Dr. Ghazanfar Ali
Department of Biotechnology
University of Azad Jammu and Kashmir, Pakistan
Assistant Professor
csp21c@163.com
Qualifications
2009 Ph.D., Quaid-i-Azam University, Islamabad, Pakistan
2004 M.Phil., Quaid-i-Azam University, Islamabad, Pakistan
2002 M.Sc., Quaid-i-Azam University, Islamabad, Pakistan
1999 B.Sc., The University of Punjab, Lahore, Pakistan
Publications (Selected)
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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, Madiah Khalid, Fazal Ur Rehman, Muhammad Qudir Javid. Sequencing and Characterization of Mitochondrial Protein-Coding Genes for Schizothorax niger (Cypriniformes: Cyprinidae) with Phylogenetic Consideration. BioMed Research International. Volume 2020;https://doi.org/10.1155/2020/5980135. IF:2.276
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Ali G*, Awan NB, Sadia, Khawaja AW, Foo JN2, Khor CC, Chang CH, Chew EG, Kiani FR, Jelani M. Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families. Journal of Gene Medicine. 2020 May: 22(5):e3167. doi: 10.1002/jgm.3167. IF:3.258
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Zahid Latif, Imen Chakchouk, Isabelle Schrauwen, Kwanghyuk Lee, Regie Lyn P. Santos-Cortez, Izoduwa Abbe, Anushree Acharya, Afeefa Jarral, Imran Ali, Ehsan Ullah, Muhammad Nasim Khan1, Ghazanfar Ali, Tufail Hussain Tahir, Michael J. Bamshad, Deborah A. Nickerson, University of Washington Center for Mendelian Genomics, Wasim Ahmad, Muhammad Ansar, Suzanne M. Leal. Confirmation of the role of DHX38 in the etiology of early-onset retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 2018 Sep 4;59(11):4552-4557. IF:3.470
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Santos-Cortez RLP, Khan V, Khan FS, Mughal ZU, Chakchouk I, Lee K, Rasheed M, Hamza R, Acharya A, Ullah E, Saqib MAN, Abbe I, Ali G, Hassan MJ, Khan S, Azeem Z, Ullah I, Bamshad MJ, Nickerson DA, Schrauwen I, Ahmad W, Ansar M, Leal SM. Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability. Human Genetics. 2018 Sep;137(9):735-752. IF:5.743
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Asmat Ullah, Muhammad Umair, Maryam Yousaf, Sher Alam Khan, Nizamud Din, Khadim Shah, Farooq Ahmad, Zahid Azeem, Ghazanfar Ali, Bader Alhaddad, Afzal Rafique, Abid Jan, Tobias B. Haack, Tim M. Strom, Thomas Meitinger and Wasim Ahmad. Sequence Variants in four Genes Underlying Bardet-Biedl Syndrome (BBS) in Consanguineous Families. Molecular Vision, 2017; 23:482-494. IF:2.202
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Rosalind Law, Tracy Dixon-Salazar, Julie Jerber , Na Cai, Ansar A. Abbasi, Maha S. Zaki, Kirti Mittal, Stacey B. Gabriel, Muhammad Arshad Rafiq, Valeed Khan, Maria Nguyen, Ghazanfar Ali, Brett Copeland, Eric Scott, Nasim Vasli, Anna Mikhailov, Muhammad Nasim Khan, Danielle M. Andrade, Muhammad Ayaz, Muhammad Ansar, Muhammad Ayub, John B. Vincent, Joseph G. Gleeson. Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Non-Syndromic Autosomal Recessive Intellectual Disability. American Journal of Human Genetics. 2014; 95(6):721-728. IF:10.502
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Ali G, Amer HM, Almajhdi FN. Hemagglutinin and Neuraminidase Genes of Influenza B viruses circulating in Riyadh, Saudi Arabia during 2010-2011: Evolution and Sequence Analysis. Journal of Medical Virology. 2013; 86(6):1003-16. IF:2.021
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Almajhdi FN, Ali G*. Report on Influenza A and B Viruses: their Co-infection in a Saudi Leukemia Patient. BioMed Research International. 2013 Jul. doi: 10.1155/2013/290609. IF:2.276
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Nasim S, Shahid A, Mustufa MA, Arain GM, Ali G, Taseer IU, Talreja KL, Firdous R, Iqbal R, Siddique SA, Naz S, Akhter T. Biosafety perspective of clinical laboratory workers: a profile of Pakistan. Journal of Infection in Developing Countries. 2012 Aug 21; 6(8):611-9. IF:0.703
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Khan MA, Rafiq MA, Noor A, Hussain S, Flores JV, Rupp V, Vincent AK, Malli R, Ali G, Khan FS, Ishak GE, Doherty D, Weksberg R, Ayub M, Windpassinger C, Ibrahim S, Frye M, Ansar M, Vincent JB. Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability. American Journal of Human Genetics. 2012 May 4; 90(5):856-63. IF:10.502
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Rafiq MA, Kuss AW, Puettmann L, Noor A, Ramiah A, Ali G, Hu H, Kerio NA, Xiang Y, Garshasbi M, Khan MA, Ishak GE, Weksberg R, Ullmann R, Tzschach A, Kahrizi K, Mahmood K, Naeem F, Ayub M, Moremen KW, Vincent JB, Ropers HH, Ansar M, Najmabadi H. Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability. American Journal of Human Genetics. 2011 Jul 15; 89(1):176-82. IF:10.502
Profile Details
https://scholar.google.com/citations?user=pkTP8c4AAAAJ&hl=zh-CN&oi=sra