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Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families

Journal of medical genetics, 2016-01, Vol.53 (1), p.34-42

2016

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Clinical Classification of BRCA1 and BRCA2 DNA Sequence Variants: The Value of Cytokeratin Profiles and Evolutionary Analysis—A Report From the kConFab Investigators

Journal of clinical oncology, 2008-04, Vol.26 (10), p.1657-1663

2008

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Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity

Human mutation, 2010-06, Vol.31 (6), p.E1484-E1505

2010

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Rare variants in the ATMgene and risk of breast cancer

Breast cancer research : BCR, 2011-07, Vol.13 (4), Article R73

2011

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ENIGMA-Evidence-based network for the interpretation of germline mutant alleles: An international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes

Human mutation, 2012-01, Vol.33 (1), p.2-7

2012

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Mapping of a candidate colorectal cancer tumor-suppressor gene to a 900-kilobase region on the short arm of chromosome 8

Genes chromosomes & cancer, 2004-07, Vol.40 (3), p.247-260

2004

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Rare variants in the ATM gene and risk of breast cancer

Breast cancer research : BCR, 2011-07, Vol.13 (4), p.R73-R73

2011

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Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer

American journal of human genetics, 2009-10, Vol.85 (4), p.427-446

2009

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Gene expression profiling of formalin-fixed, paraffin-embedded familial breast tumours using the whole genome-DASL assay

The Journal of pathology, 2010-08, Vol.221 (4), p.452-461

2010

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HER3 and downstream pathways are involved in colonization of brain metastases from breast cancer

Breast cancer research : BCR, 2010-01, Vol.12 (4), p.R46-R46, Article R46

2010

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Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance

Cancer research (Chicago, Ill.), 2006-02, Vol.66 (4), p.2019-2027

2006

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Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families

Breast cancer research and treatment, 2011-08, Vol.129 (1), p.255-263

2011

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Cognition and the temporal arts: Investigating audience response to dance using PDAs that record continuous data during live performance

International journal of human-computer studies, 2009-09, Vol.67 (9), p.800-813

2009

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Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundary

Human mutation, 2011-06, Vol.32 (6), p.678-687

2011

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A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

Human reproduction (Oxford), 2010-06, Vol.25 (6), p.1569-1580

2010

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Atopy in Australia

Nature genetics, 1995-07, Vol.10 (3), p.260-260

1995

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The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

Breast cancer research and treatment, 2012-04, Vol.132 (3), p.1119-1126

2012

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Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?

Breast cancer research : BCR, 2007-01, Vol.9 (6), p.R82-R82, Article R82

2007

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BRCA1 R 1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk

Journal of medical genetics, 2012, Vol.49 (8), p.525-532

2012

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Mutation analysis of five candidate genes in familial breast cancer

Breast cancer research and treatment, 2007-11, Vol.105 (3), p.377-389

2007

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Visionary Leaders for Information

Winzenried, Arthur

1, 2010

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Common alleles at 6q25.1 and 1 p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

Human molecular genetics, 2011, Vol.20 (16), p.3304-3321

2011

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Correction: Common Genetic Variants and Modification of Penetrance of -Associated Breast Cancer

PLoS genetics, 2010-11, Vol.6 (11)

2010

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Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families

Clinical Classification of BRCA1 and BRCA2 DNA Sequence Variants: The Value of Cytokeratin Profiles and Evolutionary Analysis—A Report From the kConFab Investigators

Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity

Rare variants in the ATMgene and risk of breast cancer

ENIGMA-Evidence-based network for the interpretation of germline mutant alleles: An international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes

Mapping of a candidate colorectal cancer tumor-suppressor gene to a 900-kilobase region on the short arm of chromosome 8

Rare variants in the ATM gene and risk of breast cancer

Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer

Gene expression profiling of formalin-fixed, paraffin-embedded familial breast tumours using the whole genome-DASL assay

HER3 and downstream pathways are involved in colonization of brain metastases from breast cancer

Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance

Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families

Cognition and the temporal arts: Investigating audience response to dance using PDAs that record continuous data during live performance

Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundary

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Atopy in Australia

Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers

The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?

BRCA1 R 1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk

Mutation analysis of five candidate genes in familial breast cancer

Visionary Leaders for Information

Common alleles at 6q25.1 and 1 p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

Correction: Common Genetic Variants and Modification of Penetrance of -Associated Breast Cancer

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