Pragna I Patel, Ph.D., M.Ed.
Affiliations: | 1982-2004 | Baylor College of Medicine, Houston, TX | |
| 2004- | University of Southern California Keck School of Medicine |
Area:
Genetics of inherited diseases; population genetics of Asian IndiansGoogle:
"Pragna Patel"Parents
Sign in to add mentor| Michael R. Miller | grad student | West Virginia University Health Sciences Center (Chemistry Tree) | |
| C. Thomas Caskey | post-doc | Baylor College of Medicine (Neurotree) | |
| Craig Chinault | post-doc | Baylor College of Medicine |
Children
Sign in to add trainee| Yuting Cheng | grad student | University of Southern California Keck School of Medicine | |
| Mehreen Hai | grad student | Baylor College of Medicine | |
| Diego Rincon-Limas | grad student | Baylor College of Medicine | |
| Yutai Zhao | grad student | University of Southern California Keck School of Medicine | |
| Sofya Abazyan | post-doc | University of Southern California Keck School of Medicine | |
| Sanjay Bidichandani | post-doc | Baylor College of Medicine (Cell Biology Tree) | |
| Parimal Das | post-doc | Baylor College of Medicine | |
| Luis Figuera | post-doc | Baylor College of Medicine | |
| Brunella Franco | post-doc | Baylor College of Medicine | |
| Xueya Hauge | post-doc | Baylor College of Medicine | |
| Ramesh Juyal | post-doc | Baylor College of Medicine | |
| Fangyuan Li | post-doc | University of Southern California Keck School of Medicine | |
| Trevor Pemberton | post-doc | University of Southern California Keck School of Medicine | |
| Smita Purandare | post-doc | Baylor College of Medicine | |
| Sarah H. Elsea | post-doc | 1995-1998 | Baylor College of Medicine |
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Publications
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| Pemberton TJ, Choi S, Mayer JA, et al. (2014) A mutation in the canine gene encoding folliculin-interacting protein 2 (FNIP2) associated with a unique disruption in spinal cord myelination. Glia. 62: 39-51 |
| Beck TF, Veenma D, Shchelochkov OA, et al. (2013) Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice. Human Molecular Genetics. 22: 1026-38 |
| Ng CS, Wu P, Foley J, et al. (2012) The chicken frizzle feather is due to an α-keratin (KRT75) mutation that causes a defective rachis. Plos Genetics. 8: e1002748 |
| Pemberton TJ, Li FY, Hanson EK, et al. (2012) Impact of restricted marital practices on genetic variation in an endogamous Gujarati group. American Journal of Physical Anthropology. 149: 92-103 |
| Zhu H, Shang D, Sun M, et al. (2011) X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3. American Journal of Human Genetics. 88: 819-26 |
| Mendoza-Fandino GA, Gee JM, Ben-Dor S, et al. (2011) A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia. Clinical Genetics. 80: 265-72 |
| Pemberton TJ, Jakobsson M, Conrad DF, et al. (2008) Using population mixtures to optimize the utility of genomic databases: linkage disequilibrium and association study design in India. Annals of Human Genetics. 72: 535-46 |
| Pemberton TJ, Mehta NU, Witonsky D, et al. (2008) Prevalence of common disease-associated variants in Asian Indians. Bmc Genetics. 9: 13 |
| Pemberton TJ, Mendoza G, Gee J, et al. (2007) Inherited dental anomalies: a review and prospects for the future role of clinicians. Journal of the California Dental Association. 35: 324-6, 328-33 |
| Pemberton TJ, Li FY, Oka S, et al. (2007) Identification of novel genes expressed during mouse tooth development by microarray gene expression analysis Developmental Dynamics. 236: 2245-2257 |