A. Gardiner

803 total citations
9 papers, 348 citations indexed

About

A. Gardiner is a scholar working on Rheumatology, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, A. Gardiner has authored 9 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Rheumatology, 4 papers in Psychiatry and Mental health and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in A. Gardiner's work include Glycogen Storage Diseases and Myoclonus (4 papers), Epilepsy research and treatment (3 papers) and Genetic Neurodegenerative Diseases (3 papers). A. Gardiner is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (4 papers), Epilepsy research and treatment (3 papers) and Genetic Neurodegenerative Diseases (3 papers). A. Gardiner collaborates with scholars based in United Kingdom, Brazil and Australia. A. Gardiner's co-authors include Henry Houlden, Russell C. Dale, Jayne Antony, R. Scalco, Rosaline C. M. Quinlivan, Robert D. S. Pitceathly, Janice L. Holton, Heinz Jungbluth, Edmar Zanoteli and Jéfferson Becker and has published in prestigious journals such as Brain, Developmental Medicine & Child Neurology and Orphanet Journal of Rare Diseases.

In The Last Decade

A. Gardiner

9 papers receiving 340 citations

Peers

Countries citing papers authored by A. Gardiner

Since Specialization

Citations

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

Fields of papers citing papers by A. Gardiner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Gardiner

This figure shows the co-authorship network connecting the top 25 collaborators of A. Gardiner. A scholar is included among the top collaborators of A. 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 A. Gardiner. A. 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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9 of 9 papers shown

#	Work	Indexed citations
1	The need for biochemical testing in beta‐enolase deficiency in the genomic era 2019 ·JIMD Reports ·(unknown), R. Scalco, A. Gardiner, Richard Godfrey, (unknown), Richard Kirk, David Hilton‐Jones, Henry Houlden, Simon Heales, Rosaline C. M. Quinlivan	8
2	GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2) 2018 ·Neuromuscular Disorders ·M. Desikan, R. Scalco, Andreea Manole, A. Gardiner, Anthony H.V. Schapira, Robin Lachmann, Henry Houlden, Janice L. Holton, Rahul Phadke, Rosaline C. M. Quinlivan	5
3	The clinical and genetic heterogeneity of paroxysmal dyskinesias 2015 ·Brain ·A. Gardiner, Fatima Jaffer, Russell C. Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, María Stamelou, Matthew C. Walker, Dimitri M. Kullmann, Thomas T. Warner, Paul Jarman, Michael G. Hanna, Manju A. Kurian, Kailash P. Bhatia, Henry Houlden	101
4	Rhabdomyolysis: a genetic perspective 2015 ·Orphanet Journal of Rare Diseases ·R. Scalco, A. Gardiner, Robert D. S. Pitceathly, Edmar Zanoteli, Jéfferson Becker, Janice L. Holton, Henry Houlden, Heinz Jungbluth, Rosaline C. M. Quinlivan	103
5	G.P.22 2014 ·Neuromuscular Disorders ·R. Scalco, Robert D. S. Pitceathly, A. Gardiner, (unknown), James M. Polke, M G Sweeney, S. E. Olpin, Richard Kirk, Elaine Murphy, David Hilton‐Jones, Heinz Jungbluth, Henry Houlden, Michael G. Hanna, Rosaline C. M. Quinlivan	3
6	Paroxysmal Kinesigenic Dyskinesia May Be Misdiagnosed in Co‐occurring Gilles de la Tourette Syndrome 2014 ·Movement Disorders Clinical Practice ·Christos Ganos, Niccolò E. Mencacci, A. Gardiner, Roberto Erro, Amit Batla, Henry Houlden, Kailash P. Bhatia	9
7	Clinical features of childhood‐onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations 2013 ·Developmental Medicine & Child Neurology ·Laura Silveira‐Moriyama, A. Gardiner, Esther Meyer, Mary D. King, Martin A. Smith, Karl Rakshi, Alasdair Parker, Andrew A. Mallick, R. Malcolm Brown, Grace Vassallo, Philip Jardine, Marilisa M. Guerreiro, Andrew Lees, Henry Houlden, Manju A. Kurian	34
8	Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine 2012 ·Developmental Medicine & Child Neurology ·Russell C. Dale, A. Gardiner, Jayne Antony, Henry Houlden	80
9	Prrt2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine 2012 ·ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway) ·A. Gardiner, Kailash P. Bhatia, (unknown), Russell C. Dale, Marina Kurian, (unknown), (unknown), (unknown), (unknown), Sian Spacey, (unknown), Laura Silveira‐Moriyama, (unknown), Sergey Raskin, (unknown), A. J. Lees, Thomas T. Warner, (unknown), (unknown), Michael G. Hanna, Henry Houlden	5

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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