Sylvie Mazoyer

11.4k total citations
50 papers, 2.5k citations indexed

About

Sylvie Mazoyer is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Sylvie Mazoyer has authored 50 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 30 papers in Genetics and 7 papers in Cancer Research. Recurrent topics in Sylvie Mazoyer's work include BRCA gene mutations in cancer (25 papers), Genomic variations and chromosomal abnormalities (16 papers) and CRISPR and Genetic Engineering (15 papers). Sylvie Mazoyer is often cited by papers focused on BRCA gene mutations in cancer (25 papers), Genomic variations and chromosomal abnormalities (16 papers) and CRISPR and Genetic Engineering (15 papers). Sylvie Mazoyer collaborates with scholars based in France, United States and United Kingdom. Sylvie Mazoyer's co-authors include Nadine Puget, Gilbert Lenoir, Olga M. Sinilnikova, Monique Buisson, Henry T. Lynch, Olga Anczuków, Dominique Stoppa‐Lyonnet, Rosette Lidereau, D. Gareth Evans and Bruce A.J. Ponder and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and PLoS ONE.

In The Last Decade

Sylvie Mazoyer

47 papers receiving 2.4k citations

Peers

Countries citing papers authored by Sylvie Mazoyer

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Mazoyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvie Mazoyer

This figure shows the co-authorship network connecting the top 25 collaborators of Sylvie Mazoyer. A scholar is included among the top collaborators of Sylvie Mazoyer 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 Sylvie Mazoyer. Sylvie Mazoyer 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	A Taybi-Linder syndrome-related RTTN variant impedes neural rosette formation in human cortical organoids 2024 ·PLoS Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), Lucile Boutaud, (unknown), (unknown), (unknown), Virginie Hamel, Sophie Thomas, Bertrand Pain, Patrick Edery, Audrey Putoux, Tang K. Tang, Sylvie Mazoyer, Marion Delous	0
2	PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect 2023 ·European Journal of Medical Genetics ·(unknown), Chloé Quēlin, Laurent Pasquier, Philippe Loget, (unknown), Sylvie Odent, Annie Laquerrière, Maïa Proisy, Sylvie Mazoyer, Marion Delous, Patrick Edery, Nicolas Chatron, Gaëtan Lesca, Audrey Putoux	0
3	Clinical interpretation of variants identified in RNU4ATAC, a non-coding spliceosomal gene 2020 ·PLoS ONE ·Clara Benoit‐Pilven, (unknown), Audrey Putoux, Claire Benetollo, (unknown), (unknown), Gabriel Sala, (unknown), Marion Delous, Gaëtan Lesca, Richard A. Padgett, Anne‐Louise Leutenegger, Vincent Lacroix, Patrick Edery, Sylvie Mazoyer	10
4	A de novo frameshift pathogenic variant in TBR1 identified in autism without intellectual disability 2020 ·Human Genomics ·Laurie‐Anne Sapey‐Triomphe, (unknown), Gaëtan Lesca, Nicolas Chatron, (unknown), Sylvie Mazoyer, Christina Schmitz, Sandrine Sonié, Patrick Edery	5
5	New insights into minor splicing—a transcriptomic analysis of cells derived from TALS patients 2019 ·RNA ·(unknown), Clara Benoit‐Pilven, (unknown), Audrey Putoux, Amandine Campan-Fournier, Michael B. Bober, Christine de Die‐Smulders, Aimée Paulussen, Lucile Pinson, Annick Toutain, Chaim M. Roifman, Anne‐Louise Leutenegger, Sylvie Mazoyer, Patrick Edery, Vincent Lacroix	26
6	Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2 2015 ·PLoS ONE ·Sophie Blein, Laure Barjhoux, (unknown), Francesca Damiola, Marie‐Gabrielle Dondon, (unknown), (unknown), Olivier Caron, Alain Lortholary, Bruno Buecher, Philippe Vennin, Pascaline Berthet, Catherine Noguès, Christine Lasset, Marion Gauthier‐Villars, Sylvie Mazoyer, Dominique Stoppa‐Lyonnet, Nadine Andrieu, Gilles Thomas, Olga M. Sinilnikova, David G. Cox	9
7	BRCA2 Deep Intronic Mutation Causing Activation of a Cryptic Exon: Opening toward a New Preventive Therapeutic Strategy 2012 ·Clinical Cancer Research ·Olga Anczuków, Monique Buisson, Mélanie Léoné, (unknown), Christine Lasset, Alain Calender, Olga M. Sinilnikova, Sylvie Mazoyer	52
8	The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers 2011 ·Human Mutation ·(unknown), David G. Cox, Laure Barjhoux, (unknown), Daniel R. Barnes, (unknown), Antonis C. Antoniou, Dominique Stoppa‐Lyonnet, Olga M. Sinilnikova, Sylvie Mazoyer	39
9	Comparison of nonsense-mediated mRNA decay efficiency in various murine tissues 2008 ·BMC Genetics ·(unknown), Sandra Fontanière, Delphine Magnin, Olga Anczuków, Monique Buisson, Chang Zhang, Sylvie Mazoyer	100
10	BRCA1 and BRCA2 Mutations in Breast and Ovarian Cancer Syndrome: Reflection on the Creighton University Historical Series of High Risk Families 2006 ·Familial Cancer ·Olga M. Sinilnikova, Sylvie Mazoyer, (unknown), Henry T. Lynch, Steven A. Narod, Gilbert Lenoir	17
11	The BRCA1 exon 13 duplication in the Swedish population 2005 ·Familial Cancer ·Bárbara Kremeyer, Maria Soller, Kristina Lagerstedt‐Robinson, Paula Maguire, Sylvie Mazoyer, Margareta Nordling, Jan Wahlström, Annika Lindblom	14
12	Genomic rearrangements in theBRCA1 andBRCA2 genes 2005 ·Human Mutation ·Sylvie Mazoyer	122
13	Real‐time PCR‐based gene dosage assay for detecting BRCA1 rearrangements in breast–ovarian cancer families 2004 ·Clinical Genetics ·Michel Barrois, Ivan Bièche, Sylvie Mazoyer, (unknown), Brigitte Bressac–de Paillerets, Rosette Lidereau	40
14	Distinct BRCA1 Rearrangements Involving the BRCA1 Pseudogene Suggest the Existence of a Recombination Hot Spot 2002 ·The American Journal of Human Genetics ·Nadine Puget, Sophie Gad, (unknown), Olga M. Sinilnikova, Dominique Stoppa‐Lyonnet, Gilbert Lenoir, Sylvie Mazoyer	88
15	Color bar coding the BRCA1 gene on combed DNA: A useful strategy for detecting large gene rearrangements 2001 ·Genes Chromosomes and Cancer ·Sophie Gad, Alain Aurias, Nadine Puget, Aline Mairal, Catherine Schurra, Marco Montagna, Sabine Pagès, (unknown), Sylvie Mazoyer, Aaron Bensimon, Dominique Stoppa‐Lyonnet	50
16	Screening for Genomic Rearrangements in Families with Breast and Ovarian Cancer Identifies BRCA1 Mutations Previously Missed by Conformation-Sensitive Gel Electrophoresis or Sequencing 2000 ·The American Journal of Human Genetics ·(unknown), Katherine L. Nathanson, (unknown), Danielle Antin‐Ozerkis, Helen A. Shih, Anne‐Marie Martin, Gilbert Lenoir, Sylvie Mazoyer, Barbara L. Weber	117
17	AnAlu-mediated 7.1 kb deletion ofBRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10 2000 ·Genes Chromosomes and Cancer ·Elizabeth M. Rohlfs, Nadine Puget, Mark L. Graham, Barbara L. Weber, Judy E. Garber, (unknown), (unknown), Gilbert Lenoir, Lawrence M. Silverman, Sylvie Mazoyer	60
18	Isolation of a Gene (DLG3) Encoding a Second Member of the Discs-Large Family on Chromosome 17q12–q21 1996 ·Genomics ·Simon A. Smith, (unknown), Jeff Stevens, Sylvie Mazoyer, Roberta Melis, Briana J. Williams, R. White, Hans Albertsen	31
19	Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation 1995 ·Nature Genetics ·Simon A. Gayther, William Warren, Sylvie Mazoyer, Paul A. Russell, Patricia Harrington, Mathias Chiano, Sheila Seal, Rifat Hamoudi, Elizabeth J. van Rensburg, Alison M. Dunning, Richard R. Love, D. Gareth Evans, Doug Easton, David Clayton, Michael R. Stratton, Bruce A.J. Ponder	376
20	Genetic heterogeneity of early-onset familial breast cancer 1992 ·Human Genetics ·(unknown), Sylvie Mazoyer, (unknown), (unknown), (unknown), Pierre Kerbrat, (unknown), Ellen Solomon, (unknown), (unknown)	12

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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