Diana Wellesley

9.4k total citations
76 papers, 1.9k citations indexed

About

Diana Wellesley is a scholar working on Surgery, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Diana Wellesley has authored 76 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Surgery, 32 papers in Pediatrics, Perinatology and Child Health and 22 papers in Genetics. Recurrent topics in Diana Wellesley's work include Congenital Anomalies and Fetal Surgery (23 papers), Prenatal Screening and Diagnostics (22 papers) and Urological Disorders and Treatments (15 papers). Diana Wellesley is often cited by papers focused on Congenital Anomalies and Fetal Surgery (23 papers), Prenatal Screening and Diagnostics (22 papers) and Urological Disorders and Treatments (15 papers). Diana Wellesley collaborates with scholars based in United Kingdom, Denmark and France. Diana Wellesley's co-authors include Helen Dolk, Patricia A. Boyd, Ester Garne, Judith Rankin, Maria Loane, David Howe, Joan K. Morris, Elizabeth S. Draper, Sarah F. Slaney and Lenore Abramsky and has published in prestigious journals such as SHILAP Revista de lepidopterología, Environmental Health Perspectives and BMJ.

In The Last Decade

Diana Wellesley

72 papers receiving 1.8k citations

Peers

Diana Wellesley
Angela E. Scheuerle United States
Anna Pierini Italy
Elisa Calzolari Italy
Ingeborg Barišić Croatia
Jennifer Isenburg United States
Tunu Ramadhani United States
S. Shahrukh Hashmi United States
Elisabeth Robert Sweden
Angela E. Scheuerle United States
Diana Wellesley
Citations per year, relative to Diana Wellesley Diana Wellesley (= 1×) peers Angela E. Scheuerle

Countries citing papers authored by Diana Wellesley

Since Specialization
Citations

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

Fields of papers citing papers by Diana Wellesley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diana Wellesley

This figure shows the co-authorship network connecting the top 25 collaborators of Diana Wellesley. A scholar is included among the top collaborators of Diana Wellesley 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 Diana Wellesley. Diana Wellesley 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.
Santoro, Michele, Ingeborg Barišić, Alessio Coi, et al.. (2025). Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study. Orphanet Journal of Rare Diseases. 20(1). 76–76.
2.
Arrondel, Christelle, Giulia Barcia, Zahra Assouline, et al.. (2025). Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism. Pediatric Nephrology. 40(9). 2823–2828. 1 indexed citations
3.
Urhøj, Stine Kjær, Joan K. Morris, Maria Loane, et al.. (2024). Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study. Acta Paediatrica. 113(5). 1024–1031. 1 indexed citations
4.
Bergman, Jorieke E. H., Ingeborg Barišić, Agnieszka Kinsner‐Ovaskainen, et al.. (2024). Updated EUROCAT guidelines for classification of cases with congenital anomalies. Birth Defects Research. 116(2). e2314–e2314. 8 indexed citations
5.
Urhøj, Stine Kjær, Joachim Tan, Clara Cavero‐Carbonell, et al.. (2023). The burden of disease for children born alive with Turner syndrome—A European cohort study. Birth Defects Research. 115(16). 1459–1468. 1 indexed citations
6.
Glinianaia, Svetlana V., Judith Rankin, Joachim Tan, et al.. (2023). Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study. Archives of Disease in Childhood. 108(6). 461–467. 6 indexed citations
7.
Garne, Ester, Joachim Tan, Maria Loane, et al.. (2022). Gastrostomy and congenital anomalies: a European population-based study. BMJ Paediatrics Open. 6(1). e001526–e001526. 3 indexed citations
8.
Shangaris, Panicos, Alison Ho, Simi George, et al.. (2021). A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report. BMC Medical Genomics. 14(1). 58–58. 1 indexed citations
9.
Parkes, Brandon, Anna Hansell, Rebecca Ghosh, et al.. (2019). Risk of congenital anomalies near municipal waste incinerators in England and Scotland: Retrospective population-based cohort study. Environment International. 134. 104845–104845. 20 indexed citations
10.
Osmond, Clive, et al.. (2016). Relationship between neonatal gastroschisis and maternal body mass index in a United Kingdom population. European Journal of Obstetrics & Gynecology and Reproductive Biology. 210. 292–294. 7 indexed citations
11.
Luteijn, Michiel, Marie‐Claude Addor, Larraitz Arriola, et al.. (2015). The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe. Epidemiology. 26(6). 853–861. 5 indexed citations
12.
Barišić, Ingeborg, Maria Loane, Ester Garne, et al.. (2014). Meckel–Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe. European Journal of Human Genetics. 23(6). 746–752. 46 indexed citations
13.
Wellesley, Diana & Anneke Lucassen. (2014). Prenatal diagnosis of chromosomal imbalances. Archives of Disease in Childhood Fetal & Neonatal. 99(4). F338–F341. 4 indexed citations
14.
Boyd, P A, Catherine Rounding, P. Chamberlain, Diana Wellesley, & JJ Kurinczuk. (2012). The evolution of prenatal screening and diagnosis and its impact on an unselected population over an 18‐year period. BJOG An International Journal of Obstetrics & Gynaecology. 119(9). 1131–1140. 23 indexed citations
15.
Ramsay, Lauren, David Howe, & Diana Wellesley. (2009). Parental attitude to participating in long‐term follow‐up studies of their children's health after in utero diagnosis of abnormalities. Prenatal Diagnosis. 29(3). 207–212. 13 indexed citations
16.
Blyth, Moira, Danielle Howe, James Gnanapragasam, & Diana Wellesley. (2008). The hidden mortality of transposition of the great arteries and survival advantage provided by prenatal diagnosis. BJOG An International Journal of Obstetrics & Gynaecology. 115(9). 1096–1100. 61 indexed citations
17.
Nieuwenhuijsen, Mark, Mireille B. Toledano, James E. Bennett, et al.. (2007). Chlorination Disinfection By-Products and Risk of Congenital Anomalies in England and Wales. Environmental Health Perspectives. 116(2). 216–222. 62 indexed citations
18.
Barišić, Ingeborg, Maria Loane, Fabrizio Bianchi, et al.. (2007). Descriptive epidemiology of Cornelia de Lange syndrome in Europe. American Journal of Medical Genetics Part A. 146A(1). 51–59. 59 indexed citations
19.
Wellesley, Diana, et al.. (2005). An aetiological classification of birth defects for epidemiological research. Journal of Medical Genetics. 42(1). 54–57. 28 indexed citations
20.
Thomas, N. Simon, et al.. (2004). SHOX mutations in a family and a fetus with Langer mesomelic dwarfism. American Journal of Medical Genetics Part A. 128A(2). 179–184. 14 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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