Publications

Journal Articles

  1. Mitchell C, Hobcroft J, McLanahan SS, Rutherford Siegel S, Berg A, Brooks-Gunn J, Garfunkel I, Notterman D. (2014) Social Disadvantage, Genetic Sensitivity and Children’s Telomere Length. PNAS. 111(16):5944-5949 http://doi: 10.1073/pnas.1404293111. [PMID:24711381].
  2. Franceschini N, Tao R, Liu L, Rutherford S, Haack K, Almasy L, Göring HHH, Laston S, Lee ET, Best L, Fabsitz R, Cole SA, North KE. (2014) Mapping of a Blood Pressure QTL on Chromosome 17 in American Indians of the Strong Heart Family Study. BMC Cardiovasc Disord, 14:158. https://doi.org/10.1186/1471-2261-14-158. [PMID:25387527].
  3. Rutherford Siegel S, MacKenzie J, Chaplin G, Jablonski NG, Griffiths LR. (2012) Circulating microRNAs involved in multiple sclerosis. Molecular Biology Reports, 39(5): 6219-25. doi: 10.1007/s11033-011-1441-7. [PMID: 22231906]
  4. Quillen E, Rainwater D, Dyer T, Carless M, Curran J, Johnson M, Goring H, Cole S, Rutherford S, MacCluer J Moses E, Blangero J, Almasy L, Mahaney M. (2012) Novel associations of non-structural loci with paraoxonase activity. J Lipids, 2012:189681. doi: 10.1155/2012/189681[PMID: 22577559]
  5. Ramagopalan SV, Hoang U, Handel A, Giovannoni G, Rutherford Siegel S, Ebers GC, Goldacre MJ, Chaplin G. (2011) Period Prevalence of Multiple Sclerosis in England: Relationship to UV Exposure, Neurology, 76:1410-1414. doi: 10.1212/WNL.0b013e318216715e. [PMID:21502600]
  6. Melton PE, Rutherford S, Voruganti VS, Göring HHH, Laston S, Haack K, Comuzzie AG, Dyer TD, Johnson MP, Kent JW Jr, Curran JE, Moses EK, Blangero J, Barac A, Lee ET, Best LG, Fabsitz RR, Devereux RB, Okin PM, Bella JN, Broeckel U, Howard BV, MacCluer JW, Cole SA, Almasy L. (2010) Bivariate genetic association of KIAA1797 with heart rate in American Indians: The Strong Heart Family Study. Hum Mol Genetics, 9:3662-71. doi: 10.1093/hmg/ddq274. [PMID:20601674]
  7. Franceschini N, Rose KM, Storti KL, Rutherford S, Voruganti VS, Laston S, Göring HH, Dyer TD, Umans JG, Lee ET, Best LG, Fabsitz RR, Cole SA, MacCluer JW, North KE.. (2009) Social- and behavioral-specific genetic effects on blood pressure traits: the Strong Heart Family Study. Circ Cardiovasc Genet; 2:396-401. doi: 10.1161/CIRCGENETICS.109.853630. [PMID:20031612]
  8. Rainwater DL, Rutherford S, Dyer TD, Rainwater ED, Cole SA, VandeBerg JL, Stern MP, MacCluer JW, Blangero J, Mahaney MC. (2009) Determinants of Variation in Human Serum Paraoxonase Activity; Heredity; 102:147-154. doi: 10.1038/hdy.2008.110. [PMID:18971955]
  9. McArdle PF, Rutherford S, Mitchell BD, Damcott CM, Wang Y, Ott S, Chang YPC, Levy D, Shuldiner AR, Steinle N. (2008) Nicotinic acetylcholine receptor subunit variants on chromosome 2q are associated with blood pressure; findings in the Old Order Amish and replication in the Framingham Heart Study. BMC Medical Genetics; 9:67. 67 doi: 10.1186/1471-2350-9-67. [PMID:18625075].
  10. Franceschini N, MacCluer JW, Rose KM, Rutherford S, Cole SA, Laston S, Göring HHH, Diego V, Roman MJ, Lee ET, Best LG, Howard BV, Fabsitz RR, North KE. (2008) Genome-wide linkage analysis of pulse pressure in American Indians: The Strong Heart Study. American Journal of Hypertension; 21:194-199. doi: 10.1038/ajh.2007.34. [PMID:18188160]
  11. Rutherford S, Cai G, Lopez-Alvarenga JC, Kent JW, Voruganti VS, Proffitt JM, Curran JE, Johnson MP, Jowett JB, Bastarrachea RA, Atwood LD, Göring HHH, MacCluer JW, Moses EK, Blangero J, Comuzzie AG, Cole, SA. (2007) A chromosome 11q QTL influences change of blood pressure measures over time in Mexican Americans of the San Antonio Family Heart Study. Am J Hum Genet; 81(4):744-755. DOI: 10.1086/521151. [PMID:17846999].
  12. Rutherford S, Yongtoa Y, Frierson HF, Moskaluk CA. (2006) Chromosome 6 deletion and candidate tumor suppressor genes in adenoid cystic carcinoma. Cancer Letters, 236:309-317. DOI: 10.1016/j.canlet.2005.05.049 [PMID:16054751]
  13. Rutherford S, Hampton GM, Frierson HF, Moskaluk CA. (2005) Mapping of candidate tumor suppressor genes on chromosome 12 in adenoid cystic carcinoma. Lab Invest, 85:1076-1085. DOI: 10.1038/labinvest.3700314 [PMID:16025147]
  14. Rutherford S, Johnson MP, Griffiths LR. (2004). Sib pair studies implicate chromosome 18 in essential hypertension, Am J Med Genet, 126: 241-247. DOI: 10.1002/ajmg.a.20586 [PMID:15054836]
  15. Rutherford S, Johnson MP, Curtain RP, Griffiths LR. (2001) Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension, Hum Genetics, 109: 408-415. DOI: 10.1007/s004390100565 [PMID:11702222]
  16. El-Rifai W, Rutherford S, Knuutila S, Frierson HF, Moskaluk CA. (2001) Novel DNA copy number losses in chromosome 12q12-q13 in adenoid cystic carcinoma. Neoplasia, 3:173-178. DOI: 10.1038/sj/neo/7900158 [PMID:11494110]
  17. Curran J, Lea RA, Rutherford S, Weinstein SR, Griffiths LR. (2001) Association of estrogen receptor and glucocorticoid receptor gene polymorphisms with sporadic breast cancer, Int J Cancer, 95: 271-275. [PMID:11400122]
  18. Rutherford S, Boatwright SD, Samwell GA, Morris BJ, Griffiths LR (1998) A linkage and cross-sectional study of hypertension and obesity using a poly (A) Alu-repeat polymorphism at the glucagon receptor gene locus (17q25). Clin Exp Pharmacol Physiol 25:627-629. [PMID:9673441]
  19. Griffiths LR, Rutherford S, Nyholt D. (1998) Linkage of AGT microsatellite to Australian hypertensive Caucasians. J Hypertens, 16: S50.
  20. Nyholt DR, Rutherford S, Morris BJ, Griffiths LR. (1997) Analysis of angiotensinogen genotypes in hypertension sibships. Am J Med Genet, 61: A288
  21. Rutherford S, Nyholt DR, Curtain RP, Quinlan SR, Gaffney PT, Morris BJ, Griffiths LR (1997) Association of an Low Density Lipoprotein Receptor (LDLR) microsatellite marker with obesity, Int J Obes Relat Metab Disord, 21:1032-1037. [PMID:9368827]

Acknowledgements

  1. James S, McLanahan SS, Brooks-Gunn J, Mitchell C, Schneper L, Wagner B, Notterman D. (2017) Sleep duration and telomere length in children. J Pediatr 187: 247-252 doi: 10.1016/j.jpeds.2017.05.014. [PMID: 28602380]. Acknowledgement for work performed in article

Book Chapter

  1. Rutherford S, Shuldiner AR, Mitchell BD. (2004) Genome scans of type 2 diabetes mellitus. In: DeFronzo, R.A., Ferrannini, E., Keen, H., Zimmet, P eds. International Textbook of Diabetes Mellitus – 3rd Edition. John Wiley & Sons Ltd, Chichester, pp 439-450.

 Theses

  1. Sue Rutherford (1993) GradDip Sc thesis: Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson’s disease
  2. Sue Rutherford (2001) PhD Thesis:  The use of microsatellite markers to study essential hypertension genes