Mark Gardiner

913 total citations
18 papers, 528 citations indexed

About

Mark Gardiner is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Mark Gardiner has authored 18 papers receiving a total of 528 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Physiology and 6 papers in Genetics. Recurrent topics in Mark Gardiner's work include Lysosomal Storage Disorders Research (4 papers), Ion channel regulation and function (4 papers) and Epilepsy research and treatment (4 papers). Mark Gardiner is often cited by papers focused on Lysosomal Storage Disorders Research (4 papers), Ion channel regulation and function (4 papers) and Epilepsy research and treatment (4 papers). Mark Gardiner collaborates with scholars based in United Kingdom, Sweden and Finland. Mark Gardiner's co-authors include Bo K. Siesjö, Bengt Nilsson, Stig Rehncrona, Maj‐Lis Smith, Erik Kågström, Esther Shohami, Sara Mole, William Cookson, Hans Eiberg and Joanna Poulton and has published in prestigious journals such as Journal of Neurochemistry, Journal of Cerebral Blood Flow & Metabolism and Epilepsia.

In The Last Decade

Mark Gardiner

17 papers receiving 503 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark Gardiner United Kingdom 11 203 170 142 99 83 18 528
Jonathon S. Dunn United States 9 148 0.7× 130 0.8× 107 0.8× 27 0.3× 113 1.4× 10 590
Hiroko Iwamoto Japan 11 383 1.9× 141 0.8× 85 0.6× 108 1.1× 109 1.3× 33 652
Kenneth Livingston Canada 6 187 0.9× 136 0.8× 180 1.3× 85 0.9× 17 0.2× 7 587
Koteswara R. Chundu United States 6 233 1.1× 335 2.0× 121 0.9× 23 0.2× 42 0.5× 8 608
Hiroshi Asaba Japan 8 251 1.2× 80 0.5× 86 0.6× 38 0.4× 71 0.9× 11 723
Allen D. Roses United States 10 483 2.4× 302 1.8× 354 2.5× 120 1.2× 79 1.0× 12 854
Juan C. Cresto Argentina 13 210 1.0× 267 1.6× 48 0.3× 29 0.3× 93 1.1× 32 555
A. Larnaout Tunisia 12 244 1.2× 48 0.3× 137 1.0× 32 0.3× 49 0.6× 26 528
Alice Todeschini Italy 12 255 1.3× 101 0.6× 74 0.5× 82 0.8× 13 0.2× 21 525
Clarissa J. Liew United States 8 161 0.8× 55 0.3× 115 0.8× 134 1.4× 36 0.4× 9 475

Countries citing papers authored by Mark Gardiner

Since Specialization
Citations

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

Fields of papers citing papers by Mark Gardiner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Gardiner

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

All Works

18 of 18 papers shown
1.
Gardiner, Mark, et al.. (2012). Pyloric stenosis a 100 years after Ramstedt. Archives of Disease in Childhood. 97(8). 741–745. 26 indexed citations
2.
Lehesjoki, Anna‐Elina & Mark Gardiner. (2012). Progressive myoclonus epilepsy: Unverricht-Lundborg disease and Neuronal ceroid lipofuscinoses. 4 indexed citations
3.
Svenningsson, Anna, Cilla Söderhäll, Fredrik Lundberg, et al.. (2011). Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci. Journal of Human Genetics. 57(2). 115–121. 10 indexed citations
4.
Gardiner, Mark. (2006). Molecular genetics of infantile nervous system channelopathies. Early Human Development. 82(12). 775–779. 11 indexed citations
5.
Gardiner, Mark. (2005). Genetics of Idiopathic Generalized Epilepsies. Epilepsia. 46(s9). 15–20. 85 indexed citations
6.
Robinson, Robert A. & Mark Gardiner. (2004). Molecular basis of Mendelian idiopathic epilepsies. Annals of Medicine. 36(2). 89–97. 16 indexed citations
7.
Gardiner, Mark, et al.. (2003). Paroxysms of excitement: sodium channel dysfunction in heart and brain. BioEssays. 25(10). 981–993. 10 indexed citations
9.
Mole, Sara & Mark Gardiner. (1999). Molecular Genetics of the Neuronal Ceroid Lipofuscinoses. Epilepsia. 40(s3). 29–32. 19 indexed citations
10.
Gardiner, Mark, et al.. (1999). Molecular genetics of human epilepsies. Expert Reviews in Molecular Medicine. 1(19). 1–22. 9 indexed citations
11.
Gardiner, Mark, et al.. (1999). Genetics of inherited epilepsies. Epileptic Disorders. 1(1). 7–19. 23 indexed citations
12.
Parkinson, Nick, J. Elaine Barclay, Mark Gardiner, & Michele Rees. (1997). An inverse PCR strategy for the recovery of end fragments from the pRML YAC vector. 2(1). 133–135. 1 indexed citations
13.
Meeks, Maggie & Mark Gardiner. (1996). Molecular genetics for the paediatrician. Current Paediatrics. 6(1). 51–55.
14.
Sharp, Julie D., Minna Savukoski, Ruth B. Wheeler, et al.. (1995). Linkage analysis of late‐infantile neuronal ceroid‐lipofuscinosis. American Journal of Medical Genetics. 57(2). 348–349. 5 indexed citations
15.
Elmslie, Frances & Mark Gardiner. (1995). Genetics of the epilepsies. Current Opinion in Neurology. 8(2). 126–130. 11 indexed citations
16.
Gardiner, Mark, Andrew J. Sandford, Mary E. Deadman, et al.. (1990). Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16. Genomics. 8(2). 387–390. 85 indexed citations
17.
Gardiner, Mark, Maj‐Lis Smith, Erik Kågström, Esther Shohami, & Bo K. Siesjö. (1982). Influence of Blood Glucose Concentration on Brain Lactate Accumulation during Severe Hypoxia and Subsequent Recovery of Brain Energy Metabolism. Journal of Cerebral Blood Flow & Metabolism. 2(4). 429–438. 88 indexed citations
18.
Gardiner, Mark, Bengt Nilsson, Stig Rehncrona, & Bo K. Siesjö. (1981). Free Fatty Acids in the Rat Brain in Moderate and Severe Hypoxia. Journal of Neurochemistry. 36(4). 1500–1505. 123 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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