K Hart

927 total citations
15 papers, 786 citations indexed

About

K Hart is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, K Hart has authored 15 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in K Hart's work include Muscle Physiology and Disorders (11 papers), Genetic Neurodegenerative Diseases (4 papers) and Virus-based gene therapy research (3 papers). K Hart is often cited by papers focused on Muscle Physiology and Disorders (11 papers), Genetic Neurodegenerative Diseases (4 papers) and Virus-based gene therapy research (3 papers). K Hart collaborates with scholars based in United Kingdom, United States and Netherlands. K Hart's co-authors include Martin Bobrow, Ronald G. Worton, Peter N. Ray, Sharon Bodrug, Victor Dubowitz, M. W. Thompson, Peter S. Harper, Arthur H.M. Burghes, Shirley Hodgson and Henry J. Klamut and has published in prestigious journals such as Science, Cell and Nucleic Acids Research.

In The Last Decade

K Hart

15 papers receiving 767 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
K Hart United Kingdom 12 703 201 182 150 113 15 786
Jeffrey Murray United Kingdom 7 605 0.9× 284 1.4× 90 0.5× 141 0.9× 100 0.9× 8 766
Elizabeth F. Gillard United Kingdom 11 758 1.1× 233 1.2× 328 1.8× 85 0.6× 141 1.2× 14 888
Eri Kondo-Iida Japan 8 842 1.2× 105 0.5× 105 0.6× 99 0.7× 209 1.8× 13 939
John Hildyard United Kingdom 12 775 1.1× 197 1.0× 103 0.6× 66 0.4× 47 0.4× 23 856
G. A. Danieli Italy 15 538 0.8× 85 0.4× 328 1.8× 58 0.4× 152 1.3× 37 804
K. Azibi France 14 583 0.8× 146 0.7× 162 0.9× 81 0.5× 220 1.9× 18 770
T O'Brien United Kingdom 8 382 0.5× 147 0.7× 48 0.3× 73 0.5× 115 1.0× 11 483
Alice Steinbrecher Germany 5 638 0.9× 93 0.5× 83 0.5× 66 0.4× 125 1.1× 7 725
Flavia Blàsevich Italy 14 412 0.6× 44 0.2× 72 0.4× 57 0.4× 65 0.6× 31 525
Chun Long United States 9 852 1.2× 400 2.0× 311 1.7× 69 0.5× 74 0.7× 13 947

Countries citing papers authored by K Hart

Since Specialization
Citations

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

Fields of papers citing papers by K Hart

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Hart

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

All Works

15 of 15 papers shown
1.
Andresen, Brage Storstein, Peter Bross, Szabolcs Udvari, et al.. (1997). The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?. Human Molecular Genetics. 6(5). 695–707. 105 indexed citations
2.
Roberts, Roland G., et al.. (1989). Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy. Nucleic Acids Research. 17(2). 811–811. 48 indexed citations
3.
Hart, K, Stephen Abbs, Martin C. Wapenaar, et al.. (1989). Molecular deletions in the Duchenne/Becker muscular dystrophy gene. Clinical Genetics. 35(4). 251–260. 8 indexed citations
4.
Hart, K, Stephen Abbs, & Martin Bobrow. (1989). Pathogenic and nonpathogenic deletions in two families with Duchenne muscular dystrophy. American Journal of Medical Genetics. 33(1). 142–145. 4 indexed citations
5.
Benham, Frances, K Hart, John A. Crolla, et al.. (1989). A method for generating hybrids containing nonselected fragments of human chromosomes. Genomics. 4(4). 509–517. 78 indexed citations
6.
Hodgson, Shirley, K Hart, Stephen Abbs, et al.. (1989). Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.. Journal of Medical Genetics. 26(11). 682–693. 74 indexed citations
7.
Wapenaar, Martin C., Tim Kievits, K Hart, et al.. (1988). A deletion hot spot in the Duchenne muscular dystrophy gene. Genomics. 2(2). 101–108. 99 indexed citations
8.
Hart, K, Henry J. Klamut, Nick Thomas, et al.. (1988). Frame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy. Science. 242(4879). 755–759. 240 indexed citations
9.
Hart, K, Anthony P. Monaco, Louis M. Kunkel, & Martin Bobrow. (1987). A small deletion in the Duchenne/Becker muscular dystrophy locus ?a functionally important region?. Human Genetics. 77(1). 88–91. 6 indexed citations
10.
Hart, K, et al.. (1987). DNA deletions in mild and severe Becker muscular dystrophy. Human Genetics. 75(3). 281–285. 39 indexed citations
11.
Hodgson, Shirley, A.P. Walker, K Hart, et al.. (1987). The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.. Journal of Medical Genetics. 24(3). 152–159. 17 indexed citations
12.
Walker, A.P., K Hart, Charlotte G. Cole, et al.. (1986). Linkage studies in Duchenne and Becker muscular dystrophies.. Journal of Medical Genetics. 23(6). 538–547. 14 indexed citations
13.
14.
Hart, K, Charlotte G. Cole, A.P. Walker, et al.. (1986). The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.. Journal of Medical Genetics. 23(6). 516–520. 19 indexed citations
15.
Gillespie, David A., K Hart, & John A. Wyke. (1985). Rearrangements of viral and cellular DNA are often associated with expression of Rous sarcoma virus in rat cells. Cell. 41(1). 279–287. 20 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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