L M Kunkel

1.1k total citations
19 papers, 914 citations indexed

About

L M Kunkel is a scholar working on Molecular Biology, Cell Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, L M Kunkel has authored 19 papers receiving a total of 914 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Cell Biology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in L M Kunkel's work include Muscle Physiology and Disorders (10 papers), Biotin and Related Studies (3 papers) and RNA modifications and cancer (3 papers). L M Kunkel is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Biotin and Related Studies (3 papers) and RNA modifications and cancer (3 papers). L M Kunkel collaborates with scholars based in United States, Japan and Australia. L M Kunkel's co-authors include Andrew H. Ahn, Alan H. Beggs, Frederick M. Boyce, Xiaoyan Huang, Ingrid A. Holm, E Ozawa, Eric P. Hoffman, Mark S. Anderson, Kiichi Arahata and Ikuya Nonaka and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Cell Biology and Neurology.

In The Last Decade

L M Kunkel

19 papers receiving 894 citations

Peers

L M Kunkel

PHYSI

CCM

GENET

CMN

M. Wehling United States

Patrizia Ciscato Italy

Michele Hadhazy United States

Barbara C. Byth Canada

Marilyn Davies Australia

Amanda M. Haidet United States

Kinji Kobayashi Japan

Simona Zanotti Italy

Christian Pastoret France

Karine Nguyen France

M. Wehling United States

L M Kunkel

912 ×1.2

370 ×1.7

PHYSI

176 ×0.9

CCM

100 ×0.7

GENET

84 ×0.6

CMN

Citations per year, relative to L M Kunkel L M Kunkel (= 1×) peers M. Wehling

Countries citing papers authored by L M Kunkel

Since Specialization

Citations

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

Fields of papers citing papers by L M Kunkel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L M Kunkel. 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 L M Kunkel. The network helps show where L M Kunkel may publish in the future.

Co-authorship network of co-authors of L M Kunkel

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

All Works

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19 of 19 papers shown

Vardarajan, Badri N., et al.. (2013). Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder. Translational Psychiatry. 3(5). e262–e262. 20 indexed citations

Lidov, Hart G.W. & L M Kunkel. (1998). Dystrophin and Dp140 in the adult rodent kidney.. PubMed. 78(12). 1543–51. 18 indexed citations

Wong, Jenny, et al.. (1997). LGMD 2E in Tunisia is caused by a missense mutation Arg91Leu in β-sarcoglycan. Neuromuscular Disorders. 7(6-7). 460–460. 1 indexed citations

Holm, Ingrid A., Xiaoyan Huang, & L M Kunkel. (1997). Mutational analysis of the PEX gene in patients with X-linked hypophosphatemic rickets.. PubMed. 60(4). 790–7. 119 indexed citations

Taratuto, A.L., Alberto Dubrovsky, L. Mesa, et al.. (1997). α SARCOGLYCAN DEFICIENCY, TWO NOVEL MUTATIONS. Journal of Neuropathology & Experimental Neurology. 56(5). 619–619. 1 indexed citations

Ahn, Andrew H. & L M Kunkel. (1995). Syntrophin binds to an alternatively spliced exon of dystrophin.. The Journal of Cell Biology. 128(3). 363–371. 182 indexed citations

McNally, Elizabeth M., Sara Selig, & L M Kunkel. (1994). Adhalin, the 50 kD dystrophin associated protein, is not the locus for severe childhood autosomal recessive dystrophy (SCARMD). The American Journal of Human Genetics. 55. 2 indexed citations

Ahn, Andrew H., Minoru Yoshida, Mark S. Anderson, et al.. (1994). Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.. Proceedings of the National Academy of Sciences. 91(10). 4446–4450. 110 indexed citations

Brzustowicz, Linda M., Patrick W. Kleyn, Frederick M. Boyce, et al.. (1992). Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6. Genomics. 13(4). 991–998. 23 indexed citations

10.

Byers, T J, Paul E. Neumann, Alan H. Beggs, & L M Kunkel. (1992). ELISA quantitation of dystrophin for the diagnosis of Duchenne and Becker muscular dystrophies.. PubMed. 42(3 Pt 1). 570–6. 14 indexed citations

11.

Beggs, Alan H., Paul E. Neumann, Kiichi Arahata, et al.. (1992). Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.. Proceedings of the National Academy of Sciences. 89(2). 623–627. 21 indexed citations

12.

Laing, Nigel G., Bernadette T. Majda, P. Anthony Akkari, et al.. (1992). Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.. PubMed. 50(3). 576–83. 52 indexed citations

13.

Boyce, Frederick M., et al.. (1991). Dystrophin is transcribed in brain from a distant upstream promoter.. Proceedings of the National Academy of Sciences. 88(4). 1276–1280. 162 indexed citations

14.

Angelini, C., et al.. (1990). Enormous dystrophin in a patient with Becker muscular dystrophy. Neurology. 40(5). 808–808. 30 indexed citations

15.

Arahata, Kiichi, Eric P. Hoffman, L M Kunkel, et al.. (1989). Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses.. Proceedings of the National Academy of Sciences. 86(18). 7154–7158. 134 indexed citations

16.

Kunkel, L M, et al.. (1986). Molecular Genetics of Duchenne Muscular Dystrophy. Cold Spring Harbor Symposia on Quantitative Biology. 51(0). 349–351. 11 indexed citations

17.

Gal, A., T. F. Wienker, Kelvin J.A. Davies, et al.. (1985). Further linkage studies between retinoschisis and cloned dna sequences from the distal xp. 40. 634. 8 indexed citations

18.

Latt, S.A., David M. Kurnit, G Bruns, et al.. (1984). Molecular genetic approaches to human diseases involving mental retardation.. PubMed. 88(5). 561–71. 2 indexed citations

19.

Smith, Kirby D., L M Kunkel, & Samuel H. Boyer. (1976). Isolation and uses of chromosome-specific reiterated DNA. Cytogenetic and Genome Research. 16(1-5). 401–404. 4 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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