Glenn Barnes

5.7k total citations
15 papers, 994 citations indexed

About

Glenn Barnes is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Glenn Barnes has authored 15 papers receiving a total of 994 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 9 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Glenn Barnes's work include Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (5 papers) and Fungal and yeast genetics research (3 papers). Glenn Barnes is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (5 papers) and Fungal and yeast genetics research (3 papers). Glenn Barnes collaborates with scholars based in United States, United Kingdom and Italy. Glenn Barnes's co-authors include Richard H. Myers, Mabel P. Duyao, Jayalakshmi Srinidhi, Marcy E. MacDonald, James F. Gusella, C M Ambrose, Michael R. Altherr, Joel Gottesfeld, James R. Rusche and Steve Jones and has published in prestigious journals such as Nature Genetics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Glenn Barnes

15 papers receiving 973 citations

Peers

Countries citing papers authored by Glenn Barnes

Since Specialization

Citations

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

Fields of papers citing papers by Glenn Barnes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Glenn Barnes

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Cardiovascular involvement among collegiate athletes following COVID-19 infection 2022 ·Journal of Clinical and Translational Research ·(unknown), Nicholas G. Murray, Daniel Cipriani, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Glenn Barnes, (unknown)	8
2	Prolonged treatment with pimelic o-aminobenzamide HDAC inhibitors ameliorates the disease phenotype of a Friedreich ataxia mouse model 2011 ·Neurobiology of Disease ·Chiranjeevi Sandi, Ricardo Mouro Pinto, Sahar Al‐Mahdawi, Vahid Ezzatizadeh, Glenn Barnes, Steve Jones, James R. Rusche, Joel Gottesfeld, Mark A. Pook	93
3	Two New Pimelic Diphenylamide HDAC Inhibitors Induce Sustained Frataxin Upregulation in Cells from Friedreich's Ataxia Patients and in a Mouse Model 2010 ·PLoS ONE ·Myriam Rai, Elisabetta Soragni, C. James Chou, Glenn Barnes, Steve Jones, James R. Rusche, Joel Gottesfeld, Massimo Pandolfo	114
4	Reduced Penetrance of the Huntington's Disease Mutation 1997 ·Human Molecular Genetics ·Sandra McNeil, Andrea Novelletto, Jayalakshmi Srinidhi, Glenn Barnes, (unknown), Michael R. Altherr, John J. Wasmuth, J.F. Gusella, Marcy E. MacDonald, Richard H. Myers	99
5	1996 ·Cold Spring Harbor Symposia on Quantitative Biology ·Marcy E. MacDonald, Mabel P. Duyao, (unknown), Anna B. Auerbach, Angela Ryan, Glenn Barnes, Jacqueline K. White, Wojtek Auerbach, J.-P. G. Vonsattel, J.F. Gusella, Alexandra L. Joyner	8
6	De novo expansion of a (CAG)n repeat in sporadic Huntington's disease 1993 ·Nature Genetics ·Richard H. Myers, Marcy E. MacDonald, Walter J. Koroshetz, Mabel P. Duyao, C M Ambrose, Sherryl A. Taylor, Glenn Barnes, Jayalakshmi Srinidhi, Carol Sze Ki Lin, William L. Whaley, Alice Lazzarini, Michael Schwarz, G. Wolff, E. D. Bird, J.-P. G. Vonsattel, James F. Gusella	184
7	A gene from chromosome 4p 16.3 with similarity to a superfamily of transporter proteins 1993 ·Human Molecular Genetics ·Mabel P. Duyao, Sherryl A. Taylor, Alan Buckler, Christine Ambrose, Carol Sze Ki Lin, (unknown), Deanna M. Church, Glenn Barnes, John J. Wasmuth, David E. Housman, Marcy E. MacDonald, James F. Gusella	18
8	Gametic but not somatic instability of CAG repeat length in Huntington's disease. 1993 ·Journal of Medical Genetics ·Marcy E. MacDonald, Glenn Barnes, Jayalakshmi Srinidhi, Mabel P. Duyao, C M Ambrose, Richard H. Myers, J. Gray, P. M. Conneally, A. B. Young, John B. Penney	159
9	Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate region 1992 ·Genomics ·James F. Gusella, Michael R. Altherr, Andrea I. McClatchey, Lynn Doucette‐Stamm, (unknown), Sarah J. Plummer, (unknown), Glenn Barnes, Holger Hummerich, Francis S. Collins, David E. Housman, Hans Lehrach, Marcy E. MacDonald, Gillian P. Bates, John J. Wasmuth	12
10	Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4 1992 ·Molecular and Cellular Probes ·Bernice A. Allitto, Andrea I. McClatchey, Glenn Barnes, Michael R. Altherr, John J. Wasmuth, A.-M. Frischauf, Marcy E. MacDonald, James F. Gusella	4
11	A novel G protein-coupled receptor kinase gene cloned from 4p16.3 1992 ·Human Molecular Genetics ·Christopher S. Ambrose, (unknown), Glenn Barnes, Chentao Lin, Gillian P. Bates, Michael R. Altherr, Mabel P. Duyao, Natalia Sánchez de Groot, Deanna M. Church, (unknown), Hans Lehrach, David E. Housman, Alan Buckler, James F. Gusella, Marcy E. MacDonald	83
12	The Huntington's disease candidate region exhibits many different haplotypes 1992 ·Nature Genetics ·Marcy E. MacDonald, Andrea Novelletto, Carol Sze Ki Lin, (unknown), Glenn Barnes, Gillian P. Bates, Sherry Taylor, Bernice A. Allitto, Michael R. Altherr, Richard H. Myers, Hans Lehrach, Francis S. Collins, John J. Wasmuth, Marina Frontali, James F. Gusella	118
13	Cloning of the α–adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification 1992 ·Nature Genetics ·Stacy Taylor, Russell G. Snell, Alan Buckler, Charles T. Ambrose, Mabel P. Duyao, Deanna M. Church, Choun‐Sea Lin, Michael R. Altherr, Gillian P. Bates, Natasja G. de Groot, Glenn Barnes, Duncan J. Shaw, Hans Lehrach, J.J. Wasmuth, Peter S. Harper, David E. Housman, Marcy E. MacDonald, James F. Gusella	32
14	Management of Dysphagia in Inclusion Body Myositis 1992 ·Archives of Otolaryngology - Head and Neck Surgery ·David H. Darrow, Henry T. Hoffman, Glenn Barnes, Clayton A. Wiley	47
15	A recombination event that redefines the Huntington disease region. 1992 ·PubMed ·Russell G. Snell, Leslie M. Thompson, (unknown), Tracey Holloway, Glenn Barnes, H G Harley, Lodewijk A. Sandkuijl, Marcy E. MacDonald, FS Collins, James F. Gusella	15

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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