Sumita Danda[Author] - Search Results

Year	Number of Results
2006	1
2007	1
2008	3
2009	3
2010	3
2011	5
2012	10
2013	4
2014	9
2015	10
2016	10
2017	9
2018	7
2019	9
2020	11
2021	18
2022	22
2023	10
2024	8

1

Exploring the clinical utility of exome sequencing/mono, duo, trio in prenatal testing: a retrospective study in a tertiary care centre in south India.

Ilangovan H, Elangovan J, Danda S, Beck MM, Navaneethan P, Athiyarath R. Ilangovan H, et al. Among authors: danda s. J Perinat Med. 2024 May 7. doi: 10.1515/jpm-2023-0485. Online ahead of print. J Perinat Med. 2024. PMID: 38709224

2

Investigation of mutation spectrum amongst patients with familial primary cardiomyopathy using targeted NGS in Indian population.

Krishnaswamy SM, Arunachal G, Singh KG, Thomson VS, George P, Rao S, Danda S. Krishnaswamy SM, et al. Among authors: danda s. J Appl Genet. 2024 Mar 29. doi: 10.1007/s13353-024-00855-2. Online ahead of print. J Appl Genet. 2024. PMID: 38551768

3

A rare variant c.1802T>C (p. Ile601Thr) associated with severe phenotype among people with cystic fibrosis from south India, and potential genetic admixture in Réunion, France.

Kumar M, Aaron R, Varkki SD, Danda S, Ranganathan S, Paul GR. Kumar M, et al. Among authors: danda s. Pediatr Pulmonol. 2024 Mar 19. doi: 10.1002/ppul.26965. Online ahead of print. Pediatr Pulmonol. 2024. PMID: 38501349 No abstract available.

4

High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia.

Ravichandran L, Paul S, A R, Hs A, Mathai S, Simon A, Danda S, Thomas N, Chapla A. Ravichandran L, et al. Among authors: danda s. Endocrine. 2024 Mar 5. doi: 10.1007/s12020-024-03747-x. Online ahead of print. Endocrine. 2024. PMID: 38441846

5

Homozygous CARD14 variant presenting as infantile erythroderma.

Shajil C, Sathishkumar D, Kumar S, Danda S. Shajil C, et al. Among authors: danda s. BMJ Case Rep. 2024 Jan 16;17(1):e254090. doi: 10.1136/bcr-2022-254090. BMJ Case Rep. 2024. PMID: 38233005

6

KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature.

Yoganathan S, Whitney R, Thomas M, Danda S, Chettali AM, Prasad AN, Farhan SMK, AlSowat D, Abukhaled M, Aldhalaan H, Gowda VK, Kinhal UV, Bylappa AY, Konanki R, Lingappa L, Parchuri BM, Appendino JP, Scantlebury MH, Cunningham J, Hadjinicolaou A, El Achkar CM, Kamate M, Menon RN, Jose M, Riordan G, Kannan L, Jain V, Manokaran RK, Chau V, Donner EJ, Costain G, Minassian BA, Jain P. Yoganathan S, et al. Among authors: danda s. Epilepsia. 2024 Mar;65(3):709-724. doi: 10.1111/epi.17880. Epub 2024 Jan 17. Epilepsia. 2024. PMID: 38231304

7

Diagnostic exome identifies a novel PRKG2 mutation in a proband with skeletal dysplasia.

Kamdar P, Geetha TS, Palocaren T, Kandagaddala M, Chinniah PK, Murugan S, Vedam R, Danda S. Kamdar P, et al. Among authors: danda s. Clin Genet. 2024 Apr;105(4):453-454. doi: 10.1111/cge.14465. Epub 2023 Dec 10. Clin Genet. 2024. PMID: 38072398

8

Danda D, Goel R, Kabeerdoss J, Sun C, Danda S, Lincy Franklin A, Joseph G, Nath SK. Danda D, et al. Among authors: danda s. J Hum Genet. 2024 Jan;69(1):13-18. doi: 10.1038/s10038-023-01198-2. Epub 2023 Oct 17. J Hum Genet. 2024. PMID: 37848720

9

Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India.

Nagarajan B, Gowda VK, Yoganathan S, Sharawat IK, Srivastava K, Vora N, Badheka R, Danda S, Kalane U, Kaur A, Madaan P, Mehta S, Negi S, Panda PK, Rajadhyaksha S, Saini AG, Saini L, Shah S, Srinivasan VM, Suthar R, Thomas M, Vyas S, Sankhyan N, Sahu JK. Nagarajan B, et al. Among authors: danda s. Epilepsia Open. 2023 Dec;8(4):1383-1404. doi: 10.1002/epi4.12811. Epub 2023 Aug 25. Epilepsia Open. 2023. PMID: 37583270 Free PMC article.

10

Adult-onset leukodystrophies: a practical guide, recent treatment updates, and future directions.

Muthusamy K, Sivadasan A, Dixon L, Sudhakar S, Thomas M, Danda S, Wszolek ZK, Wierenga K, Dhamija R, Gavrilova R. Muthusamy K, et al. Among authors: danda s. Front Neurol. 2023 Jul 26;14:1219324. doi: 10.3389/fneur.2023.1219324. eCollection 2023. Front Neurol. 2023. PMID: 37564735 Free PMC article. Review.

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