R. Mark Gardiner

4.9k total citations · 2 hit papers
34 papers, 3.3k citations indexed

About

R. Mark Gardiner is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, R. Mark Gardiner has authored 34 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Physiology and 6 papers in Cell Biology. Recurrent topics in R. Mark Gardiner's work include Lysosomal Storage Disorders Research (12 papers), Cellular transport and secretion (6 papers) and Ion channel regulation and function (6 papers). R. Mark Gardiner is often cited by papers focused on Lysosomal Storage Disorders Research (12 papers), Cellular transport and secretion (6 papers) and Ion channel regulation and function (6 papers). R. Mark Gardiner collaborates with scholars based in United Kingdom, United States and Netherlands. R. Mark Gardiner's co-authors include Richard J. Thompson, Sandra Strautnieks, Eddie M.K. Chung, Patricia B. Munroe, Michele Rees, Keith A. Parker, M S Tanner, Nelson B. Freimer, Amir F. Kagalwalla and John N. Wood and has published in prestigious journals such as The Lancet, Neuron and Nature Genetics.

In The Last Decade

R. Mark Gardiner

34 papers receiving 3.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

1998 738 citations Sandra Strautnieks, Alexander S. Knisely et al. Nature Genetics profile →
SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes

2006 559 citations Caroline Fertleman, Mark D. Baker et al. Neuron profile →

Peers

R. Mark Gardiner

PHYSI

ONCOL

SURGE

CMN

David J. Figueroa United States

Junji Ishida Japan

Kazuwa Nakao Japan

Andrew Shenker United States

Bethel Stannard United States

Mirella Gonzalez‐Zulueta United States

Laura F. Michael United States

J. A. Maassen Netherlands

Constance Tom Noguchi United States

T. J. Visser Netherlands

David J. Figueroa United States

R. Mark Gardiner

2.0k ×1.3

551 ×0.6

PHYSI

568 ×0.7

ONCOL

428 ×0.6

SURGE

758 ×1.5

CMN

Citations per year, relative to R. Mark Gardiner R. Mark Gardiner (= 1×) peers David J. Figueroa

Countries citing papers authored by R. Mark Gardiner

Since Specialization

Citations

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

Fields of papers citing papers by R. Mark Gardiner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Mark Gardiner

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

All Works

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20 of 20 papers shown

Everett, Kate V., Francesca Capon, Barry A. Chioza, et al.. (2008). Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24. European Journal of Human Genetics. 16(9). 1151–1154. 19 indexed citations

Reece, Ashley, et al.. (2008). Competency domains in an undergraduate Objective Structured Clinical Examination: their impact on compensatory standard setting. Medical Education. 42(6). 600–606. 10 indexed citations

Fertleman, Caroline, Mark D. Baker, Keith A. Parker, et al.. (2006). SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes. Neuron. 52(5). 767–774. 559 indexed citations breakdown →

Sharp, Julie D., Ruth B. Wheeler, Keith A. Parker, et al.. (2003). Spectrum ofCLN6mutations in variant late infantile neuronal ceroid lipofuscinosis. Human Mutation. 22(1). 35–42. 60 indexed citations

Saxena, Anjana, Israel Hanukoglu, Deepak Saxena, et al.. (2002). Novel Mutations Responsible for Autosomal Recessive Multisystem Pseudohypoaldosteronism and Sequence Variants in Epithelial Sodium Channel α-, β-, and γ-Subunit Genes. The Journal of Clinical Endocrinology & Metabolism. 87(7). 3344–3350. 37 indexed citations

Mitchell, Wayne, Ruth B. Wheeler, Julie D. Sharp, et al.. (2001). Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8. European Journal of Paediatric Neurology. 5. 21–27. 39 indexed citations

Sharp, Julie D., Ruth B. Wheeler, Roger A. Schultz, et al.. (2001). Analysis of candidate genes in the CLN6 critical regionusing in silico cloning. European Journal of Paediatric Neurology. 5. 29–31. 4 indexed citations

Lehesjoki, Anna‐Elina, Victoria Reed, R. Mark Gardiner, & Nicholas D. E. Greene. (2001). Expression of MUL, a gene encoding a novel RBCC family ring-finger protein, in human and mouse embryogenesis. Mechanisms of Development. 108(1-2). 221–225. 15 indexed citations

Mitchison, Hannah M., David J. Bernard, Nicholas D. E. Greene, et al.. (1999). Targeted Disruption of the Cln3 Gene Provides a Mouse Model for Batten Disease. Neurobiology of Disease. 6(5). 321–334. 170 indexed citations

10.

Gardiner, R. Mark. (1999). Genetic basis of the human epilepsies. Epilepsy Research. 36(2-3). 91–95. 16 indexed citations

11.

Munroe, Patricia B., Rana Olguntürk, Jean‐Pierre Fryns, et al.. (1999). Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome. Nature Genetics. 21(1). 142–144. 314 indexed citations

12.

Strautnieks, Sandra, Alexander S. Knisely, Samuel A. Kocoshis, et al.. (1998). A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis. Nature Genetics. 20(3). 233–238. 738 indexed citations breakdown →

13.

Saxena, Anjana, Israel Hanukoglu, Sandra Strautnieks, et al.. (1998). Gene Structure of the Human Amiloride-Sensitive Epithelial Sodium Channel Beta Subunit. Biochemical and Biophysical Research Communications. 252(1). 208–213. 27 indexed citations

14.

Strautnieks, Sandra, Richard J. Thompson, Aaron Hanukoglu, et al.. (1996). Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping. Human Molecular Genetics. 5(2). 293–299. 57 indexed citations

15.

Strautnieks, Sandra, Richard J. Thompson, R. Mark Gardiner, & Eddie M.K. Chung. (1996). A novel spice–site mutation in the γ subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families. Nature Genetics. 13(2). 248–250. 185 indexed citations

16.

Janes, Robert W., Patricia B. Munroe, Hannah M. Mitchison, et al.. (1996). A model for Batten disease protein CLN3: Functional implications from homology and mutations. FEBS Letters. 399(1-2). 75–77. 70 indexed citations

17.

Järvelä, Irma, Hannah M. Mitchison, David F. Callen, et al.. (1995). Physical map of the region containing the gene for Batten disease (CLN3). American Journal of Medical Genetics. 57(2). 316–319. 9 indexed citations

18.

Taschner, Peter E.M., Jan G. Post, E.J. Meijers-Heijboer, et al.. (1995). Carrier detection of Batten disease (Juvenile neuronal ceroid‐lipofuscinosis). American Journal of Medical Genetics. 57(2). 333–337. 11 indexed citations

19.

Mitchison, Hannah M., Andrew Thompson, John C. Mulley, et al.. (1993). Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci. Genomics. 16(2). 455–460. 43 indexed citations

20.

Poulton, Joanna, Mary E. Deadman, & R. Mark Gardiner. (1989). DUPLICATIONS OF MITOCHONDRIAL DNA IN MITOCHONDRIAL MYOPATHY. The Lancet. 333(8632). 236–240. 153 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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