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The BabySeq project: implementing genomic sequencing in newborns

BMC pediatrics, 2018-07, Vol.18 (1), p.225-225, Article 225

2018

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Assessing the Costs and Cost-Effectiveness of Genomic Sequencing

Journal of personalized medicine, 2015-12, Vol.5 (4), p.470-486

2015

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Disclosing genetic risk of Alzheimer’s disease to cognitively impaired patients and visit companions: Findings from the REVEAL Study

Patient education and counseling, 2017-05, Vol.100 (5), p.927-935

2017

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Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Frontiers in genetics, 2022-04, Vol.13, p.867371-867371

2022

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The impact of genetic counselors’ use of facilitative strategies on cognitive and emotional processing of genetic risk disclosure for Alzheimer’s disease

Patient education and counseling, 2018-05, Vol.101 (5), p.817-823

2018

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A Cost-Consequence Analysis of Preemptive SLCO1B1 Testing for Statin Myopathy Risk Compared to Usual Care

Journal of personalized medicine, 2021-10, Vol.11 (11), p.1123

2021

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Workforce Considerations When Building a Precision Medicine Program

Journal of personalized medicine, 2022-11, Vol.12 (11), p.1929

2022

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Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos

HGG advances, 2023-01, Vol.4 (1), p.100160-100160, Article 100160

2023

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Behavioral and psychological impact of genome sequencing: a pilot randomized trial of primary care and cardiology patients

Npj genomic medicine, 2021-08, Vol.6 (1), p.72-72, Article 72

2021

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Disclosing genetic risk for Alzheimer's dementia to individuals with mild cognitive impairment

Alzheimer's & dementia : translational research & clinical interventions, 2020, Vol.6 (1), p.e12002-n/a

2020

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The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial

Annals of internal medicine, 2017-08, Vol.167 (3), p.159

2017

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Communicating Genetic Risk Information for Common Disorders in the Era of Genomic Medicine

Annual review of genomics and human genetics, 2013-01, Vol.14 (1), p.491-513

2013

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Methodological Issues in Assessing the Economic Value of Next-Generation Sequencing Tests: Many Challenges and Not Enough Solutions

Value in health, 2018-09, Vol.21 (9), p.1033-1042

2018

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Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

American journal of human genetics, 2021-12, Vol.108 (12), p.2224-2237

2021

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Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project

Genetics in medicine, 2018-09, Vol.20 (9), p.1069-1076

2018

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Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

Genetics in medicine, 2019-05, Vol.21 (5), p.1100-1110

2019

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Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial

JAMA pediatrics, 2021-11, Vol.175 (11), p.1132

2021

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Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies

Genetics in medicine, 2019-12, Vol.21 (12), p.2781-2790

2019

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Population-Based Newborn Screening for Germline TP53 Variants: Clinical Benefits, Cost-Effectiveness, and Value of Further Research

JNCI : Journal of the National Cancer Institute, 2022-05, Vol.114 (5), p.722-731

2022

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Cost Analyses of Genomic Sequencing: Lessons Learned from the MedSeq Project

Value in health, 2018-09, Vol.21 (9), p.1054-1061

2018

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Clinical impact of preemptive pharmacogenomic testing on antiplatelet therapy in a real-world setting

European journal of human genetics : EJHG, 2024-02

2024

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Primary care providers’ responses to unsolicited Lynch syndrome secondary findings of varying clinical significance

Genetics in medicine, 2021-10, Vol.23 (10), p.1977-1983

2021

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Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

American journal of human genetics, 2023-07, Vol.110 (7), p.1034-1045

2023

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Adopting genetics: motivations and outcomes of personal genomic testing in adult adoptees

Genetics in medicine, 2016-09, Vol.18 (9), p.924-932

2016

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The BabySeq project: implementing genomic sequencing in newborns

Assessing the Costs and Cost-Effectiveness of Genomic Sequencing

Disclosing genetic risk of Alzheimer’s disease to cognitively impaired patients and visit companions: Findings from the REVEAL Study

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

The impact of genetic counselors’ use of facilitative strategies on cognitive and emotional processing of genetic risk disclosure for Alzheimer’s disease

A Cost-Consequence Analysis of Preemptive SLCO1B1 Testing for Statin Myopathy Risk Compared to Usual Care

Workforce Considerations When Building a Precision Medicine Program

Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos

Behavioral and psychological impact of genome sequencing: a pilot randomized trial of primary care and cardiology patients

Disclosing genetic risk for Alzheimer's dementia to individuals with mild cognitive impairment

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial

Communicating Genetic Risk Information for Common Disorders in the Era of Genomic Medicine

Methodological Issues in Assessing the Economic Value of Next-Generation Sequencing Tests: Many Challenges and Not Enough Solutions

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial

Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies

Population-Based Newborn Screening for Germline TP53 Variants: Clinical Benefits, Cost-Effectiveness, and Value of Further Research

Cost Analyses of Genomic Sequencing: Lessons Learned from the MedSeq Project

Improved provider preparedness through an 8-part genetics and genomic education program

Clinical impact of preemptive pharmacogenomic testing on antiplatelet therapy in a real-world setting

Primary care providers’ responses to unsolicited Lynch syndrome secondary findings of varying clinical significance

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

Adopting genetics: motivations and outcomes of personal genomic testing in adult adoptees

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