Jonathan Pevsner
Affiliations: | Neuroscience | Johns Hopkins University School of Medicine, Baltimore, MD, United States |
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Children
Sign in to add trainee| Christopher M. Bouton | grad student | 2002 | Johns Hopkins |
| Carlo Colantuoni | grad student | 2002 | Johns Hopkins |
| Amy E. Purcell | grad student | 2002 | Johns Hopkins |
| Piper R. Hunt | grad student | 2003 | Johns Hopkins |
| Rong Mao | grad student | 2001-2005 | Johns Hopkins |
| Elisha D. Roberson | grad student | 2009 | Johns Hopkins |
| Joseph D. Baugher | grad student | 2012 | Johns Hopkins |
| Matthew D. Shirley | grad student | 2013 | Johns Hopkins |
| Eric L. Stevens | grad student | 2013 | Johns Hopkins |
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Publications
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| Thorpe J, Osei-Owusu IA, Avigdor BE, et al. (2020) Mosaicism in Human Health and Disease. Annual Review of Genetics |
| Sharim H, Grunwald A, Gabrieli T, et al. (2019) Long-read single-molecule maps of the functional methylome. Genome Research |
| McConnell MJ, Moran JV, Abyzov A, et al. (2017) Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network. Science (New York, N.Y.). 356 |
| Horiuchi Y, Kondo MA, Okada K, et al. (2016) Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium. Translational Psychiatry. 6: e915 |
| Shirley MD, Frelin L, López JS, et al. (2016) Copy Number Variants Associated with 14 Cases of Self-Injurious Behavior. Plos One. 11: e0149646 |
| Debeljak M, Freed DN, Welch JA, et al. (2015) Abstract 4270: NGS based microhaplotype counting for ultrasensitive human DNA detection Cancer Research. 75: 4270-4270 |
| Freed D, Stevens EL, Pevsner J. (2014) Somatic mosaicism in the human genome. Genes. 5: 1064-94 |
| Horiuchi Y, Kano S, Ishizuka K, et al. (2013) Olfactory cells via nasal biopsy reflect the developing brain in gene expression profiles: utility and limitation of the surrogate tissues in research for brain disorders. Neuroscience Research. 77: 247-50 |
| Comi AM, Marchuk DA, Pevsner J. (2013) A needle in a haystack: Sturge-Weber syndrome gene discovery. Pediatric Neurology. 49: 391-2 |
| Baugher JD, Baugher BD, Shirley MD, et al. (2013) Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method. Bmc Genomics. 14: 367 |