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성함이나 학술지명, PMID로 찾아보십시오.
Geirsson G에 대해
18건.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
외 269명 — 모두 보기
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Aragam KG,
Jiang T,
Goel A,
Kanoni S,
Wolford BN,
Atri DS,
Weeks EM,
Wang M,
Hindy G,
Zhou W,
Grace C,
Roselli C
외 83명 — 모두 보기
Marston NA,
Kamanu FK,
Surakka I,
Venegas LM,
Sherliker P,
Koyama S,
Ishigaki K,
Åsvold BO,
Brown MR,
Brumpton B,
de Vries PS,
Giannakopoulou O,
Giardoglou P,
Gudbjartsson DF,
Güldener U,
Haider SMI,
Helgadottir A,
Ibrahim M,
Kastrati A,
Kessler T,
Kyriakou T,
Konopka T,
Li L,
Ma L,
Meitinger T,
Mucha S,
Munz M,
Murgia F,
Nielsen JB,
Nöthen MM,
Pang S,
Reinberger T,
Schnitzler G,
Smedley D,
Thorleifsson G,
von Scheidt M,
Ulirsch JC,
Arnar DO,
Burtt NP,
Costanzo MC,
Flannick J,
Ito K,
Jang DK,
Kamatani Y,
Khera AV,
Komuro I,
Kullo IJ,
Lotta LA,
Nelson CP,
Roberts R,
Thorgeirsson G,
Thorsteinsdottir U,
Webb TR,
Baras A,
Björkegren JLM,
Boerwinkle E,
Dedoussis G,
Holm H,
Hveem K,
Melander O,
Morrison AC,
Orho-Melander M,
Rallidis LS,
Ruusalepp A,
Sabatine MS,
Stefansson K,
Zalloua P,
Ellinor PT,
Farrall M,
Danesh J,
Ruff CT,
Finucane HK,
Hopewell JC,
Clarke R,
Gupta RM,
Erdmann J,
Samani NJ,
Schunkert H,
Watkins H,
Willer CJ,
Deloukas P,
Kathiresan S,
Butterworth AS
Biobank Japan · EPIC-CVD 외 컨소시엄 1곳
Nature genetics · 2022 · PMID 36474045 · 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,
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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+
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
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
Gudmundsson J,
Sigurdsson JK,
Stefansdottir L,
Agnarsson BA,
Isaksson HJ,
Stefansson OA,
Gudjonsson SA,
Gudbjartsson DF,
Masson G,
Frigge ML,
Stacey SN,
Sulem P
외 16명 — 모두 보기
Halldorsson GH,
Tragante V,
Holm H,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Jonsson T,
Jonsson E,
Barkardottir RB,
Hilmarsson R,
Asselbergs FW,
Geirsson G,
Thorsteinsdottir U,
Rafnar T,
Thorleifsson G,
Stefansson K
Nature communications · 2018 · PMID 30410027 · open access
페이지 9개
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Schunkert H,
König IR,
Kathiresan S,
Reilly MP,
Assimes TL,
Holm H,
Preuss M,
Stewart AF,
Barbalic M,
Gieger C,
Absher D,
Aherrahrou Z
외 155명 — 모두 보기
Allayee H,
Altshuler D,
Anand SS,
Andersen K,
Anderson JL,
Ardissino D,
Ball SG,
Balmforth AJ,
Barnes TA,
Becker DM,
Becker LC,
Berger K,
Bis JC,
Boekholdt SM,
Boerwinkle E,
Braund PS,
Brown MJ,
Burnett MS,
Buysschaert I,
Carlquist JF,
Chen L,
Cichon S,
Codd V,
Davies RW,
Dedoussis G,
Dehghan A,
Demissie S,
Devaney JM,
Diemert P,
Do R,
Doering A,
Eifert S,
Mokhtari NE,
Ellis SG,
Elosua R,
Engert JC,
Epstein SE,
de Faire U,
Fischer M,
Folsom AR,
Freyer J,
Gigante B,
Girelli D,
Gretarsdottir S,
Gudnason V,
Gulcher JR,
Halperin E,
Hammond N,
Hazen SL,
Hofman A,
Horne BD,
Illig T,
Iribarren C,
Jones GT,
Jukema JW,
Kaiser MA,
Kaplan LM,
Kastelein JJ,
Khaw KT,
Knowles JW,
Kolovou G,
Kong A,
Laaksonen R,
Lambrechts D,
Leander K,
Lettre G,
Li M,
Lieb W,
Loley C,
Lotery AJ,
Mannucci PM,
Maouche S,
Martinelli N,
McKeown PP,
Meisinger C,
Meitinger T,
Melander O,
Merlini PA,
Mooser V,
Morgan T,
Mühleisen TW,
Muhlestein JB,
Münzel T,
Musunuru K,
Nahrstaedt J,
Nelson CP,
Nöthen MM,
Olivieri O,
Patel RS,
Patterson CC,
Peters A,
Peyvandi F,
Qu L,
Quyyumi AA,
Rader DJ,
Rallidis LS,
Rice C,
Rosendaal FR,
Rubin D,
Salomaa V,
Sampietro ML,
Sandhu MS,
Schadt E,
Schäfer A,
Schillert A,
Schreiber S,
Schrezenmeir J,
Schwartz SM,
Siscovick DS,
Sivananthan M,
Sivapalaratnam S,
Smith A,
Smith TB,
Snoep JD,
Soranzo N,
Spertus JA,
Stark K,
Stirrups K,
Stoll M,
Tang WH,
Tennstedt S,
Thorgeirsson G,
Thorleifsson G,
Tomaszewski M,
Uitterlinden AG,
van Rij AM,
Voight BF,
Wareham NJ,
Wells GA,
Wichmann HE,
Wild PS,
Willenborg C,
Witteman JC,
Wright BJ,
Ye S,
Zeller T,
Ziegler A,
Cambien F,
Goodall AH,
Cupples LA,
Quertermous T,
März W,
Hengstenberg C,
Blankenberg S,
Ouwehand WH,
Hall AS,
Deloukas P,
Thompson JR,
Stefansson K,
Roberts R,
Thorsteinsdottir U,
O'Donnell CJ,
McPherson R,
Erdmann J,
Samani NJ
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
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,
Hjorleifsson KE,
Melsted P,
Gylfason A,
Arnadottir GA
외 16명 — 모두 보기
Oddsson A,
Jensson BO,
Jonasdottir A,
Jonasdottir A,
Juliusdottir T,
Stefansdottir L,
Tragante V,
Halldorsson BV,
Petersen H,
Thorgeirsson G,
Thorsteinsdottir U,
Sulem P,
Hinriksdottir I,
Jonsdottir I,
Gudbjartsson DF,
Stefansson K
Communications biology · 2021 · PMID 34108613 · 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
Genetic correction of PSA values using sequence variants associated with PSA levels
Gudmundsson J,
Besenbacher S,
Sulem P,
Gudbjartsson DF,
Olafsson I,
Arinbjarnarson S,
Agnarsson BA,
Benediktsdottir KR,
Isaksson HJ,
Kostic JP,
Gudjonsson SA,
Stacey SN
외 37명 — 모두 보기
Gylfason A,
Sigurdsson A,
Holm H,
Bjornsdottir US,
Eyjolfsson GI,
Navarrete S,
Fuertes F,
Garcia-Prats MD,
Polo E,
Checherita IA,
Jinga M,
Badea P,
Aben KK,
Schalken JA,
van Oort IM,
Sweep FC,
Helfand BT,
Davis M,
Donovan JL,
Hamdy FC,
Kristjansson K,
Gulcher JR,
Masson G,
Kong A,
Catalona WJ,
Mayordomo JI,
Geirsson G,
Einarsson GV,
Barkardottir RB,
Jonsson E,
Jinga V,
Mates D,
Kiemeney LA,
Neal DE,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Science translational medicine · 2010 · PMID 21160077
페이지 4개
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
Variants conferring risk of atrial fibrillation on chromosome 4q25
Gudbjartsson DF,
Arnar DO,
Helgadottir A,
Gretarsdottir S,
Holm H,
Sigurdsson A,
Jonasdottir A,
Baker A,
Thorleifsson G,
Kristjansson K,
Palsson A,
Blondal T
외 28명 — 모두 보기
Sulem P,
Backman VM,
Hardarson GA,
Palsdottir E,
Helgason A,
Sigurjonsdottir R,
Sverrisson JT,
Kostulas K,
Ng MC,
Baum L,
So WY,
Wong KS,
Chan JC,
Furie KL,
Greenberg SM,
Sale M,
Kelly P,
MacRae CA,
Smith EE,
Rosand J,
Hillert J,
Ma RC,
Ellinor PT,
Thorgeirsson G,
Gulcher JR,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature · 2007 · PMID 17603472
페이지 2개
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,
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