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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
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
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
Haluska F, Pemberton T, Ibrahim N, et al. (2007) The RTK/RAS/BRAF/PI3K pathways in melanoma: biology, small molecule inhibitors, and potential applications. Seminars in Oncology. 34: 546-554
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
Tarpey P, Pemberton TJ, Stockton DW, et al. (2007) A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia. American Journal of Medical Genetics Part A. 143: 390-394
Se Fum Wong S, Kuei JJ, Prasad N, et al. (2007) A simple method for DNA isolation from clotted blood extricated rapidly from serum separator tubes. Clinical Chemistry. 53: 522-4
Mendoza G, Pemberton TJ, Lee K, et al. (2007) A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3. Human Genetics. 120: 653-62
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