K. Bushby

2.6k citations

49 papers · 1.6k indexed · h-index 20

Impact in

Genetics top 5%
- Neurogenetic and Muscular Disorders Research
Molecular Biology top 5%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Nuclear Structure and Function

Papers in

Molecular Biology 44
- Muscle Physiology and Disorders 40
- Nuclear Structure and Function 7
- RNA Research and Splicing 6
Genetics 6
- Neurogenetic and Muscular Disorders Research 6

Co-authors: Steven H. Laval Volker Straub J. Beckmann Louise V.B. Anderson Michela Guglieri I. Mahjneh Francesco Muntoni Lucy Feng
Journals: Neuromuscular Disorders (23 papers)Neurology (2 papers)Developmental Medicine & Child Neurology (2 papers)Journal of Medical Genetics (2 papers)Neuropediatrics (2 papers)
Partner nations: United Kingdom United States France

In The Last Decade

K. Bushby

47 papers receiving 1.5k citations

Peers

Countries citing papers authored by K. Bushby

Since Specialization

Citations

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

Fields of papers citing papers by K. Bushby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	G.P.97 Neuromuscular Disorders ·Anna Sárközy, Ramesh Srinivasan, David J. Rawlings, Kim Jeffrey, Catherine Owen, Volker Straub, Tim Cheetham, K. Bushby	2014	3
2	Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials Brain ·Karen Anthony, Sebahattin Çirak, Silvia Torelli, Giorgio Tasca, Lucy Feng, Virginia Arechavala‐Gomeza, Annarita Armaroli, Michela Guglieri, C.S.M. Straathof, Jan J.G.M. Verschuuren, Annemieke Aartsma‐Rus, I Gede Dirga Surya Arya Widhyadanta, K. Bushby, Volker Straub, Caroline A. Sewry, Alessandra Ferlini, Enzo Ricci, Jennifer E. Morgan, Francesco Muntoni	2011	112
3	Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations Neuromuscular Disorders ·Fatemeh Geranmayeh, Emma Clement, Lucy Feng, Caroline A. Sewry, V.V. Zhabo, R. Mein, Stephen Abbs, Louise Brueton, Anne-Marie Childs, Heinz Jungbluth, David Alfonso Serje Martínez, Bryan Lynch, Jean‐Pierre Lin, Gabriel Chow, Carlos de Sousa, T. E. Harvey, Anirban Majumdar, Volker Straub, K. Bushby, Francesco Muntoni	2010	133
4	New aspects on patients affected by dysferlin deficient muscular dystrophy Journal of Neurology Neurosurgery & Psychiatry ·Lars Klinge, 大毅高山, 浩土田, Judith A. Hudson, Andrea Sarkozy, Gian Luca Vita, Richard Charlton, YeHyeon Shin, Volker Straub, Rita Barresi, Hanns Lochmüller, K. Bushby	2009	61
5	G.P.1.01 Long term steroid use in non-ambulatory patients with Duchenne muscular dystrophy Neuromuscular Disorders ·浩土田, Ding Dai-yong, Kim Jeffrey, Volker Straub, K. Bushby	2007	0
6	G.P.1.08 Steroids in Duchenne muscular dystrophy (DMD): Natural history and clinical evaluation using the North Star Ambulatory Assessment (NSAA) Neuromuscular Disorders ·浩土田, E. Scott, Marion Main, Jennie Sheehan, Martin Teising, Kim Jeffrey, Volker Straub, K. Bushby	2007	1
7	Myoglobinuria in boys with Duchenne muscular dystrophy on corticosteroid therapy Neuromuscular Disorders ·篠倉均, 浩土田, Sultan Albarqi, K. Bushby, Volker Straub	2007	18
8	Congenital arthrogryposis and dilated cardiomyopathy associated with a R644C substitution in the Lamin A/C gene Developmental Medicine & Child Neurology ·Tim Kerr, Dragana Josifova, K. Bushby, Elizabeth Wraige, Keith Pohl, Heinz Jungbluth	2006	3
9	Identification of putative *in vivo* substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice PROTEOMICS ·Shawn Michael Mollenhauer, Elena Kudryashova, Irina Kramerova, Louise V.B. Anderson, J. Beckmann, K. Bushby, Melissa J. Spencer	2006	43
10	Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathy Neurology ·S. Lucioli, Betti Giusti, Eugenio Mercuri, Olga Camacho Vanegas, Laura Lucarini, Gatot Handoko, Andoni Urtizberea, Rabah Ben Yaou, Marianne de Visser, Anneke J. van der Kooi, Christoph Paus, Susan T. Iannaccone, Luciano Merlini, K. Bushby, Francesco Muntoni, Enrico Bertini, Mon‐Li Chu, Guglielmina Pepe	2005	42
11	Limb‐girdle muscular dystrophies – from genetics to molecular pathology Neuropathology and Applied Neurobiology ·Steven H. Laval, K. Bushby	2004	103
12	The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12–14, 2002 Neuromuscular Disorders ·K. Bushby, J. Beckmann	2002	45
13	Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies 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	2001	32
14	Social deprivation in Duchenne muscular dystrophy: population based study BMJ ·K. Bushby, Simon Raybould, S. O’Donnell, J G Steele	2001	9
15	Distribution of cranial MRI abnormalities in patients with symptomatic and subclinical CADASIL. British Journal of Radiology ·Alan Coulthard, S. C. Blank, K. Bushby, Raj N. Kalaria, David J. Burn	2000	45
16	Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development Human Molecular Genetics ·Louise V.B. Anderson, Kenneth Davison, Jessica Moss, C Young, Michael J. Cullen, John Walsh, Mary Ann Johnson, R. Bashir, S. Britton, Sharon Keers, Zohar Argov, I. Mahjneh, Françoise Fougerousse, J. Beckmann, K. Bushby	1999	234
17	Dystrophinopathy or sarcoglycanopathy: the importance of a full diagnostic assessment in suspected manifesting carriers of Duchenne and Becker muscular dystrophy Neuromuscular Disorders ·K. Bushby, Яна Игоревна Воробьёва, Caroline A. Sewry, Robert Pogue, Jacqueline Taylor, C. Pollitt, Francesco Muntoni	1997	3
18	Duchenne Muscular Dystrophy Journal of Medical Genetics ·K. Bushby	1994	118
19	Recent advances in understanding muscular dystrophy. Archives of Disease in Childhood ·K. Bushby	1992	5
20	HEAD CIRCUMFERENCE AND INTELLECTUAL PERFORMANCE OF PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY Developmental Medicine & Child Neurology ·Richard Appleton, K. Bushby, D. Gardner‐Medwin, John L. Welch, Paul J. Kelly	1991	22

About K. Bushby

K. Bushby is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Cell Biology and Cellular and Molecular Neuroscience, having authored 49 papers that have together received 1.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (40 papers), Cardiomyopathy and Myosin Studies (10 papers), Genetic Neurodegenerative Diseases (7 papers), Nuclear Structure and Function (7 papers), Neurogenetic and Muscular Disorders Research (6 papers), RNA Research and Splicing (6 papers), Adipose Tissue and Metabolism (4 papers) and Calpain Protease Function and Regulation (3 papers). The work is most often cited by research in Genetics (265 citations), Molecular Biology (1.4k citations), Cellular and Molecular Neuroscience (303 citations), Cardiology and Cardiovascular Medicine (371 citations) and Immunology and Allergy (89 citations). K. Bushby has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Steven H. Laval, Volker Straub, J. Beckmann, Louise V.B. Anderson, Michela Guglieri, I. Mahjneh, Francesco Muntoni, Lucy Feng, Caroline A. Sewry and John Bourke. Their work appears in journals such as Neuromuscular Disorders, Neurology, Developmental Medicine & Child Neurology, Journal of Medical Genetics and Neuropediatrics.

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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