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Author Details

William A Faucett
Genomic Medicine Institute
1991
41
24
PMIDPaper TitleJournal TitlePublished Year
34646007Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genet Med2021
33926532Application of a framework to guide genetic testing communication across clinical indications.Genome Med2021
34945775Defining the Critical Components of Informed Consent for Genetic Testing.J Pers Med2021
31582007Genetic Testing: Consent and Result Disclosure for Primary Care Providers.Med Clin North Am2019
29976988Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background.Genet Med2019
29130143Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics-Based Communities.J Genet Couns2018
30100086A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.Am J Hum Genet2018
30311371ClinGen's GenomeConnect registry enables patient-centered data sharing.Hum Mutat2018
30646163Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.JAMA Netw Open2018
29733722Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience.Health Aff (Millwood)2018
29261187Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genet Med2018
28777929Human Germline Genome Editing.Am J Hum Genet2017
26810587Toward clinical genomics in everyday medicine: perspectives and recommendations.Expert Rev Mol Diagn2016
26629640Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.JAMA Psychiatry2016
28008009Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study.Science2016
26866580The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.Genet Med2016
27047758How Geisinger made the case for an institutional duty to return genomic results to biobank participants.Appl Transl Genom2016
25493922The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.JAMA Psychiatry2015
26178529GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledge.Hum Mutat2015
25992388Operationalizing the learning health care system in an integrated delivery system.EGEMS (Wash DC)2015
23347240Chromosomal microarray impacts clinical management.Clin Genet2014
24573557An assessment of time involved in pre-test case review and counseling for a whole genome sequencing clinical research program.J Genet Couns2014
24569858An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.J Genet Couns2014
23463607Towards a Universal Clinical Genomics Database: the 2012 International Standards for Cytogenomic Arrays Consortium Meeting.Hum Mutat2013
24030437Stakeholder engagement: a key component of integrating genomic information into electronic health records.Genet Med2013
23743551The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.Genet Med2013
22384761Chromosomal microarray testing.JAAPA2012
23054248A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.J Med Genet2012
22610653The laboratory-clinician team: a professional call to action to improve communication and collaboration for optimal patient care in chromosomal microarray testing.J Genet Couns2012
20466091Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.Am J Hum Genet2010
20958093International Standard Cytogenomic Array Consortium. Interview by Alyson Krokosky, Sharon F Terry.Genet Test Mol Biomarkers2010
18557184PAs and the practice of genetic medicine.JAAPA2008
18496033A model program to increase translation of rare disease genetic tests: collaboration, education, and test translation program.Genet Med2008
18496027Issues in genetic testing for ultra-rare diseases: background and introduction.Genet Med2008
16778598Genetic testing for susceptibility to breast and ovarian cancer: evaluating the impact of a direct-to-consumer marketing campaign on physicians' knowledge and practices.Genet Med2006
15894997A primer on genetic testing.J Midwifery Womens Health2005
12792426International genetic testing.Genet Med2003
12172397Can family history be used as a tool for public health and preventive medicine?Genet Med2002
11715004Public health impact of genetic tests at the end of the 20th century.Genet Med2001
1379776Congenital deficiency of alpha-fetoprotein.Am J Obstet Gynecol1992
1720281The effect of gestational age on the detection rate of Down's syndrome by maternal serum alpha-fetoprotein screening.Am J Obstet Gynecol1991
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Collaborators

University of Florida, College of Medicine-Jacksonville
Co-authored papers 16
Autism and Developmental Medicine Institute
Co-authored papers 9
Genomic Medicine Institute, Geisinger Medical Center
Co-authored papers 8
University of Washington Medical Center
Co-authored papers 8
Yale School of Medicine
Co-authored papers 7
Geisinger Medical Center
Co-authored papers 7
Genomic Medicine Institute
Co-authored papers 6
Geisinger Autism & Developmental Medicine Institute
Co-authored papers 6
Harvard Medical School, Brigham and Women's Hospital
Co-authored papers 5
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 5
Research Institute
Co-authored papers 5
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 5
Pennsylvania State University, University Park
Co-authored papers 4
Co-authored papers 4
Stanford University School of Medicine
Co-authored papers 4
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Co-authored papers 4
Nationwide Children's Hospital, The Ohio State University College of Medicine
Co-authored papers 4
Centers for Disease Control and Prevention
Co-authored papers 3
SARAH LAWRENCE COLLEGE
Co-authored papers 3
The Broad Institute of MIT and Harvard
Co-authored papers 3
Boston Children's Hospital
Co-authored papers 3
Genomic Medicine Institute, USA Heart and Vascular Institute
Co-authored papers 3
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Boston Children's Hospital, Harvard Medical School
Co-authored papers 3
Baylor College of Medicine
Co-authored papers 3
Boston Children's Hospital and Harvard Medical School
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University of Michigan School of Medicine ann arbor
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Marshfield Clinic Research Institute
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Thomas Jefferson University
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