Komatireddy S - Search Results

1

Cryptococcal Meningitis Reported With Fingolimod Treatment: Case Series.

Del Poeta M, Ward BJ, Greenberg B, Hemmer B, Cree BAC, Komatireddy S, Mishra J, Sullivan R, Kilaru A, Moore A, Hach T, Berger JR. Del Poeta M, et al. Among authors: komatireddy s. Neurol Neuroimmunol Neuroinflamm. 2022 Mar 22;9(3):e1156. doi: 10.1212/NXI.0000000000001156. Print 2022 May. Neurol Neuroimmunol Neuroinflamm. 2022. PMID: 35318259 Free PMC article.

2

Complex phenotypes in an Indian family with homozygous SCA2 mutations.

Ragothaman M, Sarangmath N, Chaudhary S, Khare V, Mittal U, Sharma S, Komatireddy S, Chakrabarti S, Mukerji M, Juyal RC, Thelma BK, Muthane UB. Ragothaman M, et al. Among authors: komatireddy s. Ann Neurol. 2004 Jan;55(1):130-3. doi: 10.1002/ana.10815. Ann Neurol. 2004. PMID: 14705123

3

Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.

Komatireddy S, Chakrabarti S, Mandal AK, Reddy AB, Sampath S, Panicker SG, Balasubramanian D. Komatireddy S, et al. Mol Vis. 2003 Feb 18;9:43-8. Mol Vis. 2003. PMID: 12592227 Free article.

4

Glaucoma-associated CYP1B1 mutations share similar haplotype backgrounds in POAG and PACG phenotypes.

Chakrabarti S, Devi KR, Komatireddy S, Kaur K, Parikh RS, Mandal AK, Chandrasekhar G, Thomas R. Chakrabarti S, et al. Among authors: komatireddy s. Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5439-44. doi: 10.1167/iovs.07-0629. Invest Ophthalmol Vis Sci. 2007. PMID: 18055790

5

Gene symbol: CYP1B1. Disease: glaucoma, primary congenital.

Chakrabarti S, Komatireddy S, Mandal AK, Balasubramanian D. Chakrabarti S, et al. Among authors: komatireddy s. Hum Genet. 2003 Nov;113(6):556. Hum Genet. 2003. PMID: 14640114 No abstract available.

6

Gene symbol: MY0C (GLC1A). Disease: glaucoma 1, open angle.

Chakrabarti S, Komatireddy S, Mandal AK, Balasubramanian D. Chakrabarti S, et al. Among authors: komatireddy s. Hum Genet. 2003 Nov;113(6):557. Hum Genet. 2003. PMID: 14640116 No abstract available.

7

Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India.

Chakrabarti S, Kaur K, Komatireddy S, Acharya M, Devi KR, Mukhopadhyay A, Mandal AK, Hasnain SE, Chandrasekhar G, Thomas R, Ray K. Chakrabarti S, et al. Among authors: komatireddy s. Mol Vis. 2005 Feb 4;11:111-3. Mol Vis. 2005. PMID: 15723004 Free article.

8

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: komatireddy s. Mol Vis. 2005 Sep 23;11:792-7. Mol Vis. 2005. PMID: 16205626 Free article.

9

Dysregulation of Neuropilin-2 Expression in Inhibitory Neurons Impairs Hippocampal Circuit Development Leading to Autism-Epilepsy Phenotype.

Santhakumar V, Subramanian D, Eisenberg C, Huang A, Baek J, Naveed H, Komatireddy S, Shiflett M, Tran T. Santhakumar V, et al. Among authors: komatireddy s. Res Sq [Preprint]. 2024 Feb 9:rs.3.rs-3922129. doi: 10.21203/rs.3.rs-3922129/v1. Res Sq. 2024. PMID: 38405865 Free PMC article. Preprint.

10

Dysregulation of Neuropilin-2 Expression in Inhibitory Neurons Impairs Hippocampal Circuit Development Leading to Autism-Epilepsy Phenotype.

Subramanian D, Eisenberg C, Huang A, Baek J, Naveed H, Komatireddy S, Shiflett MW, Tran TS, Santhakumar V. Subramanian D, et al. Among authors: komatireddy s. bioRxiv [Preprint]. 2024 Feb 6:2024.02.05.578976. doi: 10.1101/2024.02.05.578976. bioRxiv. 2024. PMID: 38370800 Free PMC article. Preprint.

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