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List of works by William A. Faucett

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

scientific article

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort

article

An assessment of time involved in pre-test case review and counseling for a whole genome sequencing clinical research program

scientific article published on 27 February 2014

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing

scientific article

Chromosomal microarray impacts clinical management ⬇️

scientific article published on February 21, 2013

Chromosomal microarray testing ⬇️

scientific article published on January 1, 2012

ClinGen's GenomeConnect registry enables patient-centered data sharing

scientific article published on 01 November 2018

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

scientific article (publication date: 14 May 2010)

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

scientific article published on 2 December 2015

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

article

Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

scientific article published on December 2016

Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

scientific article published on 26 October 2017

Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants

scientific article published on 07 September 2018

Genetic Testing: Consent and Result Disclosure for Primary Care Providers

scientific article published on 20 August 2019

Genetic testing for susceptibility to breast and ovarian cancer: evaluating the impact of a direct-to-consumer marketing campaign on physicians' knowledge and practices

scientific article published on 01 June 2006

GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledge

scientific article

How Geisinger made the case for an institutional duty to return genomic results to biobank participants

scientific article published on February 2016

Human Germline Genome Editing

scientific article

Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics-Based Communities

scientific article

International Standard Cytogenomic Array Consortium. Interview by Alyson Krokosky, Sharon F Terry

scientific article published in October 2010

International genetic testing

scientific article published in May 2003

Issues in genetic testing for ultra-rare diseases: background and introduction

scientific article published on 01 May 2008

PAs and the practice of genetic medicine

scientific article published on 01 May 2008

Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience

article

Standardizing Variant Interpretation in Genomic Sequencing: Implications for Genetic Counseling Practice

scientific article published on 30 June 2015

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future ⬇️

scientific article (publication date: October 2013)

The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.

scientific article published on 11 February 2016

The Laboratory‐Clinician Team: A Professional Call to Action to Improve Communication and Collaboration for Optimal Patient Care in Chromosomal Microarray Testing ⬇️

scientific article published on May 18, 2012

The effect of gestational age on the detection rate of Down's syndrome by maternal serum α-fetoprotein screening ⬇️

scientific article published on 01 November 1991

The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions

scientific article published in February 2015

Toward clinical genomics in everyday medicine: perspectives and recommendations

scientific article published on 25 January 2016

Towards a Universal Clinical Genomics Database: the 2012 International Standards for Cytogenomic Arrays Consortium Meeting

scientific article (publication date: June 2013)

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