Raheel Qamar

Park Road
Chak Shahzad, IS 44000, Pakistan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 92 publications

Association of dopamine transporter gene DAT1 40-bp 3' UTR VNTR polymorphism (rs28363170) with Psychiatric disorders susceptibility: A study from the Pakistani population.

Association of dopamine transporter gene DAT1 40-bp 3' UTR VNTR polymorphism (rs28363170) with Psychiatric disorders susceptibility: A study from the Pakistani population.

Journal: Molecular biology reports

Published: May 17, 2026

RELN biallelic variant as a candidate risk factor in a consanguineous Pakistani family with bipolar disorder and clinical heterogeneity.

RELN biallelic variant as a candidate risk factor in a consanguineous Pakistani family with bipolar disorder and clinical heterogeneity.

Journal: Journal of affective disorders

Published: January 26, 2026

Identification of 19 Pathogenic Variants in a Clinically Heterogeneous Cohort With Suspected Inborn Errors of Metabolism.

Identification of 19 Pathogenic Variants in a Clinically Heterogeneous Cohort With Suspected Inborn Errors of Metabolism.

Journal: Clinical genetics

Published: January 11, 2026

Autism spectrum disorder trios from consanguineous populations are enriched for rare homozygous variants, identifying 32 new candidate genes.

Autism spectrum disorder trios from consanguineous populations are enriched for rare homozygous variants, identifying 32 new candidate genes.

Journal: Scientific reports

Published: June 12, 2025

Association of Monoamine Oxidase A Gene Promoter Region (30 bp μVNTR) Polymorphism with Serum Levels in Multiple Psychiatric Disorders.

Association of Monoamine Oxidase A Gene Promoter Region (30 bp μVNTR) Polymorphism with Serum Levels in Multiple Psychiatric Disorders.

Journal: Biomedicines

Published: December 18, 2024

Prevalence of strabismus in Pakistan: a systematic review and meta-analysis.

Prevalence of strabismus in Pakistan: a systematic review and meta-analysis.

Journal: Strabismus

Published: October 01, 2024

Identification of a biallelic MMUT variant (p.Thr230Arg) and its global perspective on clinical management.

Identification of a biallelic MMUT variant (p.Thr230Arg) and its global perspective on clinical management.

Journal: Molecular biology reports

Published: September 18, 2024

Functionally deficient UBOX5 variants and primary angle-closure glaucoma.

Functionally deficient UBOX5 variants and primary angle-closure glaucoma.

Journal: Nature communications

Published: July 31, 2024

Exploring WNT2 polymorphisms in comitant strabismus: A genetic association study.

Exploring WNT2 polymorphisms in comitant strabismus: A genetic association study.

Journal: Gene

Published: May 09, 2024

Inborn errors of metabolism: Historical perspectives to contemporary management.

Inborn errors of metabolism: Historical perspectives to contemporary management.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: March 14, 2024

Increase in blood derived mitochondrial DNA copy number in strabismus patients.

Increase in blood derived mitochondrial DNA copy number in strabismus patients.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: January 31, 2024

Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani population.

Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani population.

Journal: The International journal of neuroscience

Published: August 29, 2023

Showing 1-12 of 92

Last Updated: 09/26/2026