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Page 1
Genomics of rare genetic diseases-experiences from India.
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 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: sonakar ak.
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.
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Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data.
Hariprakash JM, Vellarikkal SK, Keechilat P, Verma A, Jayarajan R, Dixit V, Ravi R, Senthivel V, Kumar A, Sehgal P, Sonakar AK, Ambawat S, Giri AK, Philip A, Sivadas A, Faruq M, Bharadwaj D, Sivasubbu S, Scaria V.
Hariprakash JM, et al. Among authors: sonakar ak.
Pharmacogenomics. 2018 Feb;19(3):227-241. doi: 10.2217/pgs-2017-0101. Epub 2017 Dec 14.
Pharmacogenomics. 2018.
PMID: 29239269
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A Novel Co-existence of Spinocerebellar Ataxia 1 and Spinocerebellar Ataxia 2 Mutations in Indian Patients.
Sharma P, Sonakar AK, Goel V, Garg A, Srivastava AK, Faruq M.
Sharma P, et al. Among authors: sonakar ak.
Mov Disord Clin Pract. 2022 May 10;9(5):688-692. doi: 10.1002/mdc3.13464. eCollection 2022 Jul.
Mov Disord Clin Pract. 2022.
PMID: 35844270
Free PMC article.
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SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series.
Sonakar AK, Shamim U, Srivastava MP, Faruq M, Srivastava AK.
Sonakar AK, et al.
Parkinsonism Relat Disord. 2021 Aug;89:139-145. doi: 10.1016/j.parkreldis.2021.07.011. Epub 2021 Jul 14.
Parkinsonism Relat Disord. 2021.
PMID: 34298214
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