Renée Perrier

659 total citations
19 papers, 192 citations indexed

About

Renée Perrier is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Renée Perrier has authored 19 papers receiving a total of 192 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Renée Perrier's work include Genetic and rare skin diseases. (4 papers), Genetic factors in colorectal cancer (3 papers) and Cancer Genomics and Diagnostics (3 papers). Renée Perrier is often cited by papers focused on Genetic and rare skin diseases. (4 papers), Genetic factors in colorectal cancer (3 papers) and Cancer Genomics and Diagnostics (3 papers). Renée Perrier collaborates with scholars based in Canada, United States and Australia. Renée Perrier's co-authors include Máire A. Duggan, Prafull Ghatage, Linda E. Kelemen, Peter Rambau, Martin Köbel, Helen Steed, Paul Burrowes, Richard M. Haber, Kyle C. Kurek and Willis H. Tsai and has published in prestigious journals such as Gynecologic Oncology, Histopathology and Lung Cancer.

In The Last Decade

Renée Perrier

17 papers receiving 191 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Renée Perrier Canada 7 61 57 51 46 42 19 192
Asad Haider United States 6 26 0.4× 75 1.3× 146 2.9× 45 1.0× 49 1.2× 13 287
Samantha Hansford Canada 4 91 1.5× 110 1.9× 64 1.3× 63 1.4× 111 2.6× 5 276
Zohreh Ketabi Denmark 7 42 0.7× 77 1.4× 52 1.0× 9 0.2× 94 2.2× 8 211
Bliss Magella United States 7 65 1.1× 254 4.5× 48 0.9× 66 1.4× 10 0.2× 11 348
Mayuko Inuzuka Japan 6 87 1.4× 78 1.4× 22 0.4× 73 1.6× 58 1.4× 11 249
Julie Irving Canada 6 35 0.6× 184 3.2× 160 3.1× 102 2.2× 80 1.9× 6 359
B Dębniak Poland 9 76 1.2× 87 1.5× 22 0.4× 17 0.4× 32 0.8× 11 229
Monica Rosèn United States 8 18 0.3× 130 2.3× 44 0.9× 7 0.2× 41 1.0× 37 314
Benjamin Goode United States 4 18 0.3× 85 1.5× 23 0.5× 44 1.0× 21 0.5× 4 210
Angela Burleigh Canada 7 14 0.2× 52 0.9× 78 1.5× 13 0.3× 56 1.3× 12 246

Countries citing papers authored by Renée Perrier

Since Specialization
Citations

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

Fields of papers citing papers by Renée Perrier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renée Perrier

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

All Works

19 of 19 papers shown
1.
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Bauman, Bradly M., Batsukh Dorjbal, Stefania Pittaluga, et al.. (2023). Subcutaneous panniculitis-like T-cell lymphoma in two unrelated individuals with BENTA disease. Clinical Immunology. 255. 109732–109732. 4 indexed citations
3.
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Selvarajah, Shamini, Kasmintan A. Schrader, Michael Kolinsky, et al.. (2022). Recommendations for the implementation of genetic testing for metastatic prostate cancer patients in Canada. Canadian Urological Association Journal. 16(10). 321–332. 5 indexed citations
5.
Bründler, Marie‐Anne, et al.. (2021). Bilateral Nephroblastic Tumors and a Complex Renal Vascular Anomaly in a Patient With a Mosaic RASopathy: Novel Histopathologic Features and Molecular Insights. Pediatric and Developmental Pathology. 24(3). 235–240. 13 indexed citations
6.
Perrier, Renée, Kyle C. Kurek, Juvianee Estrada‐Veras, et al.. (2021). Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants. American Journal of Medical Genetics Part A. 185(9). 2829–2845. 25 indexed citations
7.
Le, Doan, Anne Grete Bechensteen, Olav Klingenberg, et al.. (2021). Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype. Hemoglobin. 45(4). 215–219. 1 indexed citations
8.
Cameron, A. T., et al.. (2019). Universal Testing to Identify Lynch Syndrome Among Women With Newly Diagnosed Endometrial Carcinoma. Journal of Obstetrics and Gynaecology Canada. 42(2). 137–143. 6 indexed citations
9.
Glaze, Sarah, et al.. (2018). GO- BRCA : A collaborative service model to improve access to ovarian cancer genetic testing. Gynecologic Oncology. 149. 127–127. 1 indexed citations
10.
Chernos, Judy, Renée Perrier, A. Micheil Innes, et al.. (2017). Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype. Prenatal Diagnosis. 37(6). 602–610. 2 indexed citations
11.
Skolnik, Kate, et al.. (2016). Birt-Hogg-Dubé syndrome: a large single family cohort. Respiratory Research. 17(1). 22–22. 26 indexed citations
12.
Racher, Hilary, Sameh E. Soliman, Bob Argiropoulos, et al.. (2016). Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma. Cancer Genetics. 209(7-8). 359–363. 8 indexed citations
13.
Rambau, Peter, Máire A. Duggan, Prafull Ghatage, et al.. (2016). Significant frequency of MSH2/MSH6 abnormality in ovarian endometrioid carcinoma supports histotype‐specific Lynch syndrome screening in ovarian carcinomas. Histopathology. 69(2). 288–297. 63 indexed citations
14.
Perrier, Renée, et al.. (2016). Metachronous Type I pleuropulmonary blastoma and atypical choroid plexus papilloma in a young child. Pediatric Blood & Cancer. 63(12). 2240–2242. 3 indexed citations
15.
Lazier, Joanna, Jean K. Mah, Ana Nikolić, et al.. (2015). Bilateral congenital lumbar hernias in a patient with central core disease – A case report. Neuromuscular Disorders. 26(1). 56–59. 5 indexed citations
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Innes, A. Micheil, Erik G. Puffenberger, Ian M. MacDonald, et al.. (2010). A founder mutation in BBS2 is responsible for Bardet‐Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. Clinical Genetics. 78(5). 424–431. 16 indexed citations
18.
Perrier, Renée, et al.. (2010). An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutation. Hereditary Cancer in Clinical Practice. 8(Suppl 1). P17–P17. 1 indexed citations
19.

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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