Publications

Selected Publications

for complete list of publications see CV


  1. Santorico SA, Hendricks AE. Progress in Methods for Rare Variant Association. BMC Genetics, 2016 Feb 3;17 Suppl 2:6. (PMID: 26866487)

  2. The UK10K project: rare variants in health and disease. Nature, 2015. Oct 1;526(7571):82-90. (PMID: 26367797)

  3. Zhang X, Johnson AD, Hendricks AE, Hwang SJ, Tanriverdi K, Ganesh SK, Smith NL, Peyser PA, Freedman JE, O’Donnell CJ. Genetic Associations with Expression for Genes Implicated in GWAS Studies for Atherosclerotic Cardiovascular Disease and Blood Phenotypes. Hum Mol Gen, 2014. Feb 1;23(3):782-95. (PMID: 24057673)

  4. Hendricks AE, Dupuis J, Logue MW, Myers RH, Lunetta KL. Correction for multiple testing in a gene region. EJHG, 2014. Mar;22(3):414-8. (PMID: 23838599)

  5. Pearce LR, Atanassova N, Banton MC, Bottomley B, van der Klaauw AA, Revelli JP, Hendricks A, Keogh JM, Henning E, Doree D, Jeter-Jones S, Garg S, Bochukova EG, Bounds R, Ashford S, Gayton E, Hindmarsh PC, Shield JP, Crowne E, Barford D, Wareham NJ, UK10K Consortium, O'Rahilly S, Murphy MP, Powell DR, Barroso I, Farooqi IS. KSR2 Mutations Are Associated with Obesity, Insulin Resistance, and Impaired Cellular Fuel Oxidation. Cell, 2013. Nov 7; 155(4):765-77. (PMID: 24209692)

  6. Hendricks AE, Dupuis J, Gupta M, Logue MW, Lunetta KL: A comparison of gene region simulation methods. PLoS One, 2012; 7:e40925.

  7. Hadzi TC, Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Gillis T, Mysore JS, Gusella JF, MacDonald ME, Myers RH, Vonsattel JP: Assessment of Cortical and Striatal Involvement in 523 Huntington Disease Brains. Neurology, 2012 Oct 16;79(16):1708-1715.

  8. Chen H*, Hendricks AE*§, Cheng Y, Cupples LA, Dupuis J, Liu CT: Comparison of statistical approaches to rare variant analysis for quantitative traits. BMC Proceedings, 2011. 5 Suppl 9:S113. * Co-first authors § Corresponding author

  9. Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T: Genomewide linkage study of modifiers of LRRK2-related Parkinson’s disease. Movement Disorders, 2011 Sep; 26(11):2039-44.

  10. Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Wheeler V, MacDonald ME, Gusella JF, Myers RH: Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington Disease gene from male carriers of high normal alleles (27-35 CAG). AJMG, 2009. 149A(7): 1375-81.

  11. Hendricks AE, Zhu Y, Dupuis J: Genome-wide association and linkage analysis of quantitative traits: comparison of likelihood ratio test and conditional score statistic. BMC Proceedings 2009. 3 Suppl 7:S100.

  12. Dragileva E, Hendricks A, Teed A, Gillis T, Lopez ET, Friedberg EC, Kucherlapati R, Edelmann W, Lunetta KL, MacDonald ME, Wheeler VC: Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes. Neurobiol Dis 2009, 33:37-47.

  13. Swami M, Hendricks AE, Gillis T, Massood T, Mysore J, Myers RH, Wheeler VC: Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. Hum Mol Genet 2009, 18:3039-3047.