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Tumor-Based Genetic Testing and Familial Cancer Risk

Cold Spring Harbor perspectives in medicine, 2020-08, Vol.10 (8), p.a036590

2020

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Gene panel testing for inherited cancer risk

Journal of the National Comprehensive Cancer Network, 2014-09, Vol.12 (9), p.1339-1346

2014

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Understanding patient and provider perceptions and expectations of genomic medicine

Journal of surgical oncology, 2015-01, Vol.111 (1), p.9-17

2015

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Influence of Race/Ethnicity on Genetic Counseling and Testing for Hereditary Breast and Ovarian Cancer

The breast journal, 2009-09, Vol.15 (s1), p.S56-S62

2009

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Prevalence of pathogenic variants in DNA damage response and repair genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer

Scientific reports, 2020-08, Vol.10 (1), p.13518-13518, Article 13518

2020

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The Relevance of Hereditary Cancer Risks to Precision Oncology: What Should Providers Consider When Conducting Tumor Genomic Profiling?

Journal of the National Comprehensive Cancer Network, 2016-06, Vol.14 (6), p.795-806

2016

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‘A good decision is the one that feels right for me’: Codesign with patients to inform theoretical underpinning of a decision aid website

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13844-n/a

2024

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Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling

Journal of genetic counseling, 2016-06, Vol.25 (3), p.472-482

2016

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Proactive familial cancer risk assessment: a service development study in UK primary care

BJGP open, 2023-12, Vol.7 (4), p.BJGPO.2023.0076

2023

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Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer

Familial cancer, 2016-10, Vol.15 (4), p.529-539

2016

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The Hereditary Paraganglioma-Pheochromocytoma Syndrome: No Time to Waste

JAMA oncology, 2017-12, Vol.3 (12), p.1739

2017

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Interaction of germline variants in a family with a history of early‐onset clear cell renal cell carcinoma

Molecular genetics & genomic medicine, 2019-03, Vol.7 (3), p.e556-n/a

2019

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Digital innovation for cancer risk assessment allows large-scale service redevelopment of regional cancer genetics service delivery

Familial cancer, 2024-11, Vol.23 (4), p.591-598

2024

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Guidelines-Based Cancer Risk Assessment

Seminars in oncology nursing, 2019-02, Vol.35 (1), p.34-46

2019

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Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study

Journal of medical Internet research, 2016-02, Vol.18 (2), p.e23-e23

2016

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Feasibility of perioperative multi-gene panel testing (MGPT) in cancer patients eligible for hereditary genetic evaluation (GE): The PROTECT pilot

Journal of clinical oncology, 2018-05, Vol.36 (15_suppl), p.1536-1536

2018

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Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results

JNCI : Journal of the National Cancer Institute, 2018-09, Vol.110 (9), p.985-993

2018

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Abstract 808: Functional evaluation of novel germline DNA repair variants identified in patients with early-onset renal cancer

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.808-808

2021

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Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice

British journal of cancer, 2024-06, Vol.130 (12), p.2027-2036

2024

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Abstract 4185: Establishing sustainable research collaborations in the Caribbean through the utilization of multiple technology platforms

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.4185-4185

2019

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Compassionate Removal of Heated High-Flow Nasal Cannula for End of Life: Case Series and Protocol Development

Journal of hospice and palliative nursing, 2021-08, Vol.23 (4), p.360-366

2021

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The prevalence of hereditary pancreatitis mutations in families with pancreatic cancer

Journal of clinical oncology, 2019-05, Vol.37 (15_suppl), p.e15728-e15728

2019

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Patterns of referrals to regional clinical genetics services for women potentially at above-population level risk of breast cancer

BJC Reports, 2024-01, Vol.2 (1), Article 2

2024

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Are we still adjusting to multigene panel testing? An NCI-designated cancer center's 2-year experience

Journal of clinical oncology, 2017-05, Vol.35 (15_suppl), p.1585-1585

2017

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Tumor-Based Genetic Testing and Familial Cancer Risk

Gene panel testing for inherited cancer risk

Understanding patient and provider perceptions and expectations of genomic medicine

Influence of Race/Ethnicity on Genetic Counseling and Testing for Hereditary Breast and Ovarian Cancer

Prevalence of pathogenic variants in DNA damage response and repair genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer

The Relevance of Hereditary Cancer Risks to Precision Oncology: What Should Providers Consider When Conducting Tumor Genomic Profiling?

‘A good decision is the one that feels right for me’: Codesign with patients to inform theoretical underpinning of a decision aid website

Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling

Proactive familial cancer risk assessment: a service development study in UK primary care

Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer

The Hereditary Paraganglioma-Pheochromocytoma Syndrome: No Time to Waste

Interaction of germline variants in a family with a history of early‐onset clear cell renal cell carcinoma

Digital innovation for cancer risk assessment allows large-scale service redevelopment of regional cancer genetics service delivery

Guidelines-Based Cancer Risk Assessment

Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study

Feasibility of perioperative multi-gene panel testing (MGPT) in cancer patients eligible for hereditary genetic evaluation (GE): The PROTECT pilot

Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results

Abstract 808: Functional evaluation of novel germline DNA repair variants identified in patients with early-onset renal cancer

Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice

Abstract 4185: Establishing sustainable research collaborations in the Caribbean through the utilization of multiple technology platforms

Compassionate Removal of Heated High-Flow Nasal Cannula for End of Life: Case Series and Protocol Development

Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility

The prevalence of hereditary pancreatitis mutations in families with pancreatic cancer

Patterns of referrals to regional clinical genetics services for women potentially at above-population level risk of breast cancer

Are we still adjusting to multigene panel testing? An NCI-designated cancer center's 2-year experience

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