Hafsa Mamsa

1.2k total citations
8 papers, 336 citations indexed

About

Hafsa Mamsa is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Hafsa Mamsa has authored 8 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 2 papers in Clinical Biochemistry. Recurrent topics in Hafsa Mamsa's work include Genetic Neurodegenerative Diseases (4 papers), Ion channel regulation and function (2 papers) and Mitochondrial Function and Pathology (2 papers). Hafsa Mamsa is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Ion channel regulation and function (2 papers) and Mitochondrial Function and Pathology (2 papers). Hafsa Mamsa collaborates with scholars based in United States, Australia and Denmark. Hafsa Mamsa's co-authors include Joanna C. Jen, Robert W. Baloh, Jijun Wan, Stanley F. Nelson, Boukje de Vries, Rune R. Frants, S. L. M. Bakker, Michel D. Ferrari, Kaate R. J. Vanmolkot and Arn M. J. M. van den Maagdenberg and has published in prestigious journals such as Brain, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Hafsa Mamsa

8 papers receiving 333 citations

Peers

Countries citing papers authored by Hafsa Mamsa

Since Specialization

Citations

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

Fields of papers citing papers by Hafsa Mamsa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hafsa Mamsa

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Multi-omics analysis of sarcospan overexpression in mdx skeletal muscle reveals compensatory remodeling of cytoskeleton-matrix interactions that promote mechanotransduction pathways 2023 ·Skeletal Muscle ·(unknown), (unknown), Hafsa Mamsa, Pranav Kannan, (unknown), Cynthia Shu, Elizabeth M. Gibbs, (unknown), Yerbol Z. Kurmangaliyev, (unknown), Kirk C. Hansen, Rachelle H. Crosbie	8
2	Sarcospan increases laminin-binding capacity of α-dystroglycan to ameliorate DMD independent of Galgt2 2021 ·Human Molecular Genetics ·Hafsa Mamsa, (unknown), (unknown), Aaron M. Beedle, Rachelle H. Crosbie	6
3	Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia 2016 ·Brain ·Jijun Wan, Janos Steffen, Michael Yourshaw, Hafsa Mamsa, Erik Andersen, Sabine Rudnik‐Schöneborn, Kate Pope, Katherine B. Howell, Catriona McLean, Andrew J. Kornberg, (unknown), Paul J. Lockhart, Klaus Zerres, Monique M. Ryan, Stanley F. Nelson, Carla M. Koehler, Joanna C. Jen	69
4	A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism 2009 ·Human Molecular Genetics ·Patricia Blanco, Anja P. Einholm, Hafsa Mamsa, (unknown), Hugo Gutiérrez‐de‐Terán, J. Romero, Mads S. Toustrup-Jensen, Ãngel Carracedo, Joanna C. Jen, Bente Vilsen, M.J. Sobrido	45
5	Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake 2009 ·Archives of Neurology ·Boukje de Vries, Hafsa Mamsa, Anine H Stam, Jijun Wan, S. L. M. Bakker, Kaate R. J. Vanmolkot, Joost Haan, Gisela M. Terwindt, Elles M. J. Boon, Bruce D. Howard, Rune R. Frants, Robert W. Baloh, Michel D. Ferrari, Joanna C. Jen, Arn M. J. M. van den Maagdenberg	99
6	Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea 2007 ·Muscle & Nerve ·Steven J. Shook, Hafsa Mamsa, Joanna C. Jen, Robert W. Baloh, Lan Zhou	27
7	Prolonged hemiplegic episodes in children due to mutations in ATP1A2 2006 ·Journal of Neurology Neurosurgery & Psychiatry ·Joanna C. Jen, Andrea Klein, Eugen Boltshauser, Michael S. Cartwright, E. Steve Roach, Hafsa Mamsa, Robert W. Baloh	39
8	A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity 2005 ·Human Molecular Genetics ·Hane Lee, Joanna C. Jen, Hui Wang, Zugen Chen, Hafsa Mamsa, Chiara Sabatti, Robert W. Baloh, Stanley F. Nelson	43

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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