Muhmmad Tariq

13PUBLICATIONS
30CO-AUTHORS
Neurology and neuromuscular diseasesGene mappingChild and adolescent developmentMedical infection agents (incl. prions)Respiratory diseases
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Publications (13)

|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

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Frequent Collaborators

4 joint publications

Peter Nürnberg

3 joint publications

Ilyas Ahmad

3 joint publications

Naveed Altaf Malik

3 joint publications

Muhammad Sajid Hussain