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  1. Arnaud-Lopez L, Usala G, Ceresini G, Mitchell BD, Pilia MG, Piras MG, Sestu N, Maschio A, Busonero F, Albai G, Dei M, Lai S, Mulas A, Crisponi L, Tanaka T, Bandinelli S, Guralnik JM, Loi A, Balaci L, Sole G, Prinzis A, Mariotti S, Shuldiner AR, Cao A, Schlessinger D, Uda M, Abecasis GR, Nagaraja R, Sanna S, Naitza S. Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function. Am J Human Genet 82:1270-1280, 2008. PMCID: PMC2427267.
  2. Bielak LF, Yu PF, Ryan KA, Rumberger JA, Sheedy, II PF, Turner ST, Shuldiner AR, Mitchell BD, Peyser PA. Differences in prevalence and severity of coronary artery calcification between two European American populations with diverse lifestyles. Atherosclerosis 196:888-95, 2008 PMCID: PMC2277512.
  3. Chen W-M, Erdos MR, Jackson AU, Saxena R, Sanna S, Silver KD, Timpson NJ, Orrù M, Piras MG, Bonnycastle LL, Willer CJ, Lyssenko V, Shen H, Wang J, Ebrahim S, Sestu N, Duren WL, Spada MC, Stringham HM, Olla N, Swift AJ, Najjar S, Mitchell BD, Lawlor DA, Smith GD, Ben-Shlomo Y, Buchanan TA, Shuldiner AR, Lakatta E, Bergman RN, Uda M, Saramies J, Valle TT, Tuomilehto J, Cao A, Groop L, Mohlke KL, Laakso M, Schlessinger D, Collins FS, Altshuler D, Abecasis GR, Boehnke M, Scuteri1A, Watanabe RM. Variations in the G6PC2/ABCB11 region are associated with fasting glucose levels. J Clin Invest 118:2620-2628, 2008. PMCID: PMC2398737.
  4. Cole JW, Brown DW, Giles WH, Stine OC, O'Connell JR, Mitchell BD, Sorkin JD, Wozniak MA, Stern BJ, Sparks MJ, Dobbins MT, Shoffner LT, Zappala NK, Reinhart LJ, Kittner SJ. Ischemic stroke risk, smoking, and the genetics of inflammation in a biracial population: The Stroke Prevention in Young Women Study. Thrombosis Journal 6:11, 2008. PMCID: PMC2533289.
  5. Dotson CD, Zhang L, Xu H, Shin Y-K, Vigues S, Ott SH, Elson AET, Choi HJ, Shaw H, Egan JM, Mitchell BD, Li X, Steinle NI, Munger SD. Bitter taste receptors influence glucose homeostasis. PlosOne 3(12): e3974, 2008. PMCID: PMC2597743.
  6. Douglas JA, Marie-Hélène Roy-Gagnon M-H, Zhou C, Mitchell BD, Shuldiner AR, Chan H-P, Helvie MA. Mammographic breast density - evidence for genetic correlations with established breast cancer risk factors. Cancer Epidemiol, Biomarkers Prev 17:3509-3516, 2008. PMID: 19029399. PMCID: PMC2843541.
  7. Guan W, Pluzhnikov A, Cox NJ, Boehnke M for the International Type 2 Diabetes Linkage Analysis Consortium. Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium. Hum Hered 66: 35-49, 2008. PMCID: PMC2855874.
  8. Hong LE, Summerfelt A, Mitchell BD, Wonodi I, Buchanan RW, Thaker GK. Sensory gating endophenotype based on its neural oscillatory pattern and heritability estimate. Arch General Psychiatry 65(9):1008-1016, 2008. PMCID: PMC2774756.
  9. Hong LE, Wonodi I, Stine OC, Mitchell BD, Thaker GK. Evidence of missense mutations on the neuregulin 1 gene affecting function of prepulse inhibition. Biological Psychiatry 63:15-23, 2008. PMID: 17631867.
  10. Lin P-I, Mitchell BD. Approaches for unraveling the joint genetic determinants of schizophrenia and bipolar disorder. Schiz Bulletin 34:791-797, 2008. PMCID: PMC2632441
  11. McArdle PF, Parsa A, Chang Y-P C, Weir MR, O’Connell JR, Mitchell BD, Shuldiner AR. A common non-synonymous variant in GLUT9 is a determinant of serum uric acid levels in Old Order Amish. Arthritis & Rheumatism 58(9):2874-2881, 2008. PMCID: PMC2779583.
  12. McArdle PF, Rutherford S, Mitchell BD, Damcott CM, Wang Y, Ott S, Chang YPC, Levy D, Shuldiner AR, Steinle N. Nicotinic acetylcholine receptor subunit variants on chromosome 2q are associated with blood pressure related traits in the Old Order Amish and the Framingham Heart Study. BMC Medical Genetics Jul 14;9(1):67, 2008 PMCID: PMC2478679.
  13. Mitchell BD, McArdle PF, Shen H, Rampersaud E, Pollin TI, Bielak LF, Jaquish C, Douglas JA, Roy-Gagnon M-H, Sack P, Naglieri R, Hines S, Horenstein RB, Chang Y-P C, Post W, Ryan KA, Brereton NH, Pakyz RE, Sorkin J, Damcott CM, O’Connell JR, Mangano C, Corretti M, Vogel R, Herzog W, Weir MR, Peyser PA, Shuldiner AR. The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the HAPI Heart Study. Am Heart Journal 155:823-828, 2008. PMCID: PMC2443415.
  14. Pollin TI, Damcott CM, Shen H, Ott SH, Shelton J, Horenstein RB, Post W, McLenithan JC, Bielak LF, Peyser PA, Mitchell BD, Miller M, O’Connell JR, Shuldiner AR. A null mutation in human APOC3 confers a favorable plasma lipid profile and may be cardioprotective. Science 322:1702-1705, 2008. PMCID: PMC2673993.
  15. Pollin TI, McBride DJ, Agarwala R, Schäffer AA, Shuldiner AR, Mitchell BD, O’Connell JR. Investigations of the Y chromosome, male founder structure and YSTR mutation rates in the Old Order Amish. Hum Hered 65:91-104, 2008. PMCID: PMC2857628.
  16. Rampersaud E, Bielak LF, Parsa A, Shen H, Post W, Ryan KA, Rumberger JA, Sheedy II PF, Peyser PA, Shuldiner AR, Mitchell BD. The association of coronary artery calcification and carotid intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults. Am J Epidemiol 168:1016-1023, 2008. PMCID: PMC2720772.
  17. Rampersaud E, Mitchell BD, Naj AC, Pollin TI. Investigating parent of origin effects in studies of Type 2 diabetes and obesity. Curr Diab Rev 4:329-339, 2008. PMCID: PMC2896493
  18. Rampersaud E, Mitchell BD, Pollin TI, Fu M, Shen H, O’Connell JR, Ducharme JL, Hines S, Sack P, Naglieri R, Shuldiner AR, Snitker S. Physical activity and the association of common FTO gene variants with body mass index and obesity. Arch Intern Med 168(16):1791-1797, 2008. PMID: 18779467.
  19. Roy-Gagnon M-H, Weir MR, Sorkin JD, Post W, Ryan KA, Sack PA, Hines S, Bielak LF, Peyser PA, Post W, Mitchell BD, Shuldiner AR, Douglas JA. Genetic influences on the blood pressure response to stress: results from the HAPI Heart Study. J Hyperten 26:729-736, 2008 PMID: 18327083.
  20. Shaffer JR, Kammerer CM, Bruder JM, Cole SA, Dyer TD, Almasy L, MacCluer JW, Blangero J, Bauer RL, Mitchell BD. Genetic influences on bone loss in The San Antonio Family Osteoporosis Study. Osteopor Internat 19:1759-1767, 2008. PMCID: PMC2712667.
  21. Stirnadel H, Lin X, Ling H, Song K, Barter P, Kesäniemi YA, Mahley R, McPherson R, Waeber G, Bersot T, Cohen J, Grundy S, Mitchell B, Mooser V, Waterworth D. Genetic and phenotypic architecture of metabolic syndrome-associated components in dyslipidemic and normolipidemic subjects – The GEMS Study. Atherosclerosis 197:868-876, 2008, PMID: 17888929.
  22. Streeten EA, Beck TJ, Takala SL, McBride DJ, O’Connell JR, Pollin TI, Usi-Rasi K, Shuldiner AR, Mitchell BD. Autosome-wide linkage analysis of hip structural phenotypes in the Old Order Amish. Bone 43:607-612, 2008, PMCID: PMC2591020.