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29건, 그중 20건 표시.
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Hautakangas H,
Winsvold BS,
Ruotsalainen SE,
Bjornsdottir G,
Harder AVE,
Kogelman LJA,
Thomas LF,
Noordam R,
Benner C,
Gormley P,
Artto V,
Banasik K
외 59명 — 모두 보기
Bjornsdottir A,
Boomsma DI,
Brumpton BM,
Burgdorf KS,
Buring JE,
Chalmer MA,
de Boer I,
Dichgans M,
Erikstrup C,
Färkkilä M,
Garbrielsen ME,
Ghanbari M,
Hagen K,
Häppölä P,
Hottenga JJ,
Hrafnsdottir MG,
Hveem K,
Johnsen MB,
Kähönen M,
Kristoffersen ES,
Kurth T,
Lehtimäki T,
Lighart L,
Magnusson SH,
Malik R,
Pedersen OB,
Pelzer N,
Penninx BWJH,
Ran C,
Ridker PM,
Rosendaal FR,
Sigurdardottir GR,
Skogholt AH,
Sveinsson OA,
Thorgeirsson TE,
Ullum H,
Vijfhuizen LS,
Widén E,
van Dijk KW,
Aromaa A,
Belin AC,
Freilinger T,
Ikram MA,
Järvelin MR,
Raitakari OT,
Terwindt GM,
Kallela M,
Wessman M,
Olesen J,
Chasman DI,
Nyholt DR,
Stefánsson H,
Stefansson K,
van den Maagdenberg AMJM,
Hansen TF,
Ripatti S,
Zwart JA,
Palotie A,
Pirinen M
International Headache Genetics Consortium · HUNT All-in Headache 외 컨소시엄 1곳
Nature genetics · 2022 · PMID 35115687 · open access
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+
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Ghouse J,
Sveinbjörnsson G,
Vujkovic M,
Seidelin AS,
Gellert-Kristensen H,
Ahlberg G,
Tragante V,
Rand SA,
Brancale J,
Vilarinho S,
Lundegaard PR,
Sørensen E
외 39명 — 모두 보기
Erikstrup C,
Bruun MT,
Jensen BA,
Brunak S,
Banasik K,
Ullum H,
Verweij N,
Lotta L,
Baras A,
Mirshahi T,
Carey DJ,
Kaplan DE,
Lynch J,
Morgan T,
Schwantes-An TH,
Dochtermann DR,
Pyarajan S,
Tsao PS,
Laisk T,
Mägi R,
Kozlitina J,
Tybjærg-Hansen A,
Jones D,
Knowlton KU,
Nadauld L,
Ferkingstad E,
Björnsson ES,
Ulfarsson MO,
Sturluson Á,
Sulem P,
Pedersen OB,
Ostrowski SR,
Gudbjartsson DF,
Stefansson K,
Olesen MS,
Chang KM,
Holm H,
Bundgaard H,
Stender S
DBDS Genomic Consortium · Regeneron Genetics Center 외 컨소시엄 3곳
Nature genetics · 2024 · PMID 38632349 · open access
페이지 12개+
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Schormair B,
Zhao C,
Bell S,
Didriksen M,
Nawaz MS,
Schandra N,
Stefani A,
Högl B,
Dauvilliers Y,
Bachmann CG,
Kemlink D,
Sonka K
외 55명 — 모두 보기
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek ZK,
Ibrahim A,
Bergmann M,
Kittke V,
Harrer P,
Dowsett J,
Chenini S,
Ostrowski SR,
Sørensen E,
Erikstrup C,
Pedersen OB,
Topholm Bruun M,
Nielsen KR,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Burchell B,
Furlotte NA,
Nandakumar P,
Earley CJ,
Ondo WG,
Xiong L,
Desautels A,
Perola M,
Vodicka P,
Dina C,
Stoll M,
Franke A,
Lieb W,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rye DB,
Rouleau GA,
Berger K,
Stefansson H,
Ullum H,
Stefansson K,
Hinds DA,
Di Angelantonio E,
Oexle K,
Winkelmann J
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
페이지 12개+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
외 60명 — 모두 보기
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
페이지 12개+
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Henry A,
Mo X,
Finan C,
Chaffin MD,
Speed D,
Issa H,
Denaxas S,
Ware JS,
Zheng SL,
Malarstig A,
Gratton J,
Bond I
외 169명 — 모두 보기
Roselli C,
Miller D,
Chopade S,
Schmidt AF,
Abner E,
Adams L,
Andersson C,
Aragam KG,
Ärnlöv J,
Asselin G,
Raja AA,
Backman JD,
Bartz TM,
Biddinger KJ,
Biggs ML,
Bloom HL,
Boersma E,
Brandimarto J,
Brown MR,
Brunak S,
Bruun MT,
Buckbinder L,
Bundgaard H,
Carey DJ,
Chasman DI,
Chen X,
Cook JP,
Czuba T,
de Denus S,
Dehghan A,
Delgado GE,
Doney AS,
Dörr M,
Dowsett J,
Dudley SC,
Engström G,
Erikstrup C,
Esko T,
Farber-Eger EH,
Felix SB,
Finer S,
Ford I,
Ghanbari M,
Ghasemi S,
Ghouse J,
Giedraitis V,
Giulianini F,
Gottdiener JS,
Gross S,
Guðbjartsson DF,
Gui H,
Gutmann R,
Hägg S,
Haggerty CM,
Hedman ÅK,
Helgadottir A,
Hemingway H,
Hillege H,
Hyde CL,
Aagaard Jensen B,
Jukema JW,
Kardys I,
Karra R,
Kavousi M,
Kizer JR,
Kleber ME,
Køber L,
Koekemoer A,
Kuchenbaecker K,
Lai YP,
Lanfear D,
Langenberg C,
Lin H,
Lind L,
Lindgren CM,
Liu PP,
London B,
Lowery BD,
Luan J,
Lubitz SA,
Magnusson P,
Margulies KB,
Marston NA,
Martin H,
März W,
Melander O,
Mordi IR,
Morley MP,
Morris AP,
Morrison AC,
Morton L,
Nagle MW,
Nelson CP,
Niessner A,
Niiranen T,
Noordam R,
Nowak C,
O'Donoghue ML,
Ostrowski SR,
Owens AT,
Palmer CNA,
Paré G,
Pedersen OB,
Perola M,
Pigeyre M,
Psaty BM,
Rice KM,
Ridker PM,
Romaine SPR,
Rotter JI,
Ruff CT,
Sabatine MS,
Sallah N,
Salomaa V,
Sattar N,
Shalaby AA,
Shekhar A,
Smelser DT,
Smith NL,
Sørensen E,
Srinivasan S,
Stefansson K,
Sveinbjörnsson G,
Svensson P,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teumer A,
Thorgeirsson G,
Thorsteinsdottir U,
Torp-Pedersen C,
Tragante V,
Trompet S,
Uitterlinden AG,
Ullum H,
van der Harst P,
van Heel D,
van Setten J,
van Vugt M,
Veluchamy A,
Verschuuren M,
Verweij N,
Vissing CR,
Völker U,
Voors AA,
Wallentin L,
Wang Y,
Weeke PE,
Wiggins KL,
Williams LK,
Yang Y,
Yu B,
Zannad F,
Zheng C,
Asselbergs FW,
Cappola TP,
Dubé MP,
Dunn ME,
Lang CC,
Samani NJ,
Shah S,
Vasan RS,
Smith JG,
Holm H,
Shah S,
Ellinor PT,
Hingorani AD,
Wells Q,
Lumbers RT
Genes & Health Research Team · Estonian Biobank Research Team 외 컨소시엄 2곳
Nature genetics · 2025 · PMID 40038546 · open access
페이지 12개+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
외 145명 — 모두 보기
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center 외 컨소시엄 1곳
Nature genetics · 2025 · PMID 40050429
페이지 12개+
Translational genomics of osteoarthritis in 1,962,069 individuals
Hatzikotoulas K,
Southam L,
Stefansdottir L,
Boer CG,
McDonald ML,
Pett JP,
Park YC,
Tuerlings M,
Mulders R,
Barysenka A,
Arruda AL,
Tragante V
외 162명 — 모두 보기
Rocco A,
Bittner N,
Chen S,
Horn S,
Srinivasasainagendra V,
To K,
Katsoula G,
Kreitmaier P,
Tenghe AMM,
Gilly A,
Arbeeva L,
Chen LG,
de Pins AM,
Dochtermann D,
Henkel C,
Höijer J,
Ito S,
Lind PA,
Lukusa-Sawalena B,
Minn AKK,
Mola-Caminal M,
Narita A,
Nguyen C,
Reimann E,
Silberstein MD,
Skogholt AH,
Tiwari HK,
Yau MS,
Yue M,
Zhao W,
Zhao W,
Zhou JJ,
Alexiadis G,
Banasik K,
Brunak S,
Campbell A,
Cheung JTS,
Dowsett J,
Faquih T,
Faul JD,
Fei L,
Fenstad AM,
Funayama T,
Gabrielsen ME,
Gocho C,
Gromov K,
Hansen T,
Hudjashov G,
Ingvarsson T,
Johnson JS,
Jonsson H,
Kakehi S,
Karjalainen J,
Kasbohm E,
Lemmelä S,
Lin K,
Liu X,
Loef M,
Mangino M,
McCartney D,
Millwood IY,
Richman J,
Roberts MB,
Ryan KA,
Samartzis D,
Shivakumar M,
Skou ST,
Sugimoto S,
Suzuki K,
Takuwa H,
Teder-Laving M,
Thomas L,
Tomizuka K,
Turman C,
Weiss S,
Wu TT,
Zengini E,
Zhang Y,
Ferreira MAR,
Babis G,
Baras A,
Barker T,
Carey DJ,
Cheah KSE,
Chen Z,
Cheung JP,
Daly M,
de Mutsert R,
Eaton CB,
Erikstrup C,
Furnes ON,
Golightly YM,
Gudbjartsson DF,
Hailer NP,
Hayward C,
Hochberg MC,
Homuth G,
Huckins LM,
Hveem K,
Ikegawa S,
Ishijima M,
Isomura M,
Jones M,
Kang JH,
Kardia SLR,
Kloppenburg M,
Kraft P,
Kumahashi N,
Kuwata S,
Lee MTM,
Lee PH,
Lerner R,
Li L,
Lietman SA,
Lotta L,
Lupton MK,
Mägi R,
Martin NG,
McAlindon TE,
Medland SE,
Michaëlsson K,
Mitchell BD,
Mook-Kanamori DO,
Morris AP,
Nabika T,
Nagami F,
Nelson AE,
Ostrowski SR,
Palotie A,
Pedersen OB,
Rosendaal FR,
Sakurai-Yageta M,
Schmidt CO,
Sham PC,
Singh JA,
Smelser DT,
Smith JA,
Song YQ,
Sørensen E,
Tamiya G,
Tamura Y,
Terao C,
Thorleifsson G,
Troelsen A,
Tsezou A,
Uchio Y,
Uitterlinden AG,
Ullum H,
Valdes AM,
van Heel DA,
Walters RG,
Weir DR,
Wilkinson JM,
Winsvold BS,
Yamamoto M,
Zwart JA,
Stefansson K,
Meulenbelt I,
Teichmann SA,
van Meurs JBJ,
Styrkarsdottir U,
Zeggini E
arcOGEN Consortium · ARGO Consortium 외 컨소시엄 7곳
Nature · 2025 · PMID 40205036 · 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+
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Small AM,
Yang TY,
Itoh S,
Thériault S,
Dufresne L,
Kurosawa R,
Komuro I,
Matsuda K,
Vy HMT,
Farber-Eger EH,
Shaffer LL,
Boulier KM
외 89명 — 모두 보기
Corey KM,
Ramaker ME,
Laporte F,
Schott JJ,
Le Scouarnec S,
Singh SA,
Sonawane AR,
Smith HA,
Rafaels N,
Ghouse J,
Raja AA,
Ostrowski SR,
Sørensen E,
Mikkelsen C,
Pedersen OB,
Erikstrup C,
Ullum H,
Sveinbjornsson G,
Gudbjartsson DF,
Abner E,
Lee J,
Ganna A,
Nowak-Göttl U,
Finer S,
Schumacher J,
Maj C,
Al-Kassou B,
Nickenig G,
Trenkwalder T,
Dreβen M,
Krane M,
Nöthen MM,
Moksnes MR,
Brumpton BM,
Knight S,
Knowlton KU,
Nadauld L,
Debiec R,
Musameh MD,
Braund PS,
Nelson CP,
Czuba T,
Melander O,
Selvaraj MS,
Koyama S,
Bhukar R,
Ruan Y,
Ljungberg J,
Damrauer SM,
Levin MG,
Franke A,
Berger K,
Ruff CT,
Melloni GEM,
Kamanu FK,
Ito K,
Do R,
Loos RJF,
Schunkert H,
Wells QS,
Shah SH,
Le Tourneau T,
Messika-Zeitoun D,
Gignoux C,
Bundgaard H,
Larsson SC,
Michaëlsson K,
Holm H,
Helgadottir A,
Esko T,
van Heel DA,
Mathieu P,
Samani NJ,
Smith JG,
Söderberg S,
Rader DJ,
Marston NA,
Sabatine MS,
Pasaniuc B,
Cho K,
Wilson PWF,
O'Donnell CJ,
Stefansson K,
Bossé Y,
Aikawa E,
Engert JC,
Peloso GM,
Natarajan P,
Thanassoulis G
Colorado Center for Personalized Medicine · DBDS Genomic Consortium 외 컨소시엄 2곳
Nature genetics · 2026 · PMID 41419686 · open access
페이지 12개+
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Beaumont RN,
Flatley C,
Vaudel M,
Wu X,
Chen J,
Moen GH,
Skotte L,
Helgeland Ø,
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Banasik K,
Albiñana C,
Ronkainen J
외 76명 — 모두 보기
Fadista J,
Stinson SE,
Trajanoska K,
Wang CA,
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Andreassen OA,
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Atalay M,
Bhatta L,
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Brumpton BM,
Brunak S,
Bybjerg-Grauholm J,
Ebbing C,
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Engelbrechtsen L,
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Franks S,
Gaillard R,
Geller F,
Grove J,
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Kajantie E,
Morgen CS,
Nohr EA,
Nyegaard M,
Palmer CNA,
Pedersen OB,
Rivadeneira F,
Sebert S,
Shields BM,
Stoltenberg C,
Surakka I,
Thørner LW,
Ullum H,
Vaarasmaki M,
Vilhjalmsson BJ,
Willer CJ,
Lakka TA,
Gybel-Brask D,
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Hansen T,
Pearson ER,
Reynolds RM,
Ostrowski SR,
Pennell CE,
Jaddoe VWV,
Felix JF,
Hattersley AT,
Melbye M,
Lawlor DA,
Hveem K,
Werge T,
Nielsen HS,
Magnus P,
Evans DM,
Jacobsson B,
Järvelin MR,
Zhang G,
Hivert MF,
Johansson S,
Freathy RM,
Feenstra B,
Njølstad PR
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
페이지 10개
An atlas of genetic determinants of forearm fracture
Nethander M,
Movérare-Skrtic S,
Kämpe A,
Coward E,
Reimann E,
Grahnemo L,
Borbély É,
Helyes Z,
Funck-Brentano T,
Cohen-Solal M,
Tuukkanen J,
Koskela A
외 23명 — 모두 보기
Wu J,
Li L,
Lu T,
Gabrielsen ME,
Mägi R,
Hoff M,
Lerner UH,
Henning P,
Ullum H,
Erikstrup C,
Brunak S,
Langhammer A,
Tuomi T,
Oddsson A,
Stefansson K,
Pettersson-Kymmer U,
Ostrowski SR,
Pedersen OBV,
Styrkarsdottir U,
Mäkitie O,
Hveem K,
Richards JB,
Ohlsson C
Estonian Biobank Research Team · DBDS Genomic Consortium
Nature genetics · 2023 · PMID 37919453 · open access
페이지 10개
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,
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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
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,
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Banasik K
외 19명 — 모두 보기
Sørensen E,
Mikkelsen C,
Schwinn M,
Sturluson A,
Ostrowski SR,
Kettunen J,
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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 외 컨소시엄 1곳
Nature communications · 2026 · PMID 42178310 · open access
페이지 8개
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
외 20명 — 모두 보기
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
페이지 7개
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
외 32명 — 모두 보기
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
페이지 5개
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Zheng T,
Ellinghaus D,
Juzenas S,
Cossais F,
Burmeister G,
Mayr G,
Jørgensen IF,
Teder-Laving M,
Skogholt AH,
Chen S,
Strege PR,
Ito G
외 73명 — 모두 보기
Banasik K,
Becker T,
Bokelmann F,
Brunak S,
Buch S,
Clausnitzer H,
Datz C,
Degenhardt F,
Doniec M,
Erikstrup C,
Esko T,
Forster M,
Frey N,
Fritsche LG,
Gabrielsen ME,
Gräßle T,
Gsur A,
Gross J,
Hampe J,
Hendricks A,
Hinz S,
Hveem K,
Jongen J,
Junker R,
Karlsen TH,
Hemmrich-Stanisak G,
Kruis W,
Kupcinskas J,
Laubert T,
Rosenstiel PC,
Röcken C,
Laudes M,
Leendertz FH,
Lieb W,
Limperger V,
Margetis N,
Mätz-Rensing K,
Németh CG,
Ness-Jensen E,
Nowak-Göttl U,
Pandit A,
Pedersen OB,
Peleikis HG,
Peuker K,
Rodriguez CL,
Rühlemann MC,
Schniewind B,
Schulzky M,
Skieceviciene J,
Tepel J,
Thomas L,
Uellendahl-Werth F,
Ullum H,
Vogel I,
Volzke H,
von Fersen L,
von Schönfels W,
Vanderwerff B,
Wilking J,
Wittig M,
Zeissig S,
Zobel M,
Zawistowski M,
Vacic V,
Sazonova O,
Noblin ES,
Farrugia G,
Beyder A,
Wedel T,
Kahlke V,
Schafmayer C,
D'Amato M,
Franke A
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
페이지 4개
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Skotte L,
Fadista J,
Bybjerg-Grauholm J,
Appadurai V,
Hildebrand MS,
Hansen TF,
Banasik K,
Grove J,
Albiñana C,
Geller F,
Bjurström CF,
Vilhjálmsson BJ
외 27명 — 모두 보기
Coleman M,
Damiano JA,
Burgess R,
Scheffer IE,
Pedersen OBV,
Erikstrup C,
Westergaard D,
Nielsen KR,
Sørensen E,
Bruun MT,
Liu X,
Hjalgrim H,
Pers TH,
Mortensen PB,
Mors O,
Nordentoft M,
Dreier JW,
Børglum AD,
Christensen J,
Hougaard DM,
Buil A,
Hviid A,
Melbye M,
Ullum H,
Berkovic SF,
Werge T,
Feenstra B
Brain : a journal of neurology · 2022 · PMID 35022648 · open access
페이지 4개
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
Hindy G,
Tyrrell DJ,
Vasbinder A,
Wei C,
Presswalla F,
Wang H,
Blakely P,
Ozel AB,
Graham S,
Holton GH,
Dowsett J,
Fahed AC
외 30명 — 모두 보기
Amadi KM,
Erne GK,
Tekmulla A,
Ismail A,
Launius C,
Sotoodehnia N,
Pankow JS,
Thørner LW,
Erikstrup C,
Pedersen OB,
Banasik K,
Brunak S,
Ullum H,
Eugen-Olsen J,
Ostrowski SR,
Haas ME,
Nielsen JB,
Lotta LA,
Engström G,
Melander O,
Orho-Melander M,
Zhao L,
Murthy VL,
Pinsky DJ,
Willer CJ,
Heckbert SR,
Reiser J,
Goldstein DR,
Desch KC,
Hayek SS
DBDS Consortium · Regeneron Genetics Center
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
페이지 4개
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