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The Role of Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer

The New England journal of medicine, 2016-02, Vol.374 (5), p.454-468

2016

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Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

Cancer epidemiology, biomarkers & prevention, 2017-03, Vol.26 (3), p.404-412

2017

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American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility

Journal of clinical oncology, 2015-11, Vol.33 (31), p.3660-3667

2015

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Risk of breast cancer in Lynch syndrome: a systematic review

Breast cancer research : BCR, 2013-03, Vol.15 (2), p.R27-R27, Article R27

2013

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American Society of Clinical Oncology Expert Statement: Collection and Use of a Cancer Family History for Oncology Providers

Journal of clinical oncology, 2014-03, Vol.32 (8), p.833-840

2014

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Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models

Genetics in medicine, 2019-01, Vol.21 (1), p.71-80

2019

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Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches

American journal of human genetics, 2018-02, Vol.102 (2), p.233-248

2018

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Potential impact of family history–based screening guidelines on the detection of early‐onset colorectal cancer

Cancer, 2020-07, Vol.126 (13), p.3013-3020

2020

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Whole-Genome Sequencing in Healthy People

Mayo Clinic proceedings, 2017-01, Vol.92 (1), p.159-172

2017

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Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer

Mayo Clinic proceedings, 2010-12, Vol.85 (12), p.1111-1120

2010

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A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS)

Human mutation, 2012-01, Vol.33 (1), p.8-21

2012

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The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations

Gastroenterology (New York, N.Y. 1943), 2008-08, Vol.135 (2), p.419-428.e1

2008

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A general framework for functionally informed set-based analysis: Application to a large-scale colorectal cancer study

PLoS genetics, 2020-08, Vol.16 (8), p.e1008947-e1008947

2020

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Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of health

Genetics in medicine, 2020-09, Vol.22 (9), p.1552-1559

2020

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Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencing

Genetics in medicine, 2021-07, Vol.23 (7), p.1192-1201

2021

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A New Comprehensive Colorectal Cancer Risk Prediction Model Incorporating Family History, Personal Characteristics, and Environmental Factors

Cancer epidemiology, biomarkers & prevention, 2020-03, Vol.29 (3), p.549-557

2020

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Increased Cancer Risks in Myotonic Dystrophy

Mayo Clinic proceedings, 2012-02, Vol.87 (2), p.130-135

2012

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RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress

Journal of cell science, 2012-05, Vol.125 (Pt 10), p.2509-2522

2012

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Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome

JNCI : Journal of the National Cancer Institute, 2015-09, Vol.107 (9), p.djv170

2015

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DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome

Modern pathology, 2018-10, Vol.31 (10), p.1608-1618

2018

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BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management

The oncologist (Dayton, Ohio), 2013-05, Vol.18 (5), p.518-524

2013

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A Classification Model for BRCA2 DNA Binding Domain Missense Variants Based on Homology-Directed Repair Activity

Cancer research (Chicago, Ill.), 2013-01, Vol.73 (1), p.265-275

2013

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Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening

Genetics in medicine, 2021-05, Vol.23 (5), p.934-941

2021

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Leptin gene variants and colorectal cancer risk: Sex-specific associations

PloS one, 2018-10, Vol.13 (10), p.e0206519

2018

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The Role of Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility

Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and the American Society of Clinical Oncology

Risk of breast cancer in Lynch syndrome: a systematic review

American Society of Clinical Oncology Expert Statement: Collection and Use of a Cancer Family History for Oncology Providers

Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models

Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches

Potential impact of family history–based screening guidelines on the detection of early‐onset colorectal cancer

Whole-Genome Sequencing in Healthy People

Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer

A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS)

The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations

A general framework for functionally informed set-based analysis: Application to a large-scale colorectal cancer study

Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of health

Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencing

A New Comprehensive Colorectal Cancer Risk Prediction Model Incorporating Family History, Personal Characteristics, and Environmental Factors

Increased Cancer Risks in Myotonic Dystrophy

RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress

Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome

DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome

BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management

A Classification Model for BRCA2 DNA Binding Domain Missense Variants Based on Homology-Directed Repair Activity

Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening

Leptin gene variants and colorectal cancer risk: Sex-specific associations

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