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Page 1
KBG Syndrome in 16 Indian Individuals.
Bajaj S, Nampoothiri S, Chugh R, Sheth J, Sheth F, Sheth H, Narayan V, Deshpande A, Hegde A, Dwivedi A, Yeshodharan D, Khosla I, Mittal M, Kore M, Ramprasad V, C AK, Girisha KM. Bajaj S, et al. Am J Med Genet A. 2025 Feb;197(2):e63907. doi: 10.1002/ajmg.a.63907. Epub 2024 Oct 15. Am J Med Genet A. 2025. PMID: 39404460
An Indian Child with CONDSIAS Due to a Novel Variant in ADPRHL2 Gene.
Bajaj S, Shah P, Shah A, Setty PN, Seenappa V, Hingwala D. Bajaj S, et al. Ann Indian Acad Neurol. 2022 Nov-Dec;25(6):1190-1192. doi: 10.4103/aian.aian_558_22. Epub 2022 Oct 20. Ann Indian Acad Neurol. 2022. PMID: 36911439 Free PMC article. No abstract available.
Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test.
Sheth F, Shah J, Jain D, Shah S, Patel H, Patel K, Solanki DI, Iyer AS, Menghani B, Mhatre P, Mehta S, Bajaj S, Patel V, Pandya M, Dhami D, Patel D, Sheth J, Sheth H. Sheth F, et al. Among authors: bajaj s. BMC Neurol. 2023 Aug 5;23(1):292. doi: 10.1186/s12883-023-03341-0. BMC Neurol. 2023. PMID: 37543562 Free PMC article.
Hemiconvulsion-hemiplegia syndrome.
Bajaj S, Tullu MS, Agrawal M. Bajaj S, et al. Neurol India. 2016 Sep-Oct;64(5):1094-5. doi: 10.4103/0028-3886.190303. Neurol India. 2016. PMID: 27625282 Free article. No abstract available.
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities.
Kaur P, do Rosario MC, Hebbar M, Sharma S, Kausthubham N, Nair K, A S, Bhat Y R, Lewis LES, Nampoothiri S, Patil SJ, Suresh N, Bijarnia Mahay S, Dua Puri R, Pai S, Kaur A, Kc R, Kamath N, Bajaj S, Kumble A, Shetty R, Shenoy R, Kamate M, Shah H, Muranjan MN, Bl Y, Avabratha KS, Subramaniam G, Kadavigere R, Bielas S, Girisha KM, Shukla A. Kaur P, et al. Among authors: bajaj s. Clin Genet. 2021 Nov;100(5):542-550. doi: 10.1111/cge.14037. Epub 2021 Jul 30. Clin Genet. 2021. PMID: 34302356 Free PMC article.
810 results