Sadaf Naz

18PUBLICATIONS

62CO-AUTHORS

Neurology and neuromuscular diseasesAnthropological geneticsGene mappingSocial and affective neuroscienceNeurogenetics

Get your video featured.

Publish with JoVE

Get your video featured.

Publish with JoVE

Publications (18)

Sort by Publication Date:

|Jun 30, 2026

A CLN8 biallelic missense variant causes epilepsy with severe treatment-resistant psychosis.

|Jun 26, 2026

Compound Heterozygous ATM Variants Cause Adolescent-Onset Cerebellar and Extrapyramidal Disease Without Telangiectasia in a Consanguineous Pakistani Family.

|Apr 13, 2026

Genetic Variants from Large Cohorts and Familial Studies Implicate Common Mechanisms in Schizophrenia.

Ambreen Kanwal, José V Pardo, Sadaf Naz

|Jun 21, 2024

Identification and analyses of exonic and copy number variants in spastic paraplegia.

Anum Shafique, Ayesha Nadeem, Faiza Aslam

|Mar 08, 2024

PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss.

Shelby E Redfield, Pedro De-la-Torre, Mina Zamani

|Oct 28, 2023

Genome Sequencing of Consanguineous Family Implicates Ubiquitin-Specific Protease 53 (<i>USP53</i>) Variant in Psychosis/Schizophrenia: Wild-Type Expression in Murine Hippocampal CA 1-3 and Granular Dentate with AMPA Synapse Interactions.

Ambreen Kanwal, Sohail A Sheikh, Faiza Aslam

Pageof 3

Frequent Collaborators

Thomas B Friedman

Faiza Aslam

Mina Zamani

Shelby E Redfield

Nara Sobreria

Pedro De-la-Torre

P Dane Witmer

Zunaira Munir

Cristina Fenollar-Ferrer

2 joint publications

Rabia Faridi

Frequent Collaborators

Thomas B Friedman

Faiza Aslam

Mina Zamani

Shelby E Redfield