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David T. Miller | Researchclopedia

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David T. Miller

Boston Children's Hospital ORCID

195

Works

15,220

Citations

53

h-index

105

i10-index

Research Topics

Genomics and Rare Diseases Genomic variations and chromosomal abnormalities Neurofibromatosis and Schwannoma Cases

Affiliations

Boston University2016–2016

Louisiana State University2019–2019

AT&T (United States)1984–2003

Brigham and Women's Hospital2005–2020

Cincinnati Children's Hospital Medical Center2016–2016

Top Works

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,et al.

20102,855 citations

Congenital heart defects research

Nuclear physics research studies

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,et al.

20161,688 citations

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

Siddharth Srivastava,Jamie Love‐Nichols,et al.

2019704 citations

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

David T. Miller,Kristy Lee,et al.

2021553 citations

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

David T. Miller,Yiping Shen,et al.

2008430 citations

Clinical Genetic Testing for Patients With Autism Spectrum Disorders

Yiping Shen,Kira A. Dies,et al.

2010393 citations

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

David T. Miller,Kristy Lee,et al.

2023390 citations

Clinical trial of a farnesyltransferase inhibitor in children with Hutchinson–Gilford progeria syndrome

Leslie B. Gordon,Monica E. Kleinman,et al.

2012365 citations

Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders

Michael S. Ching,Yiping Shen,et al.

2010309 citations