David H. Ledbetter
Affiliations: | Human Genetics | Emory University School of Medicine, Atlanta, GA, United States |
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Sign in to add traineeDaniel Moreno-De-Luca | post-doc | 2008-2012 | Emory University School of Medicine |
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Publications
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Martin CL, Wain KE, Oetjens MT, et al. (2020) Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population. Jama Psychiatry |
Buchanan AH, Lester Kirchner H, Schwartz MLB, et al. (2020) Clinical outcomes of a genomic screening program for actionable genetic conditions. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Hudac CM, Bove J, Barber S, et al. (2020) Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers. Autism Research : Official Journal of the International Society For Autism Research |
Finucane BM, Myers SM, Martin CL, et al. (2020) Long overdue: including adults with brain disorders in precision health initiatives. Current Opinion in Genetics & Development. 65: 47-52 |
Myers SM, Challman TD, Bernier R, et al. (2020) Insufficient Evidence for "Autism-Specific" Genes. American Journal of Human Genetics |
Oetjens MT, Kelly MA, Sturm AC, et al. (2019) Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders. Nature Communications. 10: 4897 |
Sanders SJ, Sahin M, Hostyk J, et al. (2019) A framework for the investigation of rare genetic disorders in neuropsychiatry. Nature Medicine |
Srivastava S, Love-Nichols JA, Dies KA, et al. (2019) Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Martin C, Finucane B, Taylor CM, et al. (2019) Shared Genomic Contributors To Developmental And Neuropsychiatric Disorders European Neuropsychopharmacology. 29 |
Savatt JM, Azzariti DR, Faucett WA, et al. (2018) ClinGen's GenomeConnect registry enables patient-centered data sharing. Human Mutation. 39: 1668-1676 |