Charles Schwartz
Charles Schwartz
Director of Research, Greenwood Genetic Center
Verified email at
Cited by
Cited by
Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes
HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ...
New England Journal of Medicine 359 (16), 1685-1699, 2008
Electron scattering from hydrogen
C Schwartz
Physical Review 124 (5), 1468, 1961
A recurrent 15q13. 3 microdeletion syndrome associated with mental retardation and seizures
AJ Sharp, HC Mefford, K Li, C Baker, C Skinner, RE Stevenson, ...
Nature genetics 40 (3), 322-328, 2008
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
PS Tarpey, R Smith, E Pleasance, A Whibley, S Edkins, C Hardy, ...
Nature genetics 41 (5), 535-543, 2009
A geometric distance to the galaxy NGC4258 from orbital motions in a nuclear gas disk
JR Herrnstein, JM Moran, LJ Greenhill, PJ Diamond, M Inoue, N Nakai, ...
Nature 400 (6744), 539-541, 1999
Importance of angular correlations between atomic electrons
C Schwartz
Physical Review 126 (3), 1015, 1962
Targeted mutagenesis, precise gene editing, and site-specific gene insertion in maize using Cas9 and guide RNA
S Svitashev, JK Young, C Schwartz, H Gao, SC Falco, AM Cigan
Plant physiology 169 (2), 931-945, 2015
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
I Henry, C Bonaiti-Pellie, V Chehensse, C Beldjord, C Schwartz, ...
Nature 351 (6328), 665-667, 1991
Theory of hyperfine structure
C Schwartz
Physical Review 97 (2), 380, 1955
Genome editing in maize directed by CRISPR–Cas9 ribonucleoprotein complexes
S Svitashev, C Schwartz, B Lenderts, JK Young, AM Cigan
Nature communications 7 (1), 1-7, 2016
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes
RG Ruf, PX Xu, D Silvius, EA Otto, F Beekmann, UT Muerb, S Kumar, ...
Proceedings of the National Academy of Sciences 101 (21), 8090-8095, 2004
Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans
SP Robertson, SRF Twigg, AJ Sutherland-Smith, V Biancalana, RJ Gorlin, ...
Nature genetics 33 (4), 487-491, 2003
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative RhoRac guanine nucleotide exchange factor
NG Pasteris, A Cadle, LJ Logie, MEM Porteous, CE Schwartz, ...
Cell 79 (4), 669-678, 1994
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12. 3: the first 2,253 cases
F Rousseau, D Heitz, J Tarleton, J MacPherson, H Malmgren, N Dahl, ...
American journal of human genetics 55 (2), 225, 1994
High frequency of neurexin 1β signal peptide structural variants in patients with autism
J Feng, R Schroer, J Yan, W Song, C Yang, A Bockholt, EH Cook Jr, ...
Neuroscience letters 409 (1), 10-13, 2006
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene
CE Schwartz, MM May, NJ Carpenter, RC Rogers, J Martin, MG Bialer, ...
The American Journal of Human Genetics 77 (1), 41-53, 2005
Center-of-mass motion in many-particle systems
S Gartenhaus, C Schwartz
Physical Review 108 (2), 482, 1957
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
RM Plenge, BD Hendrich, C Schwartz, JF Arena, A Naumova, C Sapienza, ...
Nature genetics 17 (3), 353-356, 1997
5, 10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
CY Ou, RE Stevenson, VK Brown, CE Schwartz, WP Allen, MJ Khoury, ...
American journal of medical genetics 63 (4), 610-614, 1996
Lamb shift in the helium atom
C Schwartz
Physical Review 123 (5), 1700, 1961
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