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 — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Gardiner United Kingdom	6	140	89	83	77	71	9	348
Ester Cuenca-León Spain	13	170 1.2×	59 0.7×	144 1.7×	74 1.0×	141 2.0×	17	428
Helen Young Australia	9	57 0.4×	72 0.8×	56 0.7×	77 1.0×	116 1.6×	16	388
Anita Devlin United Kingdom	9	268 1.9×	79 0.9×	106 1.3×	51 0.7×	126 1.8×	28	595
Rosario Berardi Italy	14	84 0.6×	36 0.4×	47 0.6×	189 2.5×	146 2.1×	29	422
Véronique Humbertclaude France	14	225 1.6×	100 1.1×	137 1.7×	194 2.5×	319 4.5×	29	631
Anne Koy Germany	14	115 0.8×	299 3.4×	105 1.3×	59 0.8×	114 1.6×	40	535
Anine H Stam Netherlands	12	341 2.4×	102 1.1×	139 1.7×	27 0.4×	158 2.2×	15	513
Christopher Rittey United Kingdom	10	193 1.4×	147 1.7×	113 1.4×	69 0.9×	73 1.0×	16	498
Ian J. Hopkins Australia	13	247 1.8×	58 0.7×	116 1.4×	44 0.6×	109 1.5×	18	472
Yoshihisa Tatsuoka Japan	12	168 1.2×	81 0.9×	85 1.0×	11 0.1×	120 1.7×	32	409

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

Scalco, R., A. Gardiner, Richard Godfrey, et al.. (2019). The need for biochemical testing in beta‐enolase deficiency in the genomic era. JIMD Reports. 50(1). 40–43. 8 indexed citations

Desikan, M., R. Scalco, Andreea Manole, et al.. (2018). GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2). Neuromuscular Disorders. 28(4). 346–349. 5 indexed citations

Gardiner, A., Fatima Jaffer, Russell C. Dale, et al.. (2015). The clinical and genetic heterogeneity of paroxysmal dyskinesias. Brain. 138(12). 3567–3580. 101 indexed citations

Scalco, R., A. Gardiner, Robert D. S. Pitceathly, et al.. (2015). Rhabdomyolysis: a genetic perspective. Orphanet Journal of Rare Diseases. 10(1). 51–51. 103 indexed citations

Scalco, R., Robert D. S. Pitceathly, A. Gardiner, et al.. (2014). G.P.22. Neuromuscular Disorders. 24(9-10). 801–801. 3 indexed citations

Ganos, Christos, Niccolò E. Mencacci, A. Gardiner, et al.. (2014). Paroxysmal Kinesigenic Dyskinesia May Be Misdiagnosed in Co‐occurring Gilles de la Tourette Syndrome. Movement Disorders Clinical Practice. 1(1). 84–86. 9 indexed citations

Silveira‐Moriyama, Laura, A. Gardiner, Esther Meyer, et al.. (2013). Clinical features of childhood‐onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. Developmental Medicine & Child Neurology. 55(4). 327–334. 34 indexed citations

Dale, Russell C., A. Gardiner, Jayne Antony, & Henry Houlden. (2012). Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine. Developmental Medicine & Child Neurology. 54(10). 958–960. 80 indexed citations

Gardiner, A., Kailash P. Bhatia, Russell C. Dale, et al.. (2012). Prrt2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway). 5 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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