Background: Objectives: Characterize 1) the frequency of mutations in patients with clinical criteria for HBOC using a 25-gene panel in a Spanish population (FAMOSA study). 2) The psychological impact of these tests and patient''s counseling preferences. Methods: Patients with breast or ovarian cancer who met the NCCN criteria for genetic testing with a) prior testing for BRCA genes with NO mutation identified; or b) recently diagnosed (<6 months) and not genetically tested, were enrolled for multiplex cancer testing (MyRisk 25-gene panel). Participants completed self-questionnaires regarding geneting counseling preferences and three psychological scales (MICRA, CWS, R-IES) at base-line, one week, three and twelve months after results discl...
Hereditary breast and ovarian cancer (HBOC) is an inherited cancer syndrome that is associated with ...
Background: Over recent years genetic testing for germline mutations in BRCA1/BRCA2 has become more ...
Objectives: To evaluate the accuracy of algorithms for predicting BRCAI/2 germ-line mutation carrier...
Background: Hereditary breast cancer (BC), ovarian cancer (OC), and pancreatic cancer (PC) are the m...
Purpose: The aim of the study was to evaluate the clinical implication of multigene panel testing of...
Objective: Pathogenic BRCA variants account for between 5.8-24.8% of ovarian cancers. The identifica...
Background: Hereditary breast and ovarian cancer (HBOC) syndrome is an autosomal dominant inherited ...
IF 5.008 (2015/2016)International audienceUntil recently, the molecular diagnosis of hereditary brea...
[Background]: In the context of our Regional Program of Hereditary Cancer, individuals fulfilling th...
Funding Information: This work was supported by State Research Program “Biomedicine for the public h...
AbstractObjectiveGenetic predisposition to ovarian cancer is well documented. With the advent of nex...
Author: Justas Krištopaitis Title: Prevalence of BRCA1 and BRCA2 genes mutations and their impact on...
PURPOSE: Recent advances in DNA sequencing have led to the development of breast cancer susceptibili...
Purpose: Gene panel sequencing is revolutionizing germline risk assessment for hereditary breast can...
BRCA1 and BRCA2 are gene mutations that drastically increase chances of developing breast and ovaria...
Hereditary breast and ovarian cancer (HBOC) is an inherited cancer syndrome that is associated with ...
Background: Over recent years genetic testing for germline mutations in BRCA1/BRCA2 has become more ...
Objectives: To evaluate the accuracy of algorithms for predicting BRCAI/2 germ-line mutation carrier...
Background: Hereditary breast cancer (BC), ovarian cancer (OC), and pancreatic cancer (PC) are the m...
Purpose: The aim of the study was to evaluate the clinical implication of multigene panel testing of...
Objective: Pathogenic BRCA variants account for between 5.8-24.8% of ovarian cancers. The identifica...
Background: Hereditary breast and ovarian cancer (HBOC) syndrome is an autosomal dominant inherited ...
IF 5.008 (2015/2016)International audienceUntil recently, the molecular diagnosis of hereditary brea...
[Background]: In the context of our Regional Program of Hereditary Cancer, individuals fulfilling th...
Funding Information: This work was supported by State Research Program “Biomedicine for the public h...
AbstractObjectiveGenetic predisposition to ovarian cancer is well documented. With the advent of nex...
Author: Justas Krištopaitis Title: Prevalence of BRCA1 and BRCA2 genes mutations and their impact on...
PURPOSE: Recent advances in DNA sequencing have led to the development of breast cancer susceptibili...
Purpose: Gene panel sequencing is revolutionizing germline risk assessment for hereditary breast can...
BRCA1 and BRCA2 are gene mutations that drastically increase chances of developing breast and ovaria...
Hereditary breast and ovarian cancer (HBOC) is an inherited cancer syndrome that is associated with ...
Background: Over recent years genetic testing for germline mutations in BRCA1/BRCA2 has become more ...
Objectives: To evaluate the accuracy of algorithms for predicting BRCAI/2 germ-line mutation carrier...