Abdul Wali

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 7

Top Venues

Congenital anomalies

BioMed research international

The journal of gene medicine

Genetics research

Balochistan University of Information Technology, Engineering and Management Sciences

Quaid-i-Azam University Faculty of Biological Sciences (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Balochistan University of Information Technology, Engineering and Management Sciences Mar 01 2010

Pakistan

Associate Professor :: Biotechnology

Education History

Quaid-i-Azam University Faculty of Biological Sciences Sep 16 2004 - Jun 09 2008

Pakistan

PHD :: Department of Biochemistry

Publications

Ghazanfar Ali, Sadia Sadia, Syeda Ain-Ul-Batool, Zahid Azeem, Naheed Bashir Awan, Syed Akif Raza Kazmi, Zia- Ur-Rehman, Zeeshan Anjum, Fazal- Ur-Rehman, Abdul Wali, Kafaitullah Khan, Nasib Zaman, Muhammad Ayub, Muhammad Sajid, Noor Hassan
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family. Genetics research 2023 (2023)
Ghazanfar Ali, Sadia Sadia, Jia Nee Foo, Abdul Nasir, Chu-Hua Chang, Elaine GuoYan Chew, Zahid Latif, Zahid Azeem, Syeda Ain-Ul-Batool, Syed Akif Raza Kazmi, Naheed Bashir Awan, Abdul Hameed Khan, Fazal-Ur- Rehman, Madiha Khalid, Abdul Wali, Samina Sarwar, Wasim Akhtar, Ansar Ahmed Abbasi, Rameez Nisar
Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome. BioMed research international 2021 (2021)
Syeda Maria Fiaz Bukhari, Ghazanfar Ali, Syed Rizwan Abbas, Zeeshan Anjum, Nasim Ahmed, Ammara Munir, Abdul Wali, Muhammad Ayub, Kafaitullah Khan, Ahmed Khames, Muneeb Muhamed Musthafa
Ethnobotanical and Biochemical Study of Berberis lycium Royle Collected from Different Areas of Azad Jammu and Kashmir. Evidence-based complementary and alternative medicine : eCAM 2021 (2021)
Tasleem Akhtar, Ghazanfar Ali, Nuzhat Shafi, Wasim Akhtar, Abdul Hameed Khan, Zahid Latif, Abdul Wali, Syeda Ain-Ul-Batool, Abdul Rehman Khan, Sadia Mumtaz, Syed Iftikhar Altaf, Sundus Khawaja, Sadia Sadia, Madiha Khalid, Fazal-Ur- Rehman, Qudir Javid
Sequencing and Characterization of Mitochondrial Protein-Coding Genes for Schizothorax niger (Cypriniformes: Cyprinidae) with Phylogenetic Consideration. BioMed research international 2020 (2020)
Nuha Alrayes, Abdul Aziz, Farman Ullah, Muhammad Ishfaq, Musharraf Jelani, Abdul Wali
Novel missense alteration in LRP4 gene underlies Cenani-Lenz syndactyly syndrome in a consanguineous family. The journal of gene medicine 22 (1) (2020)
Ambreen Ijaz, Sulman Basit, Ajab Gul, Lilas Batool, Abrar Hussain, Sibtain Afzal, Khushnooda Ramzan, Jamil Ahmad, Abdul Wali
XPC gene mutations in families with xeroderma pigmentosum from Pakistan; prevalent founder effect. Congenital anomalies 59 (1) (2018)
Ambreen Ijaz, Musharraf Jelani, Anila Panezai, Tahmina Rabbani, Iftikhar A Rasool, Jamil Ahmad, Abdul Wali
Novel insertion and a previously reported nonsense variant of ALOXE3 gene lead to autosomal recessive ichthyosis in two Balochi families. Congenital anomalies 59 (5) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Abdul Wali