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2006

  1. Damcott CM, Reinhart LJ, Pollin TI, Ott SH, Shen H, Silver K, Mitchell BD, Shuldiner AR. Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: Replication and evidence for a role in both insulin resistance and insulin secretion. Diabetes 55: 2654-2659, 2006.
  2. Guo X, Saad MF, Langefeld CD, Williams AH, Cui J, Taylor KD, Norris JM, Jinagouda S, Darwin CH, Mitchell BD, Bergman RN, Sutton B, Chen YD, Wagenknecht LE, Bowden DW, Rotter JI. Genome-wide linkage of plasma adiponectin reveals a major locus on chromosome 3q distinct from the adiponectin structural gene: The IRAS Family Study. Diabetes 55: 1723-1730, 2006.
  3. Hong LE, Mitchell BD, Avila MT, Adami H, McMahon RP, Thaker GK. Familial aggregation of eye tracking endophenotypes in schizophrenia families. Arch Gen Psych 63:259-264, 2006.
  4. Kharlip J, Naglieri R, Mitchell BD, Ryan KA, Donner TW. Screening for silent coronary heart disease in type 2 diabetes: Clinical application of ADA guidelines. Diab Care 29:692-694, 2006.
  5. MacClellan LR, Mitchell BD, Cole JW, Wozniak MA, Stern BJ, Giles WH, Brown DW, Sparks MJ, Kittner SJ, for the Stroke Prevention in Young Women Study Group. Familial aggregation of ischemic stroke in young women: The Stroke Prevention in Young Women Study. Genet Epidemiol 30:602-608, 2006.
  6. McArdle PF, Pollin TI, O’Connell JR, Sorkin JD, Agarwala R, Schäffer AA, Streeten EA, King TM, Shuldiner AR, Mitchell BD. Does having children extend lifespan? A genealogical study of parity and longevity in the Amish. J Gerontol A Biol Sci Med Sci 61:190-195, 2006.
  7. Silver K, Magnuson VL, Tolea M, Wang J, Hagopian WA, Mitchell BD. Polymorphisms in the betacellulin gene and susceptibility to type 1 diabetes mellitus. J Molec Med 84:616-623, 2006.
  8. Song Q, Cole JW, O'Connell JR, Stine OC, Gallagher M, Giles WH, Mitchell BD, Wozniak MA, Stern BJ, Reinhart LJ, Xu Q, Wang J, Gibbons GH, Kittner SJ. Phosphodiesterase 4D polymorphisms and the risk of cerebral infarction in a biracial population: The Stroke Prevention in Young Women Study. Human Molecular Genetics 15:2468-2478, 2006.
  9. Streeten EA, McBride DJ, Pollin TI, Ryan KA, Shapiro J, Ott S, Mitchell BD, Shuldiner AR, O’Connell JR. Quantitative trait loci for bone mineral density identified by genome-wide linkage scan to chromosomes 7q and 21q in men from the Amish Family Osteoporosis Study. J Bone Miner Res 21:1433-1442, 2006.
  10. Wonodi I, Mitchell BD, Stine OC, Hong LE, Carpenter Jr. WT, Thaker GK, Buchanan RW. Lack of association between COMT gene and deficit/nondeficit schizophrenia. Behav Brain Funct 2:42, 2006.
  11. Zeggini E, Damcott C, Karim MA, Rayner NW, Groves CJ, Baier LJ, Cox NJ, Hale TC, Hanson RL, Hattersley AT, Hitman GA, Hunt SE, Knowler WC, Mitchell BD, Ng MCY, O’Connell J, Pollin TI, Prochazka M, Vaxillaire M, Walker M, Wang X, Whittaker P, Xiang K, Jia W, Chan JC, Froguel P, Bogardus C, Deloukas P, Shuldiner AR, Elbein SC, McCarthy MI, for the International type 2 diabetes 1q consortium. Variation within the gene encoding the upstream stimulatory factor 1 (USF1) does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence of linkage to chromosome 1q. Diabetes 55: 2541-2548, 2006.