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

Breast cancer research : BCR, 2021-12, Vol.23 (1)

2021

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A germline mutation in PBRM1 predisposes to renal cell carcinoma

Journal of medical genetics, 2015-06, Vol.52 (6), p.426-430

2015

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Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma

Journal of medical genetics, 2011-04, Vol.48 (4), p.226-34

2011

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Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

PloS one, 2015-04, Vol.10 (4), p.e0120020

2015

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Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study

American journal of obstetrics and gynecology, 2021-07, Vol.225 (1), p.51.e1-51.e17

2021

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BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosis

Genetics in medicine, 2012-05, Vol.14 (5), p.527-534

2012

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GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers

Frontiers in oncology, 2018-10, Vol.8, p.490-490

2018

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

BMC medical research methodology, 2021-07, Vol.21 (1), p.1-155, Article 155

2021

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Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in BRCA1/2 Carriers

Cancer epidemiology, biomarkers & prevention, 2015-04, Vol.24 (4), p.698-707

2015

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

International journal of cancer, 2019-01, Vol.144 (8), p.1962-1974

2019

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Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma

Journal of medical genetics, 2017-09, Vol.54 (9), p.607-612

2017

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Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO)

Breast cancer research and treatment, 2011-12, Vol.130 (3), p.927-938

2011

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

Cancers, 2021-07, Vol.13 (15), p.3659

2021

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Mutation analysis of PALB2 gene in French breast cancer families

Breast cancer research and treatment, 2015-12, Vol.154 (3), p.463-471

2015

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The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

Human mutation, 2011-09, Vol.32 (9), p.1004-1007

2011

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Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

Nature (London), 2016-03, Vol.531 (7592), p.126-126

2016

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The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer

NPJ breast cancer, 2019, Vol.5 (1), p.38-14, Article 38

2019

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

BMC cancer, 2016-01, Vol.16 (12), p.13-13, Article 13

2016

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Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients

Human mutation, 2009-04, Vol.30 (4), p.564-574

2009

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Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations

Oncogene, 2004-01, Vol.23 (4), p.914-919

2004

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Correction: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

Nature (London), 2016-03, Vol.531 (7592), p.126-126

2016

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Germline copy number variation of genes involved in chromatin remodelling in families suggestive of Li-Fraumeni syndrome with brain tumours

European journal of human genetics : EJHG, 2013-12, Vol.21 (12), p.1369-1376

2013

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Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing

European journal of cancer (1990), 2006-05, Vol.42 (7), p.871-881

2006

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

A germline mutation in PBRM1 predisposes to renal cell carcinoma

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study

BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosis

GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers

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

Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in BRCA1/2 Carriers

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

Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma

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

Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO)

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

Mutation analysis of PALB2 gene in French breast cancer families

The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer

Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO)

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

Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients

Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations

Correction: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

Germline copy number variation of genes involved in chromatin remodelling in families suggestive of Li-Fraumeni syndrome with brain tumours

Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing

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