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868 results

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Mutational dynamics across VOCs in International travellers and Community transmission underscores importance of Spike-ACE2 interaction.
Mehta P, Ravi V, Devi P, Maurya R, Parveen S, Mishra P, Yadav A, Swaminathan A, Saifi S, Khare K, Chattopadhyay P, Yadav M, Chauhan NS, Tarai B, Budhiraja S, Shamim U, Pandey R. Mehta P, et al. Among authors: parveen s. Microbiol Res. 2022 Sep;262:127099. doi: 10.1016/j.micres.2022.127099. Epub 2022 Jun 25. Microbiol Res. 2022. PMID: 35779308 Free PMC article.
An Indian child with Coats plus syndrome due to mutations in STN1.
Passi GR, Shamim U, Rathore S, Joshi A, Mathur A, Parveen S, Sharma P, Crow YJ, Faruq M. Passi GR, et al. Among authors: parveen s. Am J Med Genet A. 2020 Sep;182(9):2139-2144. doi: 10.1002/ajmg.a.61737. Epub 2020 Jul 6. Am J Med Genet A. 2020. PMID: 32627942
Cerebellar Ataxia in Adults with SQSTM1-Associated Frontotemporal Dementia-Amyotrophic Lateral Sclerosis Spectrum of Disorders.
Mishra B, Rajan R, Gupta A, Faruq M, Shamim U, Parveen S, Garg A, Tripathi M, Vishnu VY, Singh MB, Bhatia R, Srivastava P. Mishra B, et al. Among authors: parveen s. Mov Disord Clin Pract. 2021 Apr 28;8(5):800-802. doi: 10.1002/mdc3.13218. eCollection 2021 Jul. Mov Disord Clin Pract. 2021. PMID: 34307757 Free PMC article. No abstract available.
Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel LOXL3 Mutation.
Sood A, Shamim U, Kharbanda OP, Kabra M, Gupta N, Mathur A, Joshi A, Parveen S, Zahra S, Sharma P, Seth M, Khan A, Faruq M, Mishra D. Sood A, et al. Among authors: parveen s. Cleft Palate Craniofac J. 2022 Nov;59(11):1329-1339. doi: 10.1177/10556656211052781. Epub 2021 Nov 17. Cleft Palate Craniofac J. 2022. PMID: 34787502
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: parveen s. 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.
LncRNAs harbouring regulatory motifs within repeat elements modulate immune response towards COVID-19 disease severity and clinical outcomes.
Chattopadhyay P, Mishra P, Khare K, Yadav A, Mehta P, Saifi S, Swaminathan A, Devi P, Parveen S, Tyagi A, Jha V, Tarai B, Jha S, Budhiraja S, Narayan J, Pandey R. Chattopadhyay P, et al. Among authors: parveen s. Clin Transl Med. 2022 Jul;12(7):e932. doi: 10.1002/ctm2.932. Clin Transl Med. 2022. PMID: 35808807 Free PMC article. No abstract available.
Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool.
Sharma P, Sonakar AK, Tyagi N, Suroliya V, Kumar M, Kutum R, Asokchandran V, Ambawat S, Shamim U, Anand A, Ahmad I, Shakya S, Uppili B, Mathur A, Parveen S, Jain S, Singh J, Seth M, Zahra S, Joshi A, Goel D, Sahni S, Kamai A, Wadhwa S, Murali A, Saifi S, Chowdhury D, Pandey S, Anand KS, Narasimhan RL, Laskar S, Kushwaha S, Kumar M, Shaji CV, Srivastava MVP, Srivastava AK, Faruq M; GOMED‐Ataxia study group. Sharma P, et al. Among authors: parveen s. Adv Genet (Hoboken). 2022 Mar 10;3(2):2100078. doi: 10.1002/ggn2.202100078. eCollection 2022 Jun. Adv Genet (Hoboken). 2022. PMID: 36618024 Free PMC article.
Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort.
Tyagi N, Uppili B, Sharma P, Parveen S, Saifi S, Jain A, Sonakar A, Ahmed I, Sahni S, Shamim U, Anand A, Suroliya V, Asokachandran V, Srivastava A, Sivasubbu S, Scaria V, Faruq M. Tyagi N, et al. Among authors: parveen s. Neurogenetics. 2024 Jan;25(1):13-25. doi: 10.1007/s10048-023-00736-6. Epub 2023 Nov 2. Neurogenetics. 2024. PMID: 37917284
868 results