Get started
Author

Sandra Fert‐Ferrer

NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique
2006 · S P Romana, I Radford-Weiss, et al. · Leukemia · 138
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing
2018 · Elodie Girard, Séverine Eon‐Marchais, et al. · International Journal of Cancer · 82
PDF
Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stages
2009 · Elise Chapiro, Nathalie Leporrier, et al. · Leukemia Research · 78
Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia
2006 · E. Chapiro, L. Russell, et al. · Blood · 75
Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course
2011 · on behalf of the BCGHo and the GFCH, Natalie Put, et al. · Annals of Hematology · 74
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study
2021 · Lieske H. Schrijver, Antonis C. Antoniou, et al. · American Journal of Obstetrics and Gynecology · 68
PDF
Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53
2019 · Elise Chapiro, Elodie Pramil, et al. · Blood · 53
PDF
Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers
2010 · S. J. Ramus, C. Kartsonaki, et al. · JNCI Journal of the National Cancer Institute · 50
PDF
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
2019 · Gisella Figlioli, Massimo Bogliolo, et al. · npj Breast Cancer · 43
PDF
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach
2021 · Sandrine M. Caputo, Lisa Golmard, et al. · The American Journal of Human Genetics · 37
PDF
14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma
2014 · Adrien Cosson, Elise Chapiro, et al. · Genes Chromosomes and Cancer · 30
“Double‐hit” chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain
2017 · Elise Chapiro, Claude Lesty, et al. · American Journal of Hematology · 27
PDF
GENESIS: a French national resource to study the missing heritability of breast cancer
2016 · Olga M. Sinilnikova, Marie-Gabrielle Dondon, et al. · BMC Cancer · 26
PDF
Specific chromosomal IG translocations have different prognoses in chronic lymphocytic leukemia.
2011 · Florence Nguyen-Khac, Elise Chapiro, et al. · PubMed · 22
Association and Performance of Polygenic Risk Scores for Breast Cancer Among French Women Presenting or Not a Familial Predisposition to the Disease
2022 · Yue Jiao, Thérèse Truong, et al. · European Journal of Cancer · 19
PDF
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer
2022 · Julie Leclerc, Marie Beaumont, et al. · Genes Chromosomes and Cancer · 18
PDF
GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers
2018 · Fabienne Lesueur, Noura Mebirouk, et al. · Frontiers in Oncology · 18
PDF
A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES)
2004 · J. Lespinasse, H. Testard, et al. · Annales de Génétique · 18
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation
2021 · Maximiliano Ribeiro Guerra, Juliette Coignard, et al. · Breast Cancer Research · 16
PDF
Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32)
2003 · Joris Andrieux, Sandra Fert-Ferrer, et al. · Cancer Genetics and Cytogenetics · 16
Interstitial deletion of the short arm of chromosome 1: Attempt to establish a clinical phenotype (46,XX,del (1)(p22p32))
2002 · Clotilde Mircher, Marie‐Odile Rethore, et al. · American Journal of Medical Genetics Part A · 16
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features
2000 · Sandra Fert-Ferrer, Agn�s Guichet, et al. · Prenatal Diagnosis · 15
Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases
2004 · J. Lespinasse, M.O. Réthoré, et al. · Annales de Génétique · 13
Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort
2023 · Ahmed Bouras, Souhir Guidara, et al. · Cancers · 11
PDF
Endoscopic Phenotype of Monoallelic Carriers of MUTYH Gene Mutations in the Family of Polyposis Patients: A Prospective Study
2019 · Noha El Hachem, Caroline Abadie, et al. · Diseases of the Colon & Rectum · 10
Works count: 38
Citation count: 996
H-index: 18
I10-index: 25
Year
Topic
Type