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Current Opinion in Pediatrics|September 2, 2011
Whole exome and whole genome sequencingDavid Bick, David DimmockCurrent Protocols in Human Genetics|April 19, 2013
Whole genome sequencing: a considered approach to clinical implementationDavid DimmockGenome Medicine|May 29, 2020
The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinicChristian R Marshall, David Bick, John W Belmont, et al.NPJ Genomic Medicine|December 15, 2020
Clinical utility of genomic sequencing: a measurement toolkitRobin Z Hayeems, David Dimmock, David Bick, et al.NPJ Genomic Medicine|February 26, 2024
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disordersKristen M Wigby, Deanna Brockman, Gregory Costain, et al.Fertility and Sterility|March 27, 2010
Is it the patient or the IVF? Beckwith-Wiedemann syndrome in both spontaneous and assisted reproductive conceptionsEstil Y Strawn, David Bick, Amy SwansonCurrent Protocols in Human Genetics|January 15, 2011
Real-time quantitative PCR analysis of mitochondrial DNA contentVictor Venegas, Jing Wang, David Dimmock, et al.WMJ : Official Publication of the State Medical Society of Wisconsin|July 24, 2007
Preimplantation genetic diagnosis: technology and clinical applicationsAmy Swanson, Estil Strawn, Eduardo Lau, et al.Journal of Pediatric Gastroenterology and Nutrition|June 21, 2013
Reduced mitochondrial DNA content and heterozygous nuclear gene mutations in patients with acute liver failureDaniel Helbling, Adam Buchaklian, Jing Wang, et al.Clinical Chemistry|May 8, 2010
Quantitative evaluation of the mitochondrial DNA depletion syndromeDavid Dimmock, Lin-Ya Tang, Eric S Schmitt, et al.Pageof 13