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Author Details

Carrie L Blout
Department of Medicine Brigham and Women's Hospital and Harvard Medical School
2014
14
11
PMIDPaper TitleJournal TitlePublished Year
32349224Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.J Pers Med2020
32413979Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.J Pers Med2020
30592300A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg<sup>a</sup>.Transfusion2019
30287922Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
30670880Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
29565423Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial.Genet Med2018
29497922Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.J Genet Couns2018
28654958The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.Ann Intern Med2017
29030401A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients.Circ Cardiovasc Genet2017
27181682Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
27392080Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
23881473Newborn screening: education, consent, and the residual blood spot. The position of the national society of genetic counselors.J Genet Couns2014
24387990Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy.Am J Hum Genet2014
25251809Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings.Am J Med Genet A2014
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Collaborators

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