Muhmmad Tariq

13PUBLICATIONS

30CO-AUTHORS

Neurology and neuromuscular diseasesGene mappingChild and adolescent developmentMedical infection agents (incl. prions)Respiratory diseases

Get your video featured.

Publish with JoVE

Get your video featured.

Publish with JoVE

Publications (13)

Sort by Publication Date:

|Jul 08, 2026

Whole-exome sequencing reveals novel and previously reported variants in genes linked to white matter pathology in neurodevelopmental disorders.

|Aug 27, 2025

Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz-Jeghers Syndrome.

Tahir N Khan, Chunyu Liu, Kai Lee Yap

|Jul 29, 2025

Exome sequencing reveals broad genetic heterogeneity for neuromuscular disorders in consanguineous Pakistani Families.

Tooba Aleem, Maliha Rashid, Naeem Ahmad

|Jun 15, 2023

A homozygous founder variant in PDE2A causes paroxysmal dyskinesia with intellectual disability.

Hammad Yousaf, Shagufta Rehmat, Muhammad Jameel

|May 15, 2023

Exome sequencing identifies a novel pathogenic variant in RAB3GAP1 causing Warburg Micro syndrome in a Pakistani family.

Wahid Ullah, Muhammad Ilyas, Muhammad Tariq

|Feb 27, 2023

Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy.

Hafiza Noor Ul Ayan, Pir Sheeraz Ali, Asad Aslam Korejo

Pageof 3

Frequent Collaborators

Peter Nürnberg

Ilyas Ahmad

Naveed Altaf Malik

Muhammad Sajid Hussain

Ayaz Khan

Sheraz Khan

Naeem Ahmad

Muhammad Farrukh Asif

2 joint publications

Birgit Budde

2 joint publications

Hafiza Noor Ul Ayan

Frequent Collaborators

Peter Nürnberg

Ilyas Ahmad

Naveed Altaf Malik

Muhammad Sajid Hussain