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Breast Cancer Research : BCR
|
November 13, 2016
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
Timothy R Rebbeck, Tara M Friebel, Nandita Mitra, et al.
Human Molecular Genetics
|
September 6, 2011
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
David G Cox, Jacques Simard, Daniel Sinnett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M M Lakeman, Alexandra J van den Broek, Juliën A M Vos, et al.
Human Genetics
|
May 21, 2011
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
Kate M Im, Tomas Kirchhoff, Xianshu Wang, et al.
Plos Genetics
|
November 10, 2010
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
Mia M Gaudet, Tomas Kirchhoff, Todd Green, et al.
Plos Genetics
|
April 2, 2013
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk
Mia M Gaudet, Karoline B Kuchenbaecker, Joseph Vijai, et al.
Human Molecular Genetics
|
August 7, 2009
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Antonis C Antoniou, Olga M Sinilnikova, Lesley McGuffog, et al.
Plos One
|
July 28, 2016
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Elena Vigorito, Karoline B Kuchenbaecker, Jonathan Beesley, et al.
Breast Cancer Research : BCR
|
February 22, 2012
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
Antonis C Antoniou, Karoline B Kuchenbaecker, Penny Soucy, et al.
Cancer Research
|
December 2, 2010
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction
Antonis C Antoniou, Jonathan Beesley, Lesley McGuffog, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Breast Cancer Research : BCR
|
November 13, 2016
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
Timothy R Rebbeck, Tara M Friebel, Nandita Mitra, et al.
Human Molecular Genetics
|
September 6, 2011
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
David G Cox, Jacques Simard, Daniel Sinnett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M M Lakeman, Alexandra J van den Broek, Juliën A M Vos, et al.
Human Genetics
|
May 21, 2011
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
Kate M Im, Tomas Kirchhoff, Xianshu Wang, et al.
Plos Genetics
|
November 10, 2010
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
Mia M Gaudet, Tomas Kirchhoff, Todd Green, et al.
Plos Genetics
|
April 2, 2013
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk
Mia M Gaudet, Karoline B Kuchenbaecker, Joseph Vijai, et al.
Human Molecular Genetics
|
August 7, 2009
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Antonis C Antoniou, Olga M Sinilnikova, Lesley McGuffog, et al.
Plos One
|
July 28, 2016
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Elena Vigorito, Karoline B Kuchenbaecker, Jonathan Beesley, et al.
Breast Cancer Research : BCR
|
February 22, 2012
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
Antonis C Antoniou, Karoline B Kuchenbaecker, Penny Soucy, et al.
Cancer Research
|
December 2, 2010
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction
Antonis C Antoniou, Jonathan Beesley, Lesley McGuffog, et al.
Page
of 4