Sandrine M. Caputo

2.6k total citations
29 papers, 607 citations indexed

About

Sandrine M. Caputo is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Sandrine M. Caputo has authored 29 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 18 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Sandrine M. Caputo's work include BRCA gene mutations in cancer (15 papers), CRISPR and Genetic Engineering (11 papers) and DNA Repair Mechanisms (9 papers). Sandrine M. Caputo is often cited by papers focused on BRCA gene mutations in cancer (15 papers), CRISPR and Genetic Engineering (11 papers) and DNA Repair Mechanisms (9 papers). Sandrine M. Caputo collaborates with scholars based in France, Brazil and United States. Sandrine M. Caputo's co-authors include Étienne Rouleau, Rosette Lidereau, Thomas van Overeem Hansen, Álvaro N.A. Monteiro, Alvaro Galli, Fergus J. Couch, Maaike P.G. Vreeswijk, Susan L. Neuhausen, Sophie Zinn‐Justin and Olga M. Sinilnikova and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

Sandrine M. Caputo

25 papers receiving 604 citations

Peers

Countries citing papers authored by Sandrine M. Caputo

Since Specialization

Citations

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

Fields of papers citing papers by Sandrine M. Caputo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandrine M. Caputo. 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 Sandrine M. Caputo. The network helps show where Sandrine M. Caputo may publish in the future.

Co-authorship network of co-authors of Sandrine M. Caputo

This figure shows the co-authorship network connecting the top 25 collaborators of Sandrine M. Caputo. A scholar is included among the top collaborators of Sandrine M. Caputo 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 Sandrine M. Caputo. Sandrine M. Caputo 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	High prevalence of constitutional BRCA1 epimutation in patients with early-onset triple-negative breast cancer 2025 ·Clinical Epigenetics ·(unknown), (unknown), (unknown), (unknown), Sandrine M. Caputo, (unknown), (unknown), Anthony Laugé, (unknown), Étienne Rouleau, Emmanuelle Mouret‐Fourme, (unknown), Éric Pasmant, (unknown), Chrystelle Colas, Ivan Bièche	0
2	RNA-based diagnostic studies in genetics: Review and guidance from a multidisciplinary French network 2025 ·European Journal of Human Genetics ·Marie‐Pierre Buisine, Christine Bellanné‐Chantelot, Nadège Calmels, Christel Vaché, Thomas Besnard, Benjamin Cogné, Antonio Vitobello, Amélie Piton, Alexandra Martins, Pascaline Gaildrat, Claire‐Marie Dhaenens, Svetlana Gorokhova, Nadia Boutry‐Kryza, Sandrine M. Caputo, Raphaël Leman, Sophie Krieger, Gérald Le Gac, Claude Houdayer	0
3	Interprétation des résultats issus du séquençage à haut débit pour les maladies génétiques 2024 ·médecine/sciences ·Svetlana Gorokhova, Cécile Rouzier, Cécile Acquaviva, Stéphanie Baert‐Desurmont, Sandrine M. Caputo, (unknown), Florence Coulet, Martine Doco‐Fenzy, Boris Keren, Cédric Le Maréchal, Gaël Nicolas, Vincent Procaccio, Pascale Richard, Pauline Romanet, (unknown), Jean Muller, (unknown), Pascale Saugier-Véber	0
4	Adaptive nanopore sequencing to determine pathogenicity ofBRCA1exonic duplication 2023 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Elodie Girard, Sandrine M. Caputo, Victor Renault, Véronique Becette, Lisa Golmard, Nicolas Servant, Dominique Stoppa‐Lyonnet, Olivier Delattre, Chrystelle Colas, Julien Masliah‐Planchon	11
5	Combined Tumor-Based BRCA1/2 and TP53 Mutation Testing in Ovarian Cancer 2023 ·International Journal of Molecular Sciences ·Édith Borcoman, (unknown), Catherine Genestie, Patricia Pautier, Ludovic Lacroix, Sandrine M. Caputo, Odile Cabaret, Marine Guillaud-Bataille, Judith Michels, Aurélie Auguste, Alexandra Léary, Étienne Rouleau	3
6	WWOX binds MERIT40 and modulates its function in homologous recombination, implications in breast cancer 2023 ·Cancer Gene Therapy ·(unknown), Sophie Vacher, Josée Guirouilh‐Barbat, Jacques Camonis, Étienne Formstecher, Tatiana Popova, Anne‐Sophie Hamy, Ambre Petitalot, Rosette Lidereau, Sandrine M. Caputo, Sophie Zinn‐Justin, Ivan Bièche, Keltouma Driouch, François Lallemand	1
7	Germline HPF1 retrogene insertion in RB1 gene involved in cancer predisposition 2023 ·Journal of Medical Genetics ·(unknown), Catherine Dehainault, (unknown), Ambre Petitalot, Sandrine M. Caputo, (unknown), Sophie Vacher, Ivan Bièche, François Radvanyi, Hélène Pacquement, François Doz, Livia Lumbroso‐Le Rouic, (unknown), Dominique Stoppa‐Lyonnet, François Lallemand, Claude Houdayer, Lisa Golmard	0
8	The high protein expression of FOXO3, but not that of FOXO1, is associated with markers of good prognosis 2020 ·Scientific Reports ·François Lallemand, Sophie Vacher, Leanne de Koning, Ambre Petitalot, Adrien Briaux, Keltouma Driouch, Céline Callens, Anne Schnitzler, (unknown), (unknown), Aurélie Barbet, Anne Vincent, Sophie Zinn‐Justin, Bernard S. López, Rosette Lidereau, Ivan Bièche, Sandrine M. Caputo	6
9	Is BRCA2 involved in early onset colorectal cancer risk? 2019 ·Clinical Genetics ·(unknown), Maud Privat, Alexandra Martins, Sandrine M. Caputo, Céline Pebrel‐Richard, (unknown), (unknown), Carole Corsini, (unknown), Nicolas Barnich, Yannick Bidet, Nancy Uhrhammer, Yves‐Jean Bignon	6
10	“Decoding hereditary breast cancer” benefits and questions from multigene panel testing 2019 ·The Breast ·Chrystelle Colas, Lisa Golmard, Antoine De Pauw, Sandrine M. Caputo, Dominique Stoppa‐Lyonnet	24
11	Combining Homologous Recombination and Phosphopeptide-binding Data to Predict the Impact of BRCA1 BRCT Variants on Cancer Risk 2018 ·Molecular Cancer Research ·Ambre Petitalot, Elodie Dardillac, Eric Jacquet, (unknown), Josée Guirouilh‐Barbat, (unknown), (unknown), Dorine Bonte, Jean Feunteun, (unknown), (unknown), Jean-Christophe Aude, (unknown), Étienne Rouleau, Rosette Lidereau, Bernard S. López, Sophie Zinn‐Justin, Sandrine M. Caputo	19
12	Non-Coding Variants in BRCA1 and BRCA2 Genes: Potential Impact on Breast and Ovarian Cancer Predisposition 2018 ·Cancers ·(unknown), François Lallemand, Leslie Burke, Dominique Stoppa‐Lyonnet, Melissa A. Brown, Sandrine M. Caputo, Étienne Rouleau	19
13	Assessment of the functional impact of germline BRCA1/2 variants located in non-coding regions in families with breast and/or ovarian cancer predisposition 2017 ·Breast Cancer Research and Treatment ·(unknown), Sandrine M. Caputo, Laurent Castéra, (unknown), Adrien Briaux, (unknown), Sophie Krieger, Peter K. Rogan, Eliseos J. Mucaki, Leslie Burke, Ivan Bièche, Claude Houdayer, Dominique Vaur, Dominique Stoppa‐Lyonnet, Melissa A. Brown, François Lallemand, Étienne Rouleau	13
14	Functional Assays for Analysis of Variants of Uncertain Significance inBRCA2 2013 ·Human Mutation ·Lucia Guidugli, Aura Carreira, Sandrine M. Caputo, Åsa Ehlén, Alvaro Galli, Álvaro N.A. Monteiro, Susan L. Neuhausen, Thomas van Overeem Hansen, Fergus J. Couch, Maaike P.G. Vreeswijk	82
15	A guide for functional analysis ofBRCA1variants of uncertain significance 2012 ·Human Mutation ·Gaël A. Millot, Marcelo A. Carvalho, Sandrine M. Caputo, Maaike P.G. Vreeswijk, Melissa A. Brown, Michelle Webb, Étienne Rouleau, Susan L. Neuhausen, Thomas van Overeem Hansen, Alvaro Galli, Rita D. Brandão, Marinus J. Blok, Aneliya Velkova, Fergus J. Couch, Álvaro N.A. Monteiro	82
16	An entire exon 3 germ-line rearrangement in the BRCA2 gene: pathogenic relevance of exon 3 deletion in breast cancer predisposition 2011 ·BMC Medical Genetics ·Danièle Muller, Étienne Rouleau, (unknown), Sandrine M. Caputo, Cédrick Lefol, Ivan Bièche, Olivier Caron, Catherine Noguès, J.M. Limacher, Liliane Demange, Rosette Lidereau, (unknown), Joseph Abecassis	15
17	The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress 2009 ·Journal of Cellular and Molecular Medicine ·Valerie L. R. M. Verstraeten, Sandrine M. Caputo, Maurice A. M. Van Steensel, Isabelle Duband‐Goulet, Sophie Zinn‐Justin, M. A. F. Kamps, Helma J.H. Kuijpers, Cecilia Östlund, Howard J. Worman, Jacob J. Briedé, Caroline Le Dour, Carlo Marcelis, Michel van Geel, Peter M. Steijlen, Arthur van den Wijngaard, Frans C. S. Ramaekers, Jos L. V. Broers	34
18	S1 Ribosomal Protein Functions in Translation Initiation and Ribonuclease RegB Activation Are Mediated by Similar RNA-Protein Interactions 2008 ·Journal of Biological Chemistry ·(unknown), Christina Sizun, Javier Pérez, Fabien Mareuil, Sandrine M. Caputo, Jean‐Louis Leroy, Benoı̂t Odaert, Soumaya Laalami, Marc Uzan, François Bontems	41
19	The Carboxyl-terminal Nucleoplasmic Region of MAN1 Exhibits a DNA Binding Winged Helix Domain 2006 ·Journal of Biological Chemistry ·Sandrine M. Caputo, Joël Couprie, Isabelle Duband‐Goulet, (unknown), Feng Lin, Sandrine Braud, Muriel Gondry, Bernard Gilquin, Howard J. Worman, Sophie Zinn‐Justin	53
20	[Helicobacter pylori and gastric cancer. The incidence of infection in personal experience]. 2002 ·PubMed ·Sandrine M. Caputo, Fabio Mosca, (unknown), (unknown), Stefano Scaringi, Giuseppina Russo, Dario Piazza	5

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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