Muhammad Ansar - Concepedia

Author

Muhammad Ansar

Also Known As

ANSAR, M., Ansar, Muhammad, Jurana Jurana, M Ansar, M. Ansar, MUHAMMAD ANSAR, Mariam Ansar, Muhammad Ansar, Muhammad Ramzan Ansar

168

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

Quaid-i-Azam University Baylor College of Medicine University of Washington Centre for Addiction and Mental Health University of Toronto

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	34	3K
2	Arts	10	10	685
3	Public Health	2	2	96
4	Health Sciences	1	1	34
5	Natural Sciences	1	1	108

Muhammad Ansar

Publications

Citations

H-Index

Page 1

	Year	Citations
Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways Liyun Sang, Julie J. Miller, Kevin C. Corbit, Cell Molecular NeuroscienceDisease MechanismGliomaMolecular BiologyComplex Disease	2011	617
WDR62 is associated with the spindle pole and is mutated in human microcephaly Adeline K. Nicholas, Maryam Khurshid, Julie Désir, Nature Genetics Spindle PoleMolecular NeuroscienceDisease MechanismGenetic DisorderMolecular Biology	2010	286
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 Saima Riazuddin, Inna A. Belyantseva, Arnaud P. J. Giese, Nature Genetics Nonsyndromic Deafness Dfnb48Type 1JSignal TransductionSynaptic SignalingCib2 Calcium-	2012	247
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
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families Ricardo Harripaul, Nasim Vasli, Muhammad Rafiq, Molecular Psychiatry Mendelian DisorderNovel Candidate GenesGenetic DisorderGeneticsConsanguineous Families	2017	177
Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35 Rob W.J. Collin, Ersan Kalay, Muhammad Tariq, The American Journal of Human Genetics Developmental BiologyGeneticsAudiologyAuditory PhysiologyAuditory Research	2008	128
Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74 Zubair M. Ahmed, Rizwan Yousaf, Byung Cheon Lee, The American Journal of Human Genetics Signal TransductionGeneticsMolecular BiologyFunctional Null MutationsHuman Deafness Dfnb74	2010	120
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
Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42 Guntram Borck, Atteeq U. Rehman, Kwanghyuk Lee, The American Journal of Human Genetics GeneticsAudiologyAuditory PhysiologyHearing DisordersLoss-of-function Mutations	2011	119
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency David B. Beck, Ana Petracovici, Chongsheng He, The American Journal of Human Genetics ChromatinMendelian DisorderGenetic DisorderNatural SciencesGenetics	2020	108

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