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A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.
Simeoni I, Stephens JC, Hu F, Deevi SV, Megy K, Bariana TK, Lentaigne C, Schulman S, Sivapalaratnam S, Vries MJ, Westbury SK, Greene D, Papadia S, Alessi MC, Attwood AP, Ballmaier M, Baynam G, Bermejo E, Bertoli M, Bray PF, Bury L, Cattaneo M, Collins P, Daugherty LC, Favier R, French DL, Furie B, Gattens M, Germeshausen M, Ghevaert C, Goodeve AC, Guerrero JA, Hampshire DJ, Hart DP, Heemskerk JW, Henskens YM, Hill M, Hogg N, Jolley JD, Kahr WH, Kelly AM, Kerr R, Kostadima M, Kunishima S, Lambert MP, Liesner R, López JA, Mapeta RP, Mathias M, Millar CM, Nathwani A, Neerman-Arbez M, Nurden AT, Nurden P, Othman M, Peerlinck K, Perry DJ, Poudel P, Reitsma P, Rondina MT, Smethurst PA, Stevenson W, Szkotak A, Tuna S, van Geet C, Whitehorn D, Wilcox DA, Zhang B, Revel-Vilk S, Gresele P, Bellissimo DB, Penkett CJ, Laffan MA, Mumford AD, Rendon A, Gomez K, Freson K, Ouwehand WH, Turro E. Simeoni I, et al. Among authors: reitsma p. Blood. 2016 Jun 9;127(23):2791-803. doi: 10.1182/blood-2015-12-688267. Epub 2016 Apr 15. Blood. 2016. PMID: 27084890 Free PMC article.
Curated disease-causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH.
Megy K, Downes K, Simeoni I, Bury L, Morales J, Mapeta R, Bellissimo DB, Bray PF, Goodeve AC, Gresele P, Lambert M, Reitsma P, Ouwehand WH, Freson K; Subcommittee on Genomics in Thrombosis and Hemostasis. Megy K, et al. Among authors: reitsma p. J Thromb Haemost. 2019 Aug;17(8):1253-1260. doi: 10.1111/jth.14479. Epub 2019 Jun 9. J Thromb Haemost. 2019. PMID: 31179617 Free PMC article. No abstract available.
New fundamentals in hemostasis.
Versteeg HH, Heemskerk JW, Levi M, Reitsma PH. Versteeg HH, et al. Physiol Rev. 2013 Jan;93(1):327-58. doi: 10.1152/physrev.00016.2011. Physiol Rev. 2013. PMID: 23303912 Free article. Review.
Recessive inheritance of von Willebrand's disease type I.
Eikenboom JC, Reitsma PH, Peerlinck KM, Briët E. Eikenboom JC, et al. Among authors: reitsma ph. Lancet. 1993 Apr 17;341(8851):982-6. doi: 10.1016/0140-6736(93)91070-3. Lancet. 1993. PMID: 8096943
Multiple SNP testing improves risk prediction of first venous thrombosis.
de Haan HG, Bezemer ID, Doggen CJ, Le Cessie S, Reitsma PH, Arellano AR, Tong CH, Devlin JJ, Bare LA, Rosendaal FR, Vossen CY. de Haan HG, et al. Blood. 2012 Jul 19;120(3):656-63. doi: 10.1182/blood-2011-12-397752. Epub 2012 May 14. Blood. 2012. PMID: 22586183 Free article.
Nomenclature of genetic variants in hemostasis.
Goodeve AC, Reitsma PH, McVey JH; Working Group on Nomenclature of the Scientific and Standardisation Committee of the International Society on Thrombosis and Haemostasis. Goodeve AC, et al. Among authors: reitsma ph. J Thromb Haemost. 2011 Apr;9(4):852-5. doi: 10.1111/j.1538-7836.2011.04191.x. J Thromb Haemost. 2011. PMID: 21595097 Free article. No abstract available.
440 results