Vivienne McConnell

5.6k total citations
20 papers, 502 citations indexed

About

Vivienne McConnell is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Vivienne McConnell has authored 20 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Vivienne McConnell's work include Connective tissue disorders research (5 papers), Genetic Syndromes and Imprinting (2 papers) and Genomics and Rare Diseases (2 papers). Vivienne McConnell is often cited by papers focused on Connective tissue disorders research (5 papers), Genetic Syndromes and Imprinting (2 papers) and Genomics and Rare Diseases (2 papers). Vivienne McConnell collaborates with scholars based in United Kingdom, United States and Ireland. Vivienne McConnell's co-authors include Giuliana Silvestri, Anne E. Hughes, Ruth Hogg, Usha Chakravarthy, C. C. Patterson, Nick Orr, Anne De Paepe, Daniela Macaya, Paul Coucke and Elise Davis and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and PLoS Medicine.

In The Last Decade

Vivienne McConnell

20 papers receiving 496 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vivienne McConnell United Kingdom 12 191 186 88 75 71 20 502
Shazia Micheal Pakistan 18 124 0.6× 274 1.5× 329 3.7× 38 0.5× 56 0.8× 36 655
Rosemary Kane Ireland 10 34 0.2× 208 1.1× 114 1.3× 24 0.3× 27 0.4× 16 447
PJ van Diest Netherlands 4 44 0.2× 235 1.3× 58 0.7× 60 0.8× 20 0.3× 13 450
Fehim Esen Türkiye 13 34 0.2× 166 0.9× 189 2.1× 204 2.7× 30 0.4× 47 678
William A. Figgett Australia 11 51 0.3× 135 0.7× 39 0.4× 442 5.9× 78 1.1× 18 768
Sebastian Costa France 10 40 0.2× 122 0.7× 33 0.4× 37 0.5× 40 0.6× 14 413
Y.W. Song South Korea 7 47 0.2× 119 0.6× 29 0.3× 271 3.6× 49 0.7× 25 525
Š Rùzicková Czechia 11 59 0.3× 168 0.9× 22 0.3× 203 2.7× 28 0.4× 20 463
J. Preston Alexander United States 10 39 0.2× 192 1.0× 159 1.8× 37 0.5× 19 0.3× 10 667
Lesley Everett United States 9 61 0.3× 167 0.9× 97 1.1× 43 0.6× 6 0.1× 39 478

Countries citing papers authored by Vivienne McConnell

Since Specialization
Citations

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

Fields of papers citing papers by Vivienne McConnell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vivienne McConnell

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

All Works

20 of 20 papers shown
1.
Shoubridge, Cheryl, et al.. (2022). IQSEC2 ‐related encephalopathy in males due to missense variants in the pleckstrin homology domain. Clinical Genetics. 102(1). 72–77. 4 indexed citations
2.
McConnell, Vivienne & Giuliana Silvestri. (2021). Age-Related Macular Degeneration. Elsevier eBooks. 74(2). 82–92. 3 indexed citations
3.
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
4.
McConnell, Vivienne, et al.. (2018). Exploring the association between SRPX2 variants and neurodevelopment: How causal is it?. Gene. 685. 50–54. 8 indexed citations
5.
Schulte, Dörte, Vivienne McConnell, Silvia Martin‐Almedina, et al.. (2018). A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon. International Journal of Molecular Sciences. 19(8). 2259–2259. 11 indexed citations
6.
Coleman, Helen G., Maurice B. Loughrey, Liam Murray, et al.. (2015). Colorectal Cancer Risk Following Adenoma Removal: A Large Prospective Population-Based Cohort Study. Cancer Epidemiology Biomarkers & Prevention. 24(9). 1373–1380. 33 indexed citations
7.
Pagnamenta, Alistair T., Moira Blyth, Sahar Mansour, et al.. (2015). Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome. Journal of Medical Genetics. 53(3). 152–162. 53 indexed citations
8.
McConnell, Vivienne, et al.. (2015). The ocular phenotype of stiff-skin syndrome. Eye. 30(1). 156–159. 3 indexed citations
9.
Vijzelaar, Raymon, Sarah Waller, Abdellatif Errami, et al.. (2013). Deletions within COL11A1in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA). BMC Medical Genetics. 14(1). 48–48. 18 indexed citations
10.
Burkitt‐Wright, Emma, Lisa Bradley, Vivienne McConnell, et al.. (2012). Neonatal lethal Costello syndrome and unusual dinucleotide deletion/insertion mutations in HRAS predicting p.Gly12Val. American Journal of Medical Genetics Part A. 158A(5). 1102–1110. 18 indexed citations
11.
Donnelly, Deirdre E., Peter D. Turnpenny, & Vivienne McConnell. (2011). Phenotypic variability in a three-generation Northern Irish family with Sotos syndrome. Clinical Dysmorphology. 20(4). 175–181. 5 indexed citations
12.
Wallace, I. R., Vivienne McConnell, P. M. Bell, & John R. Lindsay. (2011). Challenges in Management of Primary Hypoparathyroidism Associated with Autoimmune Polyglandular Syndrome Type 1. SHILAP Revista de lepidopterología. 2011. 1–3. 1 indexed citations
13.
Donnelly, Deirdre E., Vivienne McConnell, Anne Paterson, & Patrick J. Morrison. (2010). The prevalence of thanatophoric dysplasia and lethal osteogenesis imperfecta type II in Northern Ireland - a complete population study.. PubMed. 79(3). 114–8. 13 indexed citations
14.
Loeys, Bart, Elizabeth E. Gerber, Douglas L. Riegert‐Johnson, et al.. (2010). Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome. Science Translational Medicine. 2(23). 23ra20–23ra20. 165 indexed citations
15.
Hong, Min, Kelli R. Ryan, Peter D. Arkwright, et al.. (2009). Pattern recognition receptor expression is not impaired in patients with chronic mucocutanous candidiasis with or without autoimmune polyendocrinopathy candidiasis ectodermal dystrophy. Clinical & Experimental Immunology. 156(1). 40–51. 16 indexed citations
16.
Ryan, Kelli R., Min Hong, Peter D. Arkwright, et al.. (2008). Impaired dendritic cell maturation and cytokine production in patients with chronic mucocutanous candidiasis with or without APECED. Clinical & Experimental Immunology. 154(3). 406–414. 34 indexed citations
17.
Hughes, Anne E., Nick Orr, C. C. Patterson, et al.. (2007). Neovascular Age-Related Macular Degeneration Risk Based on CFH, LOC387715/HTRA1, and Smoking. PLoS Medicine. 4(12). e355–e355. 80 indexed citations
18.
McKay, Gareth J., Anne E. Hughes, Vivienne McConnell, et al.. (2004). A novel diagnostic test detects a low frequency of the hemicentin Gln5345Arg variant among Northern Irish age related macular degeneration patients.. PubMed. 10. 682–7. 11 indexed citations
19.
McConnell, Vivienne, et al.. (2004). Mosaic monosomy 14: clinical features and recognizable facies. Clinical Dysmorphology. 13(3). 155–160. 1 indexed citations
20.
McConnell, Vivienne, Theodore M. Brown, & PJ Morrison. (2003). An Irish three-generation family of Cornelia de Lange syndrome displaying autosomal dominant inheritance. Clinical Dysmorphology. 12(4). 241–244. 8 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Shazia Micheal Breakdown of academic impact, for papers by Rosemary Kane Breakdown of academic impact, for papers by PJ van Diest Breakdown of academic impact, for papers by Fehim Esen Breakdown of academic impact, for papers by William A. Figgett Breakdown of academic impact, for papers by Sebastian Costa Breakdown of academic impact, for papers by Y.W. Song Breakdown of academic impact, for papers by Š Rùzicková Breakdown of academic impact, for papers by J. Preston Alexander Breakdown of academic impact, for papers by Lesley Everett
Rankless by CCL
2026