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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
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
Development of acute kidney injury following repair of Stanford type A aortic dissection is associated with increased mortality and complications: a systematic review, meta-analysis, and meta-regression analysis.
Goyal A, Maheshwari S, Abbasi HQ, Mashkoor Y, Shamim U, Chambari M, Kelaiya A, Safi D, Saeed H, Jain H, Pokhrel P, Ullah I. Goyal A, et al. Among authors: shamim u. Cardiovasc Endocrinol Metab. 2024 Oct 21;13(4):e00314. doi: 10.1097/XCE.0000000000000314. eCollection 2024 Dec. Cardiovasc Endocrinol Metab. 2024. PMID: 39439591 Free PMC article. Review.
64 results