M. Dondon

发表

Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

M. Bihoreau, N. Servant, D. Stoppa-Lyonnet, 2018, International journal of cancer.

Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers

A. Vincent-Salomon, G. Chenevix-Trench, I. Bièche, 2018, Breast Cancer Research.

Mutation screening of MIR146A/B and BRCA1/2 3′-UTRs in the GENESIS study

D. Stoppa-Lyonnet, O. Sinilnikova, S. Mazoyer, 2016, European Journal of Human Genetics.

Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families

K. Dahan, D. Stoppa-Lyonnet, B. Gilbert-Dussardier, 2017, Carcinogenesis.

A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers

F. Révillion, Chloé-Agathe Azencott, N. Sevenet, 2020, BMC Medical Research Methodology.

Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease.

Edith Le Floch, P. Guénel, T. Truong, 2022, European journal of cancer.

Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2

G. Thomas, D. Cox, D. Stoppa-Lyonnet, 2015, PloS one.

Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers

A. Vincent-Salomon, G. Chenevix-Trench, I. Bièche, 2018, Breast Cancer Research.

Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility

E. Barillot, P. Guénel, T. Truong, 2020, International journal of cancer.

Mutation analysis of PALB2 gene in French breast cancer families

D. Stoppa-Lyonnet, O. Sinilnikova, S. Mazoyer, 2015, Breast Cancer Research and Treatment.

P53 germline mutations in childhood cancers and cancer risk for carrier individuals

C. Bonaïti‐pellié, T. Frebourg, A. Chompret, 2000, British Journal of Cancer.

Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation

D. Stoppa-Lyonnet, S. Mazoyer, F. Damiola, 2021, Breast cancer research : BCR.

Radiation dose, chemotherapy and risk of soft tissue sarcoma after solid tumours during childhood

G. Vassal, N. Daly-Schveitzer, J. Zucker, 2004, International journal of cancer.

TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing

J. Lemonnier, N. Sevenet, D. Stoppa-Lyonnet, 2021, Cancers.

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

Eliseos J. Mucaki, F. Couch, B. Bonanni, 2015, Human molecular genetics.

GENESIS: a French national resource to study the missing heritability of breast cancer

D. Stoppa-Lyonnet, O. Sinilnikova, S. Mazoyer, 2016, BMC Cancer.

Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P).

C. Bonaïti‐pellié, C. Houdayer, M. Vazquez, 2001, American journal of medical genetics.

Long‐term risk of second malignant neoplasms after neuroblastoma in childhood: Role of treatment

C. Rubino, F. de Vathaire, M. Hawkins, 2003, International journal of cancer.

Cancer mortality after radiotherapy for a skin hemangioma during childhood.

F. Eschwège, M. Avril, F. de Vathaire, 2004, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

Concomitant chemo‐radiotherapy and local dose of radiation as risk factors for second malignant neoplasms after solid cancer in childhood: A case–control study

F. de Vathaire, O. Oberlin, J. Michon, 2007, International journal of cancer.

Radiotherapy as a risk factor for malignant melanoma after childhood skin hemangioma

C. Robert, M. Avril, F. de Vathaire, 2012, Melanoma research.

Breast cancer following radiotherapy for a hemangioma during childhood

D. Lefkopoulos, C. Robert, M. Avril, 2010, Cancer Causes & Control.

Thyroid adenomas and carcinomas following radiotherapy for a hemangioma during infancy.

D. Lefkopoulos, M. Schlumberger, C. Robert, 2009, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

A new scoring system in cancer genetics: application to criteria for BRCA1 and BRCA2 mutation screening

Hervé Perdry, Sophie Pennec, Bernard Bonaïti, 2013, Journal of Medical Genetics.

Increased power to detect gene-environment interaction using siblings controls.

A. Goldstein, N. Andrieu, M. Dondon, 2005, Annals of epidemiology.