James Stavropoulos

761 total citations
9 papers, 239 citations indexed

About

James Stavropoulos is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, James Stavropoulos has authored 9 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 1 paper in Nephrology. Recurrent topics in James Stavropoulos's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). James Stavropoulos is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). James Stavropoulos collaborates with scholars based in Canada, United States and Hong Kong. James Stavropoulos's co-authors include Rosanna Weksberg, Stephen W. Scherer, David Chitayat, Christian R. Marshall, Roberto Mendoza‐Londono, Ronald D. Cohn, Sarah J. Goodman, Grace Yoon, Nicole Martin and Joanna Lazier and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Neuro-Oncology.

In The Last Decade

James Stavropoulos

9 papers receiving 237 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
James Stavropoulos Canada	6	182	118	19	16	16	9	239
Lori E Corbani United States	3	156 0.9×	40 0.3×	8 0.4×	9 0.6×	14 0.9×	4	217
Yanling Teng China	9	130 0.7×	69 0.6×	31 1.6×	15 0.9×	12 0.8×	33	195
María J. Guillen Sacoto United States	10	118 0.6×	121 1.0×	16 0.8×	5 0.3×	6 0.4×	17	203
Rebecca A. Lea United Kingdom	4	317 1.7×	67 0.6×	22 1.2×	9 0.6×	16 1.0×	6	358
Yexing Xian China	9	184 1.0×	40 0.3×	48 2.5×	20 1.3×	7 0.4×	14	293
Arunabha Majumdar United States	9	168 0.9×	167 1.4×	6 0.3×	6 0.4×	29 1.8×	16	287
Rinho Kim United States	4	205 1.1×	67 0.6×	17 0.9×	32 2.0×	18 1.1×	5	242
Nils Koelling United Kingdom	7	137 0.8×	92 0.8×	15 0.8×	5 0.3×	32 2.0×	10	214
Connie T. R. M. Stumpel Netherlands	7	92 0.5×	110 0.9×	7 0.4×	4 0.3×	11 0.7×	9	197
Tracy Dudding‐Byth Australia	10	147 0.8×	146 1.2×	37 1.9×	4 0.3×	8 0.5×	18	272

Countries citing papers authored by James Stavropoulos

Since Specialization

Citations

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

Fields of papers citing papers by James Stavropoulos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Stavropoulos

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

All Works

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9 of 9 papers shown

Deshwar, Ashish R., Lucie Dupuis, Carsten Bergmann, James Stavropoulos, & Roberto Mendoza‐Londono. (2017). Severe rhizomelic shortening in a child with a complex duplication/deletion rearrangement of chromosome X. American Journal of Medical Genetics Part A. 176(2). 450–454. 3 indexed citations

Lazier, Joanna, Nicole Martin, James Stavropoulos, & David Chitayat. (2016). Maternal uniparental disomy for chromosome 6 in a patient with IUGR, ambiguous genitalia, and persistent mullerian structures. American Journal of Medical Genetics Part A. 170(12). 3227–3230. 17 indexed citations

Rodan, Lance H., et al.. (2016). Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome. Neurology Genetics. 2(1). e43–e43. 1 indexed citations

Kemaladewi, Dwi U., Elzbieta Hyatt, Sérgio L. Pereira, et al.. (2015). Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders. The American Journal of Human Genetics. 98(1). 90–101. 83 indexed citations

Elkadri, Abdul, Cornelia Thoeni, Sophie J. Deharvengt, et al.. (2015). Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and Hypertriglyceridemia. Cellular and Molecular Gastroenterology and Hepatology. 1(4). 381–394.e7. 34 indexed citations

Foong, Justin, Marta Gîrdea, James Stavropoulos, & Michael Brudno. (2015). Prioritizing Clinically Relevant Copy Number Variation from Genetic Interactions and Gene Function Data. PLoS ONE. 10(10). e0139656–e0139656. 6 indexed citations

Zhukova, Nataliya, Daniele Merico, Patricia Rakopoulos, et al.. (2015). LG-01 * BRAF MUTATION AND CDKN2A DELETION DEFINE A CLINICALLY DISTINCT SUBGROUP OF CHILDHOOD SECONDARY HIGH-GRADE GLIOMA. Neuro-Oncology. 17(suppl 3). iii18–iii18. 2 indexed citations

Grafodatskaya, Daria, Darci T. Butcher, Andrei L. Turinsky, et al.. (2013). Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C. BMC Medical Genomics. 6(1). 1–1. 68 indexed citations

Chung, Brian Hon‐Yin, James Stavropoulos, Christian R. Marshall, et al.. (2011). 2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial features. American Journal of Medical Genetics Part A. 155(2). 424–429. 25 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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