Chris A. Feener

840 total citations
8 papers, 712 citations indexed

About

Chris A. Feener is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Chris A. Feener has authored 8 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Chris A. Feener's work include Muscle Physiology and Disorders (6 papers), Cardiomyopathy and Myosin Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Chris A. Feener is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Cardiomyopathy and Myosin Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Chris A. Feener collaborates with scholars based in United States and Japan. Chris A. Feener's co-authors include Louis M. Kunkel, M. Kœnig, Frederick M. Boyce, E Ozawa, Sara Selig, Andrew H. Ahn, Minoru Yoshida, Mark S. Anderson, L M Kunkel and Yuriko Hagiwara and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Genomics.

In The Last Decade

Chris A. Feener

8 papers receiving 699 citations

Peers

Chris A. Feener

MB

PHYSI

CCM

CB

GENET

Jim Talbot Canada

Keith Davison United Kingdom

L. Specht United States

Catherine M. Pollina United States

J.G. Dickson United Kingdom

J.Rafael M. Gorospe United States

G K Suthers Australia

Michael S. Hudecki United States

U. L. Fairbrother United Kingdom

Christian Pastoret France

Jim Talbot Canada

Chris A. Feener

553 ×0.9

MB

141 ×1.0

PHYSI

137 ×1.0

CCM

85 ×0.7

CB

57 ×0.5

GENET

Citations per year, relative to Chris A. Feener Chris A. Feener (= 1×) peers Jim Talbot

Countries citing papers authored by Chris A. Feener

Since Specialization

Citations

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

Fields of papers citing papers by Chris A. Feener

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chris A. Feener. 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 Chris A. Feener. The network helps show where Chris A. Feener may publish in the future.

Co-authorship network of co-authors of Chris A. Feener

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

All Works

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8 of 8 papers shown

1.

Kang, Peter B., Chris A. Feener, Elicia Estrella, et al.. (2007). LGMD2I in a North American population. BMC Musculoskeletal Disorders. 8(1). 115–115. 24 indexed citations

2.

Takano, Atsushi, Hideo Honda, M Sakai, et al.. (2000). Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations. Muscle & Nerve. 23(5). 807–810. 19 indexed citations

3.

Bönnemann, Carsten G., Gerald F. Cox, Frederic Shapiro, et al.. (2000). A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy. Proceedings of the National Academy of Sciences. 97(3). 1212–1217. 82 indexed citations

4.

Puccio, Hélène, Chris A. Feener, Daniel J. Schaid, et al.. (1997). The genomic organization of human dystrobrevin. Neurogenetics. 1(1). 37–42. 25 indexed citations

5.

Feener, Chris A., et al.. (1994). Cloning of Human Microtubule-Associated Protein 1B and the Identification of a Related Gene on Chromosome 15. Genomics. 22(2). 273–280. 36 indexed citations

6.

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

7.

Feener, Chris A., Frederick M. Boyce, & Louis M. Kunkel. (1991). Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene.. PubMed. 48(3). 621–7. 118 indexed citations

8.

Feener, Chris A., M. Kœnig, & Louis M. Kunkel. (1989). Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus. Nature. 338(6215). 509–511. 298 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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