Glenda Sobey

2.7k total citations
26 papers, 444 citations indexed

About

Glenda Sobey is a scholar working on Genetics, Oncology and Rheumatology. According to data from OpenAlex, Glenda Sobey has authored 26 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 6 papers in Oncology and 6 papers in Rheumatology. Recurrent topics in Glenda Sobey's work include Connective tissue disorders research (21 papers), Dermatological and Skeletal Disorders (10 papers) and Peptidase Inhibition and Analysis (5 papers). Glenda Sobey is often cited by papers focused on Connective tissue disorders research (21 papers), Dermatological and Skeletal Disorders (10 papers) and Peptidase Inhibition and Analysis (5 papers). Glenda Sobey collaborates with scholars based in United Kingdom, United States and Italy. Glenda Sobey's co-authors include Nigel Burrows, Jessica Bowen, Neeti Ghali, Bart Wagner, Fransiska Malfait, Clair A. Francomano, Mark E. Lavallee, Marina Colombi, Marta C. Cohen and Michael Parker and has published in prestigious journals such as BMJ, Journal Of Clinical Periodontology and Archives of Disease in Childhood.

In The Last Decade

Glenda Sobey

25 papers receiving 431 citations

Peers

Glenda Sobey

GENET

RHEUM

SURGE

ONCOL

G Camera Italy

Dolrudee Jumlongras United States

Katarina Lindahl Sweden

C. Peteiro Spain

Junichi Hara Japan

Alanna F. Bree United States

Youngjae Jeong United States

Gretchen Oswald United States

Sofia Babay Israel

Usha Sundaram United States

G Camera Italy

Glenda Sobey

270 ×0.8

GENET

55 ×0.4

RHEUM

187 ×1.8

73 ×1.1

SURGE

58 ×1.0

ONCOL

Citations per year, relative to Glenda Sobey Glenda Sobey (= 1×) peers G Camera

Countries citing papers authored by Glenda Sobey

Since Specialization

Citations

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

Fields of papers citing papers by Glenda Sobey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Glenda Sobey

This figure shows the co-authorship network connecting the top 25 collaborators of Glenda Sobey. A scholar is included among the top collaborators of Glenda Sobey 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 Glenda Sobey. Glenda Sobey 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

Albaba, Shadi, Glenda Sobey, Jessica Bowen, et al.. (2025). Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome. European Journal of Human Genetics. 33(10). 1309–1315.

Byers, Peter H., Neeti Ghali, Juliette Harris, et al.. (2024). The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series. American Journal of Medical Genetics Part A. 197(4). e63957–e63957. 1 indexed citations

Bowen, Jessica, Mónica Hernández Alava, Diana Johnson, et al.. (2023). Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield. European Journal of Human Genetics. 31(7). 749–760. 21 indexed citations

Harris, Juliette, Duncan Baker, Jessica Bowen, et al.. (2023). An exemplary model of genetic counselling for highly specialised services. Journal of Community Genetics. 14(2). 115–119. 2 indexed citations

Dijk, Fleur S. van, Matthew Cauldwell, Rachel Harrison, et al.. (2022). Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UK. European Journal of Medical Genetics. 65(10). 104592–104592. 4 indexed citations

Ghali, Neeti, Duncan Baker, Jessica Bowen, et al.. (2020). Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility. Genetics in Medicine. 22(10). 1576–1582. 17 indexed citations

Ghali, Neeti, Duncan Baker, Angela F. Brady, et al.. (2020). Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome. American Journal of Medical Genetics Part A. 182(5). 994–1007. 14 indexed citations

Kapferer‐Seebacher, Ines, Diana Johnson, Neeti Ghali, et al.. (2020). Prospective clinical investigations of children with periodontal Ehlers–Danlos syndrome identify generalized lack of attached gingiva as a pathognomonic feature. Genetics in Medicine. 23(2). 316–322. 16 indexed citations

Metcalfe, Kay, et al.. (2019). DSE associated musculocontractural EDS, a milder phenotype or phenotypic variability. European Journal of Medical Genetics. 63(4). 103798–103798. 17 indexed citations

10.

Ghali, Neeti, Glenda Sobey, & Nigel Burrows. (2019). Ehlers-Danlos syndromes. BMJ. 366. l4966–l4966. 35 indexed citations

11.

Bowen, Jessica, Glenda Sobey, Nigel Burrows, et al.. (2017). Ehlers–Danlos syndrome, classical type. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(1). 27–39. 101 indexed citations

12.

Pollitt, Rebecca C., Vrinda Saraff, Ann Dalton, et al.. (2016). Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations. American Journal of Medical Genetics Part A. 170(12). 3150–3156. 27 indexed citations

13.

Balasubramanian, Meena, Glenda Sobey, Bart Wagner, et al.. (2016). Osteogenesis imperfecta: Ultrastructural and histological findings on examination of skin revealing novel insights into genotype-phenotype correlation. Ultrastructural Pathology. 40(2). 71–76. 12 indexed citations

14.

Sobey, Glenda. (2014). Ehlers–Danlos syndrome – a commonly misunderstood group of conditions. Clinical Medicine. 14(4). 432–436. 13 indexed citations

15.

Balasubramanian, Meena, Bart Wagner, Luíz César Peres, et al.. (2014). Ultrastructural and histological findings on examination of skin in osteogenesis imperfecta. Clinical Dysmorphology. 24(2). 45–54. 11 indexed citations

16.

Solomons, Joyce, Paul Coucke, Sofie Symoens, et al.. (2013). Dermatosparaxis (Ehlers–Danlos Type VIIC): Prenatal Diagnosis Following a Previous Pregnancy With Unexpected Skull Fractures at Delivery. American Journal of Medical Genetics Part A. 161(5). 1122–1125. 17 indexed citations

17.

Singh, Michael, Sapna Puppala, Rebecca C. Pollitt, Glenda Sobey, & D J A Scott. (2012). Femoral Artery Dissection in Vascular Type Ehlers–Danlos Syndrome; Leave Well Alone?. European Journal of Vascular and Endovascular Surgery. 43(3). 341–342. 6 indexed citations

18.

Kivuva, Emma, Michael Parker, Marta C. Cohen, Bart Wagner, & Glenda Sobey. (2008). De Barsy syndrome: a review of the phenotype. Clinical Dysmorphology. 17(2). 99–107. 30 indexed citations

19.

Sobey, Glenda, et al.. (2007). Mosaic Chromosome 6 Trisomy in an Epidermal Nevus. Pediatric Dermatology. 24(2). 144–146. 3 indexed citations

20.

Jessop, Sue, et al.. (2002). Pattern of admissions to a tertiary dermatology unit in South Africa. International Journal of Dermatology. 41(9). 568–570. 18 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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