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W. Faucett · SciRah

Researcher profile · Semantic Scholar

W. Faucett

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W. Faucett — researcher profile on SciRah

h-index: 26
Works: 55
Citations: 6,744

Most-cited papers

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T. Miller, M. Adam, S. Aradhya, L. Biesecker +28 more
2010American Journal of Human Genetics2,741 citations Open access
Semantic Scholar
The Electronic Medical Records and Genomics (eMERGE) Network: Past, Present and Future
O. Gottesman, H. Kuivaniemi, G. Tromp, W. Faucett +27 more
2013Genetics in Medicine686 citations Open access
Semantic Scholar
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
F. Dewey, M. Murray, J. Overton, L. Habegger +50 more
2016Science508 citations
Semantic Scholar
The Geisinger MyCode Community Health Initiative: an electronic health record-linked biobank for Precision Medicine research
D. Carey, Samantha N. Fetterolf, F. Davis, W. Faucett +6 more
2016Genetics in Medicine428 citations Open access
Semantic Scholar
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Flore Zufferey, E. Sherr, N. Beckmann, E. Hanson +32 more
2012Journal of Medical Genetics300 citations Open access
Semantic Scholar
Human Germline Genome Editing.
K. Ormond, D. Mortlock, D. Scholes, Yvonne Bombard +10 more
2017American Journal of Human Genetics239 citations Open access
Semantic Scholar
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities
Deb D'Angelo, S. Lebon, Qi-Xuan Chen, S. Martin-Brevet +51 more
2016JAMA psychiatry232 citations Open access
Semantic Scholar
Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants
Kandamurugu Manickam, A. Buchanan, Marci L. B. Schwartz, M. Hallquist +40 more
2018JAMA Network Open207 citations Open access
Semantic Scholar
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
Marci L. B. Schwartz, Cara Mccormick, Amanda L. Lazzeri, D’Andra M. Lindbuchler +19 more
2017bioRxiv151 citations Open access
Semantic Scholar
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
A. Moreno-De-Luca, D. W. Evans, K. Boomer, E. Hanson +12 more
2015JAMA psychiatry136 citations Open access
Semantic Scholar
Operationalizing the Learning Health Care System in an Integrated Delivery System
Wayne A. Psek, R. Stametz, L. Bailey-Davis, D. Davis +5 more
2015eGEMs110 citations Open access
Semantic Scholar
Chromosomal microarray impacts clinical management
E. Riggs, K. Wain, D. Riethmaier, Bethanny Smith‐Packard +5 more
2014Clinical Genetics93 citations
Semantic Scholar
Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience.
Marc S. Williams, A. Buchanan, F. Davis, W. Faucett +13 more
2018Health Affairs89 citations
Semantic Scholar
Genetic testing for susceptibility to breast and ovarian cancer: Evaluating the impact of a direct-to-consumer marketing campaign on physicians' knowledge and practices
M. Myers, Man-Huei Chang, Cynthia M. Jorgensen, W. Whitworth +8 more
2006Genetics in Medicine82 citations Open access
Semantic Scholar
Stakeholder engagement: a key component of integrating genomic information into electronic health records
A. Hartzler, C. McCarty, Luke V. Rasmussen, Marc S. Williams +14 more
2013Genetics in Medicine78 citations Open access
Semantic Scholar
Toward clinical genomics in everyday medicine: perspectives and recommendations
Susan K. Delaney, M. Hultner, H. Jacob, D. Ledbetter +41 more
2016Expert Review of Molecular Diagnostics63 citations Open access
Semantic Scholar
GenomeConnect: matchmaking between patients, clinical laboratories and researchers to improve genomic knowledge
B. Kirkpatrick, E. Riggs, Danielle R. Azzariti, V. R. Miller +5 more
2015Human Mutation61 citations Open access
Semantic Scholar
Developing a Conceptual, Reproducible, Rubric-Based Approach to Consent and Result Disclosure for Genetic Testing by Clinicians with Minimal Genetics Background
K. Ormond, M. Hallquist, Adam H. Buchanan, Danielle Dondanville +15 more
2018Genetics in Medicine52 citations Open access
Semantic Scholar
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
Adam H. Buchanan, Kandamurugu Manickam, M. Meyer, Jennifer K. Wagner +26 more
2017Genetics in Medicine51 citations Open access
Semantic Scholar
An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing
B. Bernhardt, Katherine S. Kellom, Alexandra Barbarese, W. Faucett +1 more
2014Journal of Genetic Counseling50 citations Open access
Semantic Scholar
Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics-Based Communities
H. Rocha, J. Savatt, E. Riggs, Jennifer K. Wagner +2 more
2017Journal of Genetic Counseling42 citations Open access
Semantic Scholar
ClinGen’s GenomeConnect Registry Enables Patient-Centered Data Sharing
J. Savatt, Danielle R. Azzariti, W. Faucett, S. Harrison +13 more
2018Human Mutation40 citations Open access
Semantic Scholar
Defining the Critical Components of Informed Consent for Genetic Testing
K. Ormond, Maia J Borensztein, M. Hallquist, A. Buchanan +7 more
2021medRxiv38 citations Open access
Semantic Scholar
Application of a framework to guide genetic testing communication across clinical indications
M. Hallquist, E. Tricou, K. Ormond, J. Savatt +12 more
2021Genome Medicine31 citations Open access
Semantic Scholar
How Geisinger made the case for an institutional duty to return genomic results to biobank participants
W. Faucett, F. Davis
2016Applied and Translational Genomics30 citations Open access
Semantic Scholar
Towards a Universal Clinical Genomics Database: The 2012 International Standards for Cytogenomic Arrays (ISCA) Consortium Meeting
E. Riggs, K. Wain, D. Riethmaier, Melissa Savage +6 more
2013Human Mutation29 citations Open access
Semantic Scholar
Genomic Screening at a Single Health System
J. Savatt, Melissa A. Kelly, Amy C. Sturm, Cara Mccormick +10 more
2025JAMA Network Open24 citations Open access
Semantic Scholar
An Assessment of Time Involved in Pre-test Case Review and Counseling for a Whole Genome Sequencing Clinical Research Program
Janet L. Williams, W. Faucett, Bethanny Smith‐Packard, Monisa D. Wagner +1 more
2014Journal of Genetic Counseling22 citations Open access
Semantic Scholar
A model program to increase translation of rare disease genetic tests: collaboration, education, and test translation program
W. Faucett, S. Hart, R. Pagon, Lisa Forman Neall +1 more
2008Genetics in Medicine17 citations Open access
Semantic Scholar
Genetic Testing: Consent and Result Disclosure for the Primary Care Provider
W. Faucett, H. Peay, C. Coughlin
2019The Medical clinics of North America15 citations Open access
Semantic Scholar
The Laboratory-Clinician Team: A Professional Call to Action to Improve Communication and Collaboration for Optimal Patient Care in Chromosomal Microarray Testing
K. Wain, E. Riggs, Karen Hanson, Melissa Savage +5 more
2012Journal of Genetic Counseling14 citations Open access
Semantic Scholar
Issues in genetic testing for ultra-rare diseases: background and introduction
D. Ledbetter, W. Faucett
2008Genetics in Medicine13 citations Open access
Semantic Scholar
The Limits and Lies of Human Genetic Research, Dangers for Social Policy, by Jonathan Michael Kaplan
W. Faucett
200313 citations
Semantic Scholar
Genetics and Life Insurance Medical Underwriting and Social Policy
W. Faucett
2005Journal of Genetic Counseling12 citations Open access
Semantic Scholar
International genetic testing
S. M. Cox, W. Faucett, Bin Chen, E. Dequeker +3 more
2003Genetics in Medicine9 citations
Semantic Scholar
Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes
E. Maxwell, Jonathan S. Packer, C. O'Dushlaine, Shane E. McCarthy +34 more
2017bioRxiv8 citations Open access
Semantic Scholar
Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists
M. Hallquist, Maia J Borensztein, C. Coughlin, A. Buchanan +7 more
2023European Journal of Human Genetics7 citations Open access
Semantic Scholar
Chromosomal microarray testing.
W. Faucett, Melissa Savage
2012JAAPA : official journal of the American Academy of Physician Assistants7 citations
Semantic Scholar
Harnessing big data for precision medicine: A panel of experts elucidates the data challenges and proposes key strategic decisions points
C. Barash, Keith Owen Elliston, W. Faucett, J. Hirsch +3 more
20156 citations Open access
Semantic Scholar
International genetic testing.
S. M. Cox, W. Faucett, Bin Chen, E. Dequeker +3 more
20035 citations
Semantic Scholar
Biobanks in the Era of Genomic Data
J. Savatt, Cassandra Pisieczko, Yan-Fei Zhang, M. Lee +2 more
2019Current Genetic Medicine Reports4 citations
Semantic Scholar
The effect of gestational age on the detection rate of Down's syndrome by maternal serum alpha-fetoprotein screening.
F. Greenberg, D. D. del Junco, B. Weyland, W. Faucett +3 more
1991American Journal of Obstetrics and Gynecology4 citations
Semantic Scholar
Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
A. Buchanan, Kandamurugu Manickam, M. Meyer, Jennifer K. Wagner +26 more
2021Genetics in Medicine2 citations Open access
Semantic Scholar
Standardizing Variant Interpretation in Genomic Sequencing: Implications for Genetic Counseling Practice
K. Ormond, Misha Rashkin, W. Faucett
2015Current Genetic Medicine Reports2 citations
Semantic Scholar
Invited commentary—genetic counselor's ethical and professional duty to discuss DTC tests
W. Faucett
20062 citations
Semantic Scholar
Genetic Testing: Consent and Result Disclosure for the Primary Care Provider
W. Faucett, H. Peay, Curtis R. Coghlin
20191 citations
Semantic Scholar
Presented Abstracts from the Thirty Sixth Annual Conference of the National Society of Genetic Counselors (Columbus, OH, September 2017)
E. Bednar, K. Muse, H. Oakley, M. Walsh +34 more
2017Journal of Genetic Counseling1 citations Open access
Semantic Scholar
O22: Integrating genomic medicine into healthcare: Experience disclosing >5,000 clinically relevant results within the Geisinger MyCode Community Health Initiative
Melissa Kelly, J. Savatt, Amy Sturm, Cara McCormick +6 more
2024Genetics in Medicine Open0 citations Open access
Semantic Scholar
Consent for genetic testing and disclosure of results: Shifting the paradigm to non-genetics clinicians
H. Peay, M. Hallquist, E. Tricou, C. Coughlin +11 more
20190 citations
Semantic Scholar
ASHG POSITION STATEMENT Human Germline Genome Editing
K. Ormond, D. Mortlock, D. Scholes, Yvonne Bombard +10 more
20170 citations
Semantic Scholar

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