Asif Mir

Islamabad, IS 44000, Pakistan

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 46 publications

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Journal: American journal of human genetics
Published: April 05, 2026

Draft nuclear and complete mitochondrial genome assemblies of the flare-horned markhor (Capra falconeri): genomic resources for conservation and phylogenetics.

Draft nuclear and complete mitochondrial genome assemblies of the flare-horned markhor (Capra falconeri): genomic resources for conservation and phylogenetics.

Journal: Mammalian genome : official journal of the International Mammalian Genome Society
Published: September 24, 2025

Novel Variants Identified in Families With SNX27 -Related Neurodevelopmental Disorder, Aiding in Characterizing Its Genotypic and Phenotypic Spectrum.

Novel Variants Identified in Families With SNX27 -Related Neurodevelopmental Disorder, Aiding in Characterizing Its Genotypic and Phenotypic Spectrum.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: August 27, 2025

Genome-wide association analysis reveals natural genetic variations controlling canopy architecture traits in bread wheat.

Genome-wide association analysis reveals natural genetic variations controlling canopy architecture traits in bread wheat.

Journal: Scientific reports
Published: August 26, 2025

Non-syndromic WFS1 mutations are not a rare cause of diabetes in Pakistan.

Non-syndromic WFS1 mutations are not a rare cause of diabetes in Pakistan.

Journal: Diabetes research and clinical practice
Published: May 01, 2025

Biallelic Truncating Variants in SCN3B Encoding Nav Channel Subunit β3 Lead to Neurodevelopmental Phenotype with and without Epilepsy and Ataxia.

Biallelic Truncating Variants in SCN3B Encoding Nav Channel Subunit β3 Lead to Neurodevelopmental Phenotype with and without Epilepsy and Ataxia.

Journal: Annals of neurology
Published: March 10, 2025

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Journal: American journal of human genetics
Published: July 31, 2024

Orchestration of Genetic Alterations in PSEN1 and PSEN2 Genes in Development of Alzheimer's Disease through Computational Analysis.

Orchestration of Genetic Alterations in PSEN1 and PSEN2 Genes in Development of Alzheimer's Disease through Computational Analysis.

Journal: Global medical genetics
Published: January 12, 2024

Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease.

Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease.

Journal: Brain : a journal of neurology
Published: July 12, 2023

Identification of Four Novel Candidate Genes for Non-syndromic Intellectual Disability in Pakistani Families.

Identification of Four Novel Candidate Genes for Non-syndromic Intellectual Disability in Pakistani Families.

Journal: Biochemical genetics
Published: July 03, 2023

A Novel Variant in VPS13B Underlying Cohen Syndrome.

A Novel Variant in VPS13B Underlying Cohen Syndrome.

Journal: BioMed research international
Published: December 10, 2022

Seed Coat Morphology and Sculpturing of Selected Invasive Alien Plants from Lesser Himalaya Pakistan and Their Systematic Implications.

Seed Coat Morphology and Sculpturing of Selected Invasive Alien Plants from Lesser Himalaya Pakistan and Their Systematic Implications.

Journal: BioMed research international
Published: April 16, 2022
Showing 1-12 of 46

Last Updated: 09/26/2026