Rumaisa Bashir

2.6k citations

20 papers · 1.7k indexed · 1 hit paper · h-index 18

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
Molecular Biology top 5%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Ion channel regulation and function
- Nuclear Structure and Function

Papers in ⓘ

Aging 2
Cellular and Molecular Neuroscience 7
- Genetic Neurodegenerative Diseases 6

Co-authors: I. Mahjneh (6 shared papers)Sharon Keers (6 shared papers)Isabelle Richard (5 shared papers)Elizabeth Vafiadaki (4 shared papers)Tom Strachan (4 shared papers)J. Beckmann (3 shared papers)Zohar Argov (3 shared papers)Kate Bushby (3 shared papers)
Journals: Genomics (4 papers)Neuromuscular Disorders (3 papers)Nature Genetics (2 papers)Human Molecular Genetics (2 papers)Hepatology (1 paper)
Partner nations: United Kingdom United States France

In The Last Decade

Rumaisa Bashir

20 papers receiving 1.7k citations

Hit Papers

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A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B 1998 · 526 citations

Peers

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-authors

The 25 scholars most cited alongside Rumaisa Bashir, 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 Rumaisa Bashir Line = papers co-authored together Rumaisa Bashir links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B Nature Genetics ·Rumaisa Bashir, S. Britton, Tom Strachan, Sharon Keers, Elizabeth Vafiadaki, Majlinda Lako, Isabelle Richard, Sylvie Marchand, Nathalie Bourg, Zohar Argov, Menachem Sadeh, I. Mahjneh, Gianpiero Marconi, Maria Rita Passos‐Bueno, Eloisa De Sá Moreira, Mayana Zatz, J. Beckmann, Kate Bushby Hit paper breakdown →	1998	526
2	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 ·Véronique Bolduc, Gareth Marlow, Kym M. Boycott, Khalil Saleki, Hiroshi Inoue, J. Kroon, Mitsuo Itakura, Yves Robitaille, Lucie Parent, Frank Baas, Kuniko Mizuta, Nobuyuki Kamata, Isabelle Richard, Wim H.J.P. Linssen, I. Mahjneh, Marjolein Visser, Rumaisa Bashir, Bernard Brais	2010	195
3	Investigation of the role of polymorphisms at the alcohol and aldehyde dehydrogenase loci in genetic predisposition to alcohol-related end-organ damage Hepatology ·Christopher P. Day, Rumaisa Bashir, Oliver James, Margaret F. Bassendine, David W. Crabb, Holly R. Thomasson, Ting‐Kai Li, Howard J. Edenberg	1991	131
4	Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) Neuromuscular Disorders ·Louise V.B. Anderson, Ruth M Harrison, Robert Pogue, Elizabeth Vafiadaki, C. Pollitt, Keith Davison, Jennifer A. Moss, Sharon Keers, Angela Pyle, Pamela J. Shaw, I. Mahjneh, Zohar Argov, Cheryl R. Greenberg, Klaus Wrogemann, Tulio E. Bertorini, Hans H. Goebel, J. Beckmann, Rumaisa Bashir, Kate Bushby	2000	113
5	A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis piamentosa Human Molecular Genetics ·Chris F. Inglehearn, T J Keen, Rumaisa Bashir, Marcelle Jay, Fred W. Fitzke, Alan C.Bird, A L Crombie, Shomi S. Bhattacharya	1992	101
6	Muscular dystrophy due to dysferlin deficiency in Libyan Jews Brain ·Zohar Argov, Menachem Sadeh, Kineret Mazor, Dov Soffer, Esther Kahana, Iris Eisenberg, Stella Mitrani‐Rosenbaum, Isabelle Richard, J. Beckmann, Sharon Keers, Rumaisa Bashir, Kate Bushby, Hanna Rosenmann	2000	77
7	A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p Nature Genetics ·Chris F. Inglehearn, Simon Carter, TJeffrey Keen, Janet C. Lindsey, A. Stephenson, Rumaisa Bashir, May Al-Maghtheh, Anthony T. Moore, Marcelle Jay, Alan C. Bird, Shomi S. Bhattacharya	1993	69
8	The Third Human FER-1-like Protein Is Highly Similar to Dysferlin Genomics ·S. Britton, Tom C. Freeman, Elizabeth Vafiadaki, Sharon Keers, Ruth Harrison, Kate Bushby, Rumaisa Bashir	2000	59
9	Localisation of a gene for Darier's disease Human Molecular Genetics ·Rumaisa Bashir, Colin S. Munro, Susan Vaneta Mason, A. Stephenson, Jonathan L. Rees, Tom Strachan	1993	54
10	Lack of Correlation between Outcomes of Membrane Repair Assay and Correction of Dystrophic Changes in Experimental Therapeutic Strategy in Dysferlinopathy PLoS ONE ·William Lostal, Marc Bartoli, Carinne Roudaut, Nathalie Bourg, Martin Krahn, Marina Pryadkina, Patrick Borel, Laurence Suel, Joseph A. Roche, Daniel Stockholm, Robert J. Bloch, Nicolas Lévy, Rumaisa Bashir, Isabelle Richard	2012	53
11	A new distal myopathy with mutation in anoctamin 5 Neuromuscular Disorders ·I. Mahjneh, Jyoti K. Jaiswal, Antti Lamminen, Mirja Somer, Gareth Marlow, Sari Kiuru‐Enari, Rumaisa Bashir	2010	50
12	Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation Neuroreport ·Elizabeth Vafiadaki, André Reis, Sharon Keers, Ruth Harrison, Louise V.B. Anderson, Thomas Raffelsberger, Silva Ivanova, Harald Höger, Reginald E. Bittner, Kate Bushby, Rumaisa Bashir	2001	49
13	Patients with a Non‐dysferlin Miyoshi Myopathy have a Novel Membrane Repair Defect Traffic ·Jyoti K. Jaiswal, Gareth Marlow, Gillian Summerill, I. Mahjneh, Sebastian Mueller, Maria Hill, Katsuya Miyake, Hannelore Haase, Louise V.B. Anderson, Isabelle Richard, Sari Kiuru‐Enari, Paul L. McNeil, Sanford M. Simon, Rumaisa Bashir	2006	45
14	Genetic and Physical Mapping at the Limb-Girdle Muscular Dystrophy Locus (LGMD2B) on Chromosome 2p Genomics ·Rumaisa Bashir, Sharon Keers, Tom Strachan, Rita Passos-Bueno, Mayana Zatz, Jean Weissenbach, Denis Le Paslier, Miriam H. Meisler, Kate Bushby	1996	44
15	Dysferlin Deficiency Shows Compensatory Induction of Rab27A/Slp2a That May Contribute to Inflammatory Onset American Journal Of Pathology ·Akanchha Kesari, Mitsunori Fukuda, Susan M. Knoblach, Rumaisa Bashir, Gustavo A. Nader, Deepak A. Rao, Kanneboyina Nagaraju, Eric P. Hoffman	2008	39
16	Solution Structure of the Inner DysF Domain of Myoferlin and Implications for Limb Girdle Muscular Dystrophy Type 2B Journal of Molecular Biology ·Pryank Patel, Richard Harris, Stella Geddes, Eugen‐Matthias Strehle, James D. Watson, Rumaisa Bashir, K. Bushby, Paul C. Driscoll, N.H. Keep	2008	33
17	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 ·José L. Jiménez, Rumaisa Bashir	2007	31
18	Selective pattern of muscle involvement seen in distal muscular dystrophy associated with anoctamin 5 mutations: A follow-up muscle MRI study Neuromuscular Disorders ·I. Mahjneh, Rumaisa Bashir, Sari Kiuru‐Enari, Wim H.J.P. Linssen, Antti Lamminen, Marjolein Visser	2012	24
19	Aup1, a Novel Gene on Mouse Chromosome 6 and Human Chromosome 2p13 Genomics ·Wonhee Jang, John Weber, Rumaisa Bashir, Kate Bushby, Miriam H. Meisler	1996	11
20	Linkage Analyses in British Pedigrees Suggest a Single Locus for Darier Disease and Narrow the Location to the Interval between D12S105 and D12S129 Genomics ·Simon Carter, S Bryce, Colin S. Munro, Eugene Healy, Rumaisa Bashir, Jean Weissenbach, Janine LeBlanc-Straceski, Raju Kucherlapati, A. Stephenson, Jonathan L. Rees, Tom Strachan	1994	8

About Rumaisa Bashir

Rumaisa Bashir is a scholar working on Aging, Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology and Physiology, having authored 20 papers that have together received 1.7k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (12 papers), Genetic Neurodegenerative Diseases (6 papers), Nuclear Structure and Function (4 papers), RNA Research and Splicing (3 papers), Advanced biosensing and bioanalysis techniques (2 papers), Ion channel regulation and function (2 papers), Genetic and rare skin diseases. (2 papers) and Cardiomyopathy and Myosin Studies (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (405 citations), Molecular Biology (1.5k citations), Cell Biology (286 citations), Cardiology and Cardiovascular Medicine (343 citations) and Genetics (152 citations). Rumaisa Bashir has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include I. Mahjneh, Sharon Keers, Isabelle Richard, Elizabeth Vafiadaki, Tom Strachan, J. Beckmann, Zohar Argov, Kate Bushby, S. Britton and Mayana Zatz. Their work appears in journals such as Genomics, Neuromuscular Disorders, Nature Genetics, Human Molecular Genetics and Hepatology.

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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