Agnès Hardouin

2.6k total citations
25 papers, 778 citations indexed

About

Agnès Hardouin is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Agnès Hardouin has authored 25 papers receiving a total of 778 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Agnès Hardouin's work include BRCA gene mutations in cancer (9 papers), CRISPR and Genetic Engineering (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Agnès Hardouin is often cited by papers focused on BRCA gene mutations in cancer (9 papers), CRISPR and Genetic Engineering (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Agnès Hardouin collaborates with scholars based in France, Luxembourg and United States. Agnès Hardouin's co-authors include Sophie Krieger, Thierry Frébourg, Pascaline Berthet, Antoine Rousselin, Dominique Vaur, Mario Tosi, Valérie Layet, Alexandra Martins, Catherine Dugast and Thierry Conroy and has published in prestigious journals such as Journal of Clinical Oncology, Cancer Research and International Journal of Radiation Oncology*Biology*Physics.

In The Last Decade

Agnès Hardouin

25 papers receiving 768 citations

Peers

Countries citing papers authored by Agnès Hardouin

Since Specialization

Citations

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

Fields of papers citing papers by Agnès Hardouin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Agnès Hardouin

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Dermo-hypodermites à streptocoque du groupe B chez les nourrissons de moins de 3 mois : étude rétrospective dans deux centres hospitaliers 2015 ·Archives de Pédiatrie ·Agnès Hardouin, Pascale Mariani, (unknown), (unknown), Mathie Lorrot, A. Blachier, Y. Aujard, Stéphane Bonacorsi, Albert Faye	1
2	Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes 2014 ·European Journal of Human Genetics ·Laurent Castéra, Sophie Krieger, Antoine Rousselin, Angélina Legros, (unknown), (unknown), Baptiste Brault, (unknown), Nicolas Goardon, (unknown), Stéphanie Baert‐Desurmont, Julie Tinat, Odile Béra, Catherine Dugast, Pascaline Berthet, (unknown), Valérie Layet, Agnès Hardouin, Thierry Frébourg, Dominique Vaur	175
3	Assessment ofSPAG9Transcript in Fine Needle Aspirates of Thyroid Nodules 2012 ·European Thyroid Journal ·(unknown), Sophie Krieger, G. Planchard, Agnès Hardouin, Dominique Vaur, Jean-Pierre Rame, Stéphane Bardet	2
4	Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genes 2011 ·European Journal of Human Genetics ·(unknown), Sophie Krieger, Pascaline Gaildrat, Françoise Révillion, Marie‐Pierre Buisine, Audrey Killian, Christiane Duponchel, Antoine Rousselin, Dominique Vaur, (unknown), Pascaline Berthet, Thierry Frébourg, Alexandra Martins, Agnès Hardouin, Mario Tosi	64
5	A One-Step Prescreening for Point Mutations and Large Rearrangement in BRCA1 and BRCA2 Genes Using Quantitative Polymerase Chain Reaction and High-Resolution Melting Curve Analysis 2010 ·Genetic Testing and Molecular Biomarkers ·Florence Coulet, (unknown), Étienne Rouleau, Cédrick Lefol, Sabrina Martín, Chrystelle Colas, Odile Cohen‐Haguenauer, Irina Giurgea, Anne Fajac, Catherine Noguès, Liliane Demange, Agnès Hardouin, Rosette Lidereau, Florent Soubrier	16
6	Two novel variants in the 3′UTR of the BRCA1 gene in familial breast and/or ovarian cancer 2010 ·Breast Cancer Research and Treatment ·Stéphanie Lheureux, Bernard Lambert, Sophie Krieger, Angélina Legros, Dominique Vaur, Christophe Denoyelle, Pascaline Berthet, Laurent Poulain, Agnès Hardouin	14
7	One-Year Longitudinal Study of Fatigue, Cognitive Functions, and Quality of Life After Adjuvant Radiotherapy for Breast Cancer 2010 ·International Journal of Radiation OncologyBiologyPhysics ·Sabine Noal, Christelle Lévy, Agnès Hardouin, Chantal Rieux, Natacha Heutte, (unknown), (unknown), Djelila Allouache, O. Switsers, Corinne Delcambre, T. Delozier, M. Henry‐Amar, Florence Joly	82
8	The BRCA1 c.5434C→G (p.Pro1812Ala) variant induces a deleterious exon 23 skipping by affecting exonic splicing regulatory elements 2010 ·Journal of Medical Genetics ·Pascaline Gaildrat, Sophie Krieger, (unknown), Audrey Killian, Antoine Rousselin, Pascaline Berthet, Thierry Frébourg, Agnès Hardouin, Alexandra Martins, Mario Tosi	33
9	Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene 2008 ·Journal of Medical Genetics ·Céline Bonnet, Sophie Krieger, Myriam Vézain, Antoine Rousselin, Isabelle Tournier, Alexandra Martins, Pascaline Berthet, Annie Chevrier, Catherine Dugast, Valérie Layet, Anita De Rossi, Rosette Lidereau, Thierry Frébourg, Agnès Hardouin, Mario Tosi	89
10	Influence of CA 15-3 blood level and doubling time on diagnostic performances of 18F-FDG PET in breast cancer patients with occult recurrence 2007 ·Nuclear Medicine Communications ·Nicolas Aide, Virginie Huchet, O. Switsers, Natacha Heutte, T. Delozier, Agnès Hardouin, Stéphane Bardet	15
11	Routine detection of EGFR mutations in patients with NSCLC: A comparative study of three alternative methods in 105 patients 2006 ·Journal of Clinical Oncology ·Gérard Zalcman, Nicolas Richard, Agnès Hardouin, R. Gervais, Martine Antoine, Hervé Mittre, (unknown), Françoise Galateau-Sallé, J. Cadranel, (unknown)	2
12	Significant contribution of germline BRCA2 rearrangements in male breast cancer families 2004 ·HAL (Le Centre pour la Communication Scientifique Directe) ·Isabelle Tournier, Brigitte Bressac–de Paillerets, H. Sobol, Dominique Stoppa‐Lyonnet, Rosette Lidereau, Michel Barrois, Sylvie Mazoyer, Florence Coulet, Agnès Hardouin, Agnès Chompret, Alain Lortholary, Pierre O. Chappuis, Violaine Bourdon, Valérie Bonadona, Christine Maugard, Brigitte Gilbert, Catherine Noguès, Thierry Frébourg, Mario Tosi	7
13	Significant Contribution of Germline *BRCA2* Rearrangements in Male Breast Cancer Families 2004 ·Cancer Research ·Isabelle Tournier, Brigitte Bressac–de Paillerets, (unknown), Dominique Stoppa-Lyonnet, (unknown), Michel Barrois, Sylvie Mazoyer, (unknown), Agnès Hardouin, Agnès Chompret, (unknown), Pierre O. Chappuis, Violaine Bourdon, (unknown), Christine Maugard, Brigitte Gilbert, Catherine Noguès, (unknown), (unknown)	81
14	BCL‐2/J_H translocation in peripheral blood lymphocytes of unexposed individuals: Lack of seasonal variations in frequency and molecular features 2003 ·International Journal of Cancer ·Sandrine Roulland, Pierre Lebailly, (unknown), Mélanie Briand, David Cappellen, Didier Pottier, Agnès Hardouin, Xavier Troussard, Christian Bastard, M. Henry‐Amar, Pascal Gauduchon	12
15	No BCL-2 protein over expression but BCL-2/IgH rearrangements in B cells of patients with persistent polyclonal B-cell lymphocytosis 2001 ·The Hematology Journal ·(unknown), Sandrine Roulland, Gaël Roué, Hossein Mossafa, Véronique Salaün, Stéphane Chèze, Pascal Gauduchon, Agnès Hardouin, Brigitte Sola, Xavier Troussard	7
16	Systematic sequencing of the BRCA-1 coding region for germ-line mutation detection in 70 French high-risk families. 1999 ·International Journal of Oncology ·(unknown), Nadège Presneau, (unknown), Fabrice Kwiatkowski, Alain Lortholary, Agnès Hardouin, Yves‐Jean Bignon	4
17	[Mutation by deletion-insertion in BRCA-1 gene in three unrelated French breast/ovarian cancer families: possible implication of a mobile element]. 1999 ·PubMed ·Nadège Presneau, (unknown), (unknown), Alain Lortholary, Agnès Hardouin, Dominique Bernard-Gallon, Yohan Bignon	2
18	New mechanism of BRCA-1 mutation by deletion/insertion at the same nucleotide position in three unrelated French breast/ovarian cancer families 1998 ·Human Genetics ·Nadège Presneau, (unknown), (unknown), Alain Lortholary, Agnès Hardouin, Dominique Bernard-Gallon, Y. J. Bignon	13
19	Toxicité rénale du 9-hydroxy-2-méthyl-ellipticinium. 1984 ·La Presse Médicale ·(unknown), (unknown), P Juret, (unknown), P. Herlin, Agnès Hardouin, (unknown)	1
20	Bronchiolites du nourrisson à virus respiratoire syncytial: Intérêt et limites des techniques d'immunofluorescence pour le diagnostic rapide, direct et indirect 1981 ·Annales de l Institut Pasteur Virologie ·F. Freymuth∘, Agnès Hardouin, (unknown), (unknown), Patrick Boutard, (unknown), P Charbonneau, C. Bazin, (unknown)	6

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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