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2009

  1. Bielak LF, Horenstein RB, Ryan KA, Sheedy II, PF, Post W, Mitchell BD, Shuldiner AR, Peyser PA. Circulating CD34+ cell count is associated with extent of subclinical atherosclerosis in asymptomatic Amish men, independent of 10-year Framingham risk. Clinical Medicine: Cardiology 3:53-60, 2009. PMCID: PMC2856343
  2. Cheng Y-C, Kao WH, Mitchell BD, O’Connell JR, Shen H, McArdle PF, Gibson Q, Ryan KA, Shuldiner AR, Pollin TI. Genome-wide association scan identifies variants near matrix metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. Circ Cardiovasc Genet 2(4):329-337, 2009. PMCID: PMC2801898.
  3. Gschwendtner A, Bevan S, Cole JW, Plourde A, Matarin M, Ross-Adams H, Meitinger T, Wichmann E, Mitchell BD, Furie K, Rich SS, Syme PD, MacLeod MJ, Meschia J, Rosand J, Kittner SJ, Markus HS, Müller-Myhsok B, Dichgans M, on behalf of the Ischemic Stroke Genetics Consortium. Sequence variants on chromosome 9p21 confer risk of atherosclerotic stroke. Ann Neurol 18;65(5):531-539, 2009. PMCID: PMC2702695
  4. Heard-Costa NL, Zillikens MC, Monda KL, Johansson A, Harris TB, Fu M, Haritunians T, Feitosa MF, Aspelund T, Eiriksdottir G, Garcia M, Launer LJ, Smith AV, Mitchell BD, McArdle PF, Shuldiner AR, Bielinski SJ, Boerwinkle E, Brancati F, Demerath EW, Pankow JS, Arnold AM, Chen Y-DI, Glazer NL, McKnight B, Psaty BM, Rotter JI, Amin N, Campbell H, Gyllensten U, Pattaro C, Pramstaller PP, Rudan I, Struchalin M, Vitart V, Gao X, Kraja A, Province MA, Zhang Q, Atwood LD, Dupuis J, Hirschhorn JN, Jaquish CE, O’Donnell CJ, Vasan RS, White CC, Aulchenko YS, Estrada K, Hofman A, Rivadeneira F, Uitterlinden AG, Witteman JCM, Oostra BA, Kaplan RC, Gudnason V, O’Connell JR, Borecki IB, van Duijn CM, Cupples LA, Fox CS, North KE. NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. PLOS Genetics 5(6):e1000539, 2009. PMCID: PMC2695005.
  5. Ling H, Waterworth DM, Stirnadel H, Pollin TI, Barter P, Kesäniemi YA, Mahley RW, McPherson R, Waeber G, Bersot TP, Cohen JC, Grundy SM, Mooser VE, Mitchell BD. Genome-wide linkage and association analyses to identify genetic determinants of plasma adiponectin levels: The GEMS Study. Obesity 17:737-44, 2009. PMID: 19165155
  6. MacClellan LR, Howard TD, Stine OC, Giles WH, O’Connell JR, Cole JW, Wozniak MA, Stern BJ, Mitchell BD, Kittner SJ. Relation of candidate genes that encode for endothelial function to migraine and stroke: The Stroke Prevention in Young Women Study. Stroke 40:e550-e557, 2009. PMCID: PMC2753702.
  7. Mez JB, Cole JW, Howard TD, MacClellan LR, Stine OC, O Connell JR, Wozniak MA, Stern BJ, Sorkin JD, Mitchell BD, Kittner SJ. Evaluation of self-reported ethnicity in a case-control population: The Stroke Prevention in Young Women Study. BMC Res Notes 2(1):260, 2009. PMCID: PMC2801514
  8. Michos ED, Streeten E, Ryan KA, Rampersaud E, Peyser PA, Bielak LF, Shuldiner AR, Mitchell BD, Post W. Serum 25-hydroxyvitamin D levels are not associated with subclinical vascular disease or C-reactive protein in the Old Order Amish. Calcif Tiss Internat 84(3):195-202, 2009. PMCID: PMC2908302.
  9. Mitchell BD. Clustering of schizophrenia with other co-morbidities – what can we learn? Schiz Bulletin 35:282-283, 2009. PMCID: PMC2659321
  10. Naj AC, Kao W-HL, O'Connell JR, Mitchell BD, Silver KD. Sequence variation in IGF1R is associated with differences in insulin levels in nondiabetic Old Order Amish. Diab Metab Res Rev 25:773-779, 2009. PMCID: PMC2837841
  11. Prokopenko I, Zeggini E, Hanson RL, Mitchell BD, Rayner NW, Akan P, Baier L, Das SK, Elliott KS, Fu M, Frayling TM, Groves CJ, Gwilliam R, Scott LJ, Voight BF, Hattersley AT, Hu C, Morris AD, Ng M, Palmer CAN, Tello-Ruiz M, Vaxillaire M, Wang C-R, Stein L, Chan J, Jia W, Froguel P, Elbein SC, Deloukas P, Bogardus C, Shuldiner AR, McCarthy MI for the International Type 2 Diabetes 1q consortium. Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q. Diabetes 58:1704-1709, 2009. PMCID: PMC2699860.
  12. Shaffer JR, Kammerer CM, Bruder JM, Cole SA, Dyer TD, Almasy L, MacCluer JW, Blangero J, Bauer RL, Mitchell BD. Quantitative trait locus on chromosome 1q influences bone loss in young Mexican American adults. Calcif Tissue Internat 84:75-84, 2009. PMCID: PMC2680710
  13. Shen H, Herzog W, Drolet M, Cosentino R, Newcomer S, Sack P, Karon H, Ryan KA, Zhao Y, Shi X, Mitchell BD, Shuldiner AR. Aspirin resistance in healthy drug-naïve men versus women from the Heredity and Phenotype Intervention [HAPI] Heart Study. Am J Cardiol 104(4):606-12, 2009. PMID: 19660620.
  14. Shen H, Pollin TI, Damcott CM, McLenithan JC, Mitchell BD, Shuldiner AR. Glucokinase regulatory protein (GCKR) gene polymorphism affects postprandial lipoprotein response in a dietary intervention study among Old Order Amish. Human Genet 126:567-574, 2009. PMCID: PMC2918876.
  15. Shuldiner AR, O’Connell JR, Bliden KP, Gandhi A, Ryan K, Horenstein RB, Damcott CM, Pakyz R, Gibson Q, Pollin TI, Post W, Parsa A, Mitchell BD, Faraday N, Herzog W, Gurbel PA. Association of cytochrome p450 2C19 genotype with the anti-platelet effect and clinical efficacy of clopidogrel therapy. JAMA 302: 849-858, 2009. PMID: 19706858.
  16. Tarasov KV, Sanna S, Scuteri A, Strait JB, Orrù M, Parsa A, Lin P-I, Maschio A, Lai S, Piras MG Masala M, Tanaka T, Post WS, O’Connell JR, Schlessinger D, Cao A, Nagaraja R, Mitchell BD, Abecasis GR, Shuldiner AR, Uda M, Lakatta EG, Najjar SS. COL4A1 is associated with arterial stiffness by genome wide association scan. Circ Cardiovasc Genet 2(2):151-158, 2009. PMCID: PMC2801872.
  17. Van Hout CV, Levin AM, Rampersaud E, Shen H, O’Connell JR, Mitchell BD, Shuldiner AR, Douglas JA. Extent and distribution of linkage disequilibrium in the Old Order Amish. Genet Epidemiol 20;34(2):146-150, 2009. PMCID: PMC2811753.
  18. Wang Y, McArdle PF, Wade JB, Dorff SE, Sha S, Shi X, Rampersaud E, Subramanya AR, Shen H, Kim JD, Steinle NI, Ober C, Welling PA, Chakravarti A, Weder AB, Cooper RR, Mitchell BD, Shuldiner AR, Chang Y-P Cl. Whole-genome association study in the Old Order Amish identifies STK39 as a novel hypertension susceptibility gene. Proc Natl Acad Science 106:226-231, 2009. PMCID: PMC2629209
  19. Wonodi I, Hong LE, Stine OC, Mitchell BD, Elliott A, Roberts RC, Conley RR, McMahon RP, Thaker GK. Dopamine transporter gene polymorphism modulates oculomotor function and DAT1 mRNA expression in schizophrenia. Am J Med Genet B Neuropsychiatric Genetics 150B(2):282-9, 2009 PMCID: PMC2774755.