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Universal screening of both endometrial and colon cancers increases the detection of Lynch syndrome

Cancer, 2018-08, Vol.124 (15), p.3145-3153

2018

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Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment

JAMA oncology, 2015-10, Vol.1 (7), p.943

2015

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A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome

Modern pathology, 2017-03, Vol.30 (3), p.440-447

2017

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Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center

Familial cancer, 2023-10, Vol.22 (4), p.467-474

2023

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Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria

JNCI : Journal of the National Cancer Institute, 2013-11, Vol.105 (21), p.1607-1616

2013

Volltextzugriff (PDF)

Prevalence of Thyroid Cancer in Familial Adenomatous Polyposis Syndrome and the Role of Screening Ultrasound Examinations

Clinical gastroenterology and hepatology, 2007-03, Vol.5 (3), p.367-373

2007

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A Rapid Systematic Review of Outcomes Studies in Genetic Counseling

Journal of genetic counseling, 2017-06, Vol.26 (3), p.361-378

2017

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Transition to telephone genetic counseling services during the COVID‐19 pandemic

Journal of genetic counseling, 2021-08, Vol.30 (4), p.984-988

2021

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Case 7-2020: A 52-Year-Old Man with a Mass in the Left Breast

The New England journal of medicine, 2020-02, Vol.382 (9), p.856-864

2020

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Development of an Electronic Decision Aid Tool to Facilitate Mainstream Genetic Testing in Ovarian Cancer Patients

The oncologist (Dayton, Ohio), 2024-05, Vol.29 (5), p.e665-e671

2024

Volltextzugriff (PDF)

Patient decisions regarding cancer gene panel testing: An exploratory study

Journal of genetic counseling, 2023-11

2023

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Colorectal Cancer Risk Perception on the Basis of Genetic Test Results in Individuals at Risk for Lynch Syndrome

Journal of clinical oncology, 2009-08, Vol.27 (24), p.3981-3986

2009

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ATM Variants in Breast Cancer: Implications for Breast Radiation Therapy Treatment Recommendations

International journal of radiation oncology, biology, physics, 2021-08, Vol.110 (5), p.1373-1382

2021

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Pathologic Findings in Prophylactic and Nonprophylactic Hysterectomy Specimens of Patients With Lynch Syndrome

The American journal of surgical pathology, 2016-09, Vol.40 (9), p.1177-1191

2016

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Performance of the shared decision-making process scale for use in evaluation of hereditary cancer genetic testing decisions

Journal of genetic counseling, 2023-10, Vol.32 (5), p.957-964

2023

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Prevalence and Predictors of Appropriate Colorectal Cancer Surveillance in Lynch Syndrome

The American journal of gastroenterology, 2010-08, Vol.105 (8), p.1851-1860

2010

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Perceptions of Cancer Risk, Cause, and Needs in Participants from Low Socioeconomic Background at Risk for Hereditary Cancer

Behavioral medicine (Washington, D.C.), 2017-10, Vol.43 (4), p.259-267

2017

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Prevalence and Functional Analysis of Sequence Variants in the ATR Checkpoint Mediator Claspin

Molecular cancer research, 2009-09, Vol.7 (9), p.1510-1516

2009

Volltextzugriff (PDF)

Sharing Genetic Test Results in Lynch Syndrome: Communication With Close and Distant Relatives

Clinical gastroenterology and hepatology, 2008-03, Vol.6 (3), p.333-338

2008

Volltextzugriff (PDF)

Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization

Journal of genetic counseling, 2018-12, Vol.27 (6), p.1318-1327

2018

Volltextzugriff (PDF)

Enhancing the Identification of Lynch Syndrome Through Universal Screening of Both Endometrial and Colon Cancers

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S178-S178

2017

Volltextzugriff (PDF)

A pooled electronic consultation program to improve access to genetics specialists

Genetics in Medicine Open, 2023, Vol.1 (1), p.100819, Article 100819

2023

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Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome

Gynecologic oncology, 2012-12, Vol.127 (3), p.544-551

2012

Volltextzugriff (PDF)

Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni syndrome

Cancer research (Chicago, Ill.), 2001-11, Vol.61 (22), p.8062-8067

2001

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Universal screening of both endometrial and colon cancers increases the detection of Lynch syndrome

Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment

A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome

Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center

Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria

Prevalence of Thyroid Cancer in Familial Adenomatous Polyposis Syndrome and the Role of Screening Ultrasound Examinations

A Rapid Systematic Review of Outcomes Studies in Genetic Counseling

Transition to telephone genetic counseling services during the COVID‐19 pandemic

Case 7-2020: A 52-Year-Old Man with a Mass in the Left Breast

Development of an Electronic Decision Aid Tool to Facilitate Mainstream Genetic Testing in Ovarian Cancer Patients

Patient decisions regarding cancer gene panel testing: An exploratory study

Colorectal Cancer Risk Perception on the Basis of Genetic Test Results in Individuals at Risk for Lynch Syndrome

ATM Variants in Breast Cancer: Implications for Breast Radiation Therapy Treatment Recommendations

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

Pathologic Findings in Prophylactic and Nonprophylactic Hysterectomy Specimens of Patients With Lynch Syndrome

Performance of the shared decision-making process scale for use in evaluation of hereditary cancer genetic testing decisions

Prevalence and Predictors of Appropriate Colorectal Cancer Surveillance in Lynch Syndrome

Perceptions of Cancer Risk, Cause, and Needs in Participants from Low Socioeconomic Background at Risk for Hereditary Cancer

Prevalence and Functional Analysis of Sequence Variants in the ATR Checkpoint Mediator Claspin

Sharing Genetic Test Results in Lynch Syndrome: Communication With Close and Distant Relatives

Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization

Enhancing the Identification of Lynch Syndrome Through Universal Screening of Both Endometrial and Colon Cancers

A pooled electronic consultation program to improve access to genetics specialists

Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome

Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni syndrome

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