Ghazanfar Ali - Concepedia

Author

Ghazanfar Ali

Also Known As

A Parray G, Ali G, Ali Ghazanfar, G Ali, G. Ali, GHAZANFAR ALI, Galil Ali, Geehan Nazar Ali, Ghazanfar ALI, Ghazanfar Ali

107

Publications

Citations

H-Index

Concepts

All Affiliations

Quaid-i-Azam University University of Azad Jammu and Kashmir Baylor College of Medicine University of Washington University of Balochistan

About

Ghazanfar Ali is an author at Quaid-i-Azam University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	22	1K
2	Arts	3	3	212
3	Health Sciences	2	2	36
4	Business	1	1	37
5	Engineering	1	1	75

Ghazanfar Ali

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsFragile X Spectrum	2012	228
Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39 Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed, The American Journal of Human Genetics GeneticsAudiologyPathologyAuditory PhysiologyNonsyndromic Hearing Loss	2009	120
Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability Muhammad Rafiq, Andreas W. Kuß, Lucia Puettmann, The American Journal of Human Genetics Genome InstabilityMendelian DisorderAlpha 1,2-Mannosidase GeneGenetic DisorderGenetics	2011	88
Low prevalence of Connexin 26 (<i>GJB2</i>) variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment RLP Santos, Muhammad Wajid, TL Pham, Clinical Genetics	2004	78
Green synthesis and characterization of tin dioxide nanoparticles for photocatalytic and antimicrobial studies Sirajul Haq, Wajid Rehman, Muhammad Waseem, Materials Research Express EngineeringMetal NanoparticlesInorganic PhotochemistryGreen ChemistryNanocatalysis	2020	75
Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiology	2010	71
A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis Ghazanfar Ali, Muhammad Salman Chishti, Syed Irfan Raza, Human Genetics GeneticsPathogenesisPathologyLipase HMolecular Genetics	2007	70
Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability Rosalind Law, Tracy Dixon‐Salazar, Julie Jerber, The American Journal of Human Genetics	2014	70
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene Asma Gul, Muhammad Jawad Hassan, Saqib Mahmood, Neurogenetics Aspm GeneAllelic VariantDevelopmental BiologyPakistani FamiliesGenetic Disorder	2006	60
Mutation in the <i>HPGD</i> gene encoding NAD<sup>+</sup> dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC) Muhammad Tariq, Zahid Azeem, Ghazanfar Ali, Journal of Medical Genetics	2008	57

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