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List of works by Swarkar Sharma

A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

scientific article

A genetic analysis identifies a haplotype at adiponectin locus: Association with obesity and type 2 diabetes

scientific article published on 19 February 2020

A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups

scientific article published on 10 April 2014

A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud

scientific article published on 09 August 2019

A novel subgroup Q5 of human Y-chromosomal haplogroup Q in India

scientific article

A variation in PANK2 gene is causing Pantothenate kinase-associated Neurodegeneration in a family from Jammu and Kashmir - India

scientific article

ACE2 Homo-dimerization, Human Genomic variants and Interaction of Host Proteins Explain High Population Specific Differences in Outcomes of COVID19

scientific article published on 25 April 2020

Ancient Human Migrations to and through Jammu Kashmir- India were not of Males Exclusively.

scientific article published on 16 January 2018

Association between common variants near LBX1 and adolescent idiopathic scoliosis replicated in the Chinese Han population

scientific article

Biophysical characterization of double-stranded oligonucleotides using ETBR and isothermal fluorescence spectroscopy: implication for SNP genotyping.

scientific article published on 12 November 2007

Concomitant presence of mutations in mitochondrial genome and p53 in cancer development - a study in north Indian sporadic breast and esophageal cancer patients

scientific article published on 01 December 2008

Genetic affinity among five different population groups in India reflecting a Y-chromosome gene flow

scientific article

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis

scientific article

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.

scientific article

Human mtDNA hypervariable regions, HVR I and II, hint at deep common maternal founder and subsequent maternal gene flow in Indian population groups

scientific article

IL-10 promoter single nucleotide polymorphisms are significantly associated with resistance to leprosy.

scientific article

Interaction between the UCP2-866G/A, mtDNA 10398G/A and PGC1alpha p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian population

scientific article published on 14 August 2007

Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer.

scientific article

Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous Dysplasia

scientific article published in December 2015

Normal leptin expression, lower adipogenic ability, decreased leptin receptor and hyposensitivity to Leptin in Adolescent Idiopathic Scoliosis

scientific article

Origin and spread of human mitochondrial DNA haplogroup U7.

scientific article published on 07 April 2017

PGC-1alpha Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study

scientific article published on 28 March 2007

Publisher Correction: A genetic analysis identifies a haplotype at adiponectin locus: Association with obesity and type 2 diabetes

scientific article published on 27 April 2020

Replication of type 2 diabetes candidate genes variations in three geographically unrelated Indian population groups.

scientific article

Risk factors of type 2 diabetes in population of Jammu and Kashmir, India

scientific article published on 25 August 2013

Role of telomeres and associated maintenance genes in Type 2 Diabetes Mellitus: A review

scientific article published on 21 October 2016

TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

scientific article

Telomere Maintenance Genes are associated with Type 2 Diabetes Susceptibility in Northwest Indian Population Group

scientific article published on 15 April 2020

The Indian origin of paternal haplogroup R1a1* substantiates the autochthonous origin of Brahmins and the caste system

scientific article

The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population

scientific article

The possible role of 10398A and 16189C mtDNA variants in providing susceptibility to T2DM in two North Indian populations: a replicative study

scientific article published on 26 October 2006

Understanding Genetic Heterogeneity in Type 2 Diabetes by Delineating Physiological Phenotypes: SIRT1 and its Gene Network in Impaired Insulin Secretion.

scientific article

Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India

scientific article published on 13 June 2016

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