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David T. Miller
Researcher at Boston Children's Hospital
Publications - 99
Citations - 13426
David T. Miller is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Autism & Genetic testing. The author has an hindex of 46, co-authored 99 publications receiving 11525 citations. Previous affiliations of David T. Miller include Harvard University & United States Public Health Service.
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Journal ArticleDOI
Consensus Statement : Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
David T. Miller,Margaret P Adam,Margaret P Adam,Swaroop Aradhya,Leslie G. Biesecker,Arthur R. Brothman,Nigel P. Carter,Deanna M. Church,John A. Crolla,Evan E. Eichler,Charles J. Epstein,W. Andrew Faucett,Lars Feuk,Jan M. Friedman,Ada Hamosh,Laird G. Jackson,Erin B. Kaminsky,Klaas Kok,Ian D. Krantz,Robert M. Kuhn,Charles Lee,James Ostell,Carla Rosenberg,Stephen W. Scherer,Nancy B. Spinner,Dimitri J. Stavropoulos,James Tepperberg,Erik C. Thorland,Joris Vermeesch,Darrel Waggoner,Michael S. Watson,Christa Lese Martin,David H. Ledbetter +32 more
TL;DR: Chromosomal microarray (CMA) is increasingly utilized for genetic testing of individuals with unexplained developmental delay/intellectual disability (DD/ID), autism spectrum disorders (ASD), or multiple congenital anomalies (MCA).
Journal ArticleDOI
Association between Microdeletion and Microduplication at 16p11.2 and Autism
Lauren A. Weiss,Yiping Shen,Joshua M. Korn,Joshua M. Korn,Dan E. Arking,David T. Miller,Ragnheidur Fossdal,Evald Saemundsen,Hreinn Stefansson,Todd Green,Todd Green,Orah S. Platt,Douglas M. Ruderfer,Douglas M. Ruderfer,Christopher A. Walsh,David Altshuler,David Altshuler,Aravinda Chakravarti,Aravinda Chakravarti,Rudolph E. Tanzi,Kari Stefansson,Susan L. Santangelo,James F. Gusella,James F. Gusella,Pamela Sklar,Pamela Sklar,Bai-Lin Wu,Mark J. Daly,Mark J. Daly +28 more
TL;DR: A novel, recurrent microdeletion and a reciprocal microduplication that carry substantial susceptibility to autism and appear to account for approximately 1% of cases are identified.
Journal ArticleDOI
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): A policy statement of the American College of Medical Genetics and Genomics
Sarah S. Kalia,Kathy Adelman,Sherri J. Bale,Wendy K. Chung,Christine M. Eng,James P. Evans,Gail E. Herman,Sophia B. Hufnagel,Teri E. Klein,Bruce R. Korf,Kent D. McKelvey,Kelly E. Ormond,C. Sue Richards,Christopher N. Vlangos,Michael S. Watson,Christa Lese Martin,David T. Miller +16 more
TL;DR: The new process for accepting and evaluating nominations for updates to the secondary findings list is described, and the updated secondary findings minimum list includes 59 medically actionable genes recommended for return in clinical genomic sequencing.
Journal ArticleDOI
Association between microdeletion and microduplication at 16p11.2 and autism
Lauren A. Weiss,Yiping Shen,Joshua M. Korn,Dan E. Arking,David T. Miller,Ragnheidur Fossdal,Evald Saemundsen,Hreinn Stefansson,Manuel A. R. Ferreira,Todd Green,Orah S. Piatt,Douglas M. Ruderfer,Christopher A. Walsh,David Altshuler,Aravinda Chakravarti,Rudolph E. Tanzi,Kari Stefansson,Susan L. Santangelo,James F. Gusella,Pamela Sklar,Bai-Lin Wu,Mark J. Daly +21 more
Journal ArticleDOI
The digestive function of the epithelium of the small intestine. II. Localization of disaccharide hydrolysis in the isolated brush border portion of intestinal epithelial cells.
David T. Miller,Robert K. Crane +1 more
TL;DR: The epithelial brush border membrane has been isolated as a morphologically distinct entity from homogenates of intestinal mucosa and found to contain virtually all of the invertase and maltase activities of the unfractionated homogenate.