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성함이나 학술지명, PMID로 찾아보십시오.
Jonsdottir I에 대해
41건, 그중 20건 표시.
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Wain LV,
Shrine N,
Artigas MS,
Erzurumluoglu AM,
Noyvert B,
Bossini-Castillo L,
Obeidat M,
Henry AP,
Portelli MA,
Hall RJ,
Billington CK,
Rimington TL
외 94명 — 모두 보기
Fenech AG,
John C,
Blake T,
Jackson VE,
Allen RJ,
Prins BP,
Campbell A,
Porteous DJ,
Jarvelin MR,
Wielscher M,
James AL,
Hui J,
Wareham NJ,
Zhao JH,
Wilson JF,
Joshi PK,
Stubbe B,
Rawal R,
Schulz H,
Imboden M,
Probst-Hensch NM,
Karrasch S,
Gieger C,
Deary IJ,
Harris SE,
Marten J,
Rudan I,
Enroth S,
Gyllensten U,
Kerr SM,
Polasek O,
Kähönen M,
Surakka I,
Vitart V,
Hayward C,
Lehtimäki T,
Raitakari OT,
Evans DM,
Henderson AJ,
Pennell CE,
Wang CA,
Sly PD,
Wan ES,
Busch R,
Hobbs BD,
Litonjua AA,
Sparrow DW,
Gulsvik A,
Bakke PS,
Crapo JD,
Beaty TH,
Hansel NN,
Mathias RA,
Ruczinski I,
Barnes KC,
Bossé Y,
Joubert P,
van den Berge M,
Brandsma CA,
Paré PD,
Sin DD,
Nickle DC,
Hao K,
Gottesman O,
Dewey FE,
Bruse SE,
Carey DJ,
Kirchner HL,
Jonsson S,
Thorleifsson G,
Jonsdottir I,
Gislason T,
Stefansson K,
Schurmann C,
Nadkarni G,
Bottinger EP,
Loos RJ,
Walters RG,
Chen Z,
Millwood IY,
Vaucher J,
Kurmi OP,
Li L,
Hansell AL,
Brightling C,
Zeggini E,
Cho MH,
Silverman EK,
Sayers I,
Trynka G,
Morris AP,
Strachan DP,
Hall IP,
Tobin MD
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
페이지 12개+
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Hammerschlag AR,
Stringer S,
de Leeuw CA,
Sniekers S,
Taskesen E,
Watanabe K,
Blanken TF,
Dekker K,
Te Lindert BHW,
Wassing R,
Jonsdottir I,
Thorleifsson G
외 10명 — 모두 보기
Nature genetics · 2017 · PMID 28604731 · open access
페이지 12개+
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Demenais F,
Margaritte-Jeannin P,
Barnes KC,
Cookson WOC,
Altmüller J,
Ang W,
Barr RG,
Beaty TH,
Becker AB,
Beilby J,
Bisgaard H,
Bjornsdottir US
외 163명 — 모두 보기
Bleecker E,
Bønnelykke K,
Boomsma DI,
Bouzigon E,
Brightling CE,
Brossard M,
Brusselle GG,
Burchard E,
Burkart KM,
Bush A,
Chan-Yeung M,
Chung KF,
Couto Alves A,
Curtin JA,
Custovic A,
Daley D,
de Jongste JC,
Del-Rio-Navarro BE,
Donohue KM,
Duijts L,
Eng C,
Eriksson JG,
Farrall M,
Fedorova Y,
Feenstra B,
Ferreira MA,
Freidin MB,
Gajdos Z,
Gauderman J,
Gehring U,
Geller F,
Genuneit J,
Gharib SA,
Gilliland F,
Granell R,
Graves PE,
Gudbjartsson DF,
Haahtela T,
Heckbert SR,
Heederik D,
Heinrich J,
Heliövaara M,
Henderson J,
Himes BE,
Hirose H,
Hirschhorn JN,
Hofman A,
Holt P,
Hottenga J,
Hudson TJ,
Hui J,
Imboden M,
Ivanov V,
Jaddoe VWV,
James A,
Janson C,
Jarvelin MR,
Jarvis D,
Jones G,
Jonsdottir I,
Jousilahti P,
Kabesch M,
Kähönen M,
Kantor DB,
Karunas AS,
Khusnutdinova E,
Koppelman GH,
Kozyrskyj AL,
Kreiner E,
Kubo M,
Kumar R,
Kumar A,
Kuokkanen M,
Lahousse L,
Laitinen T,
Laprise C,
Lathrop M,
Lau S,
Lee YA,
Lehtimäki T,
Letort S,
Levin AM,
Li G,
Liang L,
Loehr LR,
London SJ,
Loth DW,
Manichaikul A,
Marenholz I,
Martinez FJ,
Matheson MC,
Mathias RA,
Matsumoto K,
Mbarek H,
McArdle WL,
Melbye M,
Melén E,
Meyers D,
Michel S,
Mohamdi H,
Musk AW,
Myers RA,
Nieuwenhuis MAE,
Noguchi E,
O'Connor GT,
Ogorodova LM,
Palmer CD,
Palotie A,
Park JE,
Pennell CE,
Pershagen G,
Polonikov A,
Postma DS,
Probst-Hensch N,
Puzyrev VP,
Raby BA,
Raitakari OT,
Ramasamy A,
Rich SS,
Robertson CF,
Romieu I,
Salam MT,
Salomaa V,
Schlünssen V,
Scott R,
Selivanova PA,
Sigsgaard T,
Simpson A,
Siroux V,
Smith LJ,
Solodilova M,
Standl M,
Stefansson K,
Strachan DP,
Stricker BH,
Takahashi A,
Thompson PJ,
Thorleifsson G,
Thorsteinsdottir U,
Tiesler CMT,
Torgerson DG,
Tsunoda T,
Uitterlinden AG,
van der Valk RJP,
Vaysse A,
Vedantam S,
von Berg A,
von Mutius E,
Vonk JM,
Waage J,
Wareham NJ,
Weiss ST,
White WB,
Wickman M,
Widén E,
Willemsen G,
Williams LK,
Wouters IM,
Yang JJ,
Zhao JH,
Moffatt MF,
Ober C,
Nicolae DL
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
페이지 12개+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
외 213명 — 모두 보기
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
Okada Y,
Edwards TL,
Stefansson K,
Susztak K,
Scholz M,
Heid IM,
Hung AM,
Teumer A,
Pattaro C,
Woodward OM,
Vitart V,
Köttgen A
German Chronic Kidney Disease Study · Lifelines Cohort Study 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31578528 · open access
페이지 12개+
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Saevarsdottir S,
Olafsdottir TA,
Ivarsdottir EV,
Halldorsson GH,
Gunnarsdottir K,
Sigurdsson A,
Johannesson A,
Sigurdsson JK,
Juliusdottir T,
Lund SH,
Arnthorsson AO,
Styrmisdottir EL
외 34명 — 모두 보기
Gudmundsson J,
Grondal GM,
Steinsson K,
Alfredsson L,
Askling J,
Benediktsson R,
Bjarnason R,
Geirsson AJ,
Gudbjornsson B,
Gudjonsson H,
Hjaltason H,
Hreidarsson AB,
Klareskog L,
Kockum I,
Kristjansdottir H,
Love TJ,
Ludviksson BR,
Olsson T,
Onundarson PT,
Orvar KB,
Padyukov L,
Sigurgeirsson B,
Tragante V,
Bjarnadottir K,
Rafnar T,
Masson G,
Sulem P,
Gudbjartsson DF,
Melsted P,
Thorleifsson G,
Norddahl GL,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Nature · 2020 · PMID 32581359
페이지 12개+
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
Skuladottir AT,
Bjornsdottir G,
Ferkingstad E,
Einarsson G,
Stefansdottir L,
Nawaz MS,
Oddsson A,
Olafsdottir TA,
Saevarsdottir S,
Walters GB,
Magnusson SH,
Bjornsdottir A
외 18명 — 모두 보기
Sveinsson OA,
Vikingsson A,
Hansen TF,
Jacobsen RL,
Erikstrup C,
Schwinn M,
Brunak S,
Banasik K,
Ostrowski SR,
Troelsen A,
Henkel C,
Pedersen OB,
Jonsdottir I,
Gudbjartsson DF,
Sulem P,
Thorgeirsson TE,
Stefansson H,
Stefansson K
DBDS Genetic Consortium
Nature communications · 2022 · PMID 35332129 · open access
페이지 12개+
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Venkatesh SS,
Wittemans LBL,
Palmer DS,
Baya NA,
Ferreira T,
Hill B,
Lassen FH,
Parker MJ,
Reibe S,
Elhakeem A,
Banasik K,
Bruun MT
외 39명 — 모두 보기
Erikstrup C,
Aagard Jensen B,
Juul A,
Mikkelsen C,
Nielsen HS,
Ostrowski SR,
Pedersen OB,
Rohde PD,
Sørensen E,
Ullum H,
Westergaard D,
Haraldsson A,
Holm H,
Jonsdottir I,
Olafsson I,
Steingrimsdottir T,
Steinthorsdottir V,
Thorleifsson G,
Figueredo J,
Karjalainen MK,
Pasanen A,
Jacobs BM,
Kalantzis G,
Hubers N,
Lippincott M,
Fraser A,
Lawlor DA,
Timpson NJ,
Nyegaard M,
Stefansson K,
Magi R,
Laivuori H,
van Heel DA,
Boomsma DI,
Balasubramanian R,
Seminara SB,
Chan YM,
Laisk T,
Lindgren CM
Genes & Health Research Team · Estonian Biobank Research Team 외 컨소시엄 3곳
Nature genetics · 2025 · PMID 40229599 · open access
페이지 12개+
Genome-wide association study and polygenic risk prediction of hypothyroidism
Rand SA,
Ahlberg G,
Tragante V,
Monfort LM,
Zheng C,
Feldt-Rasmussen U,
Klose MC,
Teder-Laving M,
Metspalu A,
Poulsen HE,
Ellervik C,
Nygaard B
외 18명 — 모두 보기
Erikstrup C,
Bruun MT,
A Jensen B,
Ullum H,
Brunak S,
Schwinn M,
Ostrowski SR,
Pedersen OB,
Sørensen E,
Jonsdottir I,
Gudbjartsson DF,
Thorleifsson G,
Holm H,
Saevarsdottir S,
Stefansson K,
Salling Olesen M,
Bundgaard H,
Ghouse J
DBDS Genomic Consortium · Estonian Biobank Research Team 외 컨소시엄 1곳
Nature genetics · 2025 · PMID 41238958 · open access
페이지 12개+
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Olafsson S,
Alexandersson KF,
Gizurarson JGK,
Hauksdottir K,
Gunnarsson O,
Olafsson K,
Gudmundsson J,
Stacey SN,
Sveinbjornsson G,
Saemundsdottir J,
Bjornsson ES,
Olafsson S
외 22명 — 모두 보기
Bjornsson S,
Orvar KB,
Vikingsson A,
Geirsson AJ,
Arinbjarnarson S,
Bjornsdottir G,
Thorgeirsson TE,
Sigurdsson S,
Halldorsson GH,
Magnusson OT,
Masson G,
Holm H,
Jonsdottir I,
Sigurdardottir O,
Eyjolfsson GI,
Olafsson I,
Sulem P,
Thorsteinsdottir U,
Jonsson T,
Rafnar T,
Gudbjartsson DF,
Stefansson K
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
페이지 11개
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density
Ivarsdottir EV,
Benonisdottir S,
Thorleifsson G,
Sulem P,
Oddsson A,
Styrkarsdottir U,
Kristmundsdottir S,
Arnadottir GA,
Thorgeirsson G,
Jonsdottir I,
Zoega GM,
Thorsteinsdottir U
외 4명 — 모두 보기
Nature communications · 2019 · PMID 30894546 · open access
페이지 10개
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
외 38명 — 모두 보기
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
페이지 9개
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
Bjornsdottir G,
Stefansdottir L,
Thorleifsson G,
Sulem P,
Norland K,
Ferkingstad E,
Oddsson A,
Zink F,
Lund SH,
Nawaz MS,
Bragi Walters G,
Skuladottir AT
외 32명 — 모두 보기
Gudjonsson SA,
Einarsson G,
Halldorsson GH,
Bjarnadottir V,
Sveinbjornsson G,
Helgadottir A,
Styrkarsdottir U,
Gudmundsson LJ,
Pedersen OB,
Hansen TF,
Werge T,
Banasik K,
Troelsen A,
Skou ST,
Thørner LW,
Erikstrup C,
Nielsen KR,
Mikkelsen S,
Jonsdottir I,
Bjornsson A,
Olafsson IH,
Ulfarsson E,
Blondal J,
Vikingsson A,
Brunak S,
Ostrowski SR,
Ullum H,
Thorsteinsdottir U,
Stefansson H,
Gudbjartsson DF,
Thorgeirsson TE,
Stefansson K
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
페이지 8개
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
Bønnelykke K,
Matheson MC,
Pers TH,
Granell R,
Strachan DP,
Alves AC,
Linneberg A,
Curtin JA,
Warrington NM,
Standl M,
Kerkhof M,
Jonsdottir I
외 58명 — 모두 보기
Bukvic BK,
Kaakinen M,
Sleimann P,
Thorleifsson G,
Thorsteinsdottir U,
Schramm K,
Baltic S,
Kreiner-Møller E,
Simpson A,
St Pourcain B,
Coin L,
Hui J,
Walters EH,
Tiesler CMT,
Duffy DL,
Jones G,
Ring SM,
McArdle WL,
Price L,
Robertson CF,
Pekkanen J,
Pekkanen J,
Tang CS,
Thiering E,
Montgomery GW,
Hartikainen AL,
Dharmage SC,
Husemoen LL,
Herder C,
Kemp JP,
Elliot P,
James A,
Waldenberger M,
Abramson MJ,
Fairfax BP,
Knight JC,
Knight JC,
Gupta R,
Thompson PJ,
Holt P,
Sly P,
Hirschhorn JN,
Blekic M,
Weidinger S,
Hakonarsson H,
Stefansson K,
Heinrich J,
Postma DS,
Custovic A,
Pennell CE,
Pennell CE,
Jarvelin MR,
Koppelman GH,
Timpson N,
Ferreira MA,
Ferreira MA,
Bisgaard H,
Henderson AJ
AAGC
Nature genetics · 2013 · PMID 23817571
페이지 7개
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
외 40명 — 모두 보기
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
페이지 7개
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,
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외 16명 — 모두 보기
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Communications biology · 2021 · PMID 34108613 · open access
페이지 7개
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
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외 12명 — 모두 보기
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Nature communications · 2016 · PMID 26838040 · open access
페이지 6개
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
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외 23명 — 모두 보기
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Nature communications · 2020 · PMID 31959851 · open access
페이지 6개
Identification of sequence variants influencing immunoglobulin levels
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외 26명 — 모두 보기
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Nature genetics · 2017 · PMID 28628107
페이지 5개
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
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외 17명 — 모두 보기
Sigurdsson A,
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Nature genetics · 2018 · PMID 30374069
페이지 5개
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
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Tragante V,
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외 28명 — 모두 보기
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Bjornsdottir US,
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Gudbjartsson DF,
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Nature genetics · 2019 · PMID 30643255
페이지 5개
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