William Andrew Faucett
William Andrew Faucett
Retired, IRB Co-Chair, Geisinger Health System
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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
DT Miller, MP Adam, S Aradhya, LG Biesecker, AR Brothman, NP Carter, ...
The American Journal of Human Genetics 86 (5), 749-764, 2010
Chromosomal microarray versus karyotyping for prenatal diagnosis
RJ Wapner, CL Martin, B Levy, BC Ballif, CM Eng, JM Zachary, M Savage, ...
New England Journal of Medicine 367 (23), 2175-2184, 2012
The electronic medical records and genomics (eMERGE) network: past, present, and future
O Gottesman, H Kuivaniemi, G Tromp, WA Faucett, R Li, TA Manolio, ...
Genetics in Medicine 15 (10), 761-771, 2013
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
FE Dewey, MF Murray, JD Overton, L Habegger, JB Leader, SN Fetterolf, ...
Science 354 (6319), aaf6814, 2016
Can family history be used as a tool for public health and preventive medicine?
PW Yoon, MT Scheuner, KL Peterson-Oehlke, M Gwinn, A Faucett, ...
Genetics in Medicine 4 (4), 304-310, 2002
The Geisinger MyCode community health initiative: an electronic health record–linked biobank for precision medicine research
DJ Carey, SN Fetterolf, FD Davis, WA Faucett, HL Kirchner, U Mirshahi, ...
Genetics in medicine 18 (9), 906-913, 2016
A 600 kb deletion syndrome at 16p11. 2 leads to energy imbalance and neuropsychiatric disorders
F Zufferey, EH Sherr, ND Beckmann, E Hanson, AM Maillard, L Hippolyte, ...
Journal of medical genetics 49 (10), 660-668, 2012
Human germline genome editing
KE Ormond, DP Mortlock, DT Scholes, Y Bombard, LC Brody, WA Faucett, ...
The American Journal of Human Genetics 101 (2), 167-176, 2017
Defining the effect of the 16p11. 2 duplication on cognition, behavior, and medical comorbidities
D D’Angelo, S Lebon, Q Chen, S Martin-Brevet, LAG Snyder, L Hippolyte, ...
JAMA psychiatry 73 (1), 20-30, 2016
Exome sequencing–based screening for BRCA1/2 expected pathogenic variants among adult biobank participants
K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ...
JAMA Network Open 1 (5), e182140-e182140, 2018
A model for genome-first care: returning secondary genomic findings to participants and their healthcare providers in a large research cohort
MLB Schwartz, CZ McCormick, AL Lazzeri, ML D’Andra, MLG Hallquist, ...
The American Journal of Human Genetics 103 (3), 328-337, 2018
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11. 2 deletions
A Moreno-De-Luca, DW Evans, KB Boomer, E Hanson, R Bernier, ...
JAMA psychiatry 72 (2), 119-126, 2015
Patient-centered precision health in a learning health care system: Geisinger’s genomic medicine experience
MS Williams, AH Buchanan, FD Davis, WA Faucett, MLG Hallquist, ...
Health Affairs 37 (5), 757-764, 2018
Operationalizing the learning health care system in an integrated delivery system
WA Psek, RA Stametz, LD Bailey-Davis, D Davis, J Darer, WA Faucett, ...
Egems 3 (1), 2015
Chromosomal microarray impacts clinical management
ER Riggs, KE Wain, D Riethmaier, B Smith‐Packard, WA Faucett, ...
Clinical Genetics 85 (2), 147-153, 2014
Genetic testing for susceptibility to breast and ovarian cancer: evaluating the impact of a direct-to-consumer marketing campaign on physicians' knowledge and practices
MF Myers, MH Chang, C Jorgensen, W Whitworth, S Kassim, JA Litch, ...
Genetics in Medicine 8 (6), 361-370, 2006
Stakeholder engagement: a key component of integrating genomic information into electronic health records
A Hartzler, CA McCarty, LV Rasmussen, MS Williams, M Brilliant, ...
Genetics in Medicine 15 (10), 792-801, 2013
Toward clinical genomics in everyday medicine: perspectives and recommendations
SK Delaney, ML Hultner, HJ Jacob, DH Ledbetter, JJ McCarthy, M Ball, ...
Expert review of molecular diagnostics 16 (5), 521-532, 2016
Public Health Impact of Genetic Tests at the end of the both Century
PW Yoon, B Chen, A Faucett, M Clyne, M Gwinn, IM Lubin, W Burke, ...
Genetics in Medicine 3 (6), 405-410, 2001
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
AH Buchanan, K Manickam, MN Meyer, JK Wagner, MLG Hallquist, ...
Genetics in Medicine 20 (5), 554-558, 2018
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