K. Bushby

8.9k total citations · 4 hit papers
38 papers, 4.7k citations indexed

About

K. Bushby is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, K. Bushby has authored 38 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in K. Bushby's work include Muscle Physiology and Disorders (29 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Genetic Neurodegenerative Diseases (8 papers). K. Bushby is often cited by papers focused on Muscle Physiology and Disorders (29 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Genetic Neurodegenerative Diseases (8 papers). K. Bushby collaborates with scholars based in United Kingdom, United States and France. K. Bushby's co-authors include David J. Birnkrant, Laura E. Case, Shree Pandya, Jean Tomezsko, Paula R. Clemens, Linda Cripe, Richard S. Finkel, Frederic Shapiro, Carolyn M. Constantin and Craig M. McDonald and has published in prestigious journals such as The Lancet, Journal of Molecular Biology and Brain.

In The Last Decade

K. Bushby

38 papers receiving 4.6k 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.

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

2009 1.4k citations K. Bushby, Richard S. Finkel et al. The Lancet Neurology profile →
Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care

2009 785 citations K. Bushby, Richard S. Finkel et al. The Lancet Neurology profile →
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management

2018 781 citations David J. Birnkrant, K. Bushby et al. The Lancet Neurology profile →
Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management

2018 651 citations David J. Birnkrant, K. Bushby et al. The Lancet Neurology profile →

Peers

K. Bushby

GENET

CCM

CMN

Shree Pandya United States

David J. Birnkrant United States

Julaine Florence United States

Wendy King United States

Linda Cripe United States

Jean Tomezsko United States

Laura E. Case United States

Brenda Wong United States

Francesco Muntoni United Kingdom

Kathi Kinnett United States

Shree Pandya United States

K. Bushby

4.2k ×1.1

1.2k ×1.1

GENET

1.0k ×1.1

CCM

953 ×1.3

860 ×1.2

CMN

Citations per year, relative to K. Bushby K. Bushby (= 1×) peers Shree Pandya

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-authorship network of co-authors of K. Bushby

This figure shows the co-authorship network connecting the top 25 collaborators of K. Bushby. A scholar is included among the top collaborators of K. Bushby 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 K. Bushby. K. Bushby 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

Birnkrant, David J., K. Bushby, Carla Bann, et al.. (2018). Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. The Lancet Neurology. 17(3). 251–267. 781 indexed citations breakdown →

Birnkrant, David J., K. Bushby, Carla Bann, et al.. (2018). Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. The Lancet Neurology. 17(4). 347–361. 651 indexed citations breakdown →

Landfeldt, Erik, Anna Mayhew, Volker Straub, et al.. (2018). Psychometric analysis of the pediatric quality of life inventory 3.0 neuromuscular module administered to patients with duchenne muscular dystrophy: A rasch analysis. Muscle & Nerve. 58(3). 367–373. 9 indexed citations

Landfeldt, Erik, Peter Lindgren, Christopher F. Bell, et al.. (2015). Compliance to Care Guidelines for Duchenne Muscular Dystrophy. Journal of Neuromuscular Diseases. 2(1). 63–72. 44 indexed citations

Landfeldt, Erik, Anna Mayhew, Michelle Eagle, et al.. (2015). Development and psychometric analysis of the Duchenne muscular dystrophy Functional Ability Self-Assessment Tool (DMDSAT). Neuromuscular Disorders. 25(12). 937–944. 19 indexed citations

Birnkrant, David J., K. Bushby, Raouf Amin, et al.. (2010). The respiratory management of patients with duchenne muscular dystrophy: A DMD care considerations working group specialty article. Pediatric Pulmonology. 45(8). 739–748. 111 indexed citations

Bushby, K., Richard S. Finkel, David J. Birnkrant, et al.. (2009). Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. The Lancet Neurology. 9(1). 77–93. 1378 indexed citations breakdown →

Bushby, K., Richard S. Finkel, David J. Birnkrant, et al.. (2009). Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. The Lancet Neurology. 9(2). 177–189. 785 indexed citations breakdown →

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

10.

Reha, A., Gary Elfring, Richard S. Finkel, et al.. (2008). T.P.5.01 Phase 2b Study of PTC124 in Duchenne/Becker muscular dystrophy (DMD/BMD): Demographic and other baseline data. Neuromuscular Disorders. 18(9-10). 823–823. 5 indexed citations

11.

Salih, Mustafa A., J. Andoni Urtizberea, France Leturcq, et al.. (2007). G.P.8.12 Molecular characterization and clinical update on one of the earliest described families with severe childhood autosomal recessive muscular dystrophy (SCARMD). Neuromuscular Disorders. 17(9-10). 813–813. 2 indexed citations

12.

Clement, Emma, E. Mercuri, Mary Rutherford, et al.. (2007). C.P.3.06 Spectrum of brain changes and genotype-phenotype correlations in secondary dystroglycanopathies. Neuromuscular Disorders. 17(9-10). 871–871. 1 indexed citations

13.

Pepe, Guglielmina, Laura Lucarini, Ruizhu Zhang, et al.. (2005). COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophy. Annals of Neurology. 59(1). 190–195. 27 indexed citations

14.

McDermott, Christopher, Andrew J. Grierson, Jonathan Wood, et al.. (2003). Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation. Annals of Neurology. 54(6). 748–759. 90 indexed citations

15.

Bushby, K. & Louise V.B. Anderson. (2001). Muscular dystrophy : methods and protocols. Humana Press eBooks. 17 indexed citations

16.

Bushby, K.. (1999). Making sense of the limb-girdle muscular dystrophies. Brain. 122(8). 1403–1420. 130 indexed citations

17.

Tomkins, Janine, Janet Y. Slade, Paul G. Ince, et al.. (1998). Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS). Neuroreport. 9(17). 3967–3970. 123 indexed citations

18.

Mahjneh, I., K. Bushby, A. Pizzi, R. Bashir, & Gianpiero Marconi. (1996). Limb-girdle muscular dystrophy: a follow-up study of 79 patients. Acta Neurologica Scandinavica. 94(3). 177–189. 17 indexed citations

19.

Passos-Bueno, Maria-Rita, Eloísa S. Moreira, Mariz Vainzof, et al.. (1995). Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region. Genomics. 27(1). 192–195. 31 indexed citations

20.

Bushby, K., et al.. (1991). Prevalence and incidence of Becker muscular dystrophy. The Lancet. 337(8748). 1022–1024. 143 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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