Original Articles
1. Chidambaram A., Chakravarti A., Ferrell R.E., Iyengar S.K. Estimating the age-at-onset function using life-table methods. Genet Epidemiol 5:255-263, 1988.
2. Iyengar S.K., Hamman R.F., Marshall J.A., Baxter J., Majumder P.P., Ferrell R.E. Genetic studies of Type 2 (non-insulin dependent) diabetes mellitus: Lack of association with seven genetic markers. Diabetologia 32:690-693, 1989.
3. Iyengar S.K., Hamman R.F., Marshall J.A., Majumder P.P., Ferrell R.E. On the role of vitamin-D binding globulin in glucose homeostasis: results from the San Luis Valley Diabetes Study. Genet Epidemiol 6: 691-698, 1989.
4. Kamboh M.I., Hamman R.F., Iyengar S.K., Aston C.E., Ferrell R.E. Apolipoprotein A-IV polymorphism, and its role in determining variation in lipoprotein-lipid, glucose and insulin levels in normal and non-insulin-dependent diabetic individuals. Atherosclerosis 91: 25-34, 1991.
5. Kamboh M.I, Iyengar S.K., Aston C.E., Hamman R.F., Ferrell R.E. Apolipoprotein A-IV genetic polymorphism and its impact on quantitative traits in normoglycemic and non-insulin dependent diabetic Hispanics from the San Luis Valley, Colorado. Hum Biol 64 (4):605-16, 1992.
6. Ferrell R.E., Iyengar S.K. Molecular Studies of the genetics of non-insulin dependent diabetes mellitus. Amer J Hum Biol 5: 415-424, 1993.
7. Gill J., Reyes-Mugica M., Iyengar S.K., Kidd K.K., Touloukian R.J., Smith C., Keller M., and Genel M. Early presentation of metastatic medullary carcinoma in MEN2A: Implications for therapy. J Pediatrics 129: 459-464, 1996.
8. Merriwether D.A., Huston S., Iyengar S.K., Hamman R., Norris J.M., Shetterly S., Kamboh M.I., Ferrell R.E. Mitochondrial versus nuclear admixture estimates demonstrates a past history of directional mating. Am J of Phys Anthropol 102: 153-159, 1997.
9. Iyengar S.K., Kalinsky H., Weiss S., Korostishevsky M., Sadeh M., Kidd K. K., and Bonne-Tamir B. Homozygosity by descent for a rare mutation in the myphosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease. J Med Genet 34: 391-394, 1997.
10. Iyengar S.K., Calafell F., Kidd K.K. Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes. Genetic Epidemiology 14:809-814, 1997.
11. Iyengar S.K., Seaman M., Rosenbaum H., Sirugo G., Castiglione C., Kidd J.R., Kidd K.K. Analyses of cross-species polymerase chain reaction products to infer the ancestral state of human polymorphisms. DNA Sequence 8(5): 317-327, 1998.
12. Schelling J.R., Zarif L., Sehgal A., Iyengar S.K., Sedor J.R. Genetic susceptibility to end stage renal disease. Curr Opin Hypertens 8:465-472, 1999.
13. El-Meanawy M.A., Schelling J.R., Pozuela F., Churpek M.M., Ficker E., Iyengar S.K., Sedor J.R: Use of serial analysis of gene expression (SAGE) to generate kidney expression libraries. Am J Physiol Renal Physiol. 279(2):F383-92, 2000.
14. Ficker E., Thomas D., Viswanathan P.C., Dennis A.T., Priori S.G., Napolitano C., Memmi M., Wible B.A., Kaufman E.S., Iyengar S.K., Schwartz P.J., Rudy Y., Brown A.M. Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome. Am J Physiol Heart Circ Physiol. 279(4):H1748-56, 2000.
15. Covic A.M.C., Schelling J.R., Constantiner M., Iyengar S.K., Sedor J.R. Serum C-peptide concentrations poorly phenotype type 2 diabetic end-stage renal disease patients for genetic epidemiological analysis. Kidney Int. 58(4):1742-1750, 2000.
16. Zarif L., Covic A., Iyengar S.K., Sehgal A., Sedor J.R., Schelling J.R. Inaccuracy of clinical phenotyping parameters for hypertensive nephrosclerosis. Nephrol Dial Transplant 2000 Nov;15(11):1801-7.
17. Covic A.M., Iyengar S.K., Constantiner M., Olson J.M., Sabbagh E., Jedrey C. Sedor J.R., Schelling J.R. A family-based strategy to identify genes for diabetic nephropathy Am J Kidney Dis (in press).
18. Kaufman ES, Priori SG, Napolitano C, Schwartz PJ, Iyengar S.K., Elston RC, Schnell AH, Gorodeski EZ, Rammohan G, Bahhur NO, Connuck D, Verrilli L, Rosenbaum DS, Brown AM. Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: experience in 101 related family members. J Cardiovasc Electrophysiol. 2001 Apr;12(4):455-61.
19. Jacobs KB, Burton PR, Iyengar S.K., Elston RC, Palmer LJ. Pooling data and linkage analysis in the chromosome 5q candidate region for asthma. Genet Epidemiol. 2001;21 Suppl 1:S103-8.
20. Schick, J.H., Iyengar S.K., Elston R.C., Fijal B.A., Klein B., Klein R. The Genetic Epidemiology of Age-Related Maculopathy. InterJ Hum Genet; 1:11-24, 2001.
21. Iyengar S.K. , Jacobs KB, Palmer LJ. Improved evidence for linkage on 6p and 5p with retrospective pooling of data from three asthma genome screens. Genet Epidemiol. 2001;21 Suppl 1:S130-5.
22. Rybicki BA, Iyengar S.K., Harris T, Liptak R, Elston RC, Maliarik MJ, Iannuzzi MC. Prospects of admixture linkage disequilibrium mapping in the African-American genome. Cytometry. 2002 Jan 1;47(1):63-5.
23. Iyengar S.K. , Schelling JR, Sedor JR. Approaches to understanding susceptibility to nephropathy: From genetics to genomics. Kidney Int. 2002 Jan;61(1 Suppl):61-7.
24. Schelling JR, El-Meanawy MA, Barathan S, Dodig T, Iyengar S.K., Sedor JR. Generation of kidney transcriptomes using serial analysis of gene expression. Exp Nephrol. 2002;10(2):82-92.
25. Rybicki BA, Iyengar S.K., Harris T, Liptak R, Elston RC, Sheffer R, Chen KM, Major M, Maliarik MJ, Iannuzzi MC. The distribution of long range admixture linkage disequilibrium in an African-American population. Hum Hered. 2002;53(4):187-96.
26. Hayden PS, Iyengar S.K., Schelling JR, Sedor JR. Kidney disease, genotype and the pathogenesis of vasculopathy. Curr Opin Nephrol Hypertens. 2003 Jan;12(1):71-8.
27. Schick JH, Iyengar S.K., Klein BE, Klein R, Reading K, Liptak R, Millard C, Lee KE, Tomany SC, Moore EL, Fijal BA, Elston RC. A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study. Am J Hum Genet. 2003 Jun;72(6):1412-24. Epub 2003 Apr 24.
28. Iyengar S.K., Fox KA, Schachere M, Manzoor F, Slaughter ME, Covic AM, Orloff SM, Hayden PS, Olson JM, Schelling JR, Sedor JR. Linkage analysis of candidate loci for end-stage renal disease due to diabetic nephropathy. J Am Soc Nephrol. 2003 Jul;14(7 Suppl 2):S195-201.
29. The Family Investigation of Nephropathy & Diabetes Research Group. Genetic determinants of diabetic nephropathy: The family investigation of nephropathy and diabetes (FIND). J Am Soc Nephrol; 14: S202-S204, 2003.
30. Chattopadhyay P, Pakstis AJ, Mukherjee N, Iyengar S.K., Odunsi A, Okonofua F, Bonne-Tamir B, Speed W, Kidd JR, Kidd KK. Global survey of haplotype frequencies and linkage disequilibrium at the RET locus. Eur J Hum Genet. 2003 Oct;11(10):760-9.
31. Stein CM, Song Y, Elston RC, Jun G, Tiwari HK, Iyengar S.K.. Structural equation model-based genome scan for the metabolic syndrome. BMC Genet. 2003 Dec 31;4 Suppl 1:S99.
32. Jun G, Song Y, Stein CM, Iyengar S.K.. An autosome-wide search using longitudinal data for loci linked to type 2 diabetes progression. BMC Genet. 2003 Dec 31;4 Suppl 1:S8.
33. Iyengar S.K., Song D, Klein BE, Klein R, Schick JH, Humphrey J, Millard C, Liptak R, Russo K, Jun G, Lee KE, Fijal B, Elston RC. Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration. Am J Hum Genet. 2004 Jan;74(1):20-39. Epub 2003 Dec 19.
34. Stein CM, Schick JH, Gerry Taylor H, Shriberg LD, Millard C, Kundtz-Kluge A, Russo K, Minich N, Hansen A, Freebairn LA, Elston RC, Lewis BA, Iyengar S.K.. Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. Am J Hum Genet. 2004 Feb;74(2):283-97. Epub 2004 Jan 20.
35. Lewis BA, Freebairn LA, Hansen A, Gerry Taylor H, Iyengar S.K., Shriberg LD. Family pedigrees of children with suspected childhood apraxia of speech. J Commun Disord. 2004 Mar-Apr;37(2):157-75.
36. Lewis BA, Freebairn LA, Hansen AJ, Iyengar S.K. , Taylor HG. School-age follow-up of children with childhood apraxia of speech. Lang Speech Hear Serv Sch. 2004 Apr;35(2):122-40.
37. Iyengar S.K., Stein CM, Russo K, Erokwu BO, Strohl KP. The fa leptin receptor mutation and the heritability of respiratory frequency in a Brown Norway and Zucker intercross. J Appl Physiol. 2004 Sep;97(3):811-20. Epub 2004 Mar 19.
38. Iyengar S.K., Klein BE, Klein R, Jun G, Schick JH, Millard C, Liptak R, Russo K, Lee KE, Elston RC. Identification of a major locus for age-related cortical cataract on chromosome 6p12-q12 in the Beaver Dam Eye Study. Proc Natl Acad Sci U S A. 2004 Oct 5;101(40):14485-90. Epub 2004 Sep 27.
39. Elston RC, Song D, Iyengar S.K. Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis. Am J Hum Genet. 2005 Jan;76(1):152-6. Epub 2004 Nov 11.
40. Knowler WC, Coresh J, Elston RC, Freedman BI, Iyengar S.K., Kimmel PL, Olson JM, Plaetke R, Sedor JR, Seldin MF. The Family Investigation of Nephropathy and Diabetes (FIND); Design and methods. J Diabetes Complications. 2005 Jan-Feb;19(1):1-9.
41. Duggal P, Klein AP, Lee KE, Iyengar S.K., Klein R, Bailey-Wilson JE, Klein BE. A genetic contribution to intraocular pressure: the beaver dam eye study. Invest Ophthalmol Vis Sci. 2005 Feb;46(2):555-60
42. Jun G., Klein B.E., Klein R., Fox K., Millard C., Capriotti J., Russo K., Lee KE., Elston R.C., Iyengar S.K.. Genomewide analyses demonstrate novel loci that predispose to drusen Formation. IOVS (in press).
43. Orloff M., Iyengar S.K., Winkler C.A., Goddard K.A.B., Dart R., Ahuja T.S., Mokryzcki M., Briggs WA., Korbet SM., Kimmel PL., Simon EE. Trachtman H., Vlahov D., Michel D.M., Berns JS., Smith MC., Schelling JR., Sedor JR., Kopp JB. Variants in the Wilms tumor gene are associated with focal segmental glomerulosclerosis in the African American population. Physiological Genomics (in press).
1. Iyengar S.K., Weder A, Schork NJ. Growth and regulation of hypertension. In: R McCarty, DA Blizard and RL Chevalier (eds), Handbook of Hypertension; Development of the Hypertensive Phenotype: Basic and Clinical studies. Elsevier, New York, volume 19; 77-102, 1999.
2. Iyengar S.K. Gene conversion. In: R. Elston, J. Olson and L. Palmer (eds), Biostatistical Genetics and Genetic Epidemiology. Wiley, New York, 285-286, 2002.
3. El-Meanawy MA, Barathan S, Hayden PS, Iyengar S.K., Schelling JR, Sedor JR. Serial analysis of gene expression (SAGE). Methods Mol Med. 2003;86:257-74. Renal Disease. Guide to Technical Approaches. M.S. Goligorsky, ed. The Humana Press, Totowa, N.J. 2003.
Last modified: Mon Jan 31, 2005