Germline protein truncating variants (PTVs) in the gene have been associated with a 2-4-fold increased breast cancer risk in case-control studies conducted in different European populations. However, the distribution and the frequency of PTVs in Europe have never been investigated. In the present study, we collected the data of 114 European female breast cancer cases with PTVs ascertained in 20 centers from 13 European countries. We identified 27 different PTVs. The p.Gln1701* PTV is the most common PTV in Northern Europe with a maximum frequency in Finland and a lower relative frequency in Southern Europe. On the contrary, p.Arg1931* seems to be the most common PTV in Southern Europe. We also showed that p.Arg658*, the third most commo...
AbstractGermline copy number variants (CNVs) are pervasive in the human genome but potential disease...
Si le syndrome de prédisposition héréditaire au cancer du sein et de l’ovaire constitue uneentité re...
Abstract Breast cancer is the most common cancer among women, and inherited predisposition is one o...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2–4-...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2–4-fold i...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2-4-fold i...
FANCM germline protein truncating variants (PTVs) are moderate-risk factors for ER-negative breast c...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2-4-fold i...
Q1Q1Artículo de investigación80140-80163There are significant inter-individual differences in the le...
There are significant inter-individual differences in the levels of gene expression. Through modulat...
A three-stage genome-wide association study recently identified single nucleotide polymorphisms (SNP...
Previous genome-wide association studies among women of European ancestry identified two independent...
Rare variants in at least 10 genes, including BRCA1, BRCA2, PALB2, ATM, and CHEK2, are associated wi...
BRCA1 BRCA2 mutational spectrum in the Middle East, North Africa, and Southern Europe is not well ch...
BACKGROUND: Protein truncating variants in ATM, BRCA1, BRCA2, CHEK2, and PALB2 are associated with i...
AbstractGermline copy number variants (CNVs) are pervasive in the human genome but potential disease...
Si le syndrome de prédisposition héréditaire au cancer du sein et de l’ovaire constitue uneentité re...
Abstract Breast cancer is the most common cancer among women, and inherited predisposition is one o...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2–4-...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2–4-fold i...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2-4-fold i...
FANCM germline protein truncating variants (PTVs) are moderate-risk factors for ER-negative breast c...
Germline protein truncating variants (PTVs) in the FANCM gene have been associated with a 2-4-fold i...
Q1Q1Artículo de investigación80140-80163There are significant inter-individual differences in the le...
There are significant inter-individual differences in the levels of gene expression. Through modulat...
A three-stage genome-wide association study recently identified single nucleotide polymorphisms (SNP...
Previous genome-wide association studies among women of European ancestry identified two independent...
Rare variants in at least 10 genes, including BRCA1, BRCA2, PALB2, ATM, and CHEK2, are associated wi...
BRCA1 BRCA2 mutational spectrum in the Middle East, North Africa, and Southern Europe is not well ch...
BACKGROUND: Protein truncating variants in ATM, BRCA1, BRCA2, CHEK2, and PALB2 are associated with i...
AbstractGermline copy number variants (CNVs) are pervasive in the human genome but potential disease...
Si le syndrome de prédisposition héréditaire au cancer du sein et de l’ovaire constitue uneentité re...
Abstract Breast cancer is the most common cancer among women, and inherited predisposition is one o...