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Muhammad Tariq (Muhmmad Tariq)

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 11

Top Venues

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

National Institute for Biotechnology and Genetic Engineering

NIBGE (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Institute for Biotechnology and Genetic Engineering Jul 13o 2014

Pakistan

Senior Scientist :: Health Biotechnology Division

Education History

NIBGE

Pakistan

PHD :: NIBGE

Publications

Hafiza Noor Ul Ayan, Pir Sheraz Ali, Asad Aslam Korejo, Holger Thiele, Peter Nürnberg, Muhammad Tariq, Syed Zahid Jamal, Jeanette Erdmann, Ilyas Ahmad
Homozygous frameshift variant in desmoglein-2 causes biventricular arrhythmogenic right ventricular cardiomyopathy. Clinical genetics (2023)
Hammad Yousaf, Shagufta Rehmat, Muhammad Jameel, Rabab Ibrahim, Sohana Nadeem Hashmi, Ehtisham Ul Haq Makhdoom, Justyna Iwaszkiewicz, Saadia Maryam Saadi, Muhammad Tariq, Shahid M Baig, Mathias Toft, Ambrin Fatima, Zafar Iqbal
A homozygous founder variant in PDE2A causes paroxysmal dyskinesia with intellectual disability. Clinical genetics (2023)
Wahid Ullah, Muhammad Ilyas, Muhammad Tariq, Maria Imdad, Ikram Ullah, Stephanie Efthymiou, Muhammad Faheem, Muhammad Abbas, null null, Muhammad Aamir, Muhammad Nouman, Henry Houlden
Exome sequencing identifies a novel pathogenic variant in RAB3GAP1 causing Warburg Micro syndrome in a Pakistani family. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience (2023)
Hafiza Noor Ul Ayan, Pir Sheeraz Ali, Asad Aslam Korejo, Holger Thiele, Peter Nürnberg, Muhammad Tariq, Syed Zahid Jamal, Jeanette Erdmann, Ilyas Ahmad
Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy. Clinical genetics (2023)
Ilyas Ahmad, Ayaz Khan, Hafiza Noor Ul Ayan, Birgit Budde, Janine Altmüller, Asad Aslam Korejo, Gudrun Nürnberg, Holger Thiele, Muhammad Tariq, Peter Nürnberg, Jeanette Erdmann
A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family. Journal of human genetics (2022)
Ayaz Khan, Shixiong Tian, Muhammad Tariq, Sheraz Khan, Muhammad Safeer, Naimat Ullah, Nazia Akbar, Iram Javed, Mahnoor Asif, Ilyas Ahmad, Shahid Ullah, Humayoon Shafique Satti, Raees Khan, Muhammad Naeem, Mahwish Ali, John Rendu, Julien Fauré, Klaus Dieterich, Xenia Latypova, Shahid Mahmood Baig, Naveed Altaf Malik, Feng Zhang, Tahir Naeem Khan, Chunyu Liu
NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes. Molecular genetics and genomics : MGG 297 (6) (2022)
Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, Uzma Abdullah, Ghulam Hussain, Maria Asif, Birgit Budde, Wolfgang Höhne, Sigrid Tinschert, Saadia Maryam Saadi, Hammad Yousaf, Zafar Ali, Ambrin Fatima, Emrah Kaygusuz, Ayaz Khan, Muhammad Jameel, Sheraz Khan, Muhammad Tariq, Iram Anjum, Janine Altmüller, Holger Thiele, Stefan Höning, Shahid Mahmood Baig, Peter Nürnberg, Muhammad Sajid Hussain
Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ. Genes 12 (5) (2021)
Shafaq Ramzan, Stephanie Tennstedt, Muhammad Tariq, Sheraz Khan, Hafiza Noor Ul Ayan, Aamir Ali, Matthias Munz, Holger Thiele, Asad Aslam Korejo, Abdul Razzaq Mughal, Syed Zahid Jamal, Peter Nürnberg, Shahid Mahmood Baig, Jeanette Erdmann, Ilyas Ahmad
A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family. Genes 12 (8) (2021)
Syeda Seema Waseem, Abubakar Moawia, Birgit Budde, Muhammad Tariq, Ayaz Khan, Zafar Ali, Sheraz Khan, Maria Iqbal, Naveed Altaf Malik, Saif Ul Haque, Janine Altmüller, Holger Thiele, Muhammad Sajid Hussain, Sebahattin Cirak, Shahid Mahmood Baig, Peter Nürnberg
A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family. Genes 12 (10) (2021)
Sajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, Ilyas Ahmad, Maria Iqbal, Syeda Seema Waseem, Maria Asif, Uzma Abdullah, Ehtisham Ul Haq Makhdoom, Emrah Kaygusuz, Muhammad Zakaria, Shafaq Ramzan, Saif Ul Haque, Asif Mir, Iram Anjum, Mehak Fiaz, Zafar Ali, Muhammad Tariq, Neelam Saba, Wajid Hussain, Birgit Budde, Saba Irshad, Angelika Anna Noegel, Stefan Höning, Shahid Mahmood Baig, Peter Nürnberg, Muhammad Sajid Hussain
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan. Molecular genetics & genomic medicine 8 (9) (2020)
Joakim Klar, Jörg Piontek, Susanne Milatz, Muhammad Tariq, Muhammad Jameel, Tilman Breiderhoff, Jens Schuster, Ambrin Fatima, Maria Asif, Muhammad Sher, Katrin Mäbert, Anja Fromm, Shahid M Baig, Dorothee Günzel, Niklas Dahl
Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage. PLoS genetics 13 (7) (2017)

Muhammad Tariq.css-eqlu8i{font-size:small;padding-left:4px;} (Muhmmad Tariq)

Publication Activity (10 Years)

Top Topics

Top Venues

Muhammad Tariq (Muhmmad Tariq)