Sadaf Naz

19PUBLICATIONS
64CO-AUTHORS
Clinical nutritionNeurology and neuromuscular diseasesAnthropological geneticsGene mappingSocial and affective neuroscience
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Publications (19)

|Oct 14, 2026
Characterization of familial short stature with or without skeletal dysplasia in a Pakistani cohort reveals founder mutations as well as novel variants.

|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

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Frequent Collaborators

3 joint publications

Thomas B Friedman

3 joint publications

Nara Sobreria

3 joint publications

Faiza Aslam

3 joint publications

Muhammad Noman