David T. Miller - Concepedia

Author

David T. Miller

Also Known As

Brianna M. Paul, D Miller, D T Miller, D. MILLER, D. Miller, D. T. Miller, D.T. Miller, David T Miller, David Miller, David T Miller

194

Publications

15K

Citations

H-Index

184

Concepts

All Affiliations

Boston Children's Hospital Harvard University Brigham and Women's Hospital Massachusetts General Hospital Baylor College of Medicine

About

David T. Miller is an author at Boston Children's Hospital specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	31	4.9K
2	Engineering	12	13	699
3	Education	2	2	208
4	Health Sciences	2	2	209
5	Arts	1	1	64

David T. Miller

Publications

10K

Citations

H-Index

Page 1

	Year	Citations
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, Genetics in Medicine Secondary FindingsMedicineAmerican CollegeNext-generation SequencingPathology	2016	1.7K
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, Wendy K. Chung, Genetics in Medicine Secondary FindingsAcmg SfNext-generation SequencingGeneticsGenetic Epidemiology	2021	541
Genetic variants near <i>TIMP3</i> and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration Wei Chen, Dwight Stambolian, Albert O. Edwards, Proceedings of the National Academy of Sciences	2010	511
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders David T. Miller, Yiping Shen, Lauren A. Weiss, Journal of Medical Genetics	2008	429
Clinical Genetic Testing for Patients With Autism Spectrum Disorders Yiping Shen, Kira A. Dies, Ingrid A. Holm, PEDIATRICS	2010	392
Clinical trial of a farnesyltransferase inhibitor in children with Hutchinson–Gilford progeria syndrome Leslie B. Gordon, Monica E. Kleinman, David T. Miller, Proceedings of the National Academy of Sciences	2012	365
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, Noura S. Abul‐Husn, Genetics in Medicine Secondary FindingsSequencingAcmg SfNext-generation SequencingGenetics	2023	364
Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders Michael S. Ching, Yiping Shen, Wen‐Hann Tan, American Journal of Medical Genetics Part B Neuropsychiatric Genetics Brain DevelopmentGeneticsGenetic EpidemiologyWide SpectrumSocial Sciences	2010	308
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG) David T. Miller, Kristy Lee, Laura M. Amendola, Genetics in Medicine American CollegeClinical ExomeDiagnosisPathologyGynecology	2021	244
Association of Common <i>CRP</i> Gene Variants with CRP Levels and Cardiovascular Events David T. Miller, Robert Y.L. Zee, Jacqueline Suk Danik, Annals of Human Genetics	2005	220

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