Rumaisa Bashir

2.6k total citations · 1 hit paper
20 papers, 1.7k citations indexed

About

Rumaisa Bashir is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Rumaisa Bashir has authored 20 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 4 papers in Cell Biology. Recurrent topics in Rumaisa Bashir's work include Muscle Physiology and Disorders (12 papers), Genetic Neurodegenerative Diseases (6 papers) and Nuclear Structure and Function (4 papers). Rumaisa Bashir is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Genetic Neurodegenerative Diseases (6 papers) and Nuclear Structure and Function (4 papers). Rumaisa Bashir collaborates with scholars based in United Kingdom, United States and France. Rumaisa Bashir's co-authors include I. Mahjneh, Sharon Keers, Isabelle Richard, Elizabeth Vafiadaki, Tom Strachan, Zohar Argov, J. Beckmann, Kate Bushby, S. Britton and Mayana Zatz and has published in prestigious journals such as Nature Genetics, PLoS ONE and Journal of Molecular Biology.

In The Last Decade

Rumaisa Bashir

20 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

1998 526 citations Rumaisa Bashir, S. Britton et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rumaisa Bashir United Kingdom	18	1.5k	405	343	286	254	20	1.7k
Sharon Keers United Kingdom	18	1.8k 1.3×	553 1.4×	376 1.1×	326 1.1×	341 1.3×	28	2.1k
Kumaraswamy Sivakumar United States	22	1.3k 0.9×	564 1.4×	480 1.4×	454 1.6×	116 0.5×	41	2.1k
Rafaëlle Bernard France	20	2.3k 1.6×	354 0.9×	237 0.7×	367 1.3×	219 0.9×	54	2.8k
Judy U. Earley United States	27	1.4k 1.0×	143 0.4×	415 1.2×	254 0.9×	206 0.8×	38	1.9k
Jens Reimann Germany	22	845 0.6×	265 0.7×	221 0.6×	296 1.0×	176 0.7×	55	1.3k
I. Mahjneh Finland	18	1.7k 1.1×	522 1.3×	455 1.3×	401 1.4×	282 1.1×	36	1.9k
Martin Krahn France	19	1.1k 0.7×	289 0.7×	245 0.7×	175 0.6×	201 0.8×	64	1.4k
Noemí de Luna Spain	24	1.0k 0.7×	299 0.7×	162 0.5×	107 0.4×	341 1.3×	55	1.6k
Anna Fidziańska Poland	25	1.8k 1.2×	382 0.9×	802 2.3×	347 1.2×	122 0.5×	121	2.3k
Sasha Bogdanovich United States	21	1.9k 1.3×	213 0.5×	295 0.9×	384 1.3×	558 2.2×	33	2.3k

Countries citing papers authored by Rumaisa Bashir

Since Specialization

Citations

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

Fields of papers citing papers by Rumaisa Bashir

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rumaisa Bashir

This figure shows the co-authorship network connecting the top 25 collaborators of Rumaisa Bashir. A scholar is included among the top collaborators of Rumaisa 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 Rumaisa Bashir. Rumaisa Bashir is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lostal, William, Marc Bartoli, Carinne Roudaut, et al.. (2012). Lack of Correlation between Outcomes of Membrane Repair Assay and Correction of Dystrophic Changes in Experimental Therapeutic Strategy in Dysferlinopathy. PLoS ONE. 7(5). e38036–e38036. 53 indexed citations

Mahjneh, I., Rumaisa Bashir, Sari Kiuru‐Enari, et al.. (2012). Selective pattern of muscle involvement seen in distal muscular dystrophy associated with anoctamin 5 mutations: A follow-up muscle MRI study. Neuromuscular Disorders. 22. S130–S136. 24 indexed citations

Bolduc, Véronique, Gareth Marlow, Kym M. Boycott, et al.. (2010). Recessive Mutations in the Putative Calcium-Activated Chloride Channel Anoctamin 5 Cause Proximal LGMD2L and Distal MMD3 Muscular Dystrophies. The American Journal of Human Genetics. 86(2). 213–221. 195 indexed citations

Mahjneh, I., Jyoti K. Jaiswal, Antti Lamminen, et al.. (2010). A new distal myopathy with mutation in anoctamin 5. Neuromuscular Disorders. 20(12). 791–795. 50 indexed citations

Harris, Richard, Eugen‐Matthias Strehle, James D. Watson, et al.. (2008). Solution Structure of the Inner DysF Domain of Myoferlin and Implications for Limb Girdle Muscular Dystrophy Type 2B. Journal of Molecular Biology. 379(5). 981–990. 33 indexed citations

Kesari, Akanchha, Mitsunori Fukuda, Susan M. Knoblach, et al.. (2008). Dysferlin Deficiency Shows Compensatory Induction of Rab27A/Slp2a That May Contribute to Inflammatory Onset. American Journal Of Pathology. 173(5). 1476–1487. 39 indexed citations

Jiménez, José L. & Rumaisa Bashir. (2007). In silico functional and structural characterisation of ferlin proteins by mapping disease-causing mutations and evolutionary information onto three-dimensional models of their C2 domains. Journal of the Neurological Sciences. 260(1-2). 114–123. 31 indexed citations

Jaiswal, Jyoti K., Gareth Marlow, I. Mahjneh, et al.. (2006). Patients with a Non‐dysferlin Miyoshi Myopathy have a Novel Membrane Repair Defect. Traffic. 8(1). 77–88. 45 indexed citations

Vafiadaki, Elizabeth, André Reis, Sharon Keers, et al.. (2001). Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation. Neuroreport. 12(3). 625–629. 49 indexed citations

10.

Argov, Zohar, Dov Soffer, Esther Kahana, et al.. (2000). Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Brain. 123(6). 1229–1237. 77 indexed citations

11.

Britton, S., Tom C. Freeman, Elizabeth Vafiadaki, et al.. (2000). The Third Human FER-1-like Protein Is Highly Similar to Dysferlin. Genomics. 68(3). 313–321. 59 indexed citations

12.

Anderson, Louise V.B., Robert Pogue, Elizabeth Vafiadaki, et al.. (2000). Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Neuromuscular Disorders. 10(8). 553–559. 113 indexed citations

13.

Bashir, Rumaisa, S. Britton, Tom Strachan, et al.. (1998). A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nature Genetics. 20(1). 37–42. 526 indexed citations breakdown →

14.

Bashir, Rumaisa, Sharon Keers, Tom Strachan, et al.. (1996). Genetic and Physical Mapping at the Limb-Girdle Muscular Dystrophy Locus (LGMD2B) on Chromosome 2p. Genomics. 33(1). 46–52. 44 indexed citations

15.

Jang, Wonhee, John Weber, Rumaisa Bashir, Kate Bushby, & Miriam H. Meisler. (1996). Aup1, a Novel Gene on Mouse Chromosome 6 and Human Chromosome 2p13. Genomics. 36(2). 366–368. 11 indexed citations

16.

Carter, Simon, S Bryce, Colin S. Munro, et al.. (1994). Linkage Analyses in British Pedigrees Suggest a Single Locus for Darier Disease and Narrow the Location to the Interval between D12S105 and D12S129. Genomics. 24(2). 378–382. 8 indexed citations

17.

Inglehearn, Chris F., Simon Carter, Janet C. Lindsey, et al.. (1993). A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. Nature Genetics. 4(1). 51–53. 69 indexed citations

18.

Bashir, Rumaisa, et al.. (1993). Localisation of a gene for Darier's disease. Human Molecular Genetics. 2(11). 1937–1939. 54 indexed citations

19.

Inglehearn, Chris F., T J Keen, Rumaisa Bashir, et al.. (1992). A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis piamentosa. Human Molecular Genetics. 1(1). 41–45. 101 indexed citations

20.

Day, Christopher P., Rumaisa Bashir, Oliver James, et al.. (1991). Investigation of the role of polymorphisms at the alcohol and aldehyde dehydrogenase loci in genetic predisposition to alcohol-related end-organ damage. Hepatology. 14(5). 798–801. 131 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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