R. M. Chalmers

1.5k total citations
16 papers, 1.1k citations indexed

About

R. M. Chalmers is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Hematology. According to data from OpenAlex, R. M. Chalmers has authored 16 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Hematology. Recurrent topics in R. M. Chalmers's work include Mitochondrial Function and Pathology (9 papers), interferon and immune responses (3 papers) and RNA modifications and cancer (3 papers). R. M. Chalmers is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), interferon and immune responses (3 papers) and RNA modifications and cancer (3 papers). R. M. Chalmers collaborates with scholars based in United Kingdom, United States and Italy. R. M. Chalmers's co-authors include A E Harding, Kari Majamaa, Anu Suomalainen, Leena Peltonen, Hannu Somer, Atle Melberg, Nina N. Nupponen, I. Rautakorpi, Jyrki Kaukonen and Anders Oldfors and has published in prestigious journals such as The Lancet, Nature Genetics and Brain.

In The Last Decade

R. M. Chalmers

16 papers receiving 1.1k citations

Peers

Countries citing papers authored by R. M. Chalmers

Since Specialization

Citations

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

Fields of papers citing papers by R. M. Chalmers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. M. Chalmers

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study 2004 ·The Lancet ·Petri Luoma, Atle Melberg, Juha O. Rinne, Jyrki Kaukonen, Nina N. Nupponen, R. M. Chalmers, Anders Oldfors, I. Rautakorpi, Leena Peltonen, Kari Majamaa, Hannu Somer, Anu Suomalainen	429
2	A conserved sorting-associated protein is mutant in chorea-acanthocytosis 2001 ·Nature Genetics ·Luca Rampoldi, Carol Dobson‐Stone, Justin P. Rubio, Adrian Danek, R. M. Chalmers, Nicholas Wood, Christine Verellen, Xavier Ferrer, Alessandro Malandrini, Gian Maria Fabrizi, Robert H. Brown, Jeffery M. Vance, Margaret A. Pericak‐Vance, Gabrielle Rudolf, Sophie Carré, Elisa Alonso, M. Manfredi, Andrea H. Németh, Anthony P. Monaco	223
3	Clinical, biochemical and molecular genetic features of Leber’s hereditary optic neuropathy 1999 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·R. M. Chalmers, Anthony H.V. Schapira	55
4	Chorea-Acanthocytosis: Genetic Linkage to Chromosome 9q21 1997 ·The American Journal of Human Genetics ·Justin P. Rubio, Adrian Danek, Caroline Stone, R. M. Chalmers, Nicholas Wood, Christine Verellen, Xavier Ferrer, Alessandro Malandrini, Gian Maria Fabrizi, M. Manfredi, Jeffery M. Vance, Margaret A. Pericak‐Vance, Robert H. Brown, Gabrielle Rudolf, Fabienne Picard, Elisa Alonso, Mitchell F. Brin, Andrea H. Németh, Martin Farrall, Anthony P. Monaco	54
5	A mitochondrial DNA tRNA ^Val point mutation associated with adult-onset Leigh syndrome 1997 ·Neurology ·R. M. Chalmers, Phillipa J. Lamont, Isabelle Nelson, David W. Ellison, Neil H. Thomas, A E Harding, Simon Hammans	55
6	Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy. 1997 ·Journal of Neurology Neurosurgery & Psychiatry ·R. M. Chalmers, Paul Riordan‐Eva, Nicholas Wood	13
7	Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy. 1996 ·PubMed ·R. M. Chalmers, Mary B. Davis, Mary G. Sweeney, Nicholas Wood, A E Harding	36
8	Respiratory insufficiency in neuronopathic and neuropathic disorders 1996 ·QJM ·R. M. Chalmers, Robin Howard, C M Wiles, N.P. Hirsch, D. H. Miller, Adrian J. Williams, Geoffrey Spencer	7
9	HLA class I genotypes in Leber's hereditary optic neuropathy 1996 ·Journal of the Neurological Sciences ·R. M. Chalmers, G.G. Govan, Anthony H.V. Schapira, A. E. Harding	8
10	A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis 1996 ·Annals of Neurology ·Mengfatt Ho, R. M. Chalmers, (unknown), A E Harding, Anthony P. Monaco	42
11	Sequence of mitochondrial DNA in patients with multiple sclerosis 1996 ·Annals of Neurology ·R. M. Chalmers, A E Harding, Neil P. Robertson, D. A. S. Compston	20
12	Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features 1996 ·Journal of the Neurological Sciences ·R. M. Chalmers, Martin Brockington, Robin Howard, Bryan Lecky, J A Morgan-Hughes, A. E. Harding	41
13	A case-control study of Leber's hereditary optic neuropathy 1996 ·Brain ·R. M. Chalmers, A E Harding	58
14	Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy. 1996 ·Journal of Neurology Neurosurgery & Psychiatry ·R. M. Chalmers, A.C. Bird, A E Harding	14
15	Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis 1995 ·Journal of Neurology ·R. M. Chalmers, A E Harding, Nancy P. Robertson, H. Kellar-Wood, D. A. S. Compston	20
16	Use of the rocking bed in the treatment of neurogenic respiratory insufficiency 1994 ·QJM ·R. M. Chalmers, Robin Howard, C M Wiles, Geoffrey Spencer	7

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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