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성함이나 학술지명, PMID로 찾아보십시오.
Stefansson H에 대해
39건, 그중 19건 표시.
Many sequence variants affecting diversity of adult human height
Gudbjartsson DF,
Walters GB,
Thorleifsson G,
Stefansson H,
Halldorsson BV,
Zusmanovich P,
Sulem P,
Thorlacius S,
Gylfason A,
Steinberg S,
Helgadottir A,
Ingason A
외 25명 — 모두 보기
Steinthorsdottir V,
Olafsdottir EJ,
Olafsdottir GH,
Jonsson T,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Pedersen O,
Aben KK,
Witjes JA,
Swinkels DW,
den Heijer M,
Franke B,
Verbeek AL,
Becker DM,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Gulcher J,
Kiemeney LA,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2008 · PMID 18391951
페이지 3개
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
Li R,
Brockschmidt FF,
Kiefer AK,
Stefansson H,
Nyholt DR,
Song K,
Vermeulen SH,
Kanoni S,
Glass D,
Medland SE,
Dimitriou M,
Waterworth D
외 27명 — 모두 보기
Tung JY,
Geller F,
Heilmann S,
Hillmer AM,
Bataille V,
Eigelshoven S,
Hanneken S,
Moebus S,
Herold C,
den Heijer M,
Montgomery GW,
Deloukas P,
Eriksson N,
Heath AC,
Becker T,
Sulem P,
Mangino M,
Vollenweider P,
Spector TD,
Dedoussis G,
Martin NG,
Kiemeney LA,
Mooser V,
Stefansson K,
Hinds DA,
Nöthen MM,
Richards JB
PLoS genetics · 2012 · PMID 22693459 · open access
페이지 3개
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Anttila V,
Winsvold BS,
Gormley P,
Kurth T,
Bettella F,
McMahon G,
Kallela M,
Malik R,
de Vries B,
Terwindt G,
Medland SE,
Todt U
외 85명 — 모두 보기
McArdle WL,
Quaye L,
Koiranen M,
Ikram MA,
Lehtimäki T,
Stam AH,
Ligthart L,
Wedenoja J,
Dunham I,
Neale BM,
Palta P,
Hamalainen E,
Schürks M,
Rose LM,
Buring JE,
Ridker PM,
Steinberg S,
Stefansson H,
Jakobsson F,
Lawlor DA,
Evans DM,
Ring SM,
Färkkilä M,
Artto V,
Kaunisto MA,
Freilinger T,
Schoenen J,
Frants RR,
Pelzer N,
Weller CM,
Zielman R,
Heath AC,
Madden PAF,
Montgomery GW,
Martin NG,
Borck G,
Göbel H,
Heinze A,
Heinze-Kuhn K,
Williams FMK,
Hartikainen AL,
Pouta A,
van den Ende J,
Uitterlinden AG,
Hofman A,
Amin N,
Hottenga JJ,
Vink JM,
Heikkilä K,
Alexander M,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Wichmann HE,
Aromaa A,
Eriksson JG,
Traynor B,
Trabzuni D,
Rossin E,
Lage K,
Jacobs SBR,
Jacobs SBR,
Gibbs JR,
Birney E,
Kaprio J,
Penninx BW,
Boomsma DI,
van Duijn C,
van Duijn C,
Raitakari O,
Jarvelin MR,
Zwart JA,
Cherkas L,
Strachan DP,
Kubisch C,
Ferrari MD,
van den Maagdenberg AMJM,
Dichgans M,
Wessman M,
Smith GD,
Stefansson K,
Daly MJ,
Nyholt DR,
Chasman D,
Palotie A
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
페이지 3개
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
외 16명 — 모두 보기
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
페이지 3개
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Saevarsdottir S,
Stefansdottir L,
Sulem P,
Thorleifsson G,
Ferkingstad E,
Rutsdottir G,
Glintborg B,
Westerlind H,
Grondal G,
Loft IC,
Sorensen SB,
Lie BA
외 66명 — 모두 보기
Brink M,
Ärlestig L,
Arnthorsson AO,
Baecklund E,
Banasik K,
Bank S,
Bjorkman LI,
Ellingsen T,
Erikstrup C,
Frei O,
Gjertsson I,
Gudbjartsson DF,
Gudjonsson SA,
Halldorsson GH,
Hendricks O,
Hillert J,
Hogdall E,
Jacobsen S,
Jensen DV,
Jonsson H,
Kastbom A,
Kockum I,
Kristensen S,
Kristjansdottir H,
Larsen MH,
Linauskas A,
Hauge EM,
Loft AG,
Ludviksson BR,
Lund SH,
Markusson T,
Masson G,
Melsted P,
Moore KHS,
Munk H,
Nielsen KR,
Norddahl GL,
Oddsson A,
Olafsdottir TA,
Olason PI,
Olsson T,
Ostrowski SR,
Hørslev-Petersen K,
Rognvaldsson S,
Sanner H,
Silberberg GN,
Stefansson H,
Sørensen E,
Sørensen IJ,
Turesson C,
Bergman T,
Alfredsson L,
Kvien TK,
Brunak S,
Steinsson K,
Andersen V,
Andreassen OA,
Rantapää-Dahlqvist S,
Hetland ML,
Klareskog L,
Askling J,
Padyukov L,
Pedersen OB,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group 외 컨소시엄 1곳
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
페이지 3개
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
외 61명 — 모두 보기
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
페이지 2개
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
외 75명 — 모두 보기
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
페이지 2개
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
외 90명 — 모두 보기
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
페이지 2개
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Cichon S,
Mühleisen TW,
Degenhardt FA,
Mattheisen M,
Miró X,
Strohmaier J,
Steffens M,
Meesters C,
Herms S,
Weingarten M,
Priebe L,
Haenisch B
외 64명 — 모두 보기
Alexander M,
Vollmer J,
Breuer R,
Schmäl C,
Tessmann P,
Moebus S,
Wichmann HE,
Schreiber S,
Müller-Myhsok B,
Lucae S,
Jamain S,
Leboyer M,
Bellivier F,
Etain B,
Henry C,
Kahn JP,
Heath S,
Hamshere M,
O'Donovan MC,
Owen MJ,
Craddock N,
Schwarz M,
Vedder H,
Kammerer-Ciernioch J,
Reif A,
Sasse J,
Bauer M,
Hautzinger M,
Wright A,
Mitchell PB,
Schofield PR,
Montgomery GW,
Medland SE,
Gordon SD,
Martin NG,
Gustafsson O,
Andreassen O,
Djurovic S,
Sigurdsson E,
Steinberg S,
Stefansson H,
Stefansson K,
Kapur-Pojskic L,
Oruc L,
Rivas F,
Mayoral F,
Chuchalin A,
Babadjanova G,
Tiganov AS,
Pantelejeva G,
Abramova LI,
Grigoroiu-Serbanescu M,
Diaconu CC,
Czerski PM,
Hauser J,
Zimmer A,
Lathrop M,
Schulze TG,
Wienker TF,
Schumacher J,
Maier W,
Propping P,
Rietschel M,
Nöthen MM
Bipolar Disorder Genome Study (BiGS) Consortium
American journal of human genetics · 2011 · PMID 21353194
페이지 2개
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction
Braun A,
Shekhar S,
Levey DF,
Straub P,
Kraft J,
Panagiotaropoulou GM,
Heilbron K,
Awasthi S,
Meleka Hanna R,
Hoffmann S,
Stein M,
Lehnerer S
외 28명 — 모두 보기
Mergenthaler P,
Elnahas AG,
Topaloudi A,
Koromina M,
Palviainen T,
Asbjornsdottir B,
Stefansson H,
Skuladóttir AT,
Jónsdóttir I,
Stefansson K,
Reis K,
Esko T,
Palotie A,
Leypoldt F,
Stein MB,
Fontanillas P,
Kaprio J,
Gelernter J,
Davis LK,
Paschou P,
Tannemaat MR,
Verschuuren JJGM,
Kuhlenbäumer G,
Gregersen PK,
Huijbers MG,
Stascheit F,
Meisel A,
Ripke S
Estonian Biobank Research Team · 23andMe Research Team
Nature communications · 2024 · PMID 39537604 · open access
페이지 2개
A genetic risk factor for periodic limb movements in sleep
Stefansson H,
Rye DB,
Hicks A,
Petursson H,
Ingason A,
Thorgeirsson TE,
Palsson S,
Sigmundsson T,
Sigurdsson AP,
Eiriksdottir I,
Soebech E,
Bliwise D
외 14명 — 모두 보기
Beck JM,
Rosen A,
Waddy S,
Trotti LM,
Iranzo A,
Thambisetty M,
Hardarson GA,
Kristjansson K,
Gudmundsson LJ,
Thorsteinsdottir U,
Kong A,
Gulcher JR,
Gudbjartsson D,
Stefansson K
The New England journal of medicine · 2007 · PMID 17634447
페이지 1개
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Thorgeirsson TE,
Geller F,
Sulem P,
Rafnar T,
Wiste A,
Magnusson KP,
Manolescu A,
Thorleifsson G,
Stefansson H,
Ingason A,
Stacey SN,
Bergthorsson JT
외 45명 — 모두 보기
Thorlacius S,
Gudmundsson J,
Jonsson T,
Jakobsdottir M,
Saemundsdottir J,
Olafsdottir O,
Gudmundsson LJ,
Bjornsdottir G,
Kristjansson K,
Skuladottir H,
Isaksson HJ,
Gudbjartsson T,
Jones GT,
Mueller T,
Gottsäter A,
Flex A,
Aben KKH,
de Vegt F,
Mulders PFA,
Isla D,
Vidal MJ,
Asin L,
Saez B,
Murillo L,
Blondal T,
Kolbeinsson H,
Stefansson JG,
Hansdottir I,
Runarsdottir V,
Pola R,
Lindblad B,
van Rij AM,
Dieplinger B,
Haltmayer M,
Mayordomo JI,
Kiemeney LA,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Gudbjartsson DF,
Gulcher JR,
Jonsson S,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature · 2008 · PMID 18385739
페이지 1개
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
외 82명 — 모두 보기
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
Thompson JR,
Aulchenko YS,
Nelis M,
Aben KK,
den Heijer M,
Dirksen A,
Ashraf H,
Soranzo N,
Valdes AM,
Steves C,
Uitterlinden AG,
Hofman A,
Tönjes A,
Kovacs P,
Hottenga JJ,
Willemsen G,
Vogelzangs N,
Döring A,
Dahmen N,
Nitz B,
Pergadia ML,
Saez B,
De Diego V,
Lezcano V,
Garcia-Prats MD,
Ripatti S,
Perola M,
Kettunen J,
Hartikainen AL,
Pouta A,
Laitinen J,
Isohanni M,
Huei-Yi S,
Allen M,
Krestyaninova M,
Hall AS,
Jones GT,
van Rij AM,
Mueller T,
Dieplinger B,
Haltmayer M,
Jonsson S,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Kiemeney LA,
Mayordomo JI,
Lindholt JS,
Pedersen JH,
Franklin WA,
Wolf H,
Montgomery GW,
Heath AC,
Martin NG,
Madden PA,
Giegling I,
Rujescu D,
Järvelin MR,
Salomaa V,
Stumvoll M,
Spector TD,
Wichmann HE,
Metspalu A,
Samani NJ,
Penninx BW,
Oostra BA,
Boomsma DI,
Tiemeier H,
van Duijn CM,
Kaprio J,
Gulcher JR,
McCarthy MI,
Peltonen L,
Thorsteinsdottir U,
Stefansson K
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
페이지 1개
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Thorleifsson G,
Walters GB,
Hewitt AW,
Masson G,
Helgason A,
DeWan A,
Sigurdsson A,
Jonasdottir A,
Gudjonsson SA,
Magnusson KP,
Stefansson H,
Lam DS
외 35명 — 모두 보기
Tam PO,
Gudmundsdottir GJ,
Southgate L,
Burdon KP,
Gottfredsdottir MS,
Aldred MA,
Mitchell P,
St Clair D,
Collier DA,
Tang N,
Sveinsson O,
Macgregor S,
Martin NG,
Cree AJ,
Gibson J,
Macleod A,
Jacob A,
Ennis S,
Young TL,
Chan JC,
Karwatowski WS,
Hammond CJ,
Thordarson K,
Zhang M,
Wadelius C,
Lotery AJ,
Trembath RC,
Pang CP,
Hoh J,
Craig JE,
Kong A,
Mackey DA,
Jonasson F,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20835238
페이지 1개
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Power RA,
Tansey KE,
Buttenschøn HN,
Cohen-Woods S,
Bigdeli T,
Hall LS,
Kutalik Z,
Lee SH,
Ripke S,
Steinberg S,
Teumer A,
Viktorin A
외 64명 — 모두 보기
Wray NR,
Arolt V,
Baune BT,
Boomsma DI,
Børglum AD,
Byrne EM,
Castelao E,
Craddock N,
Craig IW,
Dannlowski U,
Deary IJ,
Degenhardt F,
Forstner AJ,
Gordon SD,
Grabe HJ,
Grove J,
Hamilton SP,
Hayward C,
Heath AC,
Hocking LJ,
Homuth G,
Hottenga JJ,
Kloiber S,
Krogh J,
Landén M,
Lang M,
Levinson DF,
Lichtenstein P,
Lucae S,
MacIntyre DJ,
Madden P,
Magnusson PKE,
Martin NG,
McIntosh AM,
Middeldorp CM,
Milaneschi Y,
Montgomery GW,
Mors O,
Müller-Myhsok B,
Nyholt DR,
Oskarsson H,
Owen MJ,
Padmanabhan S,
Penninx BWJH,
Pergadia ML,
Porteous DJ,
Potash JB,
Preisig M,
Rivera M,
Shi J,
Shyn SI,
Sigurdsson E,
Smit JH,
Smith BH,
Stefansson H,
Stefansson K,
Strohmaier J,
Sullivan PF,
Thomson P,
Thorgeirsson TE,
Van der Auwera S,
Weissman MM,
Breen G,
Lewis CM
CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium
Biological psychiatry · 2017 · PMID 27519822 · open access
페이지 1개
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Lo MT,
Hinds DA,
Tung JY,
Franz C,
Fan CC,
Wang Y,
Smeland OB,
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Holland D,
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Escott-Price V
외 10명 — 모두 보기
Nature genetics · 2017 · PMID 27918536
페이지 1개
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy
Bjornsdottir G,
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Jonasdottir A,
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Jonsdottir I
외 21명 — 모두 보기
Kristinsdottir AM,
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Nature communications · 2019 · PMID 30992453 · open access
페이지 1개
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Didriksen M,
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Sørensen E,
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Soranzo N
외 22명 — 모두 보기
Rye DB,
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Communications biology · 2020 · PMID 33239738 · open access
페이지 1개
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
Skuladottir AT,
Bjornsdottir G,
Nawaz MS,
Petersen H,
Rognvaldsson S,
Moore KHS,
Olafsson PI,
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외 19명 — 모두 보기
Ivarsdottir EV,
Stefansdottir L,
Gunnarsson B,
Muhlestein JB,
Knowlton KU,
Jones DA,
Nadauld LD,
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Strupp M,
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Communications biology · 2021 · PMID 34620984 · open access
페이지 1개
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