Rasheeda Bashir

461 total citations
27 papers, 258 citations indexed

About

Rasheeda Bashir is a scholar working on Sensory Systems, Ophthalmology and Molecular Biology. According to data from OpenAlex, Rasheeda Bashir has authored 27 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Sensory Systems, 6 papers in Ophthalmology and 5 papers in Molecular Biology. Recurrent topics in Rasheeda Bashir's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Glaucoma and retinal disorders (6 papers) and Vestibular and auditory disorders (4 papers). Rasheeda Bashir is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Glaucoma and retinal disorders (6 papers) and Vestibular and auditory disorders (4 papers). Rasheeda Bashir collaborates with scholars based in Pakistan, United Kingdom and United States. Rasheeda Bashir's co-authors include Sadaf Naz, K. Bushby, Mark Cookson, Paul G. Ince, Pamela J. Shaw, Janet C. Lindsey, M. Lusher, Ghulam Mujtaba, Imran Altaf and Muhammad Riaz Khan and has published in prestigious journals such as Neurology, Scientific Reports and Gene.

In The Last Decade

Rasheeda Bashir

24 papers receiving 254 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rasheeda Bashir Pakistan 9 102 98 76 75 43 27 258
Cristian Setz Switzerland 9 93 0.9× 150 1.5× 31 0.4× 111 1.5× 114 2.7× 19 389
Kianoush Sheykholeslami United States 11 118 1.2× 210 2.1× 26 0.3× 100 1.3× 6 0.1× 22 354
Heather B. Steele-Stallard United Kingdom 6 37 0.4× 120 1.2× 29 0.4× 297 4.0× 4 0.1× 6 349
W. Liu United States 8 163 1.6× 176 1.8× 76 1.0× 107 1.4× 10 0.2× 9 419
Xinxing Fu China 10 42 0.4× 81 0.8× 32 0.4× 75 1.0× 6 0.1× 57 301
Vidhya Munnamalai United States 9 45 0.4× 148 1.5× 63 0.8× 200 2.7× 10 0.2× 13 370
Wouter J. F. ten Cate United States 11 170 1.7× 281 2.9× 25 0.3× 85 1.1× 23 0.5× 16 364
Pietro Scimemi Italy 12 154 1.5× 436 4.4× 47 0.6× 259 3.5× 9 0.2× 23 575
Mototane Komeda Japan 8 178 1.7× 321 3.3× 28 0.4× 51 0.7× 22 0.5× 12 394
Rodrigo Martinez‐Monedero United States 7 41 0.4× 256 2.6× 46 0.6× 67 0.9× 5 0.1× 8 326

Countries citing papers authored by Rasheeda Bashir

Since Specialization
Citations

This map shows the geographic impact of Rasheeda Bashir'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 Rasheeda Bashir with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rasheeda Bashir more than expected).

Fields of papers citing papers by Rasheeda Bashir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rasheeda Bashir. 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 Rasheeda Bashir. The network helps show where Rasheeda Bashir may publish in the future.

Co-authorship network of co-authors of Rasheeda Bashir

This figure shows the co-authorship network connecting the top 25 collaborators of Rasheeda Bashir. A scholar is included among the top collaborators of Rasheeda Bashir 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 Rasheeda Bashir. Rasheeda Bashir 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
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Naz, Sadaf, Asma Mushtaq, Elizabeth Wohler, et al.. (2023). Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma. Genes. 14(2). 310–310. 4 indexed citations
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Manzoor, Jaida, et al.. (2023). Genetic association of PTPN22 polymorphisms with Type 1 diabetes in Pakistani children. Journal of King Saud University - Science. 35(10). 102967–102967. 1 indexed citations
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Altaf, Imran, et al.. (2023). Immunoprophylactic potential of recombinant outer membrane protein of Salmonella enterica serovar Typhi against enteric fever in BALB/c mice. Journal of King Saud University - Science. 36(1). 102983–102983. 2 indexed citations
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Bashir, Rasheeda, et al.. (2021). Isolation and Characterization of Polysaccharide- Degrading Microbes from Compost Samples. Journal of Environmental Science and Management. 24(2). 10–10. 3 indexed citations
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Ramzan, Memoona, Rasheeda Bashir, Ghulam Mujtaba, et al.. (2020). Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan. Scientific Reports. 10(1). 11902–11902. 10 indexed citations
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Altaf, Imran, et al.. (2020). Evaluation of the cytotoxic and antiviral effects of ethanol extract of three Opuntia species of Peste des Petits ruminant virus. Tropical Journal of Pharmaceutical Research. 19(10). 2123–2128. 2 indexed citations
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Bashir, Rasheeda, et al.. (2019). Association of hepatocyte growth factor (HGF) gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistani population. Journal of the Pakistan Medical Association. 70(0). 1–1. 1 indexed citations
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Bashir, Rasheeda, et al.. (2018). Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families.. PubMed. 68(8). 1205–1211. 2 indexed citations
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Bashir, Rasheeda, et al.. (2015). Mutations of GJB2 encoding connexin 26 contribute to non-syndromic moderate and severe hearing loss in Pakistan. European Archives of Oto-Rhino-Laryngology. 272(8). 2071–2075. 12 indexed citations
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Bashir, Rasheeda. (2014). Contribution of GLC3A locus to Primary Congenital Glaucoma in Pakistani population. Pakistan Journal of Medical Sciences. 30(6). 1341–5. 3 indexed citations
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Bashir, Rasheeda, et al.. (2013). The c.42_52del11 Mutation in TPRN and Progressive Hearing Loss in a Family from Pakistan. Biochemical Genetics. 51(5-6). 350–357. 3 indexed citations
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Khan, Muhammad Riaz, Rasheeda Bashir, & Sadaf Naz. (2013). SLC26A4 Mutations in Patients with Moderate to Severe Hearing Loss. Biochemical Genetics. 51(7-8). 514–523. 8 indexed citations
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Bashir, Rasheeda, et al.. (2011). Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss. European Journal of Medical Genetics. 55(2). 99–102. 35 indexed citations
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Bashir, Rasheeda, et al.. (2010). Mutations in CLDN14 are associated with different hearing thresholds. Journal of Human Genetics. 55(11). 767–770. 12 indexed citations
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Ince, Paul G., M. Lusher, Janet C. Lindsey, et al.. (2000). Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation. Neurology. 55(1). 89–94. 76 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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