Ghazanfar Ali

10PUBLICATIONS
39CO-AUTHORS
Neurology and neuromuscular diseasesChiropracticMedical infection agents (incl. prions)Traditional Chinese medicine and treatmentsEpigenetics (incl. genome methylation and epigenomics)
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Journal

Publications (10)

|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

|Jun 14, 2022
Efficiency of Multiple Extraction Solvents on Antioxidant, Cytotoxic, and Phytotoxic Potential of Taraxacum officinale (L.) Weber ex F.H. Wigg. from Poonch Valley, Azad Kashmir, Pakistan.

Wasim Akhtar, Ghazanfar Ali, Nadia Ashraf

|Dec 17, 2021
A homozygous missense variant in the MLC1 gene underlies megalencephalic leukoencephalopathy with subcortical cysts in large kindred: Heterozygous carriers show seizure and mild motor function deterioration.

Syeda Ain Ul Batool, Ahmad Almatrafi, Fatima Fadhli

|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

|Jun 17, 2021
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment.

Thashi Bharadwaj, Isabelle Schrauwen, Sakina Rehman

|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

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Frequent Collaborators

4 joint publications

Abdul Wali

3 joint publications

Sadia Sadia

2 joint publications

Tasleem Akhtar

2 joint publications

Fazal-Ur- Rehman