Arif I. Mahmood

Family Medicine

1600 11th St
Wichita Falls, TX 76301

Last Updated: 09/26/2026

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Found 32 publications

A Novel ATXN7L3 De Novo Variant Underlies Harel-Tora Neurodevelopmental Syndrome (HATONS) With Pre-Axial Polydactyly.

A Novel ATXN7L3 De Novo Variant Underlies Harel-Tora Neurodevelopmental Syndrome (HATONS) With Pre-Axial Polydactyly.

Journal: Clinical genetics

Published: December 10, 2025

Bi-allelic loss-of-function variants in JKAMP cause a neurodevelopmental syndrome associated with dysregulation of GPR37 trafficking.

Bi-allelic loss-of-function variants in JKAMP cause a neurodevelopmental syndrome associated with dysregulation of GPR37 trafficking.

Journal: American journal of human genetics

Published: September 26, 2025

A novel CLRN2 variant: expanding the mutation spectrum and its critical role in isolated hearing impairment.

A novel CLRN2 variant: expanding the mutation spectrum and its critical role in isolated hearing impairment.

Journal: Genes & genomics

Published: September 15, 2024

Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder.

Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder.

Journal: Frontiers in genetics

Published: October 05, 2023

Identification of novel STAT3 inhibitors for liver fibrosis, using pharmacophore-based virtual screening, molecular docking, and biomolecular dynamics simulations.

Identification of novel STAT3 inhibitors for liver fibrosis, using pharmacophore-based virtual screening, molecular docking, and biomolecular dynamics simulations.

Journal: Scientific reports

Published: August 07, 2023

Truncated DNM1 variant underlines developmental delay and epileptic encephalopathy.

Truncated DNM1 variant underlines developmental delay and epileptic encephalopathy.

Journal: Frontiers in pediatrics

Published: July 24, 2023

Structural and dynamics insights into the GBA variants associated with Parkinson's disease.

Structural and dynamics insights into the GBA variants associated with Parkinson's disease.

Journal: Journal of biomolecular structure & dynamics

Published: July 12, 2023

New drug target identification in Vibrio vulnificus by subtractive genome analysis and their inhibitors through molecular docking and molecular dynamics simulations.

New drug target identification in Vibrio vulnificus by subtractive genome analysis and their inhibitors through molecular docking and molecular dynamics simulations.

Journal: Heliyon

Published: April 13, 2023

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.

Journal: Genes

Published: April 08, 2023

Identification of novel peptide inhibitors for oncogenic KRAS G12D as therapeutic options using mutagenesis-based remodeling and MD simulations.

Identification of novel peptide inhibitors for oncogenic KRAS G12D as therapeutic options using mutagenesis-based remodeling and MD simulations.

Journal: Journal of biomolecular structure & dynamics

Published: April 03, 2023

Microglia and Astrocytes Dysfunction and Key Neuroinflammation-Based Biomarkers in Parkinson's Disease.

Microglia and Astrocytes Dysfunction and Key Neuroinflammation-Based Biomarkers in Parkinson's Disease.

Journal: Brain sciences

Published: March 03, 2023

Computer-assisted drug repurposing for thymidylate kinase drug target in monkeypox virus.

Computer-assisted drug repurposing for thymidylate kinase drug target in monkeypox virus.

Journal: Frontiers in cellular and infection microbiology

Published: February 05, 2023

Showing 1-12 of 32

Last Updated: 09/26/2026