Leslie Steele

867 total citations
23 papers, 525 citations indexed

About

Leslie Steele is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Leslie Steele has authored 23 papers receiving a total of 525 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 9 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Leslie Steele's work include Genetic Syndromes and Imprinting (8 papers), Prenatal Screening and Diagnostics (8 papers) and Epigenetics and DNA Methylation (6 papers). Leslie Steele is often cited by papers focused on Genetic Syndromes and Imprinting (8 papers), Prenatal Screening and Diagnostics (8 papers) and Epigenetics and DNA Methylation (6 papers). Leslie Steele collaborates with scholars based in Canada, United States and Australia. Leslie Steele's co-authors include Peter N. Ray, Rosanna Weksberg, Cheryl Shuman, Adam C. Smith, David Chitayat, Sanaa Choufani, Cheryl Cytrynbaum, Peter R. Durie, Paul Kortan and Annie Dupuis and has published in prestigious journals such as Journal of the American Society of Nephrology, Thorax and Human Genetics.

In The Last Decade

Leslie Steele

23 papers receiving 506 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leslie Steele Canada 14 274 232 175 105 80 23 525
Jodi D. Hoffman United States 18 365 1.3× 215 0.9× 119 0.7× 74 0.7× 52 0.7× 33 654
Natalia T. Leach United States 9 264 1.0× 199 0.9× 245 1.4× 113 1.1× 44 0.6× 17 587
M L Martínez-Frías Spain 10 152 0.6× 113 0.5× 103 0.6× 45 0.4× 140 1.8× 20 459
Ulrike Mau Germany 8 356 1.3× 349 1.5× 454 2.6× 43 0.4× 24 0.3× 10 777
Klaske D. Lichtenbelt Netherlands 16 339 1.2× 241 1.0× 331 1.9× 99 0.9× 79 1.0× 30 775
Mahmoud Aarabi United States 11 207 0.8× 196 0.8× 214 1.2× 103 1.0× 29 0.4× 20 541
Daniele De Brasi Italy 14 256 0.9× 224 1.0× 86 0.5× 38 0.4× 73 0.9× 44 478
Anna Baroncini Italy 13 256 0.9× 149 0.6× 128 0.7× 50 0.5× 61 0.8× 29 458
Claire Turner United Kingdom 13 414 1.5× 304 1.3× 183 1.0× 44 0.4× 61 0.8× 14 578
Louise C. Pyle United States 12 176 0.6× 290 1.3× 30 0.2× 143 1.4× 74 0.9× 28 479

Countries citing papers authored by Leslie Steele

Since Specialization
Citations

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

Fields of papers citing papers by Leslie Steele

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leslie Steele

This figure shows the co-authorship network connecting the top 25 collaborators of Leslie Steele. A scholar is included among the top collaborators of Leslie Steele 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 Leslie Steele. Leslie Steele 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.
Brzezinski, Jack, Cheryl Shuman, Sanaa Choufani, et al.. (2017). Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines. European Journal of Human Genetics. 25(9). 1031–1039. 21 indexed citations
2.
Cytrynbaum, Cheryl, Karen Chong, Vickie Hannig, et al.. (2016). Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell–Silver syndrome. American Journal of Medical Genetics Part A. 170(10). 2731–2739. 14 indexed citations
3.
Steele, Leslie, Johanna M. Rommens, Tracy Stockley, Berivan Baskin, & Peter N. Ray. (2014). De Novo Mutations Causing Shwachman-Diamond Syndrome and a Founder Mutation in SBDS in the French Canadian Population. 1(2). 3 indexed citations
4.
Baskin, Berivan, Dimitri J. Stavropoulos, Martin Li, et al.. (2014). Complex genomic rearrangements in the dystrophin gene due to replication‐based mechanisms. Molecular Genetics & Genomic Medicine. 2(6). 539–547. 17 indexed citations
5.
Ooi, Chee Y., Annie Dupuis, Tanja Gonska, et al.. (2014). Does Integration of Various Ion Channel Measurements Improve Diagnostic Performance in Cystic Fibrosis?. Annals of the American Thoracic Society. 11(4). 562–570. 9 indexed citations
6.
Boonyawat, Boonchai, Santhosh Dhanraj, Bozana Zlateska, et al.. (2013). Combined De-Novo Mutation and Non-Random X-Chromosome Inactivation Causing Wiskott-Aldrich Syndrome in a Female with Thrombocytopenia. Journal of Clinical Immunology. 33(7). 1150–1155. 19 indexed citations
7.
8.
Inbar‐Feigenberg, Michal, Sanaa Choufani, Cheryl Cytrynbaum, et al.. (2012). Mosaicism for genome‐wide paternal uniparental disomy with features of multiple imprinting disorders: Diagnostic and management issues. American Journal of Medical Genetics Part A. 161(1). 13–20. 46 indexed citations
9.
Winsor, E.J.T., Hani Akoury, David Chitayat, Leslie Steele, & Tracy Stockley. (2010). The role of molecular microsatellite identity testing to detect sampling errors in prenatal diagnosis. Prenatal Diagnosis. 30(8). 746–752. 9 indexed citations
10.
Moore, S. Jo, H. Dawn Marshall, Leslie Steele, et al.. (2008). The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in Newfoundland. Clinical Genetics. 74(3). 213–222. 51 indexed citations
11.
Smith, Adam C., Cheryl Shuman, David Chitayat, et al.. (2007). Severe presentation of Beckwith–Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15. American Journal of Medical Genetics Part A. 143A(24). 3010–3015. 35 indexed citations
12.
Smith, Adam C., Cheryl Shuman, Laurel L. Estabrooks, et al.. (2006). New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome. Cytogenetic and Genome Research. 113(1-4). 313–317. 23 indexed citations
13.
Shuman, Cheryl, Adam C. Smith, Leslie Steele, et al.. (2006). Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies. American Journal of Medical Genetics Part A. 140A(14). 1497–1503. 48 indexed citations
14.
Shah, Parag, Komudi Siriwardena, Glenn Taylor, et al.. (2006). Sudden infant death in a patient with FGFR3 P250R mutation. American Journal of Medical Genetics Part A. 140A(24). 2794–2796. 9 indexed citations
15.
Bishop, Michèle D., Steven D. Freedman, Julian Zielenski, et al.. (2005). The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis. Human Genetics. 118(3-4). 372–381. 72 indexed citations
16.
Skidmore, David, et al.. (2003). Prenatal diagnosis of Apert syndrome: report of two cases. Prenatal Diagnosis. 23(12). 1009–1013. 22 indexed citations
17.
Chun, Kathy, et al.. (2003). Screening of patients with craniosynostosis: Molecular strategy. American Journal of Medical Genetics Part A. 120A(4). 470–473. 21 indexed citations
18.
Goldman, Michaël, Adam C. Smith, Cheryl Shuman, et al.. (2002). Renal Abnormalities in Beckwith-Wiedemann Syndrome Are Associated with 11p15.5 Uniparental Disomy. Journal of the American Society of Nephrology. 13(8). 2077–2084. 40 indexed citations
19.
Huggins, Marlene J., et al.. (1999). Prenatal sonographic diagnosis of hypochondroplasia in a high-risk fetus. American Journal of Medical Genetics. 87(3). 226–229. 11 indexed citations
20.
Sherman, Lawrence W., et al.. (1989). Stray bullets and ?mushrooms?: Random shootings of bystanders in four cities, 1977?1988. Journal of Quantitative Criminology. 5(4). 297–316. 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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