Muhammad Ansar

4.4k citations

95 papers · 1.6k · h-index 21

Impact in

Developmental Biology top 5%
Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in

Molecular Biology 50
- RNA regulation and disease 11
Cell Biology 25
- Skin and Cellular Biology Research 13

Co-authors: Wasim Ahmad (53 shared papers)Ghazanfar Ali (19 shared papers)Suzanne M. Leal (28 shared papers)Sulman Basit (17 shared papers)Kwanghyuk Lee (9 shared papers)Syed Kamran‐ul‐Hassan Naqvi (6 shared papers)Falak Sher Khan (6 shared papers)Muzammil Ahmad Khan (5 shared papers)
Journals: Clinical Genetics (7 papers)Human Genetics (5 papers)European Journal of Human Genetics (3 papers)Human Heredity (3 papers)The American Journal of Human Genetics (3 papers)
Partner nations: Pakistan United States Saudi Arabia

In The Last Decade

Muhammad Ansar

88 papers receiving 1.5k citations

Peers

Countries citing papers authored by Muhammad Ansar

Since Specialization

Citations

This map shows the geographic impact of Muhammad Ansar's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Muhammad Ansar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Muhammad Ansar more than expected).

Fields of papers citing papers by Muhammad Ansar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Muhammad Ansar. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Muhammad Ansar. The network helps show where Muhammad Ansar may publish in the future.

Co-authors

The 25 scholars most cited alongside Muhammad Ansar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Muhammad Ansar Line = papers co-authored together Muhammad Ansar links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 95 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	WDR62 is associated with the spindle pole and is mutated in human microcephaly Nature Genetics ·Adeline K. Nicholas, Maryam Khurshid, Julie Désir, Ofélia P. Carvalho, James J. Cox, Gemma Thornton, Rizwana Kausar, Muhammad Ansar, Wasim Ahmad, Alain Verloès, Sandrine Passemard, Jean-Paul Misson, Susan Lindsay, Fanni Gergely, William B. Dobyns, Emma Roberts, Marc Abramowicz, C. Geoffrey Woods	2010	211
2	Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability The American Journal of Human Genetics ·Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, Shobbir Hussain, Joana V. Flores, Verena Rupp, Akshita K. Vincent, Roland Malli, Ghazanfar Ali, Falak Sher Khan, Gisele E. Ishak, Dan Doherty, Rosanna Weksberg, Muhammad Ayub, Christian Windpassinger, Shahnaz Ibrahim, Michaela Frye, Muhammad Ansar, John B. Vincent	2012	182
3	Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74 The American Journal of Human Genetics ·Zubair M. Ahmed, Rizwan Yousaf, Byung Cheon Lee, Shaheen N. Khan, Sue Lee, Kwanghyuk Lee, Tayyab Husnaın, Atteeq U. Rehman, Sarah Bonneux, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal, Vadim N. Gladyshev, Inna A. Belyantseva, Guy Van Camp, Sheikh Riazuddin, Thomas B. Friedman, Saima Riazuddin	2010	73
4	Mutation of ATF6 causes autosomal recessive achromatopsia Human Genetics ·Muhammad Ansar, Regie Lyn P. Santos‐Cortez, Muhammad Arif Nadeem Saqib, Fareeha Zulfiqar, Kwanghyuk Lee, Naeem Mahmood Ashraf, Ehsan Ullah, Xin Wang, Sundus Sajid, Falak Sher Khan, Muhammad Aminuddin, Joshua D. Smith, Jay Shendure, Michael J. Bamshad, Deborah A. Nickerson, Abdul Hameed, Saima Riazuddin, Zubair M. Ahmed, Wasim Ahmad, Suzanne M. Leal	2015	64
5	Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment The American Journal of Human Genetics ·Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, P.L.M. Huygen, Ghazanfar Ali, Lies H. Hoefsloot, Joris A. Veltman, Frans P.M. Cremers, Sulman Basit, Muhammad Ansar, Cor W. R. J. Cremers, Henricus P. M. Kunst, Wasim Ahmad, R.J.C. Admiraal, Suzanne M. Leal, Hannie Kremer	2010	50
6	A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family Human Molecular Genetics ·Muzammil Ahmad Khan, Verena Rupp, Meritxell Orpinell, Muhammad Sajid Hussain, Janine Altmüller, Michel O. Steinmetz, Christian Enzinger, Hölger Thiele, Wolfgang Höhne, Gudrun Nürnberg, Shahid Mahmood Baig, Muhammad Ansar, Peter Nürnberg, John B. Vincent, Michael R. Speicher, Pierre Gönczy, Christian Windpassinger	2014	50
7	Novel sequence variants in theTMC1 gene in Pakistani families with autosomal recessive hearing impairment Human Mutation ·Regie Lyn P. Santos, Muhammad Wajid, Mohammad Nasim Imtiaz Khan, Nathan McArthur, Thanh Pham, Attya Bhatti, Kwanghyuk Lee, Saba Irshad, Asif Mir, Kai Yan, Maria H. Chahrour, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal	2005	49
8	High frequency shoot regeneration and Agrobacterium-mediated DNA transfer in Canola (Brassica napus) Plant Cell Tissue and Organ Culture (PCTOC) ·Muhammad Ramzan Khan, Hamid Rashid, Muhammad Ansar, Zubeda Chaudry	2003	44
9	Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish Human Molecular Genetics ·Regie Lyn P. Santos‐Cortez, Kwanghyuk Lee, Arnaud P. J. Giese, Muhammad Ansar, Muhammad Aminuddin, K. Rehn, Xin Wang, Abdul Aziz, I. Chiu, Raja Hussain Ali, Joshua D. Smith, Jay Shendure, M. Bamshad, Deborah A. Nickerson, Zubair M. Ahmed, Wasim Ahmad, Saima Riazuddin, Suzanne M. Leal	2014	39
10	A novel homozygous missense mutation in WNT10B in familial split‐hand/foot malformation Clinical Genetics ·Suliman Khan, Sulman Basit, Faridullah Khan Zimri, Nida Ali, Ghazanfar Ali, Muhammad Ansar, Wasim Ahmad	2011	35
11	A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family BMC Medical Genetics ·Sulman Basit, Syed Kamran‐ul‐Hassan Naqvi, Naveed Wasif, Ghazanfar Ali, Muhammad Ansar, Wasim Ahmad	2008	29
12	Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance Journal of Human Genetics ·Khurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza, Kwanghyuk Lee, Shabir Hussain, Imen Chakchouk, Abdul Nasır, Anushree Acharya, Izoduwa Abbe, Muhammad Umair, Muhammad Ansar, Irfan Ullah, Khadim Shah, Michael J. Bamshad, Deborah A. Nickerson, Wasim Ahmad, Suzanne M. Leal	2018	28
13	A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability BMC Medical Genetics ·Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, Nadir Ali, Ghazanfar Ali, John B. Vincent, Muhammad Ansar	2011	27
14	Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families Human Genetics ·Naveed Wasif, Syed Kamran‐ul‐Hassan Naqvi, Sulman Basit, Nadir Ali, Muhammad Ansar, Wasim Ahmad	2010	27
15	Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophies Scientific Reports ·Muhammad Arif Nadeem Saqib, Konstantinos Nikopoulos, Ehsan Ullah, Falak Sher Khan, Jamila Iqbal, Rabia Bibi, Afeefa Jarral, Sundus Sajid, Koji M. Nishiguchi, Giulia Venturini, Muhammad Ansar, Carlo Rivolta	2015	26
16	Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly BMC Neurology ·Rizwana Kousar, Muhammad Jawad Hassan, Bushra Khan, Sulman Basit, Saqib Mahmood, Asif Mir, Wasim Ahmad, Muhammad Ansar	2011	25
17	A locus for hereditary hypotrichosis localized to human chromosome 18q21.1 European Journal of Human Genetics ·Muhammad Rafique, Muhammad Ansar, Syed M. Jamal, Sajid Malik, Muhammad Sohail, Mohammad Faiyaz-Ul-Haque, Sayedul Haque, Suzanne M. Leal, Wasim Ahmad	2003	25
18	Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genes Human Genetics ·Umm‐e‐Kalsoom, Sulman Basit, Syed Kamran‐ul‐Hassan Naqvi, Muhammad Ansar, Wasim Ahmad	2011	25
19	FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice Journal of Bone and Mineral Research ·Isabelle Schrauwen, Arnaud P. J. Giese, Abdul Aziz, David Lafont, Imen Chakchouk, Regie Lyn P. Santos‐Cortez, Kwanghyuk Lee, Anushree Acharya, Falak Sher Khan, Asmat Ullah, Deborah A. Nickerson, Michael J. Bamshad, Ghazanfar Ali, Saima Riazuddin, Muhammad Ansar, Wasim Ahmad, Zubair M. Ahmed, Suzanne M. Leal	2018	25
20	Novel CLDN14 mutations in Pakistani families with autosomal recessive non‐syndromic hearing loss American Journal of Medical Genetics Part A ·Kwanghyuk Lee, Muhammad Ansar, Paula B. Andrade, Bushra Khan, Regie Lyn P. Santos‐Cortez, Wasim Ahmad, Suzanne M. Leal	2012	21

About Muhammad Ansar

Muhammad Ansar is a scholar working on Molecular Biology, Cell Biology, Genetics, Plant Science and Sensory Systems, having authored 95 papers that have together received 1.6k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Skin and Cellular Biology Research (13 papers), RNA regulation and disease (11 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (9 papers), Hair Growth and Disorders (8 papers), Genomics and Rare Diseases (7 papers) and Congenital limb and hand anomalies (6 papers). The work is most often cited by research in Developmental Biology (96 citations), Sensory Systems (212 citations), Cell Biology (379 citations), Urology (103 citations) and Molecular Biology (1.1k citations). Muhammad Ansar has collaborated with scholars based in Pakistan, United States and Saudi Arabia. Frequent co-authors include Wasim Ahmad, Ghazanfar Ali, Suzanne M. Leal, Sulman Basit, Kwanghyuk Lee, Syed Kamran‐ul‐Hassan Naqvi, Falak Sher Khan, Muzammil Ahmad Khan, John B. Vincent and Muhammad Rafiq. Their work appears in journals such as Clinical Genetics, Human Genetics, European Journal of Human Genetics, Human Heredity and The American Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Muhammad Ansar

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About Muhammad Ansar

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