Acharya M - Search Results

1

Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.

Sanga S, Ghosh A, Kumar K, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, Bardhan M, Arunachal G, Raju S, Gayathri N, Biswas NK, Chakrabarti S, Nalini A, Roy S, Acharya M. Sanga S, et al. Among authors: acharya m. Eur J Neurol. 2021 Mar;28(3):992-1003. doi: 10.1111/ene.14616. Epub 2020 Nov 26. Eur J Neurol. 2021. PMID: 33124102

2

Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C.

Bardhan M, Anjanappa RM, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, Sanga S, Padmanabh H, Valasani RK, Nishadham V, Keerthipriya M, Geetha TS, Ramprasad V, Arunachal G, Thomas PT, Acharya M, Nalini A. Bardhan M, et al. Among authors: acharya m. Neurogenetics. 2022 Jul;23(3):187-202. doi: 10.1007/s10048-022-00690-9. Epub 2022 Apr 13. Neurogenetics. 2022. PMID: 35416532

3

Mutations in MYOC gene of Indian primary open angle glaucoma patients.

Mukhopadhyay A, Acharya M, Mukherjee S, Ray J, Choudhury S, Khan M, Ray K. Mukhopadhyay A, et al. Among authors: acharya m. Mol Vis. 2002 Nov 15;8:442-8. Mol Vis. 2002. PMID: 12447164 Free article.

4

Primary role of CYP1B1 in Indian juvenile-onset POAG patients.

Acharya M, Mookherjee S, Bhattacharjee A, Bandyopadhyay AK, Daulat Thakur SK, Bhaduri G, Sen A, Ray K. Acharya M, et al. Mol Vis. 2006 Apr 20;12:399-404. Mol Vis. 2006. PMID: 16688110 Free article.

5

Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change.

Acharya M, Mookherjee S, Bhattacharjee A, Thakur SK, Bandyopadhyay AK, Sen A, Chakrabarti S, Ray K. Acharya M, et al. BMC Mol Biol. 2007 Mar 14;8:21. doi: 10.1186/1471-2199-8-21. BMC Mol Biol. 2007. PMID: 17359525 Free PMC article.

6

Haplotype-based genomic analysis reveals novel association of CNTNAP5 genic region with primary angle closure glaucoma.

Chakraborty S, Sharma A, Sharma A, Sihota R, Bhattacharjee S, Acharya M. Chakraborty S, et al. Among authors: acharya m. J Biosci. 2021;46:15. J Biosci. 2021. PMID: 33737499 Free article.

7

A quantitative trait GWAS on lens thickness identifies novel risk loci on PTPRM in the narrow angle individuals susceptible to PACG.

Chakraborty S, Sharma A, Pal S, Sharma A, Sihota R, Bhattacharjee S, Acharya M. Chakraborty S, et al. Among authors: acharya m. Eur J Ophthalmol. 2023 Sep;33(5):1922-1930. doi: 10.1177/11206721231160988. Epub 2023 Mar 17. Eur J Ophthalmol. 2023. PMID: 36927043

8

Myocilin variants in Indian patients with open-angle glaucoma.

Bhattacharjee A, Acharya M, Mukhopadhyay A, Mookherjee S, Banerjee D, Bandopadhyay AK, Thakur SK, Sen A, Ray K. Bhattacharjee A, et al. Among authors: acharya m. Arch Ophthalmol. 2007 Jun;125(6):823-9. doi: 10.1001/archopht.125.6.823. Arch Ophthalmol. 2007. PMID: 17562996

9

Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma.

Mukhopadhyay A, Komatireddy S, Acharya M, Bhattacharjee A, Mandal AK, Thakur SK, Chandrasekhar G, Banerjee A, Thomas R, Chakrabarti S, Ray K. Mukhopadhyay A, et al. Among authors: acharya m. Mol Vis. 2005 Sep 23;11:792-7. Mol Vis. 2005. PMID: 16205626 Free article.

10

Genetics and bioinformatics of primary open angle glaucoma: an Indian perspective.

Ray K, Thakur SK, Banerjee AK, Mukhopadhyay A, Acharya M, Bhattacharjee A, Sen A, Bhaduri G. Ray K, et al. Among authors: acharya m. J Indian Med Assoc. 2004 Dec;102(12):708, 710, 712 passim. J Indian Med Assoc. 2004. PMID: 15871358 Review.

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