Bernard Peissel

9.8k total citations
63 papers, 1.7k citations indexed

About

Bernard Peissel is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Bernard Peissel has authored 63 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 34 papers in Molecular Biology and 12 papers in Oncology. Recurrent topics in Bernard Peissel's work include BRCA gene mutations in cancer (26 papers), DNA Repair Mechanisms (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Bernard Peissel is often cited by papers focused on BRCA gene mutations in cancer (26 papers), DNA Repair Mechanisms (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Bernard Peissel collaborates with scholars based in Italy, United States and United Kingdom. Bernard Peissel's co-authors include Siranoush Manoukian, Lin Geng, Paolo Radice, Cecilia Larson, Lu W, Xiaohong Fan, Gregory A. Brent, Anna Pavlova, Jing Zhou and York Pei and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and PLoS ONE.

In The Last Decade

Bernard Peissel

62 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernard Peissel Italy 21 948 942 265 253 208 63 1.7k
Steven G. Brodie United States 20 660 0.7× 1.4k 1.5× 185 0.7× 558 2.2× 276 1.3× 32 1.9k
Miguel de la Hoya Spain 26 945 1.0× 1.0k 1.1× 565 2.1× 488 1.9× 575 2.8× 92 1.9k
Gunnar Wrobel Germany 19 327 0.3× 758 0.8× 271 1.0× 275 1.1× 287 1.4× 21 1.5k
Johanna Tapper Finland 14 410 0.4× 701 0.7× 246 0.9× 339 1.3× 353 1.7× 22 1.4k
Tina Pesaran United States 16 1.2k 1.3× 827 0.9× 379 1.4× 327 1.3× 567 2.7× 43 1.9k
Kim Wilber Switzerland 14 334 0.4× 787 0.8× 117 0.4× 627 2.5× 395 1.9× 16 1.5k
Andrew Berchuck United States 10 149 0.2× 560 0.6× 249 0.9× 375 1.5× 203 1.0× 11 1.1k
Mariwil G. Wong United States 23 419 0.4× 564 0.6× 149 0.6× 430 1.7× 207 1.0× 36 1.6k
Rósa B. Barkardóttir Iceland 26 1.3k 1.4× 1.1k 1.2× 447 1.7× 482 1.9× 739 3.6× 50 2.2k
Lúcia Roque Portugal 24 304 0.3× 506 0.5× 296 1.1× 562 2.2× 199 1.0× 49 1.5k

Countries citing papers authored by Bernard Peissel

Since Specialization
Citations

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

Fields of papers citing papers by Bernard Peissel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernard Peissel

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard Peissel. A scholar is included among the top collaborators of Bernard Peissel 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 Bernard Peissel. Bernard Peissel 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.
Milani, Donatella, Alessia Dolci, Ilaria Muller, et al.. (2023). Thyroid findings in pediatric and adult patients with PTEN hamartoma tumor syndrome: A retrospective analysis, and literature review. Endocrine. 81(1). 98–106. 5 indexed citations
2.
Tomasello, Giovanni, Donatella Gambini, Fausto Petrelli, et al.. (2022). Characterization of the HER2 status in BRCA-mutated breast cancer: a single institutional series and systematic review with pooled analysis. ESMO Open. 7(4). 100531–100531. 12 indexed citations
3.
Radice, Paolo, Mara Colombo, Angelo Paradiso, et al.. (2022). The Impact of Mediterranean Dietary Intervention on Metabolic and Hormonal Parameters According to BRCA1/2 Variant Type. Frontiers in Genetics. 13. 820878–820878. 2 indexed citations
4.
Vergani, Elisabetta, Simona Frigerio, Matteo Dugo, et al.. (2021). Genetic Variants and Somatic Alterations Associated with MITF-E318K Germline Mutation in Melanoma Patients. Genes. 12(9). 1440–1440. 3 indexed citations
5.
Bruno, Eleonora, Angelo Paradiso, Antonella Daniele, et al.. (2020). Lifestyle Characteristics in Women Carriers of BRCA Mutations: Results From an Italian Trial Cohort. Clinical Breast Cancer. 21(3). e168–e176. 10 indexed citations
6.
Bruno, Eleonora, Mara Colombo, Angelo Paradiso, et al.. (2020). BRCA1/2 Variants and Metabolic Factors: Results From a Cohort of Italian Female Carriers. Cancers. 12(12). 3584–3584. 4 indexed citations
7.
Manoukian, Siranoush, Sara Alfieri, Elisabetta Bianchi, et al.. (2019). Risk‐reducing surgery in BRCA1/BRCA2 mutation carriers: Are there factors associated with the choice?. Psycho-Oncology. 28(9). 1871–1878. 12 indexed citations
8.
Pasanisi, Patrizia, Eleonora Bruno, Elisabetta Venturelli, et al.. (2018). A Dietary Intervention to Lower Serum Levels of IGF-I in BRCA Mutation Carriers. Cancers. 10(9). 309–309. 16 indexed citations
9.
Roversi, Gaia, M. Crippa, Daniela Perotti, et al.. (2015). Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors. Scientific Reports. 5(1). 15454–15454. 7 indexed citations
10.
Lusa, Lara, Loris De Cecco, Edoardo Marchesi, et al.. (2014). miR-342 Regulates BRCA1 Expression through Modulation of ID4 in Breast Cancer. PLoS ONE. 9(1). e87039–e87039. 53 indexed citations
11.
Berrino, Franco, Silvia Francisci, Bernard Peissel, et al.. (2014). Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability. Familial Cancer. 14(1). 117–128. 11 indexed citations
12.
Ripamonti, Carla B., Mara Colombo, P Mondini, et al.. (2013). First description of an acinic cell carcinoma of the breast in a BRCA1 mutation carrier: a case report. BMC Cancer. 13(1). 46–46. 32 indexed citations
13.
Pasanisi, Patrizia, Eleonora Bruno, Elisabetta Venturelli, et al.. (2011). Serum levels of IGF-I and BRCA penetrance: a case control study in breast cancer families. Familial Cancer. 10(3). 521–528. 31 indexed citations
14.
Brancati, Francesco, Valentina Gatta, Ivana Antonucci, et al.. (2010). Two Novel Mutations Affecting Splicing in the IRF6 Gene Associated With van der Woude Syndrome. Journal of Craniofacial Surgery. 21(5). 1654–1656. 8 indexed citations
15.
Colombo, Mara, Monica Giarola, Luigi Mariani, et al.. (2008). Cyclin D1 expression analysis in familial breast cancers may discriminate BRCAX from BRCA2-linked cases. Modern Pathology. 21(10). 1262–1270. 13 indexed citations
16.
Carcangiu, Maria Luisa, Bernard Peissel, Barbara Pasini, et al.. (2006). Incidental Carcinomas in Prophylactic Specimens in BRCA1 and BRCA2 Germ-line Mutation Carriers, With Emphasis on Fallopian Tube Lesions. The American Journal of Surgical Pathology. 30(10). 1222–1230. 89 indexed citations
17.
Dragani, Tommaso A., Bernard Peissel, Nicola Zanesi, et al.. (2000). Mapping of Melanoma Modifier Loci in RET Transgenic Mice. Japanese Journal of Cancer Research. 91(11). 1142–1147. 12 indexed citations
18.
Segal, Yoav, Bernard Peissel, Alessandra Renieri, et al.. (1999). LINE-1 Elements at the Sites of Molecular Rearrangements in Alport Syndrome–Diffuse Leiomyomatosis. The American Journal of Human Genetics. 64(1). 62–69. 80 indexed citations
19.
Peissel, Bernard, Geng Li, Raghu Kalluri, et al.. (1995). Comparative distribution of the alpha 1(IV), alpha 5(IV), and alpha 6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patients.. Journal of Clinical Investigation. 96(4). 1948–1957. 89 indexed citations
20.
Turco, Alberto, E Padovani, Bernard Peissel, et al.. (1995). Gene linkage analysis and DNA based detection of autosomal dominant polycystic kidney disease (ADPKD) in a newborn infant. Case report. Journal of Perinatal Medicine. 23(3). 205–212. 4 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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