Alison Evans

1.8k total citations
14 papers, 1.2k citations indexed

About

Alison Evans is a scholar working on Cardiology and Cardiovascular Medicine, Genetics and Orthopedics and Sports Medicine. According to data from OpenAlex, Alison Evans has authored 14 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cardiology and Cardiovascular Medicine, 4 papers in Genetics and 4 papers in Orthopedics and Sports Medicine. Recurrent topics in Alison Evans's work include Cardiovascular Effects of Exercise (5 papers), Sports injuries and prevention (4 papers) and Connective tissue disorders research (3 papers). Alison Evans is often cited by papers focused on Cardiovascular Effects of Exercise (5 papers), Sports injuries and prevention (4 papers) and Connective tissue disorders research (3 papers). Alison Evans collaborates with scholars based in United Kingdom, United States and Italy. Alison Evans's co-authors include William J. McKenna, Petros Syrris, Angeliki Asimaki, Srijita Sen‐Chowdhry, Deirdre Ward, Estelle Gandjbakhch, Perry Elliott, Antonios Pantazis, Glen Brice and Anne H. Child and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and The American Journal of Human Genetics.

In The Last Decade

Alison Evans

14 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alison Evans United Kingdom	12	685	273	234	160	149	14	1.2k
M C Slootweg Netherlands	14	79 0.1×	211 0.8×	481 2.1×	50 0.3×	289 1.9×	16	1.2k
Masaru Inoue Japan	20	363 0.5×	70 0.3×	220 0.9×	13 0.1×	133 0.9×	40	868
Hirokazu Kondo Japan	17	392 0.6×	31 0.1×	184 0.8×	31 0.2×	22 0.1×	77	820
Guilhèrme Pòvoa Sweden	13	169 0.2×	23 0.1×	537 2.3×	26 0.2×	193 1.3×	17	1.2k
B. Klinger Israel	23	237 0.3×	12 0.0×	521 2.2×	100 0.6×	467 3.1×	43	1.5k
Casey R. Doucette United States	5	60 0.1×	196 0.7×	195 0.8×	19 0.1×	23 0.2×	6	677
Frane Paić Croatia	8	99 0.1×	49 0.2×	242 1.0×	30 0.2×	98 0.7×	25	530
Juliane Léger France	15	35 0.1×	46 0.2×	320 1.4×	51 0.3×	357 2.4×	26	1.1k
Christelle Lecut Belgium	16	207 0.3×	22 0.1×	162 0.7×	41 0.3×	63 0.4×	28	834
Jörg‐Detlef Drenckhahn Germany	9	746 1.1×	169 0.6×	438 1.9×	7 0.0×	60 0.4×	17	1.0k

Countries citing papers authored by Alison Evans

Since Specialization

Citations

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

Fields of papers citing papers by Alison Evans

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison Evans

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

All Works

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14 of 14 papers shown

Gehmlich, Katja, Petros Syrris, Mareike Reimann, et al.. (2011). Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele. Cardiovascular Pathology. 21(4). 275–282. 28 indexed citations

Gehmlich, Katja, Petros Syrris, Emma Peskett, et al.. (2010). Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations. Cardiovascular Research. 90(1). 77–87. 41 indexed citations

Elliott, Perry, Constantinos O’Mahony, Petros Syrris, et al.. (2010). Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy. Circulation Cardiovascular Genetics. 3(4). 314–322. 125 indexed citations

Comeglio, Paolo, Philip H. Johnson, Gavin Arno, et al.. (2007). The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193FBN1 mutations. Human Mutation. 28(9). 928–928. 76 indexed citations

Syrris, Petros, Deirdre Ward, Alison Evans, et al.. (2006). Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated with Mutations in the Desmosomal Gene Desmocollin-2. The American Journal of Human Genetics. 79(5). 978–984. 261 indexed citations

Syrris, Petros, Deirdre Ward, Angeliki Asimaki, et al.. (2006). Clinical Expression of Plakophilin-2 Mutations in Familial Arrhythmogenic Right Ventricular Cardiomyopathy. Circulation. 113(3). 356–364. 161 indexed citations

Murphy, Ross T., Jens Mogensen, Ajay Bahl, et al.. (2005). Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome. Journal of the American College of Cardiology. 45(6). 922–930. 114 indexed citations

Comeglio, Paolo, Alison Evans, Glen Brice, Britt‐Marie Anderlid, & A. H. Child. (2002). Gene symbol: FBN1. Disease: Marfan syndrome.. Human Genetics. 112(1). 104–104. 5 indexed citations

Comeglio, Paolo, Alison Evans, Glen Brice, & Anne H. Child. (2001). Detection of six novel FBN1 mutations in British patients affected by Marfan syndrome. Human Mutation. 18(3). 251–251. 12 indexed citations

10.

Evans, Alison, et al.. (2000). Non-syndromic mental retardation segregating with an apparently balanced t(1;17) reciprocal translocation through three generations. American Journal of Medical Genetics. 95(2). 99–104. 3 indexed citations

11.

Mangion, Jonathan, Nazneen Rahman, Sahar Mansour, et al.. (1999). A Gene for Lymphedema-Distichiasis Maps to 16q24.3. The American Journal of Human Genetics. 65(2). 427–432. 64 indexed citations

12.

Evans, Alison, Glen Brice, Peter Mortimer, et al.. (1999). Mapping of Primary Congenital Lymphedema to the 5q35.3 Region. The American Journal of Human Genetics. 64(2). 547–555. 90 indexed citations

13.

Gotoda, Takanari, Brian S. Manning, Anthony P. Goldstone, et al.. (1997). Leptin Receptor Gene Variation and Obesity: Lack of Association in a White British Male Population. Human Molecular Genetics. 6(6). 869–876. 171 indexed citations

14.

Evans, Alison, et al.. (1981). Immotile cilia syndrome: a new cause of neonatal respiratory distress.. Archives of Disease in Childhood. 56(6). 432–435. 43 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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