BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
"""BRCAness"" syndrome in ovarian cancer: a case-control study describing the clinical features and outcome of patients with epithelial ovarian cancer associated with BRCA1 and BRCA2 mutations."
|
18955455 |
2008 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
"Methylation not a frequent ""second hit"" in tumors with germline BRCA mutations."
|
19340607 |
2009 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
"Methylation not a frequent ""second hit"" in tumors with germline BRCA mutations."
|
19340607 |
2009 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
2157delG: a frequent mutation in BRCA2 missed by PTT.
|
11106360 |
2000 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A 24-color metaphase-based radiation assay discriminates heterozygous BRCA2 mutation carriers from controls by chromosomal radiosensitivity.
|
22729890 |
2012 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A BRCA2 founder mutation and seven novel deleterious BRCA mutations in southern Chinese women with breast and ovarian cancer.
|
19353265 |
2009 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A BRCA2 founder mutation and seven novel deleterious BRCA mutations in southern Chinese women with breast and ovarian cancer.
|
19353265 |
2009 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A BRCA2 mutation, 4088insA, in a Finnish breast and ovarian cancer family associated with favourable clinical course.
|
18214034 |
2008 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity.
|
23108138 |
2013 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity.
|
23108138 |
2013 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A clinically validated diagnostic second-generation sequencing assay for detection of hereditary BRCA1 and BRCA2 mutations.
|
24094589 |
2013 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer.
|
24312913 |
2013 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay.
|
21719596 |
2011 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South Africa.
|
21204799 |
2012 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A high frequency of BRCA mutations in young black women with breast cancer residing in Florida.
|
26287763 |
2015 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A high frequency of BRCA mutations in young black women with breast cancer residing in Florida.
|
26287763 |
2015 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer.
|
14647210 |
2003 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques.
|
15951958 |
2005 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A high proportion of DNA variants of BRCA1 and BRCA2 is associated with aberrant splicing in breast/ovarian cancer patients.
|
20215541 |
2010 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A high proportion of DNA variants of BRCA1 and BRCA2 is associated with aberrant splicing in breast/ovarian cancer patients.
|
20215541 |
2010 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A high proportion of founder BRCA1 mutations in Polish breast cancer families.
|
15146557 |
2004 |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.
|
21702907 |
2011 |