Detalhe da pesquisa
1.
Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort.
Neurogenetics
; 25(1): 13-25, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37917284
2.
Spatio-temporal dynamics of intra-host variability in SARS-CoV-2 genomes.
Nucleic Acids Res
; 50(3): 1551-1561, 2022 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35048970
3.
A novel mutation in SLC39A14 causing hypermanganesemia associated with infantile onset dystonia.
J Gene Med
; 20(4): e3012, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29498153
4.
Reinfection or reactivation: Genome-based two distinct SNP profile of SARS-CoV2 repositivity in an Indian case.
J Med Virol
; 93(7): 4152-4155, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33749850
5.
STRIDE-DB: a comprehensive database for exploration of instability and phenotypic relevance of short tandem repeats in the human genome.
Database (Oxford)
; 20242024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38602506
6.
Sequencing through hyperexpanded Friedreich's ataxia-GAA repeats by nanopore technology: implications in genotype-phenotype correlation.
Brain Commun
; 5(2): fcad020, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37006329
7.
Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool.
Adv Genet (Hoboken)
; 3(2): 2100078, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36618024
8.
Respiratory Co-Infections: Modulators of SARS-CoV-2 Patients' Clinical Sub-Phenotype.
Front Microbiol
; 12: 653399, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34122366
9.
Vaccine Breakthrough Infections by SARS-CoV-2 Variants after ChAdOx1 nCoV-19 Vaccination in Healthcare Workers.
Vaccines (Basel)
; 10(1)2021 Dec 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-35062715
10.
Integrated genomic view of SARS-CoV-2 in India.
Wellcome Open Res
; 5: 184, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32995557
11.
EasyQC: Tool with Interactive User Interface for Efficient Next-Generation Sequencing Data Quality Control.
J Comput Biol
; 25(12): 1301-1311, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30204482
12.
A novel mutation in SGSH causing Sanfillipo type 3A Mucopolysaccharidoses in an Indian family.
Mol Genet Metab Rep
; 15: 124-126, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30023302