A randomized controlled trial adding fluvastatin to peginterferon and ribavirin for naïve genotype 1 hepatitis C patients von Bader, T., Hughes, L. D., Fazili, J., Frost, B., Dunnam, M., Gonterman, A., Madhoun, M., Aston, C. E.

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Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis von Gorry, MC, Gabbaizedeh, D, Furey, W, Gates, LK, Preston, RA, Aston, CE, Zhang, Y, Ulrich, C, Ehrlich, GD, Whitcomb, DC

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Reduced soluble receptor for advanced glycation end-products (sRAGE) scavenger capacity precedes pre-eclampsia in Type 1 diabetes von Yu, Y, Hanssen, KF, Kalyanaraman, V, Chirindel, A, Jenkins, AJ, Nankervis, AJ, Torjesen, PA, Scholz, H, Henriksen, T, Lorentzen, B, Garg, SK, Menard, MK, Hammad, SM, Scardo, JA, Stanley, JR, Wu, M, Basu, A, Aston, CE, Lyons, TJ

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Anti-angiogenic factors and pre-eclampsia in type 1 diabetic women von Yu, Y, Jenkins, A. J, Nankervis, A. J, Hanssen, K. F, Scholz, H, Henriksen, T, Lorentzen, B, Clausen, T, Garg, S. K, Menard, M. K, Hammad, S. M, Scardo, J. C, Stanley, J. R, Dashti, A, May, K, Lu, K, Aston, C. E, Wang, J. J, Zhang, S. X, Ma, J.-X, Lyons, T. J

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Advanced glycation end-products and methionine sulphoxide in skin collagen of patients with type 1 diabetes von Yu, Y, Thorpe, S. R, Jenkins, A. J, Shaw, J. N, Sochaski, M. A, McGee, D, Aston, C. E, Orchard, T. J, Silvers, N, Peng, Y. G, McKnight, J. A, Baynes, J. W, Lyons, T. J

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A gene for hereditary pancreatitis maps to chromosome 7q35 von Whitcomb, DC, Preston, RA, Aston, CE, Sossenheimer, MJ, Barua, PS, Zhang, Y, Wong- Chong, A, White, GJ, Wood, PG, Gates, LK, Ulrich, C, Martin, SP, Post, JC, Ehrlich, GD

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A randomized trial of dalteparin compared with ibuprofen for the treatment of superficial thrombophlebitis von RATHBUN, S. W., ASTON, C. E., WHITSETT, T. L.

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DNA Polymorphisms in Two Paraoxonase Genes (PON1 and PON2) Are Associated with the Risk of Coronary Heart Disease von Sanghera, Dharambir K., Aston, Christopher E., Saha, Nilmani, Kamboh, M. Ilyas

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Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins von Amann, S T, Gates, L K, Aston, C E, Pandya, A, Whitcomb, D C

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Mortality benefit of statin use in traumatic spinal cord injury: a retrospective analysis von Stillman, M D, Aston, C E, Rabadi, M H

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Genetic Polymorphism of Paraoxonase and the Risk of Coronary Heart Disease von Sanghera, Dharambir K, Saha, Nilmani, Aston, Christopher E, Kamboh, M. Ilyas

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Relationship of American Indian blood quantum with osteoporosis risk: a cross-sectional study of American Indian women in Oklahoma von Smith, B. J., Leyva, M. J., Stephens, L. D., Aston, C. E., Hermann, J., Payton, M., Baker, M. Z.

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The effect of Covid-19 on pediatric surgical case volume von B.L. Junqueira, L. M. Taylor, C. E. Aston, B. Bewley, J. Mason, A. J. Rensing

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Genetic screening of the lipoprotein lipase gene for mutations associated with high triglyceride/low HDL-cholesterol levels von RAZZAGHI, H, ASTON, C. E, HAMMAN, R. F, KAMBOH, M. I

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Lung cancer risk in families of nonsmoking probands: Heterogeneity by age at diagnosis von Yang, P., Schwartz, A.G., McAllister, A.E., Swanson, G.M., Aston, C.E.

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Linkage and Association between Inflammatory Bowel Disease and a Locus on Chromosome 12 von Duerr, Richard H., Barmada, M. Michael, Zhang, Leilei, Davis, Sean, Preston, Robert A., Chensny, Lara J., Brown, Jody L., Ehrlich, Garth D., Weeks, Daniel E., Aston, Christopher E.

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Preliminary report: Surgical outcomes following genitoplasty in children with moderate to severe genital atypia von Bernabé, K.J., Nokoff, N.J., Galan, D., Felsen, D., Aston, C.E., Austin, P., Baskin, L., Chan, Y.-M., Cheng, E.Y., Diamond, D.A., Ellens, R., Fried, A., Greenfield, S., Kolon, T., Kropp, B., Lakshmanan, Y., Meyer, S., Meyer, T., Delozier, A.M., Mullins, L.L., Palmer, B., Paradis, A., Reddy, P., Reyes, K.J.Scott, Schulte, M., Swartz, J.M., Yerkes, E., Wolfe-Christensen, C., Wisniewski, A.B., Poppas, D.P.

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Motivations and concerns of patients with access to genetic testing for hereditary pancreatitis von Applebaum-Shapiro, S. E., Peters, J. A., O'Connell, J. A., Aston, C. E., Whitcomb, D. C.

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A low frequency variant within the GWAS locus of MTNR1B affects fasting glucose concentrations: Genetic risk is modulated by obesity von Been, L.F, Hatfield, J.L, Shankar, A, Aston, C.E, Ralhan, S, Wander, G.S, Mehra, N.K, Singh, J.R, Mulvihill, J.J, Sanghera, D.K

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A simplified six item checklist for screening for fragile X syndrome in the pediatric population von Giangreco, Cheryl A., Steele, Mark W., Aston, Christopher E., Cummins, James H., Wenger, Sharon L.

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