Influence of CYP2C9 and VKORC1 1173C/T Genotype on the Risk of Hemorrhagic Complications in African‐American and European‐American Patients on Warfarin von Limdi, NA, McGwin, G, Goldstein, JA, Beasley, TM, Arnett, DK, Adler, BK, Baird, MF, Acton, RT

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Influence of CYP2C9 and VKORC1 on warfarin response during initiation of therapy von Limdi, N.A., Wiener, H., Goldstein, J.A., Acton, R.T., Beasley, T.M.

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DMPK-associated myotonic dystrophy and CTG repeats in Alabama African Americans von Acton, RT, Rivers, CA, Watson, B, Oh, SJ

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A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study von Acton, RT, Snively, BM, Barton, JC, McLaren, CE, Adams, PC, Rich, SS, Eckfeldt, JH, Press, RD, Sholinsky, P, Leiendecker-Foster, C, McLaren, GD, Speechley, MR, Harris, EL, Dawkins, FW, Gordeuk, VR

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Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease von Pancharuniti, N, Lewis, CA, Sauberlich, HE, Perkins, LL, Go, RC, Alvarez, JO, Macaluso, M, Acton, RT, Copeland, RB, Cousins, AL, Gore, TB, Cornwell, PE, Roseman, JM

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Racial differences in the prevalence of Factor V Leiden mutation among patients on chronic warfarin therapy von Limdi, N.A., Beasley, T.M., Allison, D.B., Rivers, C.A., Acton, R.T.

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Fibromyalgia in 300 adult index patients with primary immunodeficiency von Barton, James C, Bertoli, Luigi F, Barton, Jackson C, Acton, Ronald T

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Vibrio vulnificus Infection in a Hemodialysis Patient Receiving Intravenous Iron Therapy von Barton, James C., Coghlan, Michael E., Reymann, Michael T., Ozbirn, Thomas W., Acton, Ronald T.

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Genetic association of 11β-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks von WATSON, B. JR, BERGMAN, S. M, MYRACLE, A, CALLEN, D. F, ACTON, R. T, WARNOCK, D. G

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Variability of the pancreatic islet beta cell/liver (GLUT 2) glucose transporter gene in NIDDM patients von TANIZAWA, Y, RIGGS, A. C, CHIU, K. C, JANSSEN, R. C, BELL, D. S. H, GO, R. P. C, ROSEMAN, J. M, ACTON, R. T, PERMUTT, M. A

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Associations of MHC genes with levels of caries-inducing organisms and caries severity in African-American women von Acton, Ronald T, Dasanayake, Ananda P, Harrison, Renee A, Li, Yihong, Roseman, Jeffrey M, Go, Rodney C.P, Wiener, Howard, Caufield, Page W

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Glucokinase gene in gestational diabetes mellitus : population association study and molecular scanning von CHIU, K. C, GO, R. C. P, AOKI, M, RIGGS, A. C, TANIZAWA, Y, ACTON, R. T, BELL, D. S. H, GOLDENBERG, R. L, ROSEMAN, J. M, PERMUTT, M. A

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Relationships of serum free thyroxine and erythrocyte measures in euthyroid HFE C282Y homozygotes and control subjects: the HEIRS Study von BARTON, J. C., LEIENDECKER-FOSTER, C., REBOUSSIN, D. M., ADAMS, P. C., ACTON, R. T., ECKFELDT, J. H.

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Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics von Acton, R T, Burst, N M, Casebeer, L, Ferguson, S M, Greene, P, Laird, B L, Leviton, L

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Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative von Collins, Julianne S., Perry, Rodney T., Watson Jr, Bracie, Harrell, Lindy E., Acton, Ronald T., Blacker, Deborah, Albert, Marilyn S., Tanzi, Rudolph E., Bassett, Susan S., McInnis, Melvin G., Campbell, R. Duncan, Go, Rodney C.P.

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Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls von Perry, Rodney T., Collins, Julianne S., Harrell, Lindy E., Acton, Ronald T., Go, Rodney C.P.

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Genes within and flanking the major histocompatibility region are risk factors for diabetes, insulin resistance, hypertension, and microalbuminuria in African-American women von Acton, R.T., Bell, D.S.H., Collins, J., Giger, J.N., Go, R.C.P., Harrison, R., McDonald, R., Rivers, C., Roseman, J.M., Taylor, H.A., Vanichanan, C.

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A positive association between maternal serum zinc concentration and birth weight von Neggers, YH, Cutter, GR, Acton, RT, Alvarez, JO, Bonner, JL, Goldenberg, RL, Go, RC, Roseman, JM

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SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family von Perry, R. T., Go, R. C. P., Harrell, L. E., Acton, R. T.

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Hemochromatosis and iron therapy of Restless Legs Syndrome von Barton, James C., Wooten, Virgil D., Acton, Ronald T.

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