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Markus H에 대해
21건, 그중 20건 표시.
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Ehret GB,
Ferreira T,
Chasman DI,
Jackson AU,
Schmidt EM,
Johnson T,
Thorleifsson G,
Luan J,
Donnelly LA,
Kanoni S,
Petersen AK,
Pihur V
외 301명 — 모두 보기
Strawbridge RJ,
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Fava C,
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Theusch E,
Smith AJP,
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Pers TH,
Joehanes R,
Kim SK,
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Jansen R,
Johnson AD,
Warren H,
Kim YJ,
Zhao W,
Wu Y,
Tayo BO,
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Amin N,
Arking DE,
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Collins FS,
Connell JM,
Döring A,
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Dominiczak AF,
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CHARGE-EchoGen consortium · CHARGE-HF consortium 외 컨소시엄 1곳
Nature genetics · 2016 · PMID 27618452 · open access
페이지 12개+
Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus
Khunsriraksakul C,
Li Q,
Markus H,
Patrick MT,
Sauteraud R,
McGuire D,
Wang X,
Wang C,
Wang L,
Chen S,
Shenoy G,
Li B
외 6명 — 모두 보기
Nature communications · 2023 · PMID 36750564 · open access
페이지 12개+
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
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Patsopoulos NA,
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외 230명 — 모두 보기
Booth DR,
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International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
페이지 11개
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
Williams FM,
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Hodgkiss D,
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외 46명 — 모두 보기
Silander K,
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EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 외 컨소시엄 3곳
Annals of neurology · 2013 · PMID 23381943 · open access
페이지 11개
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
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외 198명 — 모두 보기
Tukiainen T,
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Masca N,
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Tinker A,
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Zhang H,
Donnelly LA,
Groves CJ,
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Moayyeri A,
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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 analysis identifies 13 new risk loci for schizophrenia
Ripke S,
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Akterin S,
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외 176명 — 모두 보기
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Schwab SG,
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Sawcer SJ,
Trembath RC,
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Wood NW,
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Band G,
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Su Z,
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Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 23974872 · open access
페이지 10개
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
Sabater-Lleal M,
Huang J,
Chasman D,
Naitza S,
Dehghan A,
Johnson AD,
Teumer A,
Reiner AP,
Folkersen L,
Basu S,
Rudnicka AR,
Trompet S
외 133명 — 모두 보기
Mälarstig A,
Baumert J,
Bis JC,
Guo X,
Hottenga JJ,
Shin SY,
Lopez LM,
Lahti J,
Tanaka T,
Yanek LR,
Oudot-Mellakh T,
Wilson JF,
Navarro P,
Huffman JE,
Zemunik T,
Redline S,
Mehra R,
Pulanic D,
Rudan I,
Wright AF,
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Polasek O,
Wild SH,
Campbell H,
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Wallace R,
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Becker DM,
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Bandinelli S,
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Green D,
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Harris SE,
Liewald DC,
Starr JM,
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외 70명 — 모두 보기
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외 81명 — 모두 보기
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외 146명 — 모두 보기
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외 39명 — 모두 보기
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페이지 1개
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
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외 27명 — 모두 보기
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Genetic variation at 16q24.2 is associated with small vessel stroke
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외 55명 — 모두 보기
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METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
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페이지 1개
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외 35명 — 모두 보기
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수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.