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| Assistant Professor |
| Office:
919-966-7894 |
| E-mail:
jbooker@unch.unc.edu |
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| Molecular
pathology. |
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| Putcha, G.V., Bejjani, B.A., Bleoo, S., Booker, J.B., Carey, J.C., Carson, N., Das, S., Dempsey, M.A., Gastier-Foster, J.M., Greinwald, J.H., Hoffmann, M.L., Jeng, L.J.B., Denna, M.A., Khababa, I., Lilley, M., Mao, R., Muralidharan, K., Otani, I.M., Rehm, H.L., Schaefer, F., Seltzer, W.K., Spector, E.B., Springer, M.A., Weck, K.E., Wenstrup, R.J., Withrow, S., Wu, B., Zariwala, M.A., Schrijver, I. A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort. 2007. Genet Med, 9, 413. |
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| Thorne, L.B., Civalier, C., Booker, J., Fan, H., Gulley, M.L. Analytic validation of a quantitative real-time PCR assay to measure CMV viral load in whole blood. 2007. Diagn Mol Pathol, 16, 73. |
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| Basinger, A.A., Booker J.K., Frazier, D.M., Koeberl, D.D., Sullivan, J.A., Muenzer, J. Glutaric academia type 1 in patients of Lumbee heritage from North Carolina. 2006. Mol Genet Metab, 88, 90. |
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| Libby, E.N., Booker, J.K., Gulley, M.L., Garcia, D., Moll, S. False-negative factor V Leiden genetic testing in a patient with recurrent deep venous thrombosis. 2006. Am J Hematol, 81, 284. |
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| Scanga, L., Chaing, S., Powell, C., Aylsworth, A.S., Harrell, L.J., Henshaw, N.G., Civalier, C.J., Thorne, L.B., Weck, K., Booker, J., Gulley, M.L. Diagnosis of human congenital cytomegalovirus infection by amplification of viral DNA from dried blood spots on perinatal cards. 2006. J Mol Diag, 8, 240. |
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| Fan H., Civalier, C., Booker, J.K., Gulley, M.L., Prior, T.W., Farber, R.A. Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction. 2006. J Mol Diag, 8, 277. |
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| Booker, J. Molecular Assessment of Bone Marrow Transplants. In Molecular Diagnostics for the Clinical Laboratorian, Second Edition (W.B. Coleman and G.J. Tsongalis, ed.). The Humana Press, Inc., Totowa, New Jersey, 2005. |
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| Fan, H, Booker, J., McCandless, SE, Shashi, V, Fleming, A, Farber, RA. Mosaicism for an FMR1 gene deletion in a fragile X female. 2005. Am J Med Genet A, 136, 214. |
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