Faculty Profile

Thursday August 17, 2017

Department of Biotechnology

PhD PhD(Biotechnology )
Quaid i Azam University Islamabad From:2005-02-02 To:2009-03-02
MSc MSc(Biotechnology )
Quaid i Azam University Islamabad From:2000-01-01 To:2002-01-01
MPhil MPhil(Biotechnology )
Quaid i Azam University Islamabad From:2002-09-01 To:2004-08-01
  • Organization: Biotechnology Department King Saud University Saudi Arabia
    Designation: Assistant Professor
    Since: From 2010-09-20 To 2013-05-30
    Brief Description: Teaching and Research Supervision of M.Phil and Ph.D Scholars

  • Organization: Pakistan Medical Research Council Central Research Centre NIH Islamabad
    Designation: Research Officer
    Since: From 2004-10-24 To 2010-08-18
    Brief Description: To conduct research studies regarding all the emerging health issues to Pakistani population

    Journal (2014)
  • Mehmood S, Jan A, Muhammad D, Ahmad F, Mir H, Younus M, Ali G, Ayub M, Ansar M, Ahmad W. ,Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hair. ,Australasian Journal of Dermatology , :IF: 0.97
  • Journal (2014)
  • 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, Muhamm ,Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Non-Syndromic Autosomal Recessive Intellectual Disability. ,The American Journal of Human Genetics , :IF: 11.20
  • Journal (2013)
  • 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 , :IF: 2.373 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/
  • Journal (2013)
  • Almajhdi FN, Ali G. ,Report on Influenza A and B Viruses: their Co-infection in a Saudi Leukemia Patient. ,BioMed Research International , :IF: 2.88
  • Journal (2012)
  • Mir H, Khan S, Arif MS, Ali G, Wali A, Ansar M, Ahmad W. ,736-739 ,Mutations in the gene phospholipase C, delta-1 (PLCD1) underlying hereditary leukonychia. ,Eur J Dermatol , :IF: 2.53 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/
  • Journal (2012)
  • Nasim S, Shahid A, Mustufa MA, Arain GM, Ali G, Taseer IU, Talreja KL, Firdous R, Iqbal R, Siddique SA, Naz S, Akhter T. ,611-9. ,Biosafety perspective of clinical laboratory workers: a profile of Pakistan. ,J Infect Dev Ctries , :IF: 1.92 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/
  • Journal (2012)
  • 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 ,856-863 , Am J Hum Genet. 2012 May 4;90(5):856-63. ,Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability. , :IF: 11.20 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2012)
  • Khan S, Basit S, Zimri F, Ali N, Ali G, Ansar M, Ahmad W. ,48-55 ,A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation. ,Clin Genet. , :IF: 4.25 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2011)
  • 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. ,176-82 ,Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability. ,Am J Hum Genet. , :IF: 11.20
  • Journal (2011)
  • Azeem Z, Wasif N, Basit S, Razak S, Waheed RA, Islam A, Ayub M, Kafaitullah, Kamran-ul-hassan Naqvi S, Ali G, Ahmad W. ,755-60 ,Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families. ,J Dermatol. , :IF: 1.77 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2011)
  • Ali G, Lee K, Andrade PB, Basit S, Santos-Cortez RL, Chen L, Jelani M, Ansar M, Ahmad W, Leal SM. ,106-12. ,Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3. ,Hum Hered , :IF: 1.57 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2011)
  • Khan MA, Rafiq MA, Noor A, Ali N, Ali G, Vincent JB, Ansar M. ,A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability. ,BMC Med Genet , :IF: 2.54 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2011)
  • Khan S, Habib R, Mir H, Umm-e-Kalsoom, Naz G, Ayub M, Shafique S, Yamin T, Ali N, Basit S, Wasif N, Kamran-Ul-Hassan Naqvi S, Ali G, Wali A, Ansar M, Ahmad W. ,652-4 ,Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan. ,Clin Exp Dermatol , :IF: 1.33 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2010)
  • Ali G. ,792-793. ,Hereditary Alopecia in Pakistani families. ,J Pak Med Assoc , :IF: 0.41 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2010)
  • Basit S, Ali G, Wasif N, Ansar M, Ahmad W. ,213-220 ,Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3-p22.3 in a Pakistani family and screening of the candidate genes. ,Hum Genet , :IF: 4.63 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/3?sorting=published
  • Journal (2010)
  • Ali G ,418-419 ,Genetic deafness in Pakistani population. , J Pak Med Assoc , :IF: 0.41 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/
  • Journal (2010)
  • Rafiq MA, Ansar M, Marshall CR, Noor A, Shaheen N, Mowjoodi A, Khan MA, Ali G, Amin-Ud-Din M, Feuk L, Vincent JB, Scherer SW. ,478-483 ,Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan. ,Clinical Genetics , :IF: 4.25 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/
  • Journal (2010)
  • Wasif N, Tariq M, Ali G, Hassan MJ, Ahmad W. ,106-108 ,A Novel Splice Site Mutation in the EDAR Gene Underlies Autosomal Recessive Hypohidrotic Ectodermal Dysplasia in a Pakistani Family. ,Pediatr Dermatol. , :IF: 1.04 ,https://www.researchgate.net/profile/Dr_Ghazanfar_Ali/publications/
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