C. Thomas Caskey
Affiliations: | Baylor College of Medicine, Houston, TX |
Area:
medical geneticsWebsite:
http://en.wikipedia.org/wiki/C._Thomas_CaskeyGoogle:
"C. Caskey"Mean distance: 15.1 (cluster 11) | S | N | B | C | P |
Children
Sign in to add trainee| Jeffrey Chamberlain | post-doc | Baylor College of Medicine (Cell & Gene Therapy Tree) | |
| Ying-Hui Fu | post-doc | Baylor | |
| David Nelson | post-doc | Baylor College of Medicine (GenetiTree) | |
| Pragna I Patel | post-doc | Baylor College of Medicine (GenetiTree) |
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Publications
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| Hou YC, Yu HC, Martin R, et al. (2020) Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging. Proceedings of the National Academy of Sciences of the United States of America |
| Shah N, Hou YC, Yu HC, et al. (2018) Identification of Misclassified ClinVar Variants via Disease Population Prevalence. American Journal of Human Genetics. 102: 609-619 |
| Tang H, Kirkness EF, Lippert C, et al. (2017) Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes. American Journal of Human Genetics. 101: 700-715 |
| Long T, Hicks M, Yu HC, et al. (2017) Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites. Nature Genetics |
| Guo L, Milburn MV, Ryals JA, et al. (2015) Plasma metabolomic profiles enhance precision medicine for volunteers of normal health. Proceedings of the National Academy of Sciences of the United States of America. 112: E4901-10 |
| Caskey CT, Leder P. (2014) The RNA code: nature's Rosetta Stone. Proceedings of the National Academy of Sciences of the United States of America. 111: 5758-9 |
| Brownstein CA, Beggs AH, Homer N, et al. (2014) An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. Genome Biology. 15: R53 |
| Gonzalez-Garay ML, McGuire AL, Pereira S, et al. (2013) Personalized genomic disease risk of volunteers. Proceedings of the National Academy of Sciences of the United States of America. 110: 16957-62 |
| Schaaf CP, Gonzalez-Garay ML, Xia F, et al. (2013) Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. Nature Genetics. 45: 1405-8 |
| Ohbayashi F, Balamotis MA, Kishimoto A, et al. (2005) Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors. Proceedings of the National Academy of Sciences of the United States of America. 102: 13628-33 |