R M Gardiner

2.5k total citations
70 papers, 1.8k citations indexed

About

R M Gardiner is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, R M Gardiner has authored 70 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 26 papers in Physiology and 15 papers in Genetics. Recurrent topics in R M Gardiner's work include Lysosomal Storage Disorders Research (19 papers), Metabolism and Genetic Disorders (14 papers) and Genetics and Neurodevelopmental Disorders (10 papers). R M Gardiner is often cited by papers focused on Lysosomal Storage Disorders Research (19 papers), Metabolism and Genetic Disorders (14 papers) and Genetics and Neurodevelopmental Disorders (10 papers). R M Gardiner collaborates with scholars based in United Kingdom, United States and Finland. R M Gardiner's co-authors include Joanna Poulton, Mary E. Deadman, Hannah M. Mitchison, Jan Mohr, Hans Eiberg, Sara Mole, Mark I. Rees, Ernest B. Cady, E O R Reynolds and David T. Delpy and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

R M Gardiner

70 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R M Gardiner United Kingdom 26 926 509 369 356 304 70 1.8k
Ruth Navon Israel 29 1.1k 1.2× 1.1k 2.1× 390 1.1× 361 1.0× 163 0.5× 80 2.5k
J. Jay Gargus United States 26 993 1.1× 249 0.5× 351 1.0× 498 1.4× 198 0.7× 43 1.8k
Georg Christoph Korenke Germany 25 914 1.0× 410 0.8× 138 0.4× 381 1.1× 129 0.4× 57 1.7k
Arvid Suls Belgium 22 1.0k 1.1× 289 0.6× 627 1.7× 866 2.4× 1.1k 3.7× 44 2.4k
M. B. Segal United Kingdom 27 710 0.8× 402 0.8× 919 2.5× 76 0.2× 145 0.5× 58 2.6k
D. Goossens Belgium 25 797 0.9× 455 0.9× 284 0.8× 548 1.5× 248 0.8× 75 1.9k
Lee-Jun Wong United States 28 1.8k 2.0× 199 0.4× 183 0.5× 377 1.1× 84 0.3× 59 2.6k
Marcelle Bergeron United States 19 811 0.9× 251 0.5× 262 0.7× 165 0.5× 89 0.3× 26 1.9k
Anthony Davies United Kingdom 32 2.2k 2.3× 631 1.2× 1.3k 3.4× 179 0.5× 123 0.4× 50 3.3k
Gilles Millat France 29 1.2k 1.2× 1.5k 3.0× 120 0.3× 150 0.4× 263 0.9× 80 3.1k

Countries citing papers authored by R M Gardiner

Since Specialization
Citations

This map shows the geographic impact of R M Gardiner'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 Gardiner 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 Gardiner more than expected).

Fields of papers citing papers by R M Gardiner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R M Gardiner

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

All Works

20 of 20 papers shown
1.
Mulley, John C., Bree Hodgson, Bronwyn E. Grinton, et al.. (2003). Sodium channel alpha-1 subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms. The American Journal of Human Genetics. 73(5). 11 indexed citations
2.
Bartoloni, Lucia, Jean‐Louis Blouin, Amit K. Maiti, et al.. (2001). Axonemal Beta Heavy Chain Dynein DNAH9: cDNA Sequence, Genomic Structure, and Investigation of Its Role in Primary Ciliary Dyskinesia. Genomics. 72(1). 21–33. 39 indexed citations
3.
Gardiner, R M. (2000). Impact of our understanding of the genetic aetiology of epilepsy. Journal of Neurology. 247(5). 327–334. 21 indexed citations
4.
Maiti, Amit K., Lucia Bartoloni, Hannah M. Mitchison, et al.. (2000). No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with Primary Ciliary Dyskinesia (PCD). Cytogenetic and Genome Research. 90(1-2). 119–122. 27 indexed citations
5.
Sharp, Julie D., et al.. (1999). Genetic and Physical Mapping of theCLN6Gene on Chromosome 15q21–23. Molecular Genetics and Metabolism. 66(4). 329–331. 18 indexed citations
6.
Stephenson, John B.P., Nicholas D. E. Greene, Patricia B. Munroe, et al.. (1999). The Molecular Basis of GROD-Storing Neuronal Ceroid Lipofuscinoses in Scotland. Molecular Genetics and Metabolism. 66(4). 245–247. 9 indexed citations
7.
Lewis, T., et al.. (1998). Properties of human glycine receptors containing the hyperekplexia mutation α1(K276E), expressed in Xenopus oocytes. The Journal of Physiology. 507(1). 25–40. 91 indexed citations
8.
Mitchison, Hannah M., Peter E.M. Taschner, David F. Callen, et al.. (1997). Structure of the CLN3 Gene and Predicted Structure, Location and Function of CLN3 Protein. Neuropediatrics. 28(1). 12–14. 19 indexed citations
9.
Strautnieks, Sandra, Amir F. Kagalwalla, M S Tanner, R M Gardiner, & Richard J. Thompson. (1996). Locus heterogeneity in progressive familial intrahepatic cholestasis.. Journal of Medical Genetics. 33(10). 833–836. 30 indexed citations
10.
11.
Dooley, Thomas P., Hannah M. Mitchison, Patricia B. Munroe, et al.. (1994). Mapping of Two Phenol Sulfotransferase Genes, STP and STM, to 16p: Candidate Genes for Batten Disease. Biochemical and Biophysical Research Communications. 205(1). 482–489. 31 indexed citations
12.
Kohlschütter, Alfried, R M Gardiner, & Hans H. Goebel. (1993). Human forms of neuronal ceroid‐lipofuscinosis (Batten disease): Consensus on diagnostic criteria, Hamburg 1992. Journal of Inherited Metabolic Disease. 16(2). 241–244. 48 indexed citations
13.
Whitehouse, William, Ulrike Diebold, Mark I. Rees, et al.. (1993). Exclusion of Linkage of Genetic Focal Sharp Waves to the HLA Region on Chromosome 6p in Families with Benign Partial Epilepsy with Centrotemporal Sharp Waves. Neuropediatrics. 24(4). 208–210. 12 indexed citations
14.
Rees, Mark I., Ulrike Diebold, K L Parker, et al.. (1993). Benign Childhood Epilepsy with Centrotemporal Spikes and the Focal Sharp Wave Trait is not Linked to the Fragile X Region. Neuropediatrics. 24(4). 211–213. 20 indexed citations
15.
Poulton, Joanna, Mary E. Deadman, Douglass M. Turnbull, Brian Lake, & R M Gardiner. (1991). Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non‐invasive diagnosis of mitochondrial myopathy. Clinical Genetics. 39(1). 33–38. 16 indexed citations
16.
Watmough, Nicholas J., Laurence A. Bindoff, Mark A. Birch‐Machin, et al.. (1990). Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.. Journal of Clinical Investigation. 85(1). 177–184. 61 indexed citations
17.
Gardiner, R M. (1990). The human genome: a prospect for paediatrics.. Archives of Disease in Childhood. 65(4). 457–461. 1 indexed citations
18.
Gardiner, R M, et al.. (1990). Blood-Brain Barrier Permeability to Bilirubin in the Rat Studied Using Intracarotid Bolus Injection and in Situ Brain Perfusion Techniques. Pediatric Research. 27(5). 436–441. 11 indexed citations
19.
Poulton, Joanna, Mary E. Deadman, & R M Gardiner. (1989). Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distribution. Nucleic Acids Research. 17(24). 10223–10229. 39 indexed citations
20.

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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