] Stefansson K
Eur Heart J, 44(12):1070-1080, 01 Mar 2023
Cited by: 1 article | PMID: 36747475
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Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.
Zhao L, Zhao W, International Headache Genetics Consortium (IHGC), Cao J, Tu Y
J Headache Pain, 24(1):10, 16 Feb 2023
Cited by: 6 articles | PMID: 36793015 | PMCID: PMC9933315
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Improving outpatient care for heart failure through digital innovation: a feasibility study.
Arnar DO, Oddsson SJ, Gunnarsdottir T, Gudlaugsdottir GJ, Gudmundsson EF, Ketilsdóttir A, Halldorsdottir H, Hrafnkelsdottir TJ, Hallsson H, Amundadottir ML, Thorgeirsson T
Pilot Feasibility Stud, 8(1):242, 30 Nov 2022
Cited by: 1 article | PMID: 36451212 | PMCID: PMC9709356
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Thirty novel sequence variants impacting human intracranial volume.
Nawaz MS, Einarsson G, Bustamante M, Gisladottir RS, Walters GB, Jonsdottir GA, Skuladottir AT, Bjornsdottir G, Magnusson SH, Asbjornsdottir B, Unnsteinsdottir U, Sigurdsson E, Jonsson PV, Palmadottir VK, Gudjonsson SA, Halldorsson GH, Ferkingstad E, Jonsdottir I, Thorleifsson G, [...] Stefansson K
Brain Commun, 4(6):fcac271, 25 Oct 2022
Cited by: 3 articles | PMID: 36415660 | PMCID: PMC9677475
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Genetic diversity fuels gene discovery for tobacco and alcohol use.
Saunders GRB, Wang X, Chen F, Jang SK, Liu M, Wang C, Gao S, Jiang Y, Khunsriraksakul C, Otto JM, Addison C, Akiyama M, Albert CM, Aliev F, Alonso A, Arnett DK, Ashley-Koch AE, Ashrani AA, Barnes KC, [...] Vrieze S
Nature, 612(7941):720-724, 07 Dec 2022
Cited by: 136 articles | PMID: 36477530 | PMCID: PMC9771818
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Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.
Henkel C, Styrkársdóttir U, Thorleifsson G, Stefánsdóttir L, Björnsdóttir G, Banasik K, Brunak S, Erikstrup C, Dinh KM, Hansen TF, Nielsen KR, Bruun MT, Dowsett J, Brodersen T, DBDS Genomic Consortium, Thorgeirsson TE, Gromov K, Boesen MP, Ullum H, [...] Troelsen A
Ann Rheum Dis, 82(3):384-392, 14 Nov 2022
Cited by: 9 articles | PMID: 36376028
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Search life-sciences literature (45,104,206 articles, preprints and more)

Suggested authors matching "AUTH:Thorgeirsson T" with an ORCID

Search results

Genome-wide association study of borderline personality disorder identifies six loci and highlights shared risk with mental and somatic disorders

Sequence variants associated with BMI affect disease risk through BMI itself.

Trigeminal neuralgia and its comorbidities: a nationwide disease trajectory study.

Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs

HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study.

Homozygosity for R47H in TREM2 and the Risk of Alzheimer's Disease.

Genetic causal relationship between immune diseases and migraine: a Mendelian randomization study.

GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis.

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.

Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.

Genomics yields biological and phenotypic insights into bipolar disorder

Complex effects of sequence variants on lipid levels and coronary artery disease.

Polygenic risk prediction: why and when out-of-sample prediction R² can exceed SNP-based heritability.

Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.

Migraine, chronic kidney disease and kidney function: observational and genetic analyses.

Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.

A causal effects of gut microbiota in the development of migraine.

A New Digital Health Program for Patients With Inflammatory Bowel Disease: Preliminary Program Evaluation.

Genetic variants associated with syncope implicate neural and autonomic processes.

Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.

Improving outpatient care for heart failure through digital innovation: a feasibility study.

Thirty novel sequence variants impacting human intracranial volume.

Genetic diversity fuels gene discovery for tobacco and alcohol use.

Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.

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