Muhammad Ansar

1.1k total citations
26 papers, 274 citations indexed

About

Muhammad Ansar is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Muhammad Ansar has authored 26 papers receiving a total of 274 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Muhammad Ansar's work include Genetics and Neurodevelopmental Disorders (5 papers), Blood disorders and treatments (4 papers) and Retinal Development and Disorders (4 papers). Muhammad Ansar is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Blood disorders and treatments (4 papers) and Retinal Development and Disorders (4 papers). Muhammad Ansar collaborates with scholars based in Pakistan, Switzerland and France. Muhammad Ansar's co-authors include Stylianos E. Antonarakis, Muhammad Tahir Sarwar, Federico Santoni, Sajida Hassan, Sheikh Riazuddin, Emmanuelle Ranza, Periklis Makrythanasis, Bushra Ijaz, Usman Ali Ashfaq and Sidra Rehman and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Developmental Biology.

In The Last Decade

Muhammad Ansar

26 papers receiving 267 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Muhammad Ansar Pakistan 10 198 90 43 41 28 26 274
Brian Lin United States 9 163 0.8× 62 0.7× 15 0.3× 34 0.8× 17 0.6× 16 256
A.-M. Salmon France 6 201 1.0× 95 1.1× 53 1.2× 90 2.2× 31 1.1× 8 366
Yuwei Da China 11 127 0.6× 24 0.3× 15 0.3× 41 1.0× 22 0.8× 57 401
Christine Zeschnigk Germany 7 128 0.6× 56 0.6× 33 0.8× 61 1.5× 67 2.4× 7 254
Lorelei Stoica United States 7 256 1.3× 175 1.9× 7 0.2× 29 0.7× 10 0.4× 8 355
Alisa Tubsuwan Thailand 13 185 0.9× 18 0.2× 14 0.3× 25 0.6× 14 0.5× 34 288
Qian Du Australia 9 593 3.0× 123 1.4× 5 0.1× 20 0.5× 15 0.5× 16 704
Timothy M. Piazza United States 8 130 0.7× 35 0.4× 11 0.3× 15 0.4× 90 3.2× 11 364
Corinne Bernard France 7 215 1.1× 68 0.8× 6 0.1× 49 1.2× 6 0.2× 11 389

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-authorship network of co-authors of Muhammad Ansar

This figure shows the co-authorship network connecting the top 25 collaborators of Muhammad Ansar. A scholar is included among the top collaborators of Muhammad Ansar based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Muhammad Ansar. Muhammad Ansar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ullah, Mukhtar, Mathieu Quinodoz, Abdur Rashid, et al.. (2025). A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort. npj Genomic Medicine. 10(1). 31–31. 2 indexed citations
2.
Vacca, Fabrizio, Binnaz Yalcin, & Muhammad Ansar. (2024). Exploring the pathological mechanisms underlying Cohen syndrome. Frontiers in Neuroscience. 18. 1431400–1431400. 4 indexed citations
3.
Ujjan, Ikram Din, Ijaz Anwar, Federico Santoni, et al.. (2023). Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees. Genes. 14(2). 404–404. 6 indexed citations
4.
Mattioli, Francesca, Lina Worpenberg, Shagufta Naz, et al.. (2023). Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorder. Genetics in Medicine. 25(9). 100900–100900. 12 indexed citations
5.
Nguyen, Sylvie, Fabrice Prin, Yannis Duffourd, et al.. (2023). Characterization of Vps13b-mutant mice reveals neuroanatomical and behavioral phenotypes with females less affected. Neurobiology of Disease. 185. 106259–106259. 3 indexed citations
6.
Naz, Shagufta, Francesca Mattioli, Nicolas Guex, et al.. (2023). A Biallelic Truncating Variant in the TPR Domain of GEMIN5 Associated with Intellectual Disability and Cerebral Atrophy. Genes. 14(3). 707–707. 6 indexed citations
7.
Antonarakis, Stylianos E., Aleš Holoubek, J Meylan, et al.. (2021). Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2. Human Molecular Genetics. 31(1). 1–9. 8 indexed citations
8.
Mattioli, Francesca, Hossein Darvish, Abbas Tafakhori, et al.. (2021). Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder. npj Genomic Medicine. 6(1). 94–94. 12 indexed citations
9.
Gabrielle, Pierre‐Henry, Laurence Faivre, Isabelle Audo, et al.. (2021). Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy. Scientific Reports. 11(1). 16412–16412. 6 indexed citations
10.
Ansar, Muhammad, Muhammad Asif Naeem, Mathieu Quinodoz, et al.. (2021). Genetic Analysis of Consanguineous Pakistani Families with Congenital Stationary Night Blindness. Ophthalmic Research. 65(1). 104–110. 1 indexed citations
11.
Ansar, Muhammad, et al.. (2020). Hashimoto Encephalopathy With Status Epilepticus. Cureus. 12(12). e11857–e11857. 4 indexed citations
12.
Ansar, Muhammad, Alessandro Serretti, Muhammad Tahir Sarwar, et al.. (2018). Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature. Human Molecular Genetics. 28(6). 972–979. 16 indexed citations
13.
Kausar, Humera, Waqar Ahmad, Sana Javaid Awan, et al.. (2017). Role of alternative phosphorylation and O-glycosylation of erythropoietinreceptor in modulating its function: an in silico study. TURKISH JOURNAL OF BIOLOGY. 41. 816–825. 1 indexed citations
14.
Makrythanasis, Periklis, Michel Guipponi, Federico Santoni, et al.. (2016). Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree. Human Genomics. 10(1). 26–26. 14 indexed citations
15.
Ansar, Muhammad, Astrid Oudakker, A. van Caam, et al.. (2013). Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice. Developmental Biology. 386(2). 395–407. 55 indexed citations
16.
Shahid, Imran, Bushra Ijaz, Waqar Ahmad, et al.. (2013). Stable Huh-7 cell lines expressing non-structural proteins of genotype 1a of hepatitis C virus. Journal of Virological Methods. 189(1). 65–69. 5 indexed citations
17.
Ashfaq, Usman Ali, Muhammad Ansar, Muhammad Tahir Sarwar, et al.. (2011). Post-transcriptional inhibition of hepatitis C virus replication through small interference RNA. Virology Journal. 8(1). 112–112. 9 indexed citations
18.
Sarwar, Muhammad Tahir, Humera Kausar, Bushra Ijaz, et al.. (2011). NS4A protein as a marker of HCV history suggests that different HCV genotypes originally evolved from genotype 1b. Virology Journal. 8(1). 317–317. 9 indexed citations
19.
Ansar, Muhammad, Usman Ali Ashfaq, Imran Shahid, et al.. (2011). Inhibition of full length Hepatitis C Virus particles of 1a genotype through small interference RNA. Virology Journal. 8(1). 203–203. 13 indexed citations
20.
Khaliq, Saba, Muzna Zahur, Bushra Ijaz, et al.. (2009). RNAi as a new therapeutic strategy against HCV. Biotechnology Advances. 28(1). 27–34. 29 indexed citations

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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