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Page 1
Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiency.
Deshpande D, Gupta SK, Sarma AS, Ranganath P, Jain S JMN, Sheth J, Mistri M, Gupta N, Kabra M, Phadke SR, Girisha KM, Dua Puri R, Aggarwal S, Datar C, Mandal K, Tilak P, Muranjan M, Bijarnia-Mahay S, Rama Devi A R, Tayade NB, Ranjan A, Dalal AB. Deshpande D, et al. Among authors: tayade nb. Hum Mutat. 2021 Oct;42(10):1336-1350. doi: 10.1002/humu.24263. Epub 2021 Aug 3. Hum Mutat. 2021. PMID: 34273913
Development, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in India.
Sheth H, Nair A, Bhavsar R, Kamate M, Gowda VK, Bavdekar A, Kadam S, Nampoothiri S, Panigrahi I, Kaur A, Shah S, Mehta S, Jagadeesan S, Suresh I, Kapoor S, Bajaj S, Devi RR, Prajapati A, Godbole K, Patel H, Luhar Z, Shah RC, Iyer A, Bijarnia S, Puri R, Muranjan M, Shah A, Magar S, Gupta N, Tayade N, Gandhi A, Sowani A, Kale S, Jalan A, Solanki D, Dalal A, Mane S, Prabha CR, Sheth F, Joshi CG, Joshi M, Sheth J. Sheth H, et al. Among authors: tayade n. Hum Genomics. 2024 May 10;18(1):46. doi: 10.1186/s40246-024-00613-9. Hum Genomics. 2024. PMID: 38730490 Free PMC article.
Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.
Sheth J, Nair A, Sheth F, Ajagekar M, Dhondekar T, Panigrahi I, Bavdekar A, Nampoothiri S, Datar C, Gandhi A, Muranjan M, Kaur A, Desai M, Mistri M, Patel C, Naik P, Shah M, Godbole K, Kapoor S, Gupta N, Bijarnia-Mahay S, Kadam S, Solanki D, Desai S, Iyer A, Patel K, Patel H, Shah RC, Mehta S, Shah R, Bhavsar R, Shah J, Pandya M, Patel B, Shah S, Shah H, Shah S, Bajaj S, Shah S, Thaker N, Kalane U, Kamate M, Kn VR, Tayade N, Jagadeesan S, Jain D, Chandarana M, Singh J, Mehta S, Suresh B, Sheth H. Sheth J, et al. Among authors: tayade n. Orphanet J Rare Dis. 2024 Aug 13;19(1):295. doi: 10.1186/s13023-024-03300-z. Orphanet J Rare Dis. 2024. PMID: 39138584 Free PMC article.
The Genomic Landscape of Wilson Disease in a Pan India Disease Cohort and Population-Scale Data.
Kumar M, Sharma S, Pandey S, Mammayil G, Pala Kuzhiyil A, Sreesh S, Arakkal R, Radhakrishnan DM, Rajan R, Amalnath D, Gulati R, Tayade N, Sadasivan S, Valsan A, Menon J, Kamate M, Mathur SK, Mahadevan R, Dhingra B, Rajan R, Singh K, Shalimar, Geevarghese SK, Kumar VS, Menachery J, Aliyar A, Bhoyar RC, Jolly B, Jain A, Vittal Rangan A, Moitra T, Mhaske A, Gupta V, Senthivel V, Mishra A, Saini A, Gaharwar U, Sivasubbu S, Scaria V, B K B. Kumar M, et al. Among authors: tayade n. Mov Disord Clin Pract. 2024 Nov 13. doi: 10.1002/mdc3.14266. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 39535360
Author Correction: Leveraging genetic resource diversity and identification of trait-enriched superior genotypes for accelerated improvement in linseed (Linum usitatissimum L.).
Kaur V, Gomashe SS, Yadav SK, Singh D, Sheela, Chauhan SS, Kumar V, Jat B, Tayade NR, Langyan S, Kaushik N, Singh M, Kheralia M, Wankhede DP, Aravind J, Srivastava V, Gupta K, Kumar A, Singh GP. Kaur V, et al. Among authors: tayade nr. Sci Rep. 2024 Nov 19;14(1):28600. doi: 10.1038/s41598-024-78594-x. Sci Rep. 2024. PMID: 39562769 Free PMC article. No abstract available.
Leveraging genetic resource diversity and identification of trait-enriched superior genotypes for accelerated improvement in linseed (Linum usitatissimum L.).
Kaur V, Gomashe SS, Yadav SK, Singh D, Sheela, Chauhan SS, Kumar V, Jat B, Tayade NR, Langyan S, Kaushik N, Singh M, Kheralia M, Wankhede DP, Aravind J, Srivastava V, Gupta K, Kumar A, Singh GP. Kaur V, et al. Among authors: tayade nr. Sci Rep. 2024 Aug 31;14(1):20266. doi: 10.1038/s41598-024-71044-8. Sci Rep. 2024. PMID: 39217216 Free PMC article.
Antiretroviral Therapy for the Prevention of HIV-1 Transmission.
Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour MC, Kumarasamy N, Hakim JG, Kumwenda J, Grinsztejn B, Pilotto JH, Godbole SV, Chariyalertsak S, Santos BR, Mayer KH, Hoffman IF, Eshleman SH, Piwowar-Manning E, Cottle L, Zhang XC, Makhema J, Mills LA, Panchia R, Faesen S, Eron J, Gallant J, Havlir D, Swindells S, Elharrar V, Burns D, Taha TE, Nielsen-Saines K, Celentano DD, Essex M, Hudelson SE, Redd AD, Fleming TR; HPTN 052 Study Team. Cohen MS, et al. N Engl J Med. 2016 Sep 1;375(9):830-9. doi: 10.1056/NEJMoa1600693. Epub 2016 Jul 18. N Engl J Med. 2016. PMID: 27424812 Free PMC article. Clinical Trial.
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