Louise V.B. Anderson

4.4k citations

53 papers · 3.0k indexed · h-index 31

Molecular Biology top 2%
Cellular and Molecular Neuroscience top 2%
Cell Biology top 1%
Cardiology and Cardiovascular Medicine top 5%
Physiology top 5%

Co-authors: Keith Davison Kate Bushby J. Beckmann I. Mahjneh Sharon Keers Kiichiro Matsumura Teruo Shimizu Zohar Argov
Topics: Muscle Physiology and Disorders (49 papers)Genetic Neurodegenerative Diseases (15 papers)Calpain Protease Function and Regulation (13 papers)
Cited by: Cell Biology Cellular and Molecular Neuroscience Molecular Biology
Journals: Journal of Biological Chemistry Nature Medicine Neurology
Partner nations: United Kingdom United States France

In The Last Decade

Louise V.B. Anderson

53 papers receiving 3.0k citations

Peers

Countries citing papers authored by Louise V.B. Anderson

Since Specialization

Citations

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

Fields of papers citing papers by Louise V.B. Anderson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louise V.B. Anderson. 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 Louise V.B. Anderson. The network helps show where Louise V.B. Anderson may publish in the future.

Co-authorship network of co-authors of Louise V.B. Anderson

This figure shows the co-authorship network connecting the top 25 collaborators of Louise V.B. Anderson. A scholar is included among the top collaborators of Louise V.B. Anderson 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 Louise V.B. Anderson. Louise V.B. Anderson 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

#	Work	Indexed citations
1	Patients with a Non‐dysferlin Miyoshi Myopathy have a Novel Membrane Repair Defect 2006 ·Traffic ·Jyoti K. Jaiswal,Gareth Marlow,(unknown),I. Mahjneh,(unknown),Maria Hill,Katsuya Miyake,Hannelore Haase,Louise V.B. Anderson,Isabelle Richard,Sari Kiuru‐Enari,Paul L. McNeil,Sanford M. Simon,Rumaisa Bashir	45
2	Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display 2005 ·European Journal of Human Genetics ·Yanchao Huang,Peter Verheesen,Andreas Roussis,(unknown),Ieke B. Ginjaar,Faye Haldane,Steve Laval,Louise V.B. Anderson,Theo Verrips,Rune R. Frants,Hans de Haard,Kate Bushby,Johan T. den Dunnen,Silvère M. van der Maarel	52
3	The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice 2005 ·Neuromuscular Disorders ·Maja von der Hagen,Steven H. Laval,Lynsey Cree,Faye Haldane,Matthew Pocock,Ilka Wappler,Heiko Peters,Herbert A. Reitsamer,Harald Höger,(unknown),Felicitas Oberndorfer,Louise V.B. Anderson,Volker Straub,Reginald E. Bittner,Kate Bushby	41
4	Abnormalities in α-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies 2004 ·American Journal Of Pathology ·S. Brown,Silvia Torelli,Martin Brockington,Yeliz Yuva,C. Jimenez‐Mallebrera,Lucy Feng,Louise V.B. Anderson,I. Ugo,Stephan Kröger,Kate Bushby,Thomas Voit,Caroline A. Sewry,Francesco Muntoni	134
5	Sarcoglycans of the zebrafish: orthology and localization to the sarcolemma and myosepta of muscle 2003 ·Biochemical and Biophysical Research Communications ·Stephen P. Chambers,Louise V.B. Anderson,(unknown),Andrew Dodd,Donald R. Love	18
6	Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus 2003 ·Neurogenetics ·Désirée von Tell,Carl E.G. Bruder,Louise V.B. Anderson,Maria Anvret,Gabrielle Åhlberg	6
7	Clinical variability in calpainopathy: What makes the difference? 2002 ·European Journal of Human Genetics ·Flavia Paula,Mariz Vainzof,Maria Rita Passos‐Bueno,Rita de Cássia M. Pavanello,Sérgio Russo Matioli,Louise V.B. Anderson,Vincenzo Nigro,Mayana Zatz	79
8	Muscular dystrophy : methods and protocols 2001 ·Humana Press eBooks ·K. Bushby,Louise V.B. Anderson	17
9	Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations 2001 ·Neuromuscular Disorders ·I. Mahjneh,Gianpiero Marconi,Kate Bushby,Louise V.B. Anderson,(unknown),Hannu Somer	63
10	Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies 2001 ·Neuromuscular Disorders ·Robert Pogue,Louise V.B. Anderson,Angela Pyle,Caroline A. Sewry,C. Pollitt,Margaret A. Johnson,Keith Davison,Jennifer A. Moss,Eugenio Mercuri,Francesco Muntoni,K. Bushby	32
11	Evaluation of the dystrophin–glycoprotein complex, α-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers 2001 ·Neuromuscular Disorders ·Natasha J. Olby,(unknown),Louise V.B. Anderson,Louis M. Kunkel,Carsten G. Bönnemann	7
12	Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies 2001 ·Journal of Molecular Neuroscience ·Mariz Vainzof,Louise V.B. Anderson,Elizabeth M. McNally,Dawn Belt Davis,Georgine Faulkner,(unknown),Eloísa S. Moreira,Rita C.M. Pavanello,Maria Rita Passos‐Bueno,Mayana Zatz	53
13	Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family 2000 ·European Journal of Human Genetics ·Ieke B. Ginjaar,Alexander L.J. Kneppers,(unknown),Louise V.B. Anderson,(unknown),Judith C. van Deutekom,(unknown),Johan T. den Dunnen,Egbert Bakker	73
14	Diagnostic Protein Expression in Human Muscle Biopsies 2000 ·Brain Pathology ·Antje Bornemann,Louise V.B. Anderson	27
15	Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A 1999 ·Nature Medicine ·Stephen Baghdiguian,Marianne Martin,Isabelle Richard,Françoise Pons,Catherine Astier,Nathalie Bourg,Ronald T. Hay,(unknown),Georges Halaby,Jacques Loiselet,Louise V.B. Anderson,Adolfo López de Munaín,Michel Fardeau,Paul Mangeat,J. Beckmann,Marie‐Paule Lefranc	240
16	Characterization of the Transmembrane Molecular Architecture of the Dystroglycan Complex in Schwann Cells 1999 ·Journal of Biological Chemistry ·Fumiaki Saito,Toshihiro Masaki,Keiko Kamakura,Louise V.B. Anderson,Sachiko Fujita,(unknown),Yoshihide Sunada,Teruo Shimizu,Kiichiro Matsumura	66
17	Molecular analysis of a spontaneous dystrophin `knockout' dog 1999 ·Neuromuscular Disorders ·Scott J. Schatzberg,Natasha J. Olby,Matthew Breen,Louise V.B. Anderson,Cordelia F. Langford,(unknown),Steve D. Wilton,Caroline J. Zeiss,M. M. Binns,Joe N. Kornegay,Glenn E. Morris,Nicholas Sharp	82
18	Dystroglycan Is a Dual Receptor for Agrin and Laminin-2 in Schwann Cell Membrane 1996 ·Journal of Biological Chemistry ·Hiroki Yamada,Alain J. Denzer,Hisae Hori,Takeshi Tanaka,Louise V.B. Anderson,Sachiko Fujita,(unknown),Teruo Shimizu,Markus A. Rüegg,Kiichiro Matsumura	96
19	Abnormalities in α-, β- and γ-sarcoglycan in patients with limb-girdle muscular dystrophy 1996 ·Neuromuscular Disorders ·Caroline A. Sewry,Jacqueline Taylor,Louise V.B. Anderson,E Ozawa,Robert Pogue,Fédérica Piccolo,Kate Bushby,Victor Dubowitz,Francesco Muntoni	57
20	Optimized protein diagnosis in the autosomal recessive limb-girdle muscular dystrophies 1996 ·Neuromuscular Disorders ·Louise V.B. Anderson	22

About Louise V.B. Anderson

Louise V.B. Anderson is a scholar working on Cell Biology, Cellular and Molecular Neuroscience and Molecular Biology, having authored 53 papers that have together received 3.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (49 papers), Genetic Neurodegenerative Diseases (15 papers) and Calpain Protease Function and Regulation (13 papers). The work is most often cited by research in Cell Biology (773 citations), Cellular and Molecular Neuroscience (844 citations) and Molecular Biology (2.7k citations). Louise V.B. Anderson has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Keith Davison, Kate Bushby, J. Beckmann, I. Mahjneh, Sharon Keers, Kiichiro Matsumura, Teruo Shimizu, Zohar Argov, Caroline A. Sewry and S. Britton. Their work appears in journals such as Journal of Biological Chemistry, Nature Medicine and Neurology.

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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