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Muhmmad Tariq

12PUBLICATIONS

28CO-AUTHORS

Gene mappingNeurology and neuromuscular diseasesChild and adolescent developmentMedical infection agents (incl. prions)Respiratory diseases

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Publications (12)

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|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

|Oct 10, 2022

A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family.

Ilyas Ahmad, Ayaz Khan, Hafiza Noor Ul Ayan

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Frequent Collaborators

4 joint publications

Peter Nürnberg

3 joint publications

Ilyas Ahmad

3 joint publications

Muhammad Sajid Hussain

3 joint publications

Ayaz Khan

3 joint publications

Sheraz Khan

2 joint publications

Naveed Altaf Malik

2 joint publications

Jeanette Erdmann

2 joint publications

Birgit Budde

2 joint publications

Hafiza Noor Ul Ayan

1 joint publications

Tilman Breiderhoff

Frequent Collaborators

4 joint publications

Peter Nürnberg

3 joint publications

Ilyas Ahmad

3 joint publications

Muhammad Sajid Hussain

3 joint publications

Ayaz Khan

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