Muhammad Sajid Hussain

11PUBLICATIONS
24CO-AUTHORS
Medical biochemistry - proteins and peptides (incl. medical proteomics)Epigenetics (incl. genome methylation and epigenomics)Medical mycologyGene mappingMedical infection agents (incl. prions)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (11)

|May 04, 2026
Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with <i>SGSH</i> and <i>GALNS</i> Deficiencies.

|Mar 02, 2023
Recurrence mutation in RBBP8 gene causing non-syndromic autosomal recessive primary microcephaly; geometric simulation approach for insight into predicted computational models.

Tahira Batool, Saba Irshad, Muhammad Riaz

|Feb 25, 2023
Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic Microcephaly.

Maria Asif, Uzma Abdullah, Peter Nürnberg

|Jan 21, 2023
Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability.

Maria Asif, Maryam Anayat, Faiza Tariq

|Dec 16, 2021
A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous Kurdish family.

Maria Asif, Ionut Dragos Mocanu, Uzma Abdullah

|Oct 23, 2021
A Homozygous <i>AKNA</i> Frameshift Variant Is Associated with Microcephaly in a Pakistani Family.

Syeda Seema Waseem, Abubakar Moawia, Birgit Budde

Pageof 2

Frequent Collaborators

6 joint publications

Peter Nürnberg

3 joint publications

Muhammad Tariq

3 joint publications

Uzma Abdullah

2 joint publications

Birgit Budde