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

Year Number of Results
2010 2
2011 3
2012 4
2013 2
2014 3
2015 8
2016 6
2017 2
2018 5
2019 8
2020 8
2021 3
2022 11
2023 4
2024 2

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Page 1
The Frequency of Rh Phenotype and Its Probable Genotype.
Tariq F, Ashfaq J, Ahmed R, Fatima N, Ahmed Y, Borhany M. Tariq F, et al. Among authors: borhany m. Cureus. 2022 Jun 9;14(6):e25775. doi: 10.7759/cureus.25775. eCollection 2022 Jun. Cureus. 2022. PMID: 35812560 Free PMC article.
Frequency of Intron 22 Inversion in Severe Hemophilia A Patients.
Ashfaq J, Ahmed R, Tariq F, Abedin QU, Abid M, Borhany M. Ashfaq J, et al. Among authors: borhany m. Cureus. 2022 Aug 21;14(8):e28247. doi: 10.7759/cureus.28247. eCollection 2022 Aug. Cureus. 2022. PMID: 36158401 Free PMC article.
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F. Mohsenian S, et al. Among authors: borhany m. Blood Adv. 2024 Mar 26;8(6):1392-1404. doi: 10.1182/bloodadvances.2023012186. Blood Adv. 2024. PMID: 38286442 Free PMC article.
Profiling the mutational landscape of coagulation factor V deficiency.
Paraboschi EM, Menegatti M, Rimoldi V, Borhany M, Abdelwahab M, Gemmati D, Peyvandi F, Duga S, Asselta R. Paraboschi EM, et al. Among authors: borhany m. Haematologica. 2020 Apr;105(4):e180-e185. doi: 10.3324/haematol.2019.232587. Epub 2019 Aug 8. Haematologica. 2020. PMID: 31399523 Free PMC article. No abstract available.
61 results