Mohd A. Fareed

Ghaziabad, UP 201002, India

Last Updated: 09/26/2026

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Found 15 publications

Mitochondrial uncoupling protein 2 (UCP2) gene polymorphism - 866 G/A in the promoter region is associated with type 2 diabetes mellitus among Kashmiri population of Northern India.

Mitochondrial uncoupling protein 2 (UCP2) gene polymorphism - 866 G/A in the promoter region is associated with type 2 diabetes mellitus among Kashmiri population of Northern India.

Journal: Molecular biology reports

Published: May 27, 2022

Whole-exome sequencing reveals a novel homozygous mutation in the COQ8B gene associated with nephrotic syndrome.

Whole-exome sequencing reveals a novel homozygous mutation in the COQ8B gene associated with nephrotic syndrome.

Journal: Scientific reports

Published: February 02, 2021

HNF1A-MODY Mutations in Nuclear Localization Signal Impair HNF1A-Import Receptor KPNA6 Interactions.

HNF1A-MODY Mutations in Nuclear Localization Signal Impair HNF1A-Import Receptor KPNA6 Interactions.

Journal: The protein journal

Published: December 28, 2020

Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.

Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.

Journal: Frontiers in genetics

Published: December 15, 2020

Genetics of consanguinity and inbreeding in health and disease.

Genetics of consanguinity and inbreeding in health and disease.

Journal: Annals of human biology

Published: November 29, 2016

Impact of consanguineous marriages and degrees of inbreeding on fertility, child mortality, secondary sex ratio, selection intensity, and genetic load: a cross-sectional study from Northern India.

Impact of consanguineous marriages and degrees of inbreeding on fertility, child mortality, secondary sex ratio, selection intensity, and genetic load: a cross-sectional study from Northern India.

Journal: Pediatric research

Published: April 18, 2016

Increased cardiovascular risks associated with familial inbreeding: a population-based study of adolescent cohort.

Increased cardiovascular risks associated with familial inbreeding: a population-based study of adolescent cohort.

Journal: Annals of epidemiology

Published: November 23, 2015

Prevalence and gene frequency of color vision impairments among children of six populations from North Indian region.

Prevalence and gene frequency of color vision impairments among children of six populations from North Indian region.

Journal: Genes & diseases

Published: December 08, 2014

Estimating the inbreeding depression on cognitive behavior: a population based study of child cohort.

Estimating the inbreeding depression on cognitive behavior: a population based study of child cohort.

Journal: PloS one

Published: May 27, 2014

Evidence of inbreeding depression on height, weight, and body mass index: a population-based child cohort study.

Evidence of inbreeding depression on height, weight, and body mass index: a population-based child cohort study.

Journal: American journal of human biology : the official journal of the Human Biology Council

Published: March 25, 2014

Adverse respiratory health and hematological alterations among agricultural workers occupationally exposed to organophosphate pesticides: a cross-sectional study in North India.

Adverse respiratory health and hematological alterations among agricultural workers occupationally exposed to organophosphate pesticides: a cross-sectional study in North India.

Journal: PloS one

Published: February 26, 2013

A₁A₂BO and Rh gene frequencies among six populations of Jammu and Kashmir, India.

A₁A₂BO and Rh gene frequencies among six populations of Jammu and Kashmir, India.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: December 12, 2012

Showing 1-12 of 15

Last Updated: 09/26/2026