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Page 1
The genomic landscape of rare disorders in the Middle East.
Genome Med. 2023 Jan 27;15(1):5. doi: 10.1186/s13073-023-01157-8.
Genome Med. 2023.
PMID: 36703223
Free PMC article.
Genetic determinants of severe COVID-19 in young Asian and Middle Eastern patients: a case series.
Badla BA, Hanifa MS, Jain R, Naofal ME, Halabi N, Yaslam S, Ramaswamy S, Taylor A, Alfalasi R, Shenbagam S, Khansaheb H, Al Suwaidi H, Nowotny N, Popatia R, Al Khayat A, Alsheikh-Ali A, Loney T, AlDabal LM, Abou Tayoun A.
Badla BA, et al. Among authors: alfalasi r.
Sci Rep. 2023 Nov 20;13(1):20294. doi: 10.1038/s41598-023-47718-0.
Sci Rep. 2023.
PMID: 37985737
Free PMC article.
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Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations.
Halabi N, Ramaswamy S, El Naofal M, Taylor A, Yaslam S, Jain R, Alfalasi R, Shenbagam S, Bitzan M, Yavuz L, Abulhoul H, Shankar S, Janjua D, Jadhav D, Al Maazmi MM, Abuhammour W, Alsheikh-Ali A, Al Awadhi M, Al Khayat A, Abou Tayoun AN.
Halabi N, et al. Among authors: alfalasi r.
Genome Med. 2022 May 24;14(1):56. doi: 10.1186/s13073-022-01061-7.
Genome Med. 2022.
PMID: 35606784
Free PMC article.
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A genetic overview of 23Y-STR markers in UAE population.
Nazir M, Alhaddad H, Alenizi M, Alenizi H, Taqi Z, Sanqoor S, Alrazouqi A, Hassan A, Alfalasi R, Gaur S, Al Jaber J, Ziab J, Al-Harbi E, Moura-Neto RS, Budowle B.
Nazir M, et al. Among authors: alfalasi r.
Forensic Sci Int Genet. 2016 Jul;23:150-152. doi: 10.1016/j.fsigen.2016.04.009. Epub 2016 Apr 19.
Forensic Sci Int Genet. 2016.
PMID: 27124011
No abstract available.
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Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with Congenital Hypothyroidism: Ruling Out Recessive Inheritance or a Kinship/Laboratory Sequencing Error.
Jain R, Rabea F, Alfalasi R, Elabiary MW, Abou Tayoun A.
Jain R, et al. Among authors: alfalasi r.
J Appl Lab Med. 2023 Sep 7;8(5):993-999. doi: 10.1093/jalm/jfad039.
J Appl Lab Med. 2023.
PMID: 37478349
No abstract available.
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