Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

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.

Publish with JoVE

Featured researcher

Get your video featured.

Publish with JoVE

Publications (11)

Sort by Publication Date:

|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

2 joint publications

Sheraz Khan

2 joint publications

Ayaz Khan

1 joint publications

Lotte Bang Pedersen

1 joint publications

Kjeld Møllgård

1 joint publications

Henrik Nielsen

1 joint publications

Niklas Dahl

Frequent Collaborators

6 joint publications

Peter Nürnberg

3 joint publications

Muhammad Tariq

3 joint publications

Uzma Abdullah

2 joint publications

Birgit Budde

Top Related Videos

Characterizing Histone Post-translational Modification Alterations in Yeast Neurodegenerative Proteinopathy Models

Characterizing Histone Post-translational Modification Alterations in Yeast Neurodegenerative Proteinopathy Models

Published on : Mar 24, 2019

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

See more related videos

Top Related Videos

Characterizing Histone Post-translational Modification Alterations in Yeast Neurodegenerative Proteinopathy Models

Characterizing Histone Post-translational Modification Alterations in Yeast Neurodegenerative Proteinopathy Models

Published on : Mar 24, 2019

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

See more related videos