Sandra Fert‐Ferrer

898 total citations
10 papers, 117 citations indexed

About

Sandra Fert‐Ferrer is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Sandra Fert‐Ferrer has authored 10 papers receiving a total of 117 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Sandra Fert‐Ferrer's work include Genomic variations and chromosomal abnormalities (4 papers), Genetic factors in colorectal cancer (2 papers) and Prenatal Screening and Diagnostics (2 papers). Sandra Fert‐Ferrer is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetic factors in colorectal cancer (2 papers) and Prenatal Screening and Diagnostics (2 papers). Sandra Fert‐Ferrer collaborates with scholars based in France, Denmark and Tunisia. Sandra Fert‐Ferrer's co-authors include Claes Lundsteen, M O Rethoré, M Lessard, Christian Bastard, Hélène Cavé, Odile Maarek, James Lespinasse, Lisa J. Russell, Olivier Bernard and Élise Chapiro and has published in prestigious journals such as Blood, International Journal of Molecular Sciences and Journal of Medical Genetics.

In The Last Decade

Sandra Fert‐Ferrer

9 papers receiving 115 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra Fert‐Ferrer France 7 46 39 32 30 24 10 117
Michiel Oorsprong Netherlands 2 45 1.0× 54 1.4× 18 0.6× 36 1.2× 18 0.8× 3 112
Yanara Marincevic-Zuniga Sweden 6 54 1.2× 15 0.4× 15 0.5× 36 1.2× 53 2.2× 10 108
Valeria Cazzaniga Italy 4 61 1.3× 7 0.2× 20 0.6× 29 1.0× 39 1.6× 7 129
Helen Worley United Kingdom 3 49 1.1× 69 1.8× 51 1.6× 113 3.8× 150 6.3× 4 194
Jiří Hák Czechia 6 90 2.0× 11 0.3× 18 0.6× 63 2.1× 56 2.3× 14 164
Joanna Madzio Poland 6 36 0.8× 31 0.8× 12 0.4× 23 0.8× 26 1.1× 16 110
Bruno A. Lopes Brazil 7 71 1.5× 11 0.3× 25 0.8× 54 1.8× 45 1.9× 20 126
Xujie Zhao United States 10 107 2.3× 7 0.2× 15 0.5× 46 1.5× 54 2.3× 22 184
Guillaume Hypolite France 8 77 1.7× 10 0.3× 18 0.6× 59 2.0× 44 1.8× 10 151
Sara Hetzel Germany 7 203 4.4× 32 0.8× 31 1.0× 21 0.7× 30 1.3× 12 250

Countries citing papers authored by Sandra Fert‐Ferrer

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Fert‐Ferrer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra Fert‐Ferrer. 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 Sandra Fert‐Ferrer. The network helps show where Sandra Fert‐Ferrer may publish in the future.

Co-authorship network of co-authors of Sandra Fert‐Ferrer

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

All Works

10 of 10 papers shown
1.
Jones, Natalie, Dominique Bonneau, Tiffany Busa, et al.. (2024). Classification of PTEN germline non-truncating variants: a new approach to interpretation. Journal of Medical Genetics. 61(12). 1071–1079.
2.
Bouras, Ahmed, Mélanie Léoné, Adrien Buisson, et al.. (2023). Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort. Cancers. 15(13). 3420–3420. 3 indexed citations
3.
Bouras, Ahmed, Zine‐Eddine Kherraf, Tanguy Martin‐Denavit, et al.. (2022). Identification and Characterization of an Exonic Duplication in PALB2 in a Man with Synchronous Breast and Prostate Cancer. International Journal of Molecular Sciences. 23(2). 667–667. 2 indexed citations
4.
Abadie, Caroline, Michel Longy, Chrystelle Colas, et al.. (2019). Endoscopic Phenotype of Monoallelic Carriers of MUTYH Gene Mutations in the Family of Polyposis Patients: A Prospective Study. Diseases of the Colon & Rectum. 62(4). 470–475. 6 indexed citations
5.
Chapiro, Élise, Lisa J. Russell, Christian Bastard, et al.. (2006). Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia. Blood. 108(10). 3560–3563. 48 indexed citations
6.
Lespinasse, J., et al.. (2004). Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases. Annales de Génétique. 47(3). 315–324. 11 indexed citations
7.
8.
Andrieux, Joris, Sandra Fert‐Ferrer, Marie‐Christine Copin, et al.. (2003). Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32). Cancer Genetics and Cytogenetics. 145(1). 65–69. 9 indexed citations
9.
Mircher, Clotilde, et al.. (2002). Interstitial deletion of the short arm of chromosome 1: Attempt to establish a clinical phenotype (46,XX,del (1)(p22p32)). American Journal of Medical Genetics Part A. 118A(2). 176–179. 14 indexed citations
10.
Fert‐Ferrer, Sandra, Julia Tantau, Anne Lise Delezoïde, et al.. (2000). Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features. Prenatal Diagnosis. 20(6). 511–515. 10 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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