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List of works by Mohammed Faruq

A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population

scientific article

A founder mutation MLC1 c.736delA associated with megalencephalic leukoencephalopathy with subcortical cysts-1 in north Indian kindred

scientific article published on 18 April 2018

A novel frameshift deletion in NAGLU causing sanfilipo type III-B in an Indian family

scientific article published on 26 October 2018

A novel mutation in SLC39A14 causing hypermanganesemia associated with infantile onset dystonia.

scientific article published on 2 March 2018

Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child

scientific article published on 17 March 2020

Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India

scientific article published on 09 September 2020

Generation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A)

scientific article published on 14 August 2018

Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the <i>SAMD12</i> gene

scientific article published on 19 December 2020

Integrated genomic view of SARS-CoV-2 in India

scientific article published on 03 August 2020

Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation

scientific article published on 08 July 2019

Reinfection or reactivation: Genome-based two distinct SNP profile of SARS-CoV2 repositivity in an Indian case

publication published on 03 April 2021

Spatio-temporal dynamics of intra-host variability in SARS-CoV-2 genomes

scientific article published on 01 February 2022

The EDN1 Missense Variant rs5370G &gt; T Regulates Adaptation and Maladaptation under Hypobaric Hypoxia

scientific article published in 2022

Whole exome and targeted gene sequencing to detect pathogenic recessive variants in early onset cerebellar ataxia

scientific article published on 01 September 2019

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