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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.
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: shenbagam s.
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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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: shenbagam s.
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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Carrier screening of spinal muscular atrophy in North Indian population and its public health implications.
Verma IC, Kohli S, Shenbagam S, Bijarnia-Mahay S, DuaPuri R, Saxena R.
Verma IC, et al. Among authors: shenbagam s.
Clin Genet. 2020 Aug;98(2):198-199. doi: 10.1111/cge.13796.
Clin Genet. 2020.
PMID: 32666593
No abstract available.
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Psychosocial issues in erythropoietic protoporphyria - the perspective of parents, children, and young adults: A qualitative study.
Naik H, Shenbagam S, Go AM, Balwani M.
Naik H, et al. Among authors: shenbagam s.
Mol Genet Metab. 2019 Nov;128(3):314-319. doi: 10.1016/j.ymgme.2019.01.023. Epub 2019 Jan 26.
Mol Genet Metab. 2019.
PMID: 30711301
Free PMC article.
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