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Thymic carcinoma with Lynch syndrome or microsatellite instability, a rare entity responsive to immunotherapy

European journal of cancer (1990), 2021-08, Vol.153, p.162-167

2021

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Acceptability of chemoprevention trials in high-risk subjects

Annals of oncology, 2013-11, Vol.24 Suppl 8, p.viii42-viii46

2013

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Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Cancers, 2023, Vol.15 (13), p.3313

2023

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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

Breast cancer research and treatment, 2017-01, Vol.161 (1), p.117-134

2017

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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Breast cancer research : BCR, 2011-01, Vol.13 (6), p.R110-R110, Article R110

2011

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Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

PloS one, 2016-07, Vol.11 (7), p.e0158801-e0158801

2016

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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

Human genetics, 2011-11, Vol.130 (5), p.685-699

2011

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A Combined Atomic Force Microscopy and Molecular Dynamics Simulation Study on a Plastocyanin Mutant Chemisorbed on a Gold Surface

Chemphyschem, 2003-11, Vol.4 (11), p.1189-1195

2003

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Cardiac RNase Z edited via CRISPR-Cas9 drives heart hypertrophy in Drosophila

PloS one, 2023-05, Vol.18 (5), p.e0286214-e0286214

2023

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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Nature genetics, 2020-06, Vol.52 (6), p.572-581

2020

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Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Nature genetics, 2017-05, Vol.49 (5), p.680-691

2017

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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Nature genetics, 2017-12, Vol.49 (12), p.1767-1778

2017

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Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Human mutation, 2018-05, Vol.39 (5), p.593-620

2018

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Genetics in medicine, 2020-10, Vol.22 (10), p.1653-1666

2020

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PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Journal of medical genetics, 2016-12, Vol.53 (12), p.800-811

2016

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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Nature genetics, 2020-01, Vol.52 (1), p.56-73

2020

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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Nature (London), 2014-10, Vol.514 (7520), p.92-97

2014

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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Nature genetics, 2013-04, Vol.45 (4), p.371-384

2013

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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

PLoS genetics, 2013, Vol.9 (3), p.e1003212-e1003212

2013

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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Nature genetics, 2016-04, Vol.48 (4), p.374-386

2016

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Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

Nature communications, 2016-04, Vol.7 (1), p.11375-13, Article 11375

2016

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Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

PLoS biology, 2011-11, Vol.9 (11), p.e1001199

2011

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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Breast cancer research : BCR, 2016-06, Vol.18 (1), p.64, Article 64

2016

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Proceedings of the International Consensus Conference on Breast Cancer Risk, Genetics, & Risk Management, April, 2007

Cancer, 2008-11, Vol.113 (10), p.2627-2637

2008

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An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

Breast cancer research : BCR, 2015-04, Vol.17 (1), p.61, Article 61

2015

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Thymic carcinoma with Lynch syndrome or microsatellite instability, a rare entity responsive to immunotherapy

Acceptability of chemoprevention trials in high-risk subjects

Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

A Combined Atomic Force Microscopy and Molecular Dynamics Simulation Study on a Plastocyanin Mutant Chemisorbed on a Gold Surface

Cardiac RNase Z edited via CRISPR-Cas9 drives heart hypertrophy in Drosophila

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Proceedings of the International Consensus Conference on Breast Cancer Risk, Genetics, & Risk Management, April, 2007

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

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