Abdul Wali

7PUBLICATIONS
30CO-AUTHORS
Neurology and neuromuscular diseasesTraditional Chinese medicine and treatmentsAnthropological geneticsPhylogeny and comparative analysisDevelopmental genetics (incl. sex determination)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (7)

|Oct 13, 2023
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family.

Ghazanfar Ali, Sadia Sadia, Syeda Ain-Ul-Batool

|Oct 07, 2021
Ethnobotanical and Biochemical Study of Berberis lycium Royle Collected from Different Areas of Azad Jammu and Kashmir.

Syeda Maria Fiaz Bukhari, Ghazanfar Ali, Syed Rizwan Abbas

|Mar 10, 2021
Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome.

Ghazanfar Ali, Sadia, Jia Nee Foo

|Jan 25, 2021
Sequencing and Characterization of Mitochondrial Protein-Coding Genes for Schizothorax niger (Cypriniformes: Cyprinidae) with Phylogenetic Consideration.

Tasleem Akhtar, Ghazanfar Ali, Nuzhat Shafi

|Nov 22, 2019
Novel missense alteration in LRP4 gene underlies Cenani-Lenz syndactyly syndrome in a consanguineous family.

Nuha Alrayes, Abdul Aziz, Farman Ullah

|Oct 02, 2018
Novel insertion and a previously reported nonsense variant of ALOXE3 gene lead to autosomal recessive ichthyosis in two Balochi families.

Ambreen Ijaz, Musharraf Jelani, Anila Panezai

Pageof 2

Frequent Collaborators

4 joint publications

Ghazanfar Ali

3 joint publications

Sadia Sadia

2 joint publications

Syed Akif Raza Kazmi

2 joint publications

Zeeshan Anjum