Muhammad Ansar

4.4k total citations
95 papers, 1.6k citations indexed

About

Muhammad Ansar is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Muhammad Ansar has authored 95 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 25 papers in Cell Biology and 25 papers in Genetics. Recurrent topics in Muhammad Ansar's work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Skin and Cellular Biology Research (13 papers) and RNA regulation and disease (11 papers). Muhammad Ansar is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (14 papers), Skin and Cellular Biology Research (13 papers) and RNA regulation and disease (11 papers). Muhammad Ansar collaborates with scholars based in Pakistan, United States and Saudi Arabia. Muhammad Ansar's co-authors include Wasim Ahmad, Ghazanfar Ali, Suzanne M. Leal, Sulman Basit, Kwanghyuk Lee, Muzammil Ahmad Khan, Falak Sher Khan, Syed Kamran‐ul‐Hassan Naqvi, John B. Vincent and Muhammad Rafiq and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Muhammad Ansar

88 papers receiving 1.5k 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 21 1.1k 430 379 212 126 95 1.6k
Michio Yoshida Japan 16 1.4k 1.3× 493 1.1× 146 0.4× 57 0.3× 46 0.4× 32 2.0k
Vasiliki Kalatzis France 27 1.3k 1.2× 390 0.9× 163 0.4× 214 1.0× 27 0.2× 69 2.6k
Jianbo Wang United States 20 1.9k 1.7× 437 1.0× 540 1.4× 117 0.6× 82 0.7× 31 2.2k
Valérie Delague France 28 1.7k 1.6× 647 1.5× 239 0.6× 42 0.2× 39 0.3× 91 2.6k
S Malcolm United Kingdom 31 1.2k 1.1× 1.1k 2.7× 91 0.2× 164 0.8× 118 0.9× 71 2.3k
B. Matthew Fagan United States 9 1.1k 1.0× 228 0.5× 170 0.4× 74 0.3× 27 0.2× 13 1.6k
Hope O. Sweet United States 21 1.0k 1.0× 440 1.0× 398 1.1× 41 0.2× 111 0.9× 32 1.9k
Ling Hou China 26 1.2k 1.2× 261 0.6× 967 2.6× 113 0.5× 31 0.2× 64 2.1k
M. Mark Taketo Japan 15 1.0k 1.0× 452 1.1× 96 0.3× 181 0.9× 27 0.2× 17 1.4k
Kwanghyuk Lee United States 16 566 0.5× 183 0.4× 66 0.2× 310 1.5× 56 0.4× 39 1.0k

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.
Irshad, Saba, Ambrin Fatima, Fernanda A. Correa, et al.. (2024). Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism. BMC Genomics. 25(1). 787–787. 1 indexed citations
2.
Ansar, Muhammad, et al.. (2023). AB1743-PARE PUBLIC INTEREST IN LUPUS IN AFRICA. Annals of the Rheumatic Diseases. 82. 2107–2107. 1 indexed citations
3.
Saqib, Muhammad Arif Nadeem, Edwin Mientjes, Anushree Acharya, et al.. (2023). A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndrome. European Journal of Human Genetics. 31(12). 1447–1454. 3 indexed citations
4.
Ansar, Muhammad, et al.. (2021). A Missense Variant in LAMA3 Gene Causes Microcephaly and Epidermolysis Bullosa in a Pakistani Family. SHILAP Revista de lepidopterología. 20(3). 198–203.
5.
Ullah, Asmat, Ubaid Ullah, Farooq Ahmad, et al.. (2021). Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous Families. Klinische Pädiatrie. 234(3). 123–129.
6.
Khan, Amjad, Zhichao Miao, Muhammad Umair, et al.. (2020). Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants. Genes. 11(9). 1021–1021. 11 indexed citations
7.
Umair, Muhammad, Muhammad Bilal, Raja Hussain Ali, et al.. (2019). Whole‐exome sequencing revealed a nonsense mutation in STKLD1 causing non‐syndromic pre‐axial polydactyly type A affecting only upper limb. Clinical Genetics. 96(2). 134–139. 8 indexed citations
8.
Ilyas, Muhammad, Ghulam Shabbir, Malik Ashiq Rabbani, et al.. (2018). Genetic divergence in Brassica napus L. germplasm as determined by quantitative attributes.. Pakistan Journal of Botany. 50(3). 1039–1045. 6 indexed citations
9.
Shabbir, Ghulam, et al.. (2018). Estimation of linkage disequilibrium and population structure among Brassica napus genotypes for association mapping.. Fresenius environmental bulletin. 27(9). 5980–5986. 1 indexed citations
10.
Shah, Khadim, Raja Hussain Ali, Muhammad Salman Chishti, et al.. (2017). Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. International Journal of Dermatology. 56(12). 1406–1413. 6 indexed citations
11.
Saqib, Muhammad Arif Nadeem, Konstantinos Nikopoulos, Ehsan Ullah, et al.. (2015). Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophies. Scientific Reports. 5(1). 9965–9965. 26 indexed citations
12.
Saqib, Muhammad Arif Nadeem, Ehsan Ullah, Falak Sher Khan, et al.. (2014). Homozygosity Mapping and Disease Genes Screening in Pakistani Families with Inherited Retinal Dystrophies. Investigative Ophthalmology & Visual Science. 55(13). 3292–3292. 1 indexed citations
13.
Ali, Safdar, et al.. (2014). WEED GROWTH DYNAMICS ASSOCIATED WITH RAINFED WHEAT (TRITICUM AESTIVUM L.) ESTABLISHMENT UNDER DIFFERENT TILLAGE SYSTEMS IN POTHWAR. International Journal of Plant Animal and Environmental Sciences. 4(2). 3 indexed citations
14.
Santos‐Cortez, Regie Lyn P., Kwanghyuk Lee, Arnaud P. J. Giese, et al.. (2014). Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish. Human Molecular Genetics. 23(12). 3289–3298. 39 indexed citations
15.
Lee, Kwanghyuk, Saadullah Khan, Muhammad Ansar, et al.. (2011). A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families. PubMed. 2011. 1–4. 9 indexed citations
16.
Khan, Saadullah, Rabia Habib, Hina Mir, et al.. (2011). Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan. Clinical and Experimental Dermatology. 36(6). 652–654. 13 indexed citations
17.
Schraders, Margit, Kwanghyuk Lee, Jaap Oostrik, et al.. (2010). Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment. The American Journal of Human Genetics. 86(2). 138–147. 50 indexed citations
18.
Basit, Sulman, Ghazanfar Ali, Naveed Wasif, Muhammad Ansar, & Wasim Ahmad. (2010). Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes. Human Genetics. 128(2). 213–220. 15 indexed citations
19.
Khan, Farmanullah, et al.. (2008). Response of mungbean genotypes to Rhizobium inoculum and varying levels of nitrogen fertilizer.. Pakistan Journal of Agricultural Research. 21. 33–44. 4 indexed citations
20.
Ansar, Muhammad, et al.. (1994). Cause and control of guava decline in the Punjab (Pakistan).. Pakistan Journal of Phytopathology. 6(1). 41–44. 7 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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