Françoise Parmentier

703 total citations
16 papers, 482 citations indexed

About

Françoise Parmentier is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Françoise Parmentier has authored 16 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 10 papers in Pathology and Forensic Medicine and 3 papers in Molecular Biology. Recurrent topics in Françoise Parmentier's work include Lymphoma Diagnosis and Treatment (10 papers), Chronic Lymphocytic Leukemia Research (8 papers) and Cancer Genomics and Diagnostics (3 papers). Françoise Parmentier is often cited by papers focused on Lymphoma Diagnosis and Treatment (10 papers), Chronic Lymphocytic Leukemia Research (8 papers) and Cancer Genomics and Diagnostics (3 papers). Françoise Parmentier collaborates with scholars based in France and Canada. Françoise Parmentier's co-authors include Philippe Ruminy, Christian Bastard, Emmanuel Olivier, Maryvonne Daveau, Jean‐Philippe Salier, Annie Husson, Jean‐Michel Picquenot, Hervé Tilly, Fabrice Jardin and Jean‐Marc Kuhn and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Biochemical Journal.

In The Last Decade

Françoise Parmentier

15 papers receiving 473 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Françoise Parmentier France 10 165 126 122 120 103 16 482
Toshiaki Sano Japan 12 91 0.6× 66 0.5× 127 1.0× 153 1.3× 54 0.5× 16 518
Katherine M. Jasnosz United States 10 85 0.5× 88 0.7× 120 1.0× 43 0.4× 72 0.7× 16 392
Nimrod Kiss Sweden 13 96 0.6× 284 2.3× 126 1.0× 265 2.2× 165 1.6× 15 653
Arshad A. Pandith India 14 47 0.3× 323 2.6× 112 0.9× 77 0.6× 114 1.1× 68 604
Kimio Morita Japan 14 90 0.5× 119 0.9× 50 0.4× 77 0.6× 63 0.6× 24 654
Eric T. Rush United States 13 61 0.4× 386 3.1× 126 1.0× 218 1.8× 122 1.2× 51 815
V. Facchini Italy 14 108 0.7× 117 0.9× 91 0.7× 64 0.5× 224 2.2× 33 772
Susanne Müller Germany 10 89 0.5× 290 2.3× 125 1.0× 55 0.5× 86 0.8× 28 572
B Jacobsson Sweden 14 61 0.4× 211 1.7× 45 0.4× 29 0.2× 117 1.1× 20 570
Marianne Bach Treppendahl Denmark 16 52 0.3× 496 3.9× 67 0.5× 199 1.7× 97 0.9× 24 832

Countries citing papers authored by Françoise Parmentier

Since Specialization
Citations

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

Fields of papers citing papers by Françoise Parmentier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Parmentier

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

All Works

16 of 16 papers shown
1.
Jardin, Fabrice, Philìppe Bertrand, Sylvain Mareschal, et al.. (2012). Several mechanisms lead to the inactivation of the CDKN2A (P16), P14ARF, or CDKN2B (P15) genes in the GCB and ABC molecular DLBCL subtypes. Genes Chromosomes and Cancer. 51(9). 858–867. 15 indexed citations
2.
Jardin, Fabrice, Jean-Philippe Jaı̈s, Thierry Jo Molina, et al.. (2010). Diffuse large B-cell lymphomas with CDKN2A deletion have a distinct gene expression signature and a poor prognosis under R-CHOP treatment: a GELA study. Blood. 116(7). 1092–1104. 98 indexed citations
3.
Daudignon, Agnès, Stéphanie Poulain, Pierre Morel, et al.. (2009). Increased trisomy 12 frequency and a biased IgVH 3–21 gene usage characterize small lymphocytic lymphoma. Leukemia Research. 34(5). 580–584. 13 indexed citations
4.
Jardin, Fabrice, Jean‐Michel Picquenot, Françoise Parmentier, et al.. (2009). Detection of gene copy number aberrations in mantle cell lymphoma by a single quantitative multiplex PCR assay: clinicopathological relevance and prognosis value. British Journal of Haematology. 146(6). 607–618. 21 indexed citations
5.
6.
Ruminy, Philippe, Fabrice Jardin, Jean‐Michel Picquenot, et al.. (2008). Sμ mutation patterns suggest different progression pathways in follicular lymphoma: early direct or late from FL progenitor cells. Blood. 112(5). 1951–1959. 40 indexed citations
7.
Ruminy, Philippe, Fabrice Jardin, Dominique Penther, et al.. (2007). Recurrent disruption of the Iμ splice donor site in t(14;18) positive lymphomas : A potential molecular basis for aberrant downstream class switch recombination. Genes Chromosomes and Cancer. 46(8). 735–744. 5 indexed citations
8.
Ruminy, Philippe, Fabrice Jardin, Françoise Parmentier, et al.. (2007). Genetic Reconstruction of Follicular Lymphoma Evolutions: Sμ Mutations Studies Suggest Two Progression Patterns, Early Direct or Late from FL “Stem Cells”.. Blood. 110(11). 182–182. 1 indexed citations
9.
Ruminy, Philippe, Fabrice Jardin, Jean Michel Picquenot, et al.. (2006). Promoter Shuffling by Sequential Genomic Rearrangements in Follicular Lymphoma Reveals an Ongoing Genomic Instability at the BCL6 Locus.. Blood. 108(11). 2074–2074. 1 indexed citations
10.
Bastard, Christian, Christophe Fruchart, Grégory Raux, et al.. (2006). Comparison of a Quantitative PCR Method with FISH for the Assessment of the Four Aneuploidies Commonly Evaluated in CLL Patients.. Blood. 108(11). 4950–4950. 1 indexed citations
11.
Contesse, Vincent, Yves Reznik, Estelle Louiset, et al.. (2005). Abnormal Sensitivity of Cortisol-Producing Adrenocortical Adenomas to Serotonin:In Vivoandin VitroStudies. The Journal of Clinical Endocrinology & Metabolism. 90(5). 2843–2850. 21 indexed citations
12.
Cartier, Dorthe, Sylvie Jégou, Françoise Parmentier, et al.. (2005). Expression profile of serotonin4 (5-HT4) receptors in adrenocortical aldosterone-producing adenomas. European Journal of Endocrinology. 153(6). 939–947. 45 indexed citations
13.
Jardin, Fabrice, Christian Bastard, Françoise Parmentier, et al.. (2003). Intronic BCL-6 mutations are preferentially targeted to the translocated allele in t(3;14)(q27;q32) non-Hodgkin B-cell lymphoma. Blood. 102(5). 1872–1876. 8 indexed citations
14.
Cartier, Dorthe, Isabelle Lihrmann, Françoise Parmentier, et al.. (2003). Overexpression of Serotonin4 Receptors in Cisapride-Responsive Adrenocorticotropin-Independent Bilateral Macronodular Adrenal Hyperplasia Causing Cushing’s Syndrome. The Journal of Clinical Endocrinology & Metabolism. 88(1). 248–254. 63 indexed citations
15.
Olivier, Emmanuel, Philippe Ruminy, Annie Husson, et al.. (2000). Fetuin-B, a second member of the fetuin family in mammals. Biochemical Journal. 350(2). 589–597. 123 indexed citations
16.
Olivier, Emmanuel, et al.. (2000). Fetuin-B, a second member of the fetuin family in mammals. Biochemical Journal. 350(2). 589–589. 26 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Toshiaki Sano Breakdown of academic impact, for papers by Katherine M. Jasnosz Breakdown of academic impact, for papers by Nimrod Kiss Breakdown of academic impact, for papers by Arshad A. Pandith Breakdown of academic impact, for papers by Kimio Morita Breakdown of academic impact, for papers by Eric T. Rush Breakdown of academic impact, for papers by V. Facchini Breakdown of academic impact, for papers by Susanne Müller Breakdown of academic impact, for papers by B Jacobsson Breakdown of academic impact, for papers by Marianne Bach Treppendahl
Rankless by CCL
2026