Charles Leon Schwartz
Affiliations: | 1960-1993 | Physics | University of California, Berkeley, Berkeley, CA, United States |
Area:
Theoretical physicsWebsite:
http://socrates.berkeley.edu/~schwrtz/Google:
"Charles Leon Schwartz"Bio:
https://www.aip.org/history-programs/niels-bohr-library/oral-histories/5913
https://inspirehep.net/record/989593?ln=en
Mean distance: 13552
Parents
Sign in to add mentor| Jerrold R. Zacharias | grad student | 1954 | MIT | |
| (Hyperfine Structure and Higher Nuclear Moments.) | ||||
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Publications
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| Schenkel LC, Aref-Eshghi E, Skinner C, et al. (2018) Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in. Clinical Epigenetics. 10: 21 |
| Schenkel LC, Kernohan KD, McBride A, et al. (2017) Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome. Epigenetics & Chromatin. 10: 10 |
| Schenkel LC, Schwartz C, Skinner C, et al. (2016) Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array. The Journal of Molecular Diagnostics : Jmd |
| Zhang Z, Norris J, Kalscheuer V, et al. (2013) A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome. Human Molecular Genetics. 22: 3789-97 |
| Beaulieu CL, Huang L, Innes AM, et al. (2013) Intellectual disability associated with a homozygous missense mutation in THOC6. Orphanet Journal of Rare Diseases. 8: 62 |
| Marom D, Albin A, Schwartz C, et al. (2011) X-linked mental retardation with alacrima and achalasia-Triple A syndrome or a new syndrome? American Journal of Medical Genetics. Part A. 155: 1959-63 |
| Witham S, Takano K, Schwartz C, et al. (2011) In Silico Investigation of a Missense Mutation in CLIC2 Associated with Intellectual Disability Biophysical Journal. 100 |
| Kerzendorfer C, Whibley A, Carpenter G, et al. (2010) Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks. Human Molecular Genetics. 19: 1324-34 |
| Gilfillan GD, Selmer KK, Roxrud I, et al. (2008) SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome. American Journal of Human Genetics. 82: 1003-10 |
| Field M, Tarpey PS, Smith R, et al. (2007) Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly. American Journal of Human Genetics. 81: 367-74 |