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Page 1
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India.
Narang A, Uppilli B, Vivekanand A, Naushin S, Yadav A, Singhal K, Shamim U, Sharma P, Zahra S, Mathur A, Seth M, Parveen S, Vats A, Hillman S, Dolma P, Varma B, Jain V; TRISUTRA Ayurgenomics Consortium; Prasher B, Sengupta S, Mukerji M, Faruq M. Narang A, et al. Among authors: shamim u. Hum Mutat. 2020 Nov;41(11):1833-1847. doi: 10.1002/humu.24102. Epub 2020 Sep 9. Hum Mutat. 2020. PMID: 32906206
Genomics of rare genetic diseases-experiences from India.
GUaRDIAN Consortium; Sivasubbu S, Scaria V. GUaRDIAN Consortium, et al. Hum Genomics. 2019 Sep 25;14(1):52. doi: 10.1186/s40246-019-0215-5. Hum Genomics. 2019. PMID: 31554517 Free PMC article. Review.
Genetics of 67 patients of suspected primary ciliary dyskinesia from India.
Jat KR, Faruq M, Jindal S, Bari S, Soni A, Sharma P, Mathews S, Shamim U, Ahuja V, Uppilli B, Yadav SC, Lodha R, Arava SK, Kabra SK. Jat KR, et al. Among authors: shamim u. Clin Genet. 2024 Nov;106(5):650-658. doi: 10.1111/cge.14590. Epub 2024 Jul 14. Clin Genet. 2024. PMID: 39004944
Human-host transcriptomic analysis reveals unique early innate immune responses in different sub-phenotypes of COVID-19.
Maurya R, Shamim U, Chattopadhyay P, Mehta P, Mishra P, Devi P, Swaminathan A, Saifi S, Khare K, Yadav A, Parveen S, Sharma P, A V, Tyagi A, Jha V, Tarai B, Jha S, Faruq M, Budhiraja S, Pandey R. Maurya R, et al. Among authors: shamim u. Clin Transl Med. 2022 Jun;12(6):e856. doi: 10.1002/ctm2.856. Clin Transl Med. 2022. PMID: 35696527 Free PMC article. No abstract available.
58 results