Julie Tinat

2.5k total citations · 1 hit paper
13 papers, 703 citations indexed

About

Julie Tinat is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Julie Tinat has authored 13 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Pathology and Forensic Medicine and 6 papers in Oncology. Recurrent topics in Julie Tinat's work include Genetic factors in colorectal cancer (6 papers), BRCA gene mutations in cancer (3 papers) and Cancer-related Molecular Pathways (3 papers). Julie Tinat is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), BRCA gene mutations in cancer (3 papers) and Cancer-related Molecular Pathways (3 papers). Julie Tinat collaborates with scholars based in France, Poland and Austria. Julie Tinat's co-authors include Stéphanie Baert‐Desurmont, Thierry Frébourg, Brigitte Bressac–de Paillerets, Gaëlle Bougeard, Laurence Brugières, Patrick R. Benusiglio, Catherine Bonaïti‐Pellié, Muriel Belotti, Jean‐Michel Flaman and Valérie Bonadona and has published in prestigious journals such as Journal of Clinical Oncology, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Julie Tinat

12 papers receiving 694 citations

Hit Papers

Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers 2015 2026 2018 2022 2015 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers
    2015 467 citations Gaëlle Bougeard, Mariette Renaux‐Petel et al. Journal of Clinical Oncology profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julie Tinat France 7 319 305 281 249 157 13 703
Émilie Consolino France 4 251 0.8× 260 0.9× 167 0.6× 153 0.6× 75 0.5× 4 523
Mariette Renaux‐Petel France 7 255 0.8× 310 1.0× 142 0.5× 169 0.7× 76 0.5× 12 583
Serena Masciari United States 13 320 1.0× 445 1.5× 224 0.8× 245 1.0× 207 1.3× 23 798
Tim Ripperger Germany 15 341 1.1× 135 0.4× 259 0.9× 215 0.9× 203 1.3× 46 756
Hendrik F. van Essen Netherlands 13 326 1.0× 278 0.9× 153 0.5× 276 1.1× 200 1.3× 22 775
Sheena Scroggins United States 5 449 1.4× 550 1.8× 352 1.3× 295 1.2× 142 0.9× 5 966
Giovana Tardin Torrezan Brazil 15 320 1.0× 201 0.7× 192 0.7× 211 0.8× 160 1.0× 60 715
Robyn Lukeis Australia 13 273 0.9× 202 0.7× 122 0.4× 149 0.6× 155 1.0× 25 580
Muriel Belotti France 4 210 0.7× 262 0.9× 145 0.5× 150 0.6× 76 0.5× 5 492
Denisa Ilenčíková Slovakia 15 301 0.9× 227 0.7× 190 0.7× 257 1.0× 438 2.8× 40 851

Countries citing papers authored by Julie Tinat

Since Specialization
Citations

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

Fields of papers citing papers by Julie Tinat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie Tinat

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

All Works

13 of 13 papers shown
1.
Fontaine, A., Denis Smith, Jacques Mauillon, et al.. (2025). New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patients. Familial Cancer. 24(1). 22–22. 1 indexed citations
2.
Kouwen, Mariëtte van, Birgitta Versluys, Delphine Bonnet, et al.. (2022). High yield of surveillance in patients diagnosed with constitutional mismatch repair deficiency. Journal of Medical Genetics. 60(7). 679–684. 9 indexed citations
3.
Orazio, Sébastien, Fabrice Bonnet, Natalie Jones, et al.. (2022). Increased incidence of pathogenic variants in ATM in the context of testing for breast and ovarian cancer predisposition. Journal of Human Genetics. 67(6). 339–345. 2 indexed citations
4.
Van‐Gils, Julien, Cécile Zordan, Julie Tinat, et al.. (2019). Coexistence of schwannomatosis and glioblastoma in two families. European Journal of Medical Genetics. 62(8). 103680–103680. 7 indexed citations
5.
Yauy, Kévin, Virginie Bubien, Hélène Perrochia, et al.. (2019). Ovarian Clear Cell Carcinoma in Cowden Syndrome. Journal of the National Comprehensive Cancer Network. 17(1). 7–11. 8 indexed citations
6.
Dugué, Audrey Emmanuelle, Angélina Legros, Alexandra Leconte, et al.. (2016). BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer. Familial Cancer. 16(2). 167–171.
7.
Bougeard, Gaëlle, Mariette Renaux‐Petel, Jean‐Michel Flaman, et al.. (2015). Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers. Journal of Clinical Oncology. 33(21). 2345–2352. 467 indexed citations breakdown →
8.
Castéra, Laurent, Sophie Krieger, Antoine Rousselin, et al.. (2014). Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes. European Journal of Human Genetics. 22(11). 1305–1313. 175 indexed citations
9.
Grandval, Philippe, Martine Blayau, Marie‐Pierre Buisine, et al.. (2014). The UMD-APC Database, a Model of Nation-Wide Knowledge Base: Update with Data from 3,581 Variations. Human Mutation. 35(5). 532–536. 11 indexed citations
10.
Bougeard, Gaëlle, Laurence Olivier-Faivre, Stéphanie Baert‐Desurmont, et al.. (2013). Diversity of the clinical presentation of the MMR gene biallelic mutations. Familial Cancer. 13(1). 131–135. 17 indexed citations
11.
Caron, Olivier, Thierry Frébourg, Emmanuelle Bourbouloux, et al.. (2013). Evaluation of whole body MRI for early detection of cancers in subjects with germ-line TP53 mutation (Li-Fraumeni syndrome).. Journal of Clinical Oncology. 31(15_suppl). TPS1607–TPS1607. 1 indexed citations
12.
Baert‐Desurmont, Stéphanie, Nicolas Piton, Jacqueline Bou, et al.. (2011). A remarkable APC mosaicism with two mutant alleles in a family with familial adenomatous polyposis. American Journal of Medical Genetics Part A. 155(6). 1500–1502. 3 indexed citations
13.
Tinat, Julie, Stéphanie Baert‐Desurmont, Jean‐Baptiste Latouche, et al.. (2008). The three nucleotide deletion within the 3′untranslated region of MLH1 resulting in gene expression reduction is not a causal alteration in Lynch syndrome. Familial Cancer. 7(4). 339–340. 2 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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