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Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017

Journal of genetic counseling, 2020-12, Vol.29 (6), p.1126-1141

2020

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Updates in hereditary breast cancer genetic testing and practical high risk breast management in gene carriers

Seminars in oncology, 2020-08, Vol.47 (4), p.182-186

2020

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An analysis of the impact of annual cancer genetic testing guideline updates on a past patient population

Journal of genetic counseling, 2023-10

2023

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A Randomized Trial Comparing the Effectiveness of Pre-test Genetic Counseling Using an Artificial Intelligence Automated Chatbot and Traditional In-person Genetic Counseling in Women Newly Diagnosed with Breast Cancer

Annals of surgical oncology, 2023-10, Vol.30 (10), p.5990-5996

2023

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ASO Visual Abstract: A Randomized Trial Comparing the Effectiveness of Pre-test Genetic Counseling Using an Artificial Intelligence Automated Chatbot and Traditional In-person Genetic Counseling in Women Newly Diagnosed with Breast Cancer

Annals of surgical oncology, 2023-10, Vol.30 (10), p.5997-5998

2023

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Impact of Multigene Panel Testing on Surgical Decision Making in Breast Cancer Patients

Journal of the American College of Surgeons, 2018-04, Vol.226 (4), p.560-565

2018

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Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome clinical features

Journal of medical genetics, 2011-08, Vol.48 (8), p.505-512

2011

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Impact of an embedded genetic counselor on breast cancer treatment

Breast cancer research and treatment, 2018-05, Vol.169 (1), p.43-46

2018

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Rapid implementation of telegenetic services during the COVID-19 pandemic allowed continuing patient access, but not equally for all

Health and technology, 2022-07, Vol.12 (4), p.839-844

2022

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The current state of genetic counseling assistants in the United States

Journal of genetic counseling, 2019-10, Vol.28 (5), p.962-973

2019

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Primary care physician referral practices regarding BRCA1/2 genetic counseling in a major health system

Breast cancer research and treatment, 2022-09, Vol.195 (2), p.153-160

2022

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Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study

The lancet oncology, 2024-05, Vol.25 (5), p.668-682

2024

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Equitable Parent Leadership in School Construction Design

Noss, Ryan T

2021

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The Incorporation of Predictive Genomic Testing into Genetic Counseling Programs

Journal of genetic counseling, 2014-08, Vol.23 (4), p.671-678

2014

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Inherited Thrombocytopenia Caused by Germline Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome

JIM - high impact case reports, 2020-07, Vol.8

2020

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Patient Decisions to Receive Secondary Pharmacogenomic Findings and Development of a Multidisciplinary Practice Model to Integrate Results Into Patient Care

Clinical and translational science, 2018-01, Vol.11 (1), p.71-76

2018

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Inherited Thrombocytopenia Caused by Germline ANKRD26 Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome

JIM - high impact case reports, 2020, Vol.8, p.2324709620938941-2324709620938941

2020

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Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices

Npj genomic medicine, 2016-05, Vol.1 (1), p.16010-16010, Article 16010

2016

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Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition

Melanoma research, 2011-06, Vol.21 (3), p.175-179

2011

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Getting a Delicate Process Right When Renaming Schools

School Administrator, 2023-04, Vol.80 (4), p.13-13

Noss, Ryan T

2023

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Improving species status assessments under the U.S. Endangered Species Act and implications for multispecies conservation challenges worldwide

Conservation biology, 2021-12, Vol.35 (6), p.1715-1724

2021

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A One-Year Randomized Trial of Lorcaserin for Weight Loss in Obese and Overweight Adults: The BLOSSOM Trial

The journal of clinical endocrinology and metabolism, 2011-10, Vol.96 (10), p.3067-3077

2011

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Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017

Updates in hereditary breast cancer genetic testing and practical high risk breast management in gene carriers

An analysis of the impact of annual cancer genetic testing guideline updates on a past patient population

A Randomized Trial Comparing the Effectiveness of Pre-test Genetic Counseling Using an Artificial Intelligence Automated Chatbot and Traditional In-person Genetic Counseling in Women Newly Diagnosed with Breast Cancer

ASO Visual Abstract: A Randomized Trial Comparing the Effectiveness of Pre-test Genetic Counseling Using an Artificial Intelligence Automated Chatbot and Traditional In-person Genetic Counseling in Women Newly Diagnosed with Breast Cancer

Impact of Multigene Panel Testing on Surgical Decision Making in Breast Cancer Patients

Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome clinical features

Impact of an embedded genetic counselor on breast cancer treatment

Rapid implementation of telegenetic services during the COVID-19 pandemic allowed continuing patient access, but not equally for all

The current state of genetic counseling assistants in the United States

Primary care physician referral practices regarding BRCA1/2 genetic counseling in a major health system

Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study

Equitable Parent Leadership in School Construction Design

The Incorporation of Predictive Genomic Testing into Genetic Counseling Programs

Inherited Thrombocytopenia Caused by Germline Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome

Patient Decisions to Receive Secondary Pharmacogenomic Findings and Development of a Multidisciplinary Practice Model to Integrate Results Into Patient Care

Inherited Thrombocytopenia Caused by Germline ANKRD26 Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome

Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices

Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition

Getting a Delicate Process Right When Renaming Schools

Improving species status assessments under the U.S. Endangered Species Act and implications for multispecies conservation challenges worldwide

A One-Year Randomized Trial of Lorcaserin for Weight Loss in Obese and Overweight Adults: The BLOSSOM Trial

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