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성함이나 학술지명, PMID로 찾아보십시오.
Trabetti E에 대해
7건.
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
Ligthart S,
Vaez A,
Võsa U,
Stathopoulou MG,
de Vries PS,
Prins BP,
Van der Most PJ,
Tanaka T,
Naderi E,
Rose LM,
Wu Y,
Karlsson R
외 274명 — 모두 보기
Barbalic M,
Lin H,
Pool R,
Zhu G,
Macé A,
Sidore C,
Trompet S,
Mangino M,
Sabater-Lleal M,
Kemp JP,
Abbasi A,
Kacprowski T,
Verweij N,
Smith AV,
Huang T,
Marzi C,
Feitosa MF,
Lohman KK,
Kleber ME,
Milaneschi Y,
Mueller C,
Huq M,
Vlachopoulou E,
Lyytikäinen LP,
Oldmeadow C,
Deelen J,
Perola M,
Zhao JH,
Feenstra B,
Amini M,
Lahti J,
Schraut KE,
Fornage M,
Suktitipat B,
Chen WM,
Li X,
Nutile T,
Malerba G,
Luan J,
Bak T,
Schork N,
Del Greco M F,
Thiering E,
Mahajan A,
Marioni RE,
Mihailov E,
Eriksson J,
Ozel AB,
Zhang W,
Nethander M,
Cheng YC,
Aslibekyan S,
Ang W,
Gandin I,
Yengo L,
Portas L,
Kooperberg C,
Hofer E,
Rajan KB,
Schurmann C,
den Hollander W,
Ahluwalia TS,
Zhao J,
Draisma HHM,
Ford I,
Timpson N,
Teumer A,
Huang H,
Wahl S,
Liu Y,
Huang J,
Uh HW,
Geller F,
Joshi PK,
Yanek LR,
Trabetti E,
Lehne B,
Vozzi D,
Verbanck M,
Biino G,
Saba Y,
Meulenbelt I,
O'Connell JR,
Laakso M,
Giulianini F,
Magnusson PKE,
Ballantyne CM,
Hottenga JJ,
Montgomery GW,
Rivadineira F,
Rueedi R,
Steri M,
Herzig KH,
Stott DJ,
Menni C,
Frånberg M,
St Pourcain B,
Felix SB,
Pers TH,
Bakker SJL,
Kraft P,
Peters A,
Vaidya D,
Delgado G,
Smit JH,
Großmann V,
Sinisalo J,
Seppälä I,
Williams SR,
Holliday EG,
Moed M,
Langenberg C,
Räikkönen K,
Ding J,
Campbell H,
Sale MM,
Chen YI,
James AL,
Ruggiero D,
Soranzo N,
Hartman CA,
Smith EN,
Berenson GS,
Fuchsberger C,
Hernandez D,
Tiesler CMT,
Giedraitis V,
Liewald D,
Fischer K,
Mellström D,
Larsson A,
Wang Y,
Scott WR,
Lorentzon M,
Beilby J,
Ryan KA,
Pennell CE,
Vuckovic D,
Balkau B,
Concas MP,
Schmidt R,
Mendes de Leon CF,
Bottinger EP,
Kloppenburg M,
Paternoster L,
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Willemsen G,
Evans DM,
Madden PAF,
Kähönen M,
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Karhunen V,
Kritchevsky SB,
Sattar N,
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Clarke R,
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Raitakari OT,
Attia JR,
van Heemst D,
Kajantie E,
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Scott RA,
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Lindgren CM,
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Karlsson M,
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Mohlke KL,
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Morrison AC,
Boomsma DI,
Whitfield JB,
Strachan DP,
Hofman A,
Vollenweider P,
Cucca F,
Jarvelin MR,
Jukema JW,
Spector TD,
Hamsten A,
Zeller T,
Uitterlinden AG,
Nauck M,
Gudnason V,
Qi L,
Grallert H,
Borecki IB,
Rotter JI,
März W,
Wild PS,
Lokki ML,
Boyle M,
Salomaa V,
Melbye M,
Eriksson JG,
Wilson JF,
Penninx BWJH,
Becker DM,
Worrall BB,
Gibson G,
Krauss RM,
Ciullo M,
Zaza G,
Wareham NJ,
Oldehinkel AJ,
Palmer LJ,
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Pramstaller PP,
Bandinelli S,
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Ohlsson C,
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Lehtimäki T,
Shuldiner AR,
Arnett DK,
Beilin LJ,
Robino A,
Froguel P,
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Koenig W,
Loos RJF,
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Schmidt H,
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Morris AP,
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Tracy RP,
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Boerwinkle E,
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LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
페이지 12개+
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,
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Braithwaite VS,
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Fauman EB,
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Giannakopoulou O,
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Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
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Mahajan A,
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Mook-Kanamori DO,
Mosen-Ansorena D,
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Poveda A,
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Varga TV,
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LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
외 198명 — 모두 보기
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
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Kraja AT,
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Rasheed A,
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Zhao W,
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Stančáková A,
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Havulinna AS,
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Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
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Moayyeri A,
Vergnaud AC,
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Poveda A,
Varga TV,
Caslake M,
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Palotie A,
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Salomaa V,
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Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
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Blankenberg S,
Ferrières J,
Kee F,
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Müller-Nurasyid M,
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CHARGE-Heart Failure Consortium · EchoGen Consortium 외 컨소시엄 12곳
Nature genetics · 2016 · PMID 27618447 · open access
페이지 11개
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Köttgen A,
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Hundertmark C,
Pistis G,
Ruggiero D,
O'Seaghdha CM,
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외 214명 — 모두 보기
Johnson AD,
Kutalik Z,
Smith AV,
Shi J,
Struchalin M,
Middelberg RP,
Brown MJ,
Gaffo AL,
Pirastu N,
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Hayward C,
Zemunik T,
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Tin A,
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Grotevendt A,
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Nakamura Y,
Tanaka T,
Munroe PB,
Samani NJ,
Jacobs DR Jr,
Liu K,
D'Adamo P,
Ulivi S,
Rotter JI,
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Vollenweider P,
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Salumets A,
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Plenge RM,
Portas L,
Persico I,
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Mateo Leach I,
van Gilst WH,
Goel A,
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LifeLines Cohort Study · CARDIoGRAM Consortium 외 컨소시엄 3곳
Nature genetics · 2013 · PMID 23263486
페이지 3개
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Gudbjartsson DF,
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Helgadottir A,
Sulem P,
Jonsdottir GM,
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외 61명 — 모두 보기
Beilby J,
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Nature genetics · 2009 · PMID 19198610
페이지 2개
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Gretarsdottir S,
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Thorleifsson G,
Holm H,
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de Vries JP,
Kranendonk SE,
Zeebregts CJ,
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외 90명 — 모두 보기
Boll AP,
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