David Nelson, Ph.D.
Affiliations: | Baylor College of Medicine | Baylor College of Medicine, Houston, TX |
Area:
Human genome and disease gene analysisWebsite:
http://www.bcm.edu/genetics/?pmid=11001Google:
"David Nelson"Cross-listing: GenetiTree
Parents
Sign in to add mentor| David Housman | grad student | MIT (Neurotree) | |
| C. Thomas Caskey | post-doc | Baylor College of Medicine (Neurotree) |
Children
Sign in to add trainee| Evan Eichler | grad student | 1995 | Baylor College of Medicine (GenetiTree) |
BETA: Related publications
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Publications
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| Schwartz CE, Aylsworth AS, Allanson J, et al. (2024) Personal journeys to and in human genetics and dysmorphology. American Journal of Medical Genetics. Part A. e63514 |
| Nelson DL, Caskey CT. (2021) Stephen T. Warren: Human geneticist who advanced understanding of mutational mechanisms and developmental disorders. Proceedings of the National Academy of Sciences of the United States of America. 118 |
| Amemiya CT, Alföldi J, Lee AP, et al. (2013) The African coelacanth genome provides insights into tetrapod evolution. Nature. 496: 311-6 |
| Nagamani SC, Erez A, Probst FJ, et al. (2012) Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function. Neurogenetics. 13: 333-9 |
| Gibbs RA, Rogers J, et al. (2007) Evolutionary and biomedical insights from the rhesus macaque genome. Science (New York, N.Y.). 316: 222-34 |
| Jones IM, Thomas CB, Xi T, et al. (2007) Exploration of methods to identify polymorphisms associated with variation in DNA repair capacity phenotypes. Mutation Research. 616: 213-20 |
| Muzny DM, Scherer SE, Kaul R, et al. (2006) The DNA sequence, annotation and analysis of human chromosome 3. Nature. 440: 1194-8 |
| Scherer SE, Muzny DM, Buhay CJ, et al. (2006) The finished DNA sequence of human chromosome 12. Nature. 440: 346-51 |
| Lander ES, Linton LM, Birren B, et al. (2001) Initial sequencing and analysis of the human genome. Nature. 409: 860-921 |
| Fryns JP, Borghgraef M, Brown TW, et al. (2000) 9th international workshop on fragile X syndrome and X-linked mental retardation. American Journal of Medical Genetics. 94: 345-60 |