Gillian Rea

957 total citations
12 papers, 48 citations indexed

About

Gillian Rea is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gillian Rea has authored 12 papers receiving a total of 48 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Gillian Rea's work include RNA regulation and disease (3 papers), Ocular Disorders and Treatments (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Gillian Rea is often cited by papers focused on RNA regulation and disease (3 papers), Ocular Disorders and Treatments (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Gillian Rea collaborates with scholars based in United Kingdom, Ireland and United States. Gillian Rea's co-authors include Patrick J. Morrison, Fiona J. Stewart, Alicja Wilk, Jacqueline A. James, Ferran Rosés‐Noguer, Jan Till, Roddy Walsh, Piers E.F. Daubeney, Sanjay Prasad and Deirdre E. Donnelly and has published in prestigious journals such as European Journal of Human Genetics, Molecular Genetics and Metabolism and Genes.

In The Last Decade

Gillian Rea

10 papers receiving 48 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gillian Rea United Kingdom	5	25	21	8	6	6	12	48
Hiromi Nyuzuki Japan	6	46 1.8×	19 0.9×	5 0.6×	4 0.7×	8 1.3×	21	71
Marcos Madruga Spain	4	24 1.0×	24 1.1×	4 0.5×	5 0.8×	3 0.5×	6	51
Médéric Jeanne France	5	42 1.7×	21 1.0×	2 0.3×	5 0.8×	3 0.5×	12	72
Tyra Estwick United States	3	38 1.5×	14 0.7×	4 0.5×	9 1.5×	9 1.5×	5	69
Audrey Smith United Kingdom	4	29 1.2×	20 1.0×	4 0.5×	6 1.0×	3 0.5×	4	42
Rachel Rabin United States	6	60 2.4×	33 1.6×	13 1.6×	6 1.0×	7 1.2×	9	95
Hülya Azaklı Türkiye	5	47 1.9×	20 1.0×	2 0.3×	8 1.3×	11 1.8×	10	72
Tanja Klein‐Rodewald Germany	4	33 1.3×	9 0.4×	5 0.6×	6 1.0×	3 0.5×	5	54
Fergus J. Couch United States	4	38 1.5×	25 1.2×	8 1.0×	3 0.5×	7 1.2×	9	56
Julia Kitaygorodsky Canada	3	31 1.2×	23 1.1×	3 0.4×	3 0.5×	13 2.2×	3	70

Countries citing papers authored by Gillian Rea

Since Specialization

Citations

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

Fields of papers citing papers by Gillian Rea

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gillian Rea

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

All Works

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12 of 12 papers shown

Lambert, Deborah M., Helen Stewart, Marta Bertoli, et al.. (2025). What is risk in clinical genetics? Designing and piloting tools to evaluate risk in clinical genetics using failure modes and effects analysis. European Journal of Human Genetics.

Rea, Gillian, Jane Murray, Alison Muir, et al.. (2025). Channelopathies in children in Northern Ireland 2005–2023: A national cohort study identified primarily via cascade screening. Progress in Pediatric Cardiology. 78. 101843–101843.

Lamb, Catherine E., et al.. (2023). UK recommendations for the management of transgender and gender-diverse patients with inherited cancer risks. PubMed. 1(1). 1–1. 2 indexed citations

McKenna, Caoimhe, Shirley Heggarty, Michael Donnelly, et al.. (2022). A Formative Study of the Implementation of Whole Genome Sequencing in Northern Ireland. Genes. 13(7). 1104–1104. 3 indexed citations

Rea, Gillian, Sandya Tirupathi, Jonathan Williams, Penny Clouston, & Patrick J. Morrison. (2019). Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral Palsy. The Cerebellum. 19(1). 161–163. 7 indexed citations

Ostrowski, Philip J., Anna Zachariou, Chey Loveday, et al.. (2019). Null variants and deletions in BRWD3 cause an X‐linked syndrome of mild–moderate intellectual disability, macrocephaly, and obesity: A series of 17 patients. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(4). 638–643. 5 indexed citations

Rea, Gillian, Tessa Homfray, Jan Till, et al.. (2016). Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11. Molecular Case Studies. 3(1). a001271–a001271. 11 indexed citations

Rea, Gillian, et al.. (2015). Globodontia in the otodental syndrome: a rare defect of tooth morphology occurring with hearing loss in an eight-year-old. Dental Update. 42(10). 927–932. 2 indexed citations

Rea, Gillian, et al.. (2013). Subcortical white matter abnormalities because of previously undescribed de-novo 14q12–q13.1 triplication. Clinical Dysmorphology. 22(2). 71–72. 2 indexed citations

10.

Møller, Lisbeth Birk, et al.. (2013). A silent nucleotide substitution in the ATP7A gene in a child with Menkes disease. Molecular Genetics and Metabolism. 110(4). 490–492. 4 indexed citations

11.

Rea, Gillian & Fiona J. Stewart. (2013). Genetic Biomarkers in Aortopathy. Biomarkers in Medicine. 7(4). 547–563. 5 indexed citations

12.

Rea, Gillian, et al.. (2010). Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus. European Journal of Medical Genetics. 53(3). 162–167. 7 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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