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성함이나 학술지명, PMID로 찾아보십시오.
Brunak S에 대해
23건, 그중 20건 표시.
Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease
Folkersen L,
Fauman E,
Sabater-Lleal M,
Strawbridge RJ,
Frånberg M,
Sennblad B,
Baldassarre D,
Veglia F,
Humphries SE,
Rauramaa R,
de Faire U,
Smit AJ
외 21명 — 모두 보기
Giral P,
Kurl S,
Mannarino E,
Enroth S,
Johansson Å,
Enroth SB,
Gustafsson S,
Lind L,
Lindgren C,
Morris AP,
Giedraitis V,
Silveira A,
Franco-Cereceda A,
Tremoli E,
Gyllensten U,
Ingelsson E,
Brunak S,
Eriksson P,
Ziemek D,
Hamsten A,
Mälarstig A
IMPROVE study group
PLoS genetics · 2017 · PMID 28369058 · 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+
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+
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 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+
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,
Solé-Navais P,
Banasik K,
Albiñana C,
Ronkainen J
외 76명 — 모두 보기
Fadista J,
Stinson SE,
Trajanoska K,
Wang CA,
Westergaard D,
Srinivasan S,
Sánchez-Soriano C,
Bilbao JR,
Allard C,
Groleau M,
Kuulasmaa T,
Leirer DJ,
White F,
Jacques PÉ,
Cheng H,
Hao K,
Andreassen OA,
Åsvold BO,
Atalay M,
Bhatta L,
Bouchard L,
Brumpton BM,
Brunak S,
Bybjerg-Grauholm J,
Ebbing C,
Elliott P,
Engelbrechtsen L,
Erikstrup C,
Estarlich M,
Franks S,
Gaillard R,
Geller F,
Grove J,
Hougaard DM,
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,
Bustamante M,
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,
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 9개
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,
Pedersen OB,
Banasik K
외 19명 — 모두 보기
Sørensen E,
Mikkelsen C,
Schwinn M,
Sturluson A,
Ostrowski SR,
Kettunen J,
Nielsen HS,
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
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 5개
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Degenhardt F,
Ellinghaus D,
Juzenas S,
Lerga-Jaso J,
Wendorff M,
Maya-Miles D,
Uellendahl-Werth F,
ElAbd H,
Rühlemann MC,
Arora J,
Özer O,
Lenning OB
외 317명 — 모두 보기
Myhre R,
Vadla MS,
Wacker EM,
Wienbrandt L,
Blandino Ortiz A,
de Salazar A,
Garrido Chercoles A,
Palom A,
Ruiz A,
Garcia-Fernandez AE,
Blanco-Grau A,
Mantovani A,
Zanella A,
Holten AR,
Mayer A,
Bandera A,
Cherubini A,
Protti A,
Aghemo A,
Gerussi A,
Ramirez A,
Braun A,
Nebel A,
Barreira A,
Lleo A,
Teles A,
Kildal AB,
Biondi A,
Caballero-Garralda A,
Ganna A,
Gori A,
Glück A,
Lind A,
Tanck A,
Hinney A,
Carreras Nolla A,
Fracanzani AL,
Peschuck A,
Cavallero A,
Dyrhol-Riise AM,
Ruello A,
Julià A,
Muscatello A,
Pesenti A,
Voza A,
Rando-Segura A,
Solier A,
Schmidt A,
Cortes B,
Mateos B,
Nafria-Jimenez B,
Schaefer B,
Jensen B,
Bellinghausen C,
Maj C,
Ferrando C,
de la Horra C,
Quereda C,
Skurk C,
Thibeault C,
Scollo C,
Herr C,
Spinner CD,
Gassner C,
Lange C,
Hu C,
Paccapelo C,
Lehmann C,
Angelini C,
Cappadona C,
Azuure C,
Bianco C,
Cea C,
Sancho C,
Hoff DAL,
Galimberti D,
Prati D,
Haschka D,
Jiménez D,
Pestaña D,
Toapanta D,
Muñiz-Diaz E,
Azzolini E,
Sandoval E,
Binatti E,
Scarpini E,
Helbig ET,
Casalone E,
Urrechaga E,
Paraboschi EM,
Pontali E,
Reverter E,
Calderón EJ,
Navas E,
Solligård E,
Contro E,
Arana-Arri E,
Aziz F,
Garcia F,
García Sánchez F,
Ceriotti F,
Martinelli-Boneschi F,
Peyvandi F,
Kurth F,
Blasi F,
Malvestiti F,
Medrano FJ,
Mesonero F,
Rodriguez-Frias F,
Hanses F,
Müller F,
Hemmrich-Stanisak G,
Bellani G,
Grasselli G,
Pezzoli G,
Costantino G,
Albano G,
Cardamone G,
Bellelli G,
Citerio G,
Foti G,
Lamorte G,
Matullo G,
Baselli G,
Kurihara H,
Neb H,
My I,
Kurth I,
Hernández I,
Pink I,
de Rojas I,
Galván-Femenia I,
Holter JC,
Afset JE,
Heyckendorf J,
Kässens J,
Damås JK,
Rybniker J,
Altmüller J,
Ampuero J,
Martín J,
Erdmann J,
Banales JM,
Badia JR,
Dopazo J,
Schneider J,
Bergan J,
Barretina J,
Walter J,
Hernández Quero J,
Goikoetxea J,
Delgado J,
Guerrero JM,
Fazaal J,
Kraft J,
Schröder J,
Risnes K,
Banasik K,
Müller KE,
Gaede KI,
Garcia-Etxebarria K,
Tonby K,
Heggelund L,
Izquierdo-Sanchez L,
Bettini LR,
Sumoy L,
Sander LE,
Lippert LJ,
Terranova L,
Nkambule L,
Knopp L,
Gustad LT,
Garbarino L,
Santoro L,
Téllez L,
Roade L,
Ostadreza M,
Intxausti M,
Kogevinas M,
Riveiro-Barciela M,
Berger MM,
Schaefer M,
Niemi MEK,
Gutiérrez-Stampa MA,
Carrabba M,
Figuera Basso ME,
Valsecchi MG,
Hernandez-Tejero M,
Vehreschild MJGT,
Manunta M,
Acosta-Herrera M,
D'Angiò M,
Baldini M,
Cazzaniga M,
Grimsrud MM,
Cornberg M,
Nöthen MM,
Marquié M,
Castoldi M,
Cordioli M,
Cecconi M,
D'Amato M,
Augustin M,
Tomasi M,
Boada M,
Dreher M,
Seilmaier MJ,
Joannidis M,
Wittig M,
Mazzocco M,
Ciccarelli M,
Rodríguez-Gandía M,
Bocciolone M,
Miozzo M,
Imaz Ayo N,
Blay N,
Chueca N,
Montano N,
Braun N,
Ludwig N,
Marx N,
Martínez N,
Cornely OA,
Witzke O,
Palmieri O,
Faverio P,
Preatoni P,
Bonfanti P,
Omodei P,
Tentorio P,
Castro P,
Rodrigues PM,
España PP,
Hoffmann P,
Rosenstiel P,
Schommers P,
Suwalski P,
de Pablo R,
Ferrer R,
Bals R,
Gualtierotti R,
Gallego-Durán R,
Nieto R,
Carpani R,
Morilla R,
Badalamenti S,
Haider S,
Ciesek S,
May S,
Bombace S,
Marsal S,
Pigazzini S,
Klein S,
Pelusi S,
Wilfling S,
Bosari S,
Volland S,
Brunak S,
Raychaudhuri S,
Schreiber S,
Heilmann-Heimbach S,
Aliberti S,
Ripke S,
Dudman S,
Wesse T,
Zheng T,
Bahmer T,
Eggermann T,
Illig T,
Brenner T,
Pumarola T,
Feldt T,
Folseraas T,
Gonzalez Cejudo T,
Landmesser U,
Protzer U,
Hehr U,
Rimoldi V,
Monzani V,
Skogen V,
Keitel V,
Kopfnagel V,
Friaza V,
Andrade V,
Moreno V,
Albrecht W,
Peter W,
Poller W,
Farre X,
Yi X,
Wang X,
Khodamoradi Y,
Karadeniz Z,
Latiano A,
Goerg S,
Bacher P,
Koehler P,
Tran F,
Zoller H,
Schulte EC,
Heidecker B,
Ludwig KU,
Fernández J,
Romero-Gómez M,
Albillos A,
Invernizzi P,
Buti M,
Duga S,
Bujanda L,
Hov JR,
Lenz TL,
Asselta R,
de Cid R,
Valenti L,
Karlsen TH,
Cáceres M,
Franke A
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group 외 컨소시엄 2곳
Human molecular genetics · 2022 · PMID 35848942 · open access
페이지 5개
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 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
The genetic architecture of fibromyalgia across 2.5 million individuals
Kerrebijn I,
Bjornsdottir G,
Arbabi K,
Urpa L,
Haapaniemi H,
Thorleifsson G,
Stefansdottir L,
Frangakis S,
Valliere J,
Kunorozva L,
Abner E,
Ji C
외 41명 — 모두 보기
Kangur M,
Aagaard B,
Bliddal H,
Brunak S,
Bruun MT,
Didriksen M,
Erikstrup C,
Finer S,
Geirsson AJ,
Gudbjartsson DF,
Hansen TF,
van Heel D,
Jonsdottir I,
Knight S,
Knowlton KU,
Mikkelsen C,
Nadauld LD,
Olafsdottir TA,
Ostrowski SR,
Pedersen OBV,
Saevarsdottir S,
Skuladottir AT,
Sørensen E,
Stefansson H,
Sulem P,
Sveinsson OA,
Thorlacius GE,
Thorsteinsdottir U,
Ullum H,
Vikingsson A,
Werge TM,
Saxena R,
Stefansson K,
Brummett CM,
Glintborg B,
Clauw DJ,
Thorgeirsson TE,
Williams FMK,
Sinnott-Armstrong N,
Ollila HM,
Wainberg M
Chronic Pain Genomics Consortium · FinnGen 외 컨소시엄 3곳
Nature medicine · 2026 · PMID 42521817 · open access
페이지 4개
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci
Ghouse J,
Tragante V,
Muhammad A,
Ahlberg G,
Skov MW,
Roden DM,
Jonsdottir I,
Andreasen L,
Lundegaard PR,
Trudsø LC,
Banasik K,
Brunak S
외 15명 — 모두 보기
Ostrowski SR,
Torp-Pedersen C,
Pedersen OV,
Sørensen E,
Køber L,
Iversen K,
Thorsteinsdottir U,
Thorgeirsson G,
Ullum H,
Gudbjartsson DF,
Mosley JD,
Holm H,
Stefansson K,
Bundgaard H,
Olesen MS
eMERGE consortium
European heart journal · 2022 · PMID 35751511
페이지 2개
Association of Variants Near the Bradykinin Receptor B<sub>2</sub> Gene With Angioedema in Patients Taking ACE Inhibitors
Ghouse J,
Ahlberg G,
Andreasen L,
Banasik K,
Brunak S,
Schwinn M,
Larsen IH,
Petersen O,
Sørensen E,
Ullum H,
Rasmussen ER,
Eriksson N
외 4명 — 모두 보기
Journal of the American College of Cardiology · 2021 · PMID 34384552
페이지 1개
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