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성함이나 학술지명, PMID로 찾아보십시오.
Melander O에 대해
62건, 그중 20건 표시.
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Kathiresan S,
Voight BF,
Purcell S,
Musunuru K,
Ardissino D,
Mannucci PM,
Anand S,
Engert JC,
Samani NJ,
Schunkert H,
Erdmann J,
Reilly MP
외 174명 — 모두 보기
Rader DJ,
Morgan T,
Spertus JA,
Stoll M,
Girelli D,
McKeown PP,
Patterson CC,
Siscovick DS,
O'Donnell CJ,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Melander O,
Altshuler D,
Ardissino D,
Merlini PA,
Berzuini C,
Bernardinelli L,
Peyvandi F,
Tubaro M,
Celli P,
Ferrario M,
Fetiveau R,
Marziliano N,
Casari G,
Galli M,
Ribichini F,
Rossi M,
Bernardi F,
Zonzin P,
Piazza A,
Mannucci PM,
Schwartz SM,
Siscovick DS,
Yee J,
Friedlander Y,
Elosua R,
Marrugat J,
Lucas G,
Subirana I,
Sala J,
Ramos R,
Kathiresan S,
Meigs JB,
Williams G,
Nathan DM,
MacRae CA,
O'Donnell CJ,
Salomaa V,
Havulinna AS,
Peltonen L,
Melander O,
Berglund G,
Voight BF,
Kathiresan S,
Hirschhorn JN,
Asselta R,
Duga S,
Spreafico M,
Musunuru K,
Daly MJ,
Purcell S,
Voight BF,
Purcell S,
Nemesh J,
Korn JM,
McCarroll SA,
Schwartz SM,
Yee J,
Kathiresan S,
Lucas G,
Subirana I,
Elosua R,
Surti A,
Guiducci C,
Gianniny L,
Mirel D,
Parkin M,
Burtt N,
Gabriel SB,
Samani NJ,
Thompson JR,
Braund PS,
Wright BJ,
Balmforth AJ,
Ball SG,
Hall A,
Schunkert H,
Erdmann J,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König I,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Schunkert H,
Samani NJ,
Erdmann J,
Ouwehand W,
Hengstenberg C,
Deloukas P,
Scholz M,
Cambien F,
Reilly MP,
Li M,
Chen Z,
Wilensky R,
Matthai W,
Qasim A,
Hakonarson HH,
Devaney J,
Burnett MS,
Pichard AD,
Kent KM,
Satler L,
Lindsay JM,
Waksman R,
Knouff CW,
Waterworth DM,
Walker MC,
Mooser V,
Epstein SE,
Rader DJ,
Scheffold T,
Berger K,
Stoll M,
Huge A,
Girelli D,
Martinelli N,
Olivieri O,
Corrocher R,
Morgan T,
Spertus JA,
McKeown P,
Patterson CC,
Schunkert H,
Erdmann E,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König IR,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Hólm H,
Thorleifsson G,
Thorsteinsdottir U,
Stefansson K,
Engert JC,
Do R,
Xie C,
Anand S,
Kathiresan S,
Ardissino D,
Mannucci PM,
Siscovick D,
O'Donnell CJ,
Samani NJ,
Melander O,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Altshuler D
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
페이지 4개
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C,
Johnson T,
Gateva V,
Tobin MD,
Bochud M,
Coin L,
Najjar SS,
Zhao JH,
Heath SC,
Eyheramendy S,
Papadakis K,
Voight BF
외 147명 — 모두 보기
Scott LJ,
Zhang F,
Farrall M,
Tanaka T,
Wallace C,
Chambers JC,
Khaw KT,
Nilsson P,
van der Harst P,
Polidoro S,
Grobbee DE,
Onland-Moret NC,
Bots ML,
Wain LV,
Elliott KS,
Teumer A,
Luan J,
Lucas G,
Kuusisto J,
Burton PR,
Hadley D,
McArdle WL,
Brown M,
Dominiczak A,
Newhouse SJ,
Samani NJ,
Webster J,
Zeggini E,
Beckmann JS,
Bergmann S,
Lim N,
Song K,
Vollenweider P,
Waeber G,
Waterworth DM,
Yuan X,
Groop L,
Orho-Melander M,
Allione A,
Di Gregorio A,
Guarrera S,
Panico S,
Ricceri F,
Romanazzi V,
Sacerdote C,
Vineis P,
Barroso I,
Sandhu MS,
Luben RN,
Crawford GJ,
Jousilahti P,
Perola M,
Boehnke M,
Bonnycastle LL,
Collins FS,
Jackson AU,
Mohlke KL,
Stringham HM,
Valle TT,
Willer CJ,
Bergman RN,
Morken MA,
Döring A,
Gieger C,
Illig T,
Meitinger T,
Org E,
Org E,
Pfeufer A,
Wichmann HE,
Kathiresan S,
Marrugat J,
O'Donnell CJ,
Schwartz SM,
Siscovick DS,
Subirana I,
Freimer NB,
Hartikainen AL,
McCarthy MI,
O'Reilly PF,
Peltonen L,
Pouta A,
de Jong PE,
Snieder H,
van Gilst WH,
Clarke R,
Goel A,
Hamsten A,
Peden JF,
Seedorf U,
Syvänen AC,
Tognoni G,
Lakatta EG,
Sanna S,
Scheet P,
Schlessinger D,
Scuteri A,
Dörr M,
Ernst F,
Felix SB,
Homuth G,
Lorbeer R,
Reffelmann T,
Rettig R,
Völker U,
Galan P,
Gut IG,
Hercberg S,
Lathrop GM,
Zelenika D,
Deloukas P,
Soranzo N,
Williams FM,
Zhai G,
Salomaa V,
Laakso M,
Elosua R,
Forouhi NG,
Völzke H,
Uiterwaal CS,
van der Schouw YT,
Numans ME,
Matullo G,
Navis G,
Berglund G,
Bingham SA,
Kooner JS,
Connell JM,
Bandinelli S,
Ferrucci L,
Watkins H,
Spector TD,
Tuomilehto J,
Altshuler D,
Strachan DP,
Laan M,
Meneton P,
Wareham NJ,
Uda M,
Jarvelin MR,
Mooser V,
Melander O,
Loos RJ,
Elliott P,
Abecasis GR,
Caulfield M,
Munroe PB
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
페이지 4개
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Li C,
Stoma S,
Lotta LA,
Warner S,
Albrecht E,
Allione A,
Arp PP,
Broer L,
Buxton JL,
Da Silva Couto Alves A,
Deelen J,
Fedko IO
외 84명 — 모두 보기
Gordon SD,
Jiang T,
Karlsson R,
Kerrison N,
Loe TK,
Mangino M,
Milaneschi Y,
Miraglio B,
Pervjakova N,
Russo A,
Surakka I,
van der Spek A,
Verhoeven JE,
Amin N,
Beekman M,
Blakemore AI,
Canzian F,
Hamby SE,
Hottenga JJ,
Jones PD,
Jousilahti P,
Mägi R,
Medland SE,
Montgomery GW,
Nyholt DR,
Perola M,
Pietiläinen KH,
Salomaa V,
Sillanpää E,
Suchiman HE,
van Heemst D,
Willemsen G,
Agudo A,
Boeing H,
Boomsma DI,
Chirlaque MD,
Fagherazzi G,
Ferrari P,
Franks P,
Gieger C,
Eriksson JG,
Gunter M,
Hägg S,
Hovatta I,
Imaz L,
Kaprio J,
Kaaks R,
Key T,
Krogh V,
Martin NG,
Melander O,
Metspalu A,
Moreno C,
Onland-Moret NC,
Nilsson P,
Ong KK,
Overvad K,
Palli D,
Panico S,
Pedersen NL,
Penninx BWJH,
Quirós JR,
Jarvelin MR,
Rodríguez-Barranco M,
Scott RA,
Severi G,
Slagboom PE,
Spector TD,
Tjonneland A,
Trichopoulou A,
Tumino R,
Uitterlinden AG,
van der Schouw YT,
van Duijn CM,
Weiderpass E,
Denchi EL,
Matullo G,
Butterworth AS,
Danesh J,
Samani NJ,
Wareham NJ,
Nelson CP,
Langenberg C,
Codd V
American journal of human genetics · 2020 · PMID 32109421 · open access
페이지 4개
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
외 77명 — 모두 보기
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
페이지 3개
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor
Stanne TM,
Olsson M,
Lorentzen E,
Pedersen A,
Gummesson A,
Gils A,
Jood K,
Engström G,
Melander O,
Declerck PJ,
Jern C
Thrombosis and haemostasis · 2018 · PMID 29378355 · open access
페이지 3개
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Franceschini N,
Giambartolomei C,
de Vries PS,
Finan C,
Bis JC,
Huntley RP,
Lovering RC,
Tajuddin SM,
Winkler TW,
Graff M,
Kavousi M,
Dale C
외 146명 — 모두 보기
Smith AV,
Hofer E,
van Leeuwen EM,
Nolte IM,
Lu L,
Scholz M,
Sargurupremraj M,
Pitkänen N,
Franzén O,
Joshi PK,
Noordam R,
Marioni RE,
Hwang SJ,
Musani SK,
Schminke U,
Palmas W,
Isaacs A,
Correa A,
Zonderman AB,
Hofman A,
Teumer A,
Cox AJ,
Uitterlinden AG,
Wong A,
Smit AJ,
Newman AB,
Britton A,
Ruusalepp A,
Sennblad B,
Hedblad B,
Pasaniuc B,
Penninx BW,
Langefeld CD,
Wassel CL,
Tzourio C,
Fava C,
Baldassarre D,
O'Leary DH,
Teupser D,
Kuh D,
Tremoli E,
Mannarino E,
Grossi E,
Boerwinkle E,
Schadt EE,
Ingelsson E,
Veglia F,
Rivadeneira F,
Beutner F,
Chauhan G,
Heiss G,
Snieder H,
Campbell H,
Völzke H,
Markus HS,
Deary IJ,
Jukema JW,
de Graaf J,
Price J,
Pott J,
Hopewell JC,
Liang J,
Thiery J,
Engmann J,
Gertow K,
Rice K,
Taylor KD,
Dhana K,
Kiemeney LALM,
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Launer LJ,
Holdt LM,
Dörr M,
Dichgans M,
Traylor M,
Sitzer M,
Kumari M,
Kivimaki M,
Nalls MA,
Melander O,
Raitakari O,
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Rueda-Ochoa OL,
Roussos P,
Whincup PH,
Amouyel P,
Giral P,
Anugu P,
Wong Q,
Malik R,
Rauramaa R,
Burkhardt R,
Hardy R,
Schmidt R,
de Mutsert R,
Morris RW,
Strawbridge RJ,
Wannamethee SG,
Hägg S,
Shah S,
McLachlan S,
Trompet S,
Seshadri S,
Kurl S,
Heckbert SR,
Ring S,
Harris TB,
Lehtimäki T,
Galesloot TE,
Shah T,
de Faire U,
Plagnol V,
Rosamond WD,
Post W,
Zhu X,
Zhang X,
Guo X,
Saba Y,
Dehghan A,
Seldenrijk A,
Morrison AC,
Hamsten A,
Psaty BM,
van Duijn CM,
Lawlor DA,
Mook-Kanamori DO,
Bowden DW,
Schmidt H,
Wilson JF,
Wilson JG,
Rotter JI,
Wardlaw JM,
Deanfield J,
Halcox J,
Lyytikäinen LP,
Loeffler M,
Evans MK,
Debette S,
Humphries SE,
Völker U,
Gudnason V,
Hingorani AD,
Björkegren JLM,
Casas JP,
O'Donnell CJ
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
페이지 3개
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Byun J,
Han Y,
Li Y,
Xia J,
Long E,
Choi J,
Xiao X,
Zhu M,
Zhou W,
Sun R,
Bossé Y,
Song Z
외 73명 — 모두 보기
Schwartz A,
Lusk C,
Rafnar T,
Stefansson K,
Zhang T,
Zhao W,
Pettit RW,
Liu Y,
Li X,
Zhou H,
Walsh KM,
Gorlov I,
Gorlova O,
Zhu D,
Rosenberg SM,
Pinney S,
Bailey-Wilson JE,
Mandal D,
de Andrade M,
Gaba C,
Willey JC,
You M,
Anderson M,
Wiencke JK,
Albanes D,
Lam S,
Tardon A,
Chen C,
Goodman G,
Bojeson S,
Brenner H,
Landi MT,
Chanock SJ,
Johansson M,
Muley T,
Risch A,
Wichmann HE,
Bickeböller H,
Christiani DC,
Rennert G,
Arnold S,
Field JK,
Shete S,
Le Marchand L,
Melander O,
Brunnstrom H,
Liu G,
Andrew AS,
Kiemeney LA,
Shen H,
Zienolddiny S,
Grankvist K,
Johansson M,
Caporaso N,
Cox A,
Hong YC,
Yuan JM,
Lazarus P,
Schabath MB,
Aldrich MC,
Patel A,
Lan Q,
Rothman N,
Taylor F,
Kachuri L,
Witte JS,
Sakoda LC,
Spitz M,
Brennan P,
Lin X,
McKay J,
Hung RJ,
Amos CI
Nature genetics · 2022 · PMID 35915169
페이지 3개
A genome- and phenome-wide association study of plasma procalcitonin concentrations in individuals of European ancestry
Zhang W,
van der Most PJ,
Wang S,
Kamali Z,
Giontella A,
Enhörning S,
Gansevoort RT,
van der Harst P,
Bakker SJL,
Melander O,
Keus F,
Lunter G
외 1명 — 모두 보기
EBioMedicine · 2026 · PMID 41406505 · open access
페이지 3개
Genome-wide analysis yields new loci associating with aortic valve stenosis
Helgadottir A,
Thorleifsson G,
Gretarsdottir S,
Stefansson OA,
Tragante V,
Thorolfsdottir RB,
Jonsdottir I,
Bjornsson T,
Steinthorsdottir V,
Verweij N,
Nielsen JB,
Zhou W
외 34명 — 모두 보기
Folkersen L,
Martinsson A,
Heydarpour M,
Prakash S,
Oskarsson G,
Gudbjartsson T,
Geirsson A,
Olafsson I,
Sigurdsson EL,
Almgren P,
Melander O,
Franco-Cereceda A,
Hamsten A,
Fritsche L,
Lin M,
Yang B,
Hornsby W,
Guo D,
Brummett CM,
Abecasis G,
Mathis M,
Milewicz D,
Body SC,
Eriksson P,
Willer CJ,
Hveem K,
Newton-Cheh C,
Smith JG,
Danielsen R,
Thorgeirsson G,
Thorsteinsdottir U,
Gudbjartsson DF,
Holm H,
Stefansson K
Nature communications · 2018 · PMID 29511194 · open access
페이지 2개
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Cousminer DL,
Ahlqvist E,
Mishra R,
Andersen MK,
Chesi A,
Hawa MI,
Davis A,
Hodge KM,
Bradfield JP,
Zhou K,
Guy VC,
Åkerlund M
외 41명 — 모두 보기
Wod M,
Fritsche LG,
Vestergaard H,
Snyder J,
Højlund K,
Linneberg A,
Käräjämäki A,
Brandslund I,
Kim CE,
Witte D,
Sørgjerd EP,
Brillon DJ,
Pedersen O,
Beck-Nielsen H,
Grarup N,
Pratley RE,
Rickels MR,
Vella A,
Ovalle F,
Melander O,
Harris RI,
Varvel S,
Grill VER,
Hakonarson H,
Froguel P,
Lonsdale JT,
Mauricio D,
Schloot NC,
Khunti K,
Greenbaum CJ,
Åsvold BO,
Yderstræde KB,
Pearson ER,
Schwartz S,
Voight BF,
Hansen T,
Tuomi T,
Boehm BO,
Groop L,
Leslie RD,
Grant SFA
Bone Mineral Density in Childhood Study
Diabetes care · 2018 · PMID 30254083 · open access
페이지 2개
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Gorski M,
Jung B,
Li Y,
Matias-Garcia PR,
Wuttke M,
Coassin S,
Thio CHL,
Kleber ME,
Winkler TW,
Wanner V,
Chai JF,
Chu AY
외 119명 — 모두 보기
Cocca M,
Feitosa MF,
Ghasemi S,
Hoppmann A,
Horn K,
Li M,
Nutile T,
Scholz M,
Sieber KB,
Teumer A,
Tin A,
Wang J,
Tayo BO,
Ahluwalia TS,
Almgren P,
Bakker SJL,
Banas B,
Bansal N,
Biggs ML,
Boerwinkle E,
Bottinger EP,
Brenner H,
Carroll RJ,
Chalmers J,
Chee ML,
Chee ML,
Cheng CY,
Coresh J,
de Borst MH,
Degenhardt F,
Eckardt KU,
Endlich K,
Franke A,
Freitag-Wolf S,
Gampawar P,
Gansevoort RT,
Ghanbari M,
Gieger C,
Hamet P,
Ho K,
Hofer E,
Holleczek B,
Xian Foo VH,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Josyula NS,
Kähönen M,
Khor CC,
Koenig W,
Kramer H,
Krämer BK,
Kühnel B,
Lange LA,
Lehtimäki T,
Lieb W,
Loos RJF,
Lukas MA,
Lyytikäinen LP,
Meisinger C,
Meitinger T,
Melander O,
Milaneschi Y,
Mishra PP,
Mononen N,
Mychaleckyj JC,
Nadkarni GN,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
O'Donoghue ML,
Orho-Melander M,
Pendergrass SA,
Penninx BWJH,
Preuss MH,
Psaty BM,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rosenkranz AR,
Rossing P,
Rotter JI,
Sabanayagam C,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Sedaghat S,
Shaffer CM,
Strauch K,
Szymczak S,
Taylor KD,
Tremblay J,
Chaker L,
van der Harst P,
van der Most PJ,
Verweij N,
Völker U,
Waldenberger M,
Wallentin L,
Waterworth DM,
White HD,
Wilson JG,
Wong TY,
Woodward M,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang Y,
Snieder H,
Wanner C,
Böger CA,
Köttgen A,
Kronenberg F,
Pattaro C,
Heid IM
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
페이지 2개
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes
Akbari P,
Sosina OA,
Bovijn J,
Landheer K,
Nielsen JB,
Kim M,
Aykul S,
De T,
Haas ME,
Hindy G,
Lin N,
Dinsmore IR
외 48명 — 모두 보기
Luo JZ,
Hectors S,
Geraghty B,
Germino M,
Panagis L,
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