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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1955 1
1962 3
1968 1
1969 1
1970 1
1971 2
1974 1
1978 1
1979 1
1980 1
1981 1
1982 2
1983 3
1984 2
1986 2
1987 7
1988 1
1989 2
1990 2
1991 1
1992 5
1994 1
1996 4
1997 5
1998 8
1999 13
2000 3
2001 6
2002 3
2003 4
2004 3
2005 4
2006 7
2007 2
2008 5
2009 5
2010 5
2011 1
2012 2
2021 1
2024 0

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Publication date

PubMed (OMIM) for id: 2147

119 results

Results by year

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Page 1
Ticagrelor versus Clopidogrel in CYP2C19 Loss-of-Function Carriers with Stroke or TIA.
Wang Y, Meng X, Wang A, Xie X, Pan Y, Johnston SC, Li H, Bath PM, Dong Q, Xu A, Jing J, Lin J, Niu S, Wang Y, Zhao X, Li Z, Jiang Y, Li W, Liu L, Xu J, Chang L, Wang L, Zhuang X, Zhao J, Feng Y, Man H, Li G, Wang B; CHANCE-2 Investigators. Wang Y, et al. N Engl J Med. 2021 Dec 30;385(27):2520-2530. doi: 10.1056/NEJMoa2111749. Epub 2021 Oct 28. N Engl J Med. 2021. PMID: 34708996 Clinical Trial.
Thrombosis from a prothrombin mutation conveying antithrombin resistance.
Miyawaki Y, Suzuki A, Fujita J, Maki A, Okuyama E, Murata M, Takagi A, Murate T, Kunishima S, Sakai M, Okamoto K, Matsushita T, Naoe T, Saito H, Kojima T. Miyawaki Y, et al. N Engl J Med. 2012 Jun 21;366(25):2390-6. doi: 10.1056/NEJMoa1201994. N Engl J Med. 2012. PMID: 22716977 Free article.
Failure to validate association between 12p13 variants and ischemic stroke.
International Stroke Genetics Consortium; Wellcome Trust Case-Control Consortium 2. International Stroke Genetics Consortium, et al. N Engl J Med. 2010 Apr 22;362(16):1547-50. doi: 10.1056/NEJMc0910050. N Engl J Med. 2010. PMID: 20410525 Free PMC article. No abstract available.
A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.
Morange PE, Bezemer I, Saut N, Bare L, Burgos G, Brocheton J, Durand H, Biron-Andreani C, Schved JF, Pernod G, Galan P, Drouet L, Zelenika D, Germain M, Nicaud V, Heath S, Ninio E, Delluc A, Münzel T, Zeller T, Brand-Herrmann SM, Alessi MC, Tiret L, Lathrop M, Cambien F, Blankenberg S, Emmerich J, Trégouët DA, Rosendaal FR. Morange PE, et al. Am J Hum Genet. 2010 Apr 9;86(4):592-5. doi: 10.1016/j.ajhg.2010.02.011. Epub 2010 Mar 11. Am J Hum Genet. 2010. PMID: 20226436 Free PMC article.
Functional SNP of ARHGEF10 confers risk of atherothrombotic stroke.
Matsushita T, Ashikawa K, Yonemoto K, Hirakawa Y, Hata J, Amitani H, Doi Y, Ninomiya T, Kitazono T, Ibayashi S, Iida M, Nakamura Y, Kiyohara Y, Kubo M. Matsushita T, et al. Hum Mol Genet. 2010 Mar 15;19(6):1137-46. doi: 10.1093/hmg/ddp582. Epub 2009 Dec 30. Hum Mol Genet. 2010. PMID: 20042462
Congenital prothrombin deficiency.
Lancellotti S, De Cristofaro R. Lancellotti S, et al. Semin Thromb Hemost. 2009 Jun;35(4):367-81. doi: 10.1055/s-0029-1225759. Epub 2009 Jul 13. Semin Thromb Hemost. 2009. PMID: 19598065 Review.
119 results