Ganapathy A - Search Results

1

Clinical and genetic analysis of Indian patients with NDP-related retinopathies.

Sudha D, Ganapathy A, Mohan P, Mannan AU, Krishna S, Neriyanuri S, Swaminathan M, Rishi P, Chidambaram S, Arunachalam JP. Sudha D, et al. Among authors: ganapathy a. Int Ophthalmol. 2018 Jun;38(3):1251-1260. doi: 10.1007/s10792-017-0589-0. Epub 2017 Jun 10. Int Ophthalmol. 2018. PMID: 28602015

2

Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss.

Sudha D, Patric IRP, Ganapathy A, Agarwal S, Krishna S, Neriyanuri S, Sripriya S, Sen P, Chidambaram S, Arunachalam JP. Sudha D, et al. Among authors: ganapathy a. Ophthalmic Genet. 2017 May-Jun;38(3):260-266. doi: 10.1080/13816810.2016.1214972. Epub 2016 Sep 22. Ophthalmic Genet. 2017. PMID: 28574807

3

Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease.

Battu R, Verma A, Hariharan R, Krishna S, Kiran R, Jacob J, Ganapathy A, Ramprasad VL, Kumaramanickavel G, Jeyabalan N, Ghosh A. Battu R, et al. Among authors: ganapathy a. Biomed Res Int. 2015;2015:940864. doi: 10.1155/2015/940864. Epub 2015 Apr 2. Biomed Res Int. 2015. PMID: 25922843 Free PMC article. Clinical Trial.

4

Lethal Cenani Lenz syndrome in two consecutive pregnancies: Further extension of phenotype from Maldives.

Yesodharan D, Krishnan V, Nair IR, Ganapathy A, Mannan AU, Nampoothiri S. Yesodharan D, et al. Among authors: ganapathy a. Am J Med Genet A. 2021 Feb;185(2):620-624. doi: 10.1002/ajmg.a.61971. Epub 2020 Nov 11. Am J Med Genet A. 2021. PMID: 33179409

5

Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients.

Ganapathy A, Mishra A, Soni MR, Kumar P, Sadagopan M, Kanthi AV, Patric IRP, George S, Sridharan A, Thyagarajan TC, Aswathy SL, Vidya HK, Chinnappa SM, Nayanala S, Prakash MB, Raghavendrachar VG, Parulekar M, Gowda VK, Nampoothiri S, Menon RN, Pachat D, Udani V, Naik N, Kamate M, Devi ARR, Mohammed Kunju PA, Nair M, Hegde AU, Kumar MP, Sundaram S, Tilak P, Puri RD, Shah K, Sheth J, Hasan Q, Sheth F, Agrawal P, Katragadda S, Veeramachaneni V, Chandru V, Hariharan R, Mannan AU. Ganapathy A, et al. J Neurol. 2019 Aug;266(8):1919-1926. doi: 10.1007/s00415-019-09358-1. Epub 2019 May 8. J Neurol. 2019. PMID: 31069529

6

Chronic Mucocutaneous Candidiasis in an Adolescent Boy Due to a Novel Mutation in TRAF3IP2.

Bhattad S, Dinakar C, Pinnamaraju H, Ganapathy A, Mannan A. Bhattad S, et al. Among authors: ganapathy a. J Clin Immunol. 2019 Aug;39(6):596-599. doi: 10.1007/s10875-019-00664-x. Epub 2019 Jul 10. J Clin Immunol. 2019. PMID: 31292894

7

Targeted sequencing of the DMD locus: A comprehensive diagnostic tool for all mutations.

Aravind S, Ashley B, Mannan A, Ganapathy A, Ramesh K, Ramachandran A, Nongthomba U, Shastry A. Aravind S, et al. Among authors: ganapathy a. Indian J Med Res. 2019 Sep;150(3):282-289. doi: 10.4103/ijmr.IJMR_290_18. Indian J Med Res. 2019. PMID: 31719299 Free PMC article.

8

Charcot-Marie-Tooth disease type 2S: identical novel missense mutation of IGHMBP2 gene in two unrelated families.

Chandrasekharan SV, Nair SS, Ganapathy A, Mannan AU, Sundaram S. Chandrasekharan SV, et al. Among authors: ganapathy a. Neurol Sci. 2022 Jan;43(1):719-722. doi: 10.1007/s10072-021-05668-3. Epub 2021 Oct 20. Neurol Sci. 2022. PMID: 34668123 No abstract available.

9

Assessing Utility of Clinical Exome Sequencing in Diagnosis of Rare Idiopathic Neurodevelopmental Disorders in Indian Population.

Sheth H, Pancholi D, Bhavsar R, Mannan AU, Ganapathy A, Chowdhury M, Shah S, Solanki D, Sheth F, Sheth J. Sheth H, et al. Among authors: ganapathy a. Neurol India. 2021 Nov-Dec;69(6):1729-1736. doi: 10.4103/0028-3886.333475. Neurol India. 2021. PMID: 34979677 Free article.

10

Mutation Spectrum of GNE Myopathy in the Indian Sub-Continent.

Bhattacharya S, Khadilkar SV, Nalini A, Ganapathy A, Mannan AU, Majumder PP, Bhattacharya A. Bhattacharya S, et al. Among authors: ganapathy a. J Neuromuscul Dis. 2018;5(1):85-92. doi: 10.3233/JND-170270. J Neuromuscul Dis. 2018. PMID: 29480215

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