R. Mark Gardiner

4.9k citations

34 papers · 3.3k indexed · 2 hit papers · h-index 22

Molecular Biology top 5%
Physiology top 2%
Oncology top 5%
Surgery top 5%
Cellular and Molecular Neuroscience top 5%

Co-authors: Richard J. Thompson Sandra Strautnieks Eddie M.K. Chung Patricia B. Munroe Michele Rees Keith A. Parker M S Tanner Nelson B. Freimer
Topics: Lysosomal Storage Disorders Research (12 papers)Cellular transport and secretion (6 papers)Ion channel regulation and function (6 papers)
Cited by: Physiology Oncology Clinical Biochemistry
Journals: The Lancet Neuron Nature Genetics
Partner nations: United Kingdom United States Netherlands

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

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

#	Work	Indexed citations
1	Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24 2008 ·European Journal of Human Genetics ·Kate V. Everett,Francesca Capon,(unknown),Barry A. Chioza,Ashley Reece,Mervyn Jaswon,Agostino Pierro,Prem Puri,R. Mark Gardiner,Eddie M.K. Chung	19
2	Competency domains in an undergraduate Objective Structured Clinical Examination: their impact on compensatory standard setting 2008 ·Medical Education ·Ashley Reece,Eddie M.K. Chung,R. Mark Gardiner,(unknown)	10
3	SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypesbreakdown → 2006 ·Neuron ·Caroline Fertleman,Mark D. Baker,Keith A. Parker,(unknown),Frances Elmslie,Bjarke Abrahamsen,Johan Östman,Norbert Klugbauer,John N. Wood,R. Mark Gardiner,Michele Rees	559
4	Spectrum ofCLN6mutations in variant late infantile neuronal ceroid lipofuscinosis 2003 ·Human Mutation ·Julie D. Sharp,Ruth B. Wheeler,Keith A. Parker,R. Mark Gardiner,Ruth Williams,Sara Mole	60
5	Novel Mutations Responsible for Autosomal Recessive Multisystem Pseudohypoaldosteronism and Sequence Variants in Epithelial Sodium Channel α-, β-, and γ-Subunit Genes 2002 ·The Journal of Clinical Endocrinology & Metabolism ·Anjana Saxena,Israel Hanukoglu,Deepak Saxena,Richard J. Thompson,R. Mark Gardiner,Aaron Hanukoglu	37
6	Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8 2001 ·European Journal of Paediatric Neurology ·Wayne Mitchell,Ruth B. Wheeler,Julie D. Sharp,(unknown),R. Mark Gardiner,(unknown),Liina Lonka,Ruth Williams,Anna‐Elina Lehesjoki,Sara Mole	39
7	Analysis of candidate genes in the CLN6 critical regionusing in silico cloning 2001 ·European Journal of Paediatric Neurology ·Julie D. Sharp,Ruth B. Wheeler,Roger A. Schultz,John M. Joslin,Sara Mole,Ruth Williams,R. Mark Gardiner	4
8	Expression of MUL, a gene encoding a novel RBCC family ring-finger protein, in human and mouse embryogenesis 2001 ·Mechanisms of Development ·Anna‐Elina Lehesjoki,Victoria Reed,R. Mark Gardiner,Nicholas D. E. Greene	15
9	Targeted Disruption of the Cln3 Gene Provides a Mouse Model for Batten Disease 1999 ·Neurobiology of Disease ·Hannah M. Mitchison,David J. Bernard,Nicholas D. E. Greene,Jonathan D. Cooper,Mohammed Junaid,Raju K. Pullarkat,(unknown),Martijn H. Breuning,Jennie W. Owens,William C. Mobley,R. Mark Gardiner,Brian Lake,Peter E.M. Taschner,Robert L. Nussbaum	170
10	Genetic basis of the human epilepsies 1999 ·Epilepsy Research ·R. Mark Gardiner	16
11	Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome 1999 ·Nature Genetics ·Patricia B. Munroe,Rana Olguntürk,Jean‐Pierre Fryns,Lionel Van Maldergem,France Ziereisen,Bülend Yüksel,R. Mark Gardiner,Eddie M.K. Chung	314
12	A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasisbreakdown → 1998 ·Nature Genetics ·Sandra Strautnieks,(unknown),Alexander S. Knisely,Samuel A. Kocoshis,Niklas Dahl,Henrik Arnell,Étienne Sokal,Karine Dahan,Sarah J. Childs,(unknown),M S Tanner,Amir F. Kagalwalla,Antal Németh,Joanna Pawłowska,Alastair Baker,Giorgina Mieli‐Vergani,Nelson B. Freimer,R. Mark Gardiner,Richard J. Thompson	738
13	Gene Structure of the Human Amiloride-Sensitive Epithelial Sodium Channel Beta Subunit 1998 ·Biochemical and Biophysical Research Communications ·Anjana Saxena,Israel Hanukoglu,Sandra Strautnieks,Richard J. Thompson,R. Mark Gardiner,Aaron Hanukoglu	27
14	Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping 1996 ·Human Molecular Genetics ·Sandra Strautnieks,Richard J. Thompson,Aaron Hanukoglu,Michael J. Dillon,Israel Hanukoglu,Ursula Kuhnle,Jonathan R. Seckl,R. Mark Gardiner,Eddie M.K. Chung	57
15	A novel spice–site mutation in the γ subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families 1996 ·Nature Genetics ·Sandra Strautnieks,Richard J. Thompson,R. Mark Gardiner,Eddie M.K. Chung	185
16	A model for Batten disease protein CLN3: Functional implications from homology and mutations 1996 ·FEBS Letters ·Robert W. Janes,Patricia B. Munroe,Hannah M. Mitchison,R. Mark Gardiner,Sara Mole,B.A. Wallace	70
17	Physical map of the region containing the gene for Batten disease (CLN3) 1995 ·American Journal of Medical Genetics ·Irma Järvelä,Hannah M. Mitchison,David F. Callen,Terry J. Lerner,Norman A. Doggett,Peter E.M. Taschner,R. Mark Gardiner,Sara Mole	9
18	Carrier detection of Batten disease (Juvenile neuronal ceroid‐lipofuscinosis) 1995 ·American Journal of Medical Genetics ·Peter E.M. Taschner,(unknown),Jan G. Post,E.J. Meijers-Heijboer,(unknown),Maarten J. J. E. Loonen,A. Pinckers,Elisabeth M. Bleeker‐Wagemakers,R. Mark Gardiner,Martijn H. Breuning	11
19	Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci 1993 ·Genomics ·Hannah M. Mitchison,Andrew Thompson,John C. Mulley,H.M. Kozman,Robert I. Richards,David F. Callen,R.L. Stallings,Norman A. Doggett,(unknown),Tristan R. McKay,Grant R. Sutherland,R. Mark Gardiner	43
20	DUPLICATIONS OF MITOCHONDRIAL DNA IN MITOCHONDRIAL MYOPATHY 1989 ·The Lancet ·Joanna Poulton,Mary E. Deadman,R. Mark Gardiner	153

About R. Mark Gardiner

R. Mark Gardiner is a scholar working on Physiology, Clinical Biochemistry and Physiology, having authored 34 papers that have together received 3.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (12 papers), Cellular transport and secretion (6 papers) and Ion channel regulation and function (6 papers). The work is most often cited by research in Physiology (943 citations), Oncology (784 citations) and Clinical Biochemistry (188 citations). R. Mark Gardiner has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent 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. Their work appears in journals such as The Lancet, Neuron and Nature Genetics.

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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