| Year |
Citation |
Score |
| 2020 |
Yonova-Doing E, Zhao W, Igo RP, Wang C, Sundaresan P, Lee KE, Jun GR, Alves AC, Chai X, Chan ASY, Lee MC, Fong A, Tan AG, Khor CC, Chew EY, ... ... Iyengar SK, et al. Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract. Communications Biology. 3: 755. PMID 33311586 DOI: 10.1038/s42003-020-01421-2 |
0.33 |
|
| 2020 |
Pollack S, Igo RP, Jensen RA, Christiansen M, Li X, Cheng CY, Ng MCY, Smith AV, Rossin EJ, Segrè AV, Davoudi S, Tan GS, Ida Chen YD, Kuo JZ, Dimitrov LM, ... ... Iyengar SK, et al. Erratum. Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes 2019;68:441-456. Diabetes. PMID 32341040 DOI: 10.2337/Db20-Er06A |
0.327 |
|
| 2018 |
Joachim N, Kifley A, Colijn JM, Lee KE, Buitendijk GHS, Klein BEK, Myers C, Meuer SM, Tan AG, Flood V, Schoufour JD, Franco OH, Holliday EG, Attia J, Liew G, ... Iyengar SK, et al. Joint Contribution of Genetic Susceptibility and Modifiable Factors to the Progression of Age-Related Macular Degeneration over 10 Years: The Three Continent AMD Consortium Report. Ophthalmology. Retina. 2: 684-693. PMID 31047378 DOI: 10.1016/J.Oret.2017.10.019 |
0.347 |
|
| 2018 |
Pollack S, Igo RP, Jensen RA, Christiansen M, Li X, Cheng CY, Ng MCY, Smith AV, Rossin EJ, Segrè AV, Davoudi S, Tan GS, Ida Chen YD, Kuo JZ, Dimitrov LM, ... ... Iyengar SK, et al. Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes. PMID 30487263 DOI: 10.2337/Db18-0567 |
0.43 |
|
| 2018 |
Tan AG, Kifley A, Holliday EG, Klein BEK, Iyengar SK, Lee KE, Jun GR, Cumming RG, Zhao W, Wong TY, Cheng CY, Mitchell P, Wang JJ. Aldose Reductase Polymorphisms, Fasting Blood Glucose, and Age-Related Cortical Cataract. Investigative Ophthalmology & Visual Science. 59: 4755-4762. PMID 30267098 DOI: 10.1167/Iovs.18-24353 |
0.329 |
|
| 2017 |
Loomis SJ, Klein AP, Lee KE, Chen F, Bomotti S, Truitt B, Iyengar SK, Klein R, Klein BEK, Duggal P. Exome Array Analysis of Nuclear Lens Opacity. Ophthalmic Epidemiology. 1-5. PMID 29182452 DOI: 10.1080/09286586.2017.1406122 |
0.348 |
|
| 2017 |
DeAngelis MM, Owen LA, Morrison MA, Morgan DJ, Li M, Shakoor A, Vitale A, Iyengar S, Stambolian D, Kim IK, Farrer LA. Genetics of age-related macular degeneration (AMD). Human Molecular Genetics. 26: R246. PMID 28977452 DOI: 10.1093/Hmg/Ddx343 |
0.341 |
|
| 2017 |
DeAngelis MM, Owen LA, Morrison MA, Morgan DJ, Li M, Shakoor A, Vitale A, Iyengar S, Stambolian D, Kim IK, Farrer LA. Genetics of age-related macular degeneration (AMD). Human Molecular Genetics. 26: R45-R50. PMID 28854576 DOI: 10.1093/Hmg/Ddx228 |
0.402 |
|
| 2017 |
Afshari NA, Igo RP, Morris NJ, Stambolian D, Sharma S, Pulagam VL, Dunn S, Stamler JF, Truitt BJ, Rimmler J, Kuot A, Croasdale CR, Qin X, Burdon KP, Riazuddin SA, ... ... Iyengar SK, et al. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications. 8: 14898. PMID 28358029 DOI: 10.1038/Ncomms14898 |
0.395 |
|
| 2017 |
Joachim N, Colijn JM, Kifley A, Lee KE, Buitendijk GH, Klein BE, Myers CE, Meuer SM, Tan AG, Holliday EG, Attia J, Liew G, Iyengar SK, de Jong PT, Hofman A, et al. Five-year progression of unilateral age-related macular degeneration to bilateral involvement: the Three Continent AMD Consortium report. The British Journal of Ophthalmology. PMID 28108569 DOI: 10.1136/Bjophthalmol-2016-309729 |
0.327 |
|
| 2016 |
Williams RC, Elston RC, Kumar P, Knowler WC, Abboud HE, Adler S, Bowden DW, Divers J, Freedman BI, Igo RP, Ipp E, Iyengar SK, Kimmel PL, Klag MJ, Kohn O, et al. Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND). Bmc Genomics. 17: 325. PMID 27142425 DOI: 10.1186/S12864-016-2654-X |
0.391 |
|
| 2016 |
Fan Q, Verhoeven VJ, Wojciechowski R, Barathi VA, Hysi PG, Guggenheim JA, Höhn R, Vitart V, Khawaja AP, Yamashiro K, Hosseini SM, Lehtimäki T, Lu Y, Haller T, Xie J, ... ... Iyengar SK, et al. Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Nature Communications. 7: 11008. PMID 27020472 DOI: 10.1038/Ncomms11008 |
0.373 |
|
| 2016 |
Tan AG, Kifley A, Mitchell P, Rochtchina E, Flood VM, Cumming RG, Jun G, Holliday EG, Scott RJ, Teo YY, Klein BE, Cheng CY, Iyengar SK, Wang JJ. Associations Between Methylenetetrahydrofolate Reductase Polymorphisms, Serum Homocysteine Levels, and Incident Cortical Cataract. Jama Ophthalmology. PMID 26986182 DOI: 10.1001/Jamaophthalmol.2016.0167 |
0.306 |
|
| 2016 |
Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, ... ... Iyengar SK, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/Ng.3448 |
0.424 |
|
| 2015 |
Meyers KJ, Liu Z, Millen AE, Iyengar SK, Blodi BA, Johnson E, Snodderly DM, Klein ML, Gehrs KM, Tinker L, Sarto GE, Robinson J, Wallace RB, Mares JA. Joint Associations of Diet, Lifestyle, and Genes with Age-Related Macular Degeneration. Ophthalmology. PMID 26354764 DOI: 10.1016/J.Ophtha.2015.07.029 |
0.385 |
|
| 2015 |
Millen AE, Meyers KJ, Liu Z, Engelman CD, Wallace RB, LeBlanc ES, Tinker LF, Iyengar SK, Robinson JG, Sarto GE, Mares JA. Association Between Vitamin D Status and Age-Related Macular Degeneration by Genetic Risk. Jama Ophthalmology. PMID 26312598 DOI: 10.1001/Jamaophthalmol.2015.2715 |
0.304 |
|
| 2015 |
Iyengar SK, Sedor JR, Freedman BI, Kao WH, Kretzler M, Keller BJ, Abboud HE, Adler SG, Best LG, Bowden DW, Burlock A, Chen YD, Cole SA, Comeau ME, Curtis JM, et al. Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND). Plos Genetics. 11: e1005352. PMID 26305897 DOI: 10.1371/Journal.Pgen.1005352 |
0.465 |
|
| 2015 |
Eicher JD, Stein CM, Deng F, Ciesla AA, Powers NR, Boada R, Smith SD, Pennington BF, Iyengar SK, Lewis BA, Gruen JR. The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Genes, Brain, and Behavior. 14: 377-85. PMID 25778907 DOI: 10.1111/Gbb.12214 |
0.379 |
|
| 2014 |
Klein BE, Howard KP, Iyengar SK, Sivakumaran TA, Meyers KJ, Cruickshanks KJ, Klein R. Sunlight exposure, pigmentation, and incident age-related macular degeneration. Investigative Ophthalmology & Visual Science. 55: 5855-61. PMID 25125603 DOI: 10.1167/Iovs.14-14602 |
0.336 |
|
| 2014 |
Ng MC, Shriner D, Chen BH, Li J, Chen WM, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA, Comeau ME, Rasmussen-Torvik LJ, Jensen RA, Evans DS, Sun YV, ... ... Iyengar SK, et al. Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. Plos Genetics. 10: e1004517. PMID 25102180 DOI: 10.1371/Journal.Pgen.1004517 |
0.429 |
|
| 2014 |
Liao J, Su X, Chen P, Wang X, Xu L, Li X, Thean L, Tan C, Tan AG, Tay WT, Jun G, Zheng Y, Chew M, Wang YX, Tan QS, ... ... Iyengar SK, et al. Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract. Human Molecular Genetics. 23: 6119-28. PMID 24951543 DOI: 10.1093/Hmg/Ddu315 |
0.432 |
|
| 2014 |
Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG. Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 55: 4577-84. PMID 24917144 DOI: 10.1167/Iovs.13-13517 |
0.382 |
|
| 2014 |
Ratnapriya R, Zhan X, Fariss RN, Branham KE, Zipprer D, Chakarova CF, Sergeev YV, Campos MM, Othman M, Friedman JS, Maminishkis A, Waseem NH, Brooks M, Rajasimha HK, Edwards AO, ... ... Iyengar SK, et al. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Human Molecular Genetics. 23: 5827-37. PMID 24899048 DOI: 10.1093/Hmg/Ddu276 |
0.426 |
|
| 2014 |
Klein R, Myers CE, Buitendijk GH, Rochtchina E, Gao X, de Jong PT, Sivakumaran TA, Burlutsky G, McKean-Cowdin R, Hofman A, Iyengar SK, Lee KE, Stricker BH, Vingerling JR, Mitchell P, et al. Lipids, lipid genes, and incident age-related macular degeneration: the three continent age-related macular degeneration consortium. American Journal of Ophthalmology. 158: 513-24.e3. PMID 24879949 DOI: 10.1016/J.Ajo.2014.05.027 |
0.356 |
|
| 2014 |
Stein CM, Truitt B, Deng F, Ciesla AA, Qiu F, Joseph P, Raghavendra R, Fondran J, Igo RP, Tag J, Freebairn L, Taylor HG, Lewis BA, Iyengar SK. Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders. Psychiatric Genetics. 24: 191-200. PMID 24849541 DOI: 10.1097/Ypg.0000000000000045 |
0.306 |
|
| 2014 |
Gangnon RE, Lee KE, Klein BE, Iyengar SK, Sivakumaran TA, Klein R. Misclassification can explain most apparent regression of age-related macular degeneration: results from multistate models with misclassification. Investigative Ophthalmology & Visual Science. 55: 1780-6. PMID 24550369 DOI: 10.1167/Iovs.13-12375 |
0.338 |
|
| 2014 |
Klein R, Myers CE, Cruickshanks KJ, Gangnon RE, Danforth LG, Sivakumaran TA, Iyengar SK, Tsai MY, Klein BE. Markers of inflammation, oxidative stress, and endothelial dysfunction and the 20-year cumulative incidence of early age-related macular degeneration: the Beaver Dam Eye Study. Jama Ophthalmology. 132: 446-55. PMID 24481424 DOI: 10.1001/Jamaophthalmol.2013.7671 |
0.357 |
|
| 2014 |
Klein R, Meuer SM, Myers CE, Buitendijk GH, Rochtchina E, Choudhury F, de Jong PT, McKean-Cowdin R, Iyengar SK, Gao X, Lee KE, Vingerling JR, Mitchell P, Klaver CC, Wang JJ, et al. Harmonizing the classification of age-related macular degeneration in the three-continent AMD consortium. Ophthalmic Epidemiology. 21: 14-23. PMID 24467558 DOI: 10.3109/09286586.2013.867512 |
0.339 |
|
| 2014 |
Meyers KJ, Mares JA, Igo RP, Truitt B, Liu Z, Millen AE, Klein M, Johnson EJ, Engelman CD, Karki CK, Blodi B, Gehrs K, Tinker L, Wallace R, Robinson J, ... ... Iyengar SK, et al. Genetic evidence for role of carotenoids in age-related macular degeneration in the Carotenoids in Age-Related Eye Disease Study (CAREDS). Investigative Ophthalmology & Visual Science. 55: 587-99. PMID 24346170 DOI: 10.1167/Iovs.13-13216 |
0.426 |
|
| 2014 |
Wang JJ, Buitendijk GH, Rochtchina E, Lee KE, Klein BE, van Duijn CM, Flood VM, Meuer SM, Attia J, Myers C, Holliday EG, Tan AG, Smith WT, Iyengar SK, de Jong PT, et al. Genetic susceptibility, dietary antioxidants, and long-term incidence of age-related macular degeneration in two populations. Ophthalmology. 121: 667-75. PMID 24290803 DOI: 10.1016/J.Ophtha.2013.10.017 |
0.371 |
|
| 2013 |
Thameem F, Igo RP, Freedman BI, Langefeld C, Hanson RL, Schelling JR, Elston RC, Duggirala R, Nicholas SB, Goddard KA, Divers J, Guo X, Ipp E, Kimmel PL, Meoni LA, ... ... Iyengar SK, et al. A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND). Plos One. 8: e81888. PMID 24358131 DOI: 10.1371/Journal.Pone.0081888 |
0.441 |
|
| 2013 |
Cheng CY, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJ, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, St Pourcain B, Kemp JP, McMahon G, ... ... Iyengar SK, et al. Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. American Journal of Human Genetics. 93: 264-77. PMID 24144296 DOI: 10.1016/J.Ajhg.2013.06.016 |
0.338 |
|
| 2013 |
Buitendijk GH, Rochtchina E, Myers C, van Duijn CM, Lee KE, Klein BE, Meuer SM, de Jong PT, Holliday EG, Tan AG, Uitterlinden AG, Sivakumaran TA, Sivakumaran TS, Attia J, Hofman A, ... ... Iyengar SK, et al. Prediction of age-related macular degeneration in the general population: the Three Continent AMD Consortium. Ophthalmology. 120: 2644-55. PMID 24120328 DOI: 10.1016/J.Ophtha.2013.07.053 |
0.359 |
|
| 2013 |
Nicholas SB, Iyengar SK. Does losartan prevent progression of early diabetic nephropathy in American Indians with type 2 diabetes? Diabetes. 62: 3014-6. PMID 23970520 DOI: 10.2337/Db13-0748 |
0.326 |
|
| 2013 |
Zhang X, Igo RP, Fondran J, Mootha VV, Oliva M, Hammersmith K, Sugar A, Lass JH, Iyengar SK. Association of smoking and other risk factors with Fuchs' endothelial corneal dystrophy severity and corneal thickness. Investigative Ophthalmology & Visual Science. 54: 5829-35. PMID 23882692 DOI: 10.1167/Iovs.13-11918 |
0.348 |
|
| 2013 |
Sugimoto M, Cutler A, Shen B, Moss SE, Iyengar SK, Klein R, Folkman J, Anand-Apte B. Inhibition of EGF signaling protects the diabetic retina from insulin-induced vascular leakage. The American Journal of Pathology. 183: 987-95. PMID 23831329 DOI: 10.1016/J.Ajpath.2013.05.017 |
0.311 |
|
| 2013 |
Gunzler D, Bleyer AJ, Thomas RL, O'Brien A, Russell GB, Sattar A, Iyengar SK, Thomas C, Sedor JR, Schelling JR. Diabetic nephropathy in a sibling and albuminuria predict early GFR decline: a prospective cohort study. Bmc Nephrology. 14: 124. PMID 23773264 DOI: 10.1186/1471-2369-14-124 |
0.336 |
|
| 2013 |
Li X, Bykhovskaya Y, Canedo AL, Haritunians T, Siscovick D, Aldave AJ, Szczotka-Flynn L, Iyengar SK, Rotter JI, Taylor KD, Rabinowitz YS. Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus. Investigative Ophthalmology & Visual Science. 54: 2696-704. PMID 23513063 DOI: 10.1167/Iovs.13-11601 |
0.41 |
|
| 2013 |
Klein R, Myers CE, Meuer SM, Gangnon RE, Sivakumaran TA, Iyengar SK, Lee KE, Klein BE. Risk alleles in CFH and ARMS2 and the long-term natural history of age-related macular degeneration: the Beaver Dam Eye Study. Jama Ophthalmology. 131: 383-92. PMID 23494043 DOI: 10.1001/Jamaophthalmol.2013.713 |
0.365 |
|
| 2013 |
Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, ... ... Iyengar SK, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578 |
0.443 |
|
| 2013 |
Li X, Bykhovskaya Y, Tang YG, Picornell Y, Haritunians T, Aldave AJ, Szczotka-Flynn L, Iyengar SK, Rotter JI, Taylor KD, Rabinowitz YS. An association between the calpastatin (CAST) gene and keratoconus. Cornea. 32: 696-701. PMID 23449483 DOI: 10.1097/Ico.0B013E3182821C1C |
0.331 |
|
| 2013 |
Meyers KJ, Johnson EJ, Bernstein PS, Iyengar SK, Engelman CD, Karki CK, Liu Z, Igo RP, Truitt B, Klein ML, Snodderly DM, Blodi BA, Gehrs KM, Sarto GE, Wallace RB, et al. Genetic determinants of macular pigments in women of the Carotenoids in Age-Related Eye Disease Study. Investigative Ophthalmology & Visual Science. 54: 2333-45. PMID 23404124 DOI: 10.1167/Iovs.12-10867 |
0.409 |
|
| 2013 |
Verhoeven VJ, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GH, McMahon G, ... ... Iyengar SK, et al. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nature Genetics. 45: 314-8. PMID 23396134 DOI: 10.1038/Ng.2554 |
0.391 |
|
| 2013 |
Arnold LM, Fan J, Russell IJ, Yunus MB, Khan MA, Kushner I, Olson JM, Iyengar SK. The fibromyalgia family study: a genome-wide linkage scan study. Arthritis and Rheumatism. 65: 1122-8. PMID 23280346 DOI: 10.1002/Art.37842 |
0.413 |
|
| 2013 |
Engelman CD, Meyers KJ, Iyengar SK, Liu Z, Karki CK, Igo RP, Truitt B, Robinson J, Sarto GE, Wallace R, Blodi BA, Klein ML, Tinker L, LeBlanc ES, Jackson RD, et al. Vitamin D intake and season modify the effects of the GC and CYP2R1 genes on 25-hydroxyvitamin D concentrations. The Journal of Nutrition. 143: 17-26. PMID 23190755 DOI: 10.3945/Jn.112.169482 |
0.302 |
|
| 2013 |
Lipkowitz MS, Freedman BI, Langefeld CD, Comeau ME, Bowden DW, Kao WH, Astor BC, Bottinger EP, Iyengar SK, Klotman PE, Freedman RG, Zhang W, Parekh RS, Choi MJ, Nelson GW, et al. Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans. Kidney International. 83: 114-20. PMID 22832513 DOI: 10.1038/Ki.2012.263 |
0.36 |
|
| 2013 |
Verhoeven VJM, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GHS, McMahon G, ... ... Iyengar SK, et al. Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (Nature Genetics (2013) 45 (314-318)) Nature Genetics. 45: 712-712. DOI: 10.1038/Ng0613-712B |
0.345 |
|
| 2012 |
Igo RP, Kopplin LJ, Joseph P, Truitt B, Fondran J, Bardenstein D, Aldave AJ, Croasdale CR, Price MO, Rosenwasser M, Lass JH, Iyengar SK. Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy. Plos One. 7: e46742. PMID 23110055 DOI: 10.1371/Journal.Pone.0046742 |
0.422 |
|
| 2012 |
Gangnon RE, Lee KE, Klein BE, Iyengar SK, Sivakumaran TA, Klein R. Effect of the Y402H variant in the complement factor H gene on the incidence and progression of age-related macular degeneration: results from multistate models applied to the Beaver Dam Eye Study. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 1169-76. PMID 22965593 DOI: 10.1001/Archophthalmol.2012.693 |
0.353 |
|
| 2012 |
Vithana EN, Khor CC, Qiao C, Nongpiur ME, George R, Chen LJ, Do T, Abu-Amero K, Huang CK, Low S, Tajudin LS, Perera SA, Cheng CY, Xu L, Jia H, ... ... Iyengar SK, et al. Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma. Nature Genetics. 44: 1142-6. PMID 22922875 DOI: 10.1038/Ng.2390 |
0.387 |
|
| 2012 |
Nagarsheth M, Singh A, Schmotzer B, Babineau DC, Sugar J, Lee WB, Iyengar SK, Lass JH. Relationship Between Fuchs Endothelial Corneal Dystrophy Severity and Glaucoma and/or Ocular Hypertension. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 1384-8. PMID 22777534 DOI: 10.1001/Archophthalmol.2012.1969 |
0.352 |
|
| 2012 |
Verhoeven VJ, Hysi PG, Saw SM, Vitart V, Mirshahi A, Guggenheim JA, Cotch MF, Yamashiro K, Baird PN, Mackey DA, Wojciechowski R, Ikram MK, Hewitt AW, Duggal P, Janmahasatian S, ... ... Iyengar SK, et al. Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Human Genetics. 131: 1467-80. PMID 22665138 DOI: 10.1007/S00439-012-1176-0 |
0.399 |
|
| 2012 |
Bykhovskaya Y, Li X, Epifantseva I, Haritunians T, Siscovick D, Aldave A, Szczotka-Flynn L, Iyengar SK, Taylor KD, Rotter JI, Rabinowitz YS. Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies. Investigative Ophthalmology & Visual Science. 53: 4152-7. PMID 22661479 DOI: 10.1167/Iovs.11-9268 |
0.405 |
|
| 2012 |
Kopplin LJ, Przepyszny K, Schmotzer B, Rudo K, Babineau DC, Patel SV, Verdier DD, Jurkunas U, Iyengar SK, Lass JH. Relationship of Fuchs endothelial corneal dystrophy severity to central corneal thickness. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 433-9. PMID 22491913 DOI: 10.1001/Archophthalmol.2011.1626 |
0.373 |
|
| 2012 |
Anthoni H, Sucheston LE, Lewis BA, Tapia-Páez I, Fan X, Zucchelli M, Taipale M, Stein CM, Hokkanen ME, Castrén E, Pennington BF, Smith SD, Olson RK, Tomblin JB, Schulte-Körne G, ... ... Iyengar S, et al. The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language. Behavior Genetics. 42: 509-27. PMID 22426781 DOI: 10.1007/S10519-012-9532-3 |
0.309 |
|
| 2012 |
Bostrom MA, Kao WH, Li M, Abboud HE, Adler SG, Iyengar SK, Kimmel PL, Hanson RL, Nicholas SB, Rasooly RS, Sedor JR, Coresh J, Kohn OF, Leehey DJ, Thornley-Brown D, et al. Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 59: 210-21. PMID 22119407 DOI: 10.1053/J.Ajkd.2011.09.020 |
0.416 |
|
| 2012 |
Louttit MD, Kopplin LJ, Igo RP, Fondran JR, Tagliaferri A, Bardenstein D, Aldave AJ, Croasdale CR, Price MO, Rosenwasser GO, Lass JH, Iyengar SK, Price FW, Kelly K, Hamilton S, et al. A multicenter study to map genes for Fuchs endothelial corneal dystrophy: Baseline characteristics and heritability Cornea. 31: 26-35. PMID 22045388 DOI: 10.1097/Ico.0B013E31821C9B8F |
0.352 |
|
| 2012 |
Li X, Bykhovskaya Y, Haritunians T, Siscovick D, Aldave A, Szczotka-Flynn L, Iyengar SK, Rotter JI, Taylor KD, Rabinowitz YS. A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. Human Molecular Genetics. 21: 421-9. PMID 21979947 DOI: 10.1093/Hmg/Ddr460 |
0.383 |
|
| 2012 |
Rao M, Mottl AK, Cole SA, Umans JG, Freedman BI, Bowden DW, Langefeld CD, Fox CS, Yang Q, Cupples A, Iyengar SK, Hunt SC, Trikalinos TA. Meta-analysis of genome-wide linkage scans for renal function traits. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 27: 647-56. PMID 21622988 DOI: 10.1093/Ndt/Gfr255 |
0.374 |
|
| 2011 |
Sivakumaran TA, Igo RP, Kidd JM, Itsara A, Kopplin LJ, Chen W, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, Chew EY, Ramprasad VL, Tay WT, Mitchell P, Seielstad M, ... ... Iyengar SK, et al. A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. Plos One. 6: e25598. PMID 22022419 DOI: 10.1371/Journal.Pone.0025598 |
0.391 |
|
| 2011 |
Burdon KP, Macgregor S, Bykhovskaya Y, Javadiyan S, Li X, Laurie KJ, Muszynska D, Lindsay R, Lechner J, Haritunians T, Henders AK, Dash D, Siscovick D, Anand S, Aldave A, ... ... Iyengar SK, et al. Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus. Investigative Ophthalmology & Visual Science. 52: 8514-9. PMID 22003120 DOI: 10.1167/Iovs.11-8261 |
0.423 |
|
| 2011 |
Lewis BA, Avrich AA, Freebairn LA, Hansen AJ, Sucheston LE, Kuo I, Taylor HG, Iyengar SK, Stein CM. Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes. Journal of Speech, Language, and Hearing Research : Jslhr. 54: 1628-43. PMID 21930616 DOI: 10.1044/1092-4388(2011/10-0124) |
0.308 |
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| 2011 |
Sobrin L, Green T, Sim X, Jensen RA, Tai ES, Tay WT, Wang JJ, Mitchell P, Sandholm N, Liu Y, Hietala K, Iyengar SK, Brooks M, Buraczynska M, et al. Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Investigative Ophthalmology & Visual Science. 52: 7593-602. PMID 21873659 DOI: 10.1167/Iovs.11-7510 |
0.356 |
|
| 2011 |
Igo RP, Iyengar SK, Nicholas SB, Goddard KA, Langefeld CD, Hanson RL, Duggirala R, Divers J, Abboud H, Adler SG, Arar NH, Horvath A, Elston RC, Bowden DW, Guo X, et al. Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study. American Journal of Nephrology. 33: 381-9. PMID 21454968 DOI: 10.1159/000326763 |
0.727 |
|
| 2011 |
Stein CM, Lu Q, Elston RC, Freebairn LA, Hansen AJ, Shriberg LD, Taylor HG, Lewis BA, Iyengar SK. Heritability estimation for speech-sound traits with developmental trajectories. Behavior Genetics. 41: 184-91. PMID 20623172 DOI: 10.1007/S10519-010-9378-5 |
0.324 |
|
| 2010 |
Ikram MK, Sim X, Xueling S, Jensen RA, Cotch MF, Hewitt AW, Ikram MA, Wang JJ, Klein R, Klein BE, Breteler MM, Cheung N, Liew G, Mitchell P, Uitterlinden AG, ... ... Iyengar SK, et al. Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. Plos Genetics. 6: e1001184. PMID 21060863 DOI: 10.1371/Journal.Pgen.1001184 |
0.415 |
|
| 2010 |
Kopplin LJ, Igo RP, Wang Y, Sivakumaran TA, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, SanGiovanni JP, Chew EY, Pauer GJ, Sturgill GM, Joshi T, Tian L, Xi Q, ... ... Iyengar SK, et al. Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. Genes and Immunity. 11: 609-21. PMID 20861866 DOI: 10.1038/Gene.2010.39 |
0.429 |
|
| 2010 |
Chen W, Stambolian D, Edwards AO, Branham KE, Othman M, Jakobsdottir J, Tosakulwong N, Pericak-Vance MA, Campochiaro PA, Klein ML, Tan PL, Conley YP, Kanda A, Kopplin L, Li Y, ... ... Iyengar SK, et al. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 107: 7401-6. PMID 20385819 DOI: 10.1073/Pnas.0912702107 |
0.397 |
|
| 2010 |
Kim S, Abboud HE, Pahl MV, Tayek J, Snyder S, Tamkin J, Alcorn H, Ipp E, Nast CC, Elston RC, Iyengar SK, Adler SG. Examination of association with candidate genes for diabetic nephropathy in a Mexican American population. Clinical Journal of the American Society of Nephrology : Cjasn. 5: 1072-8. PMID 20299368 DOI: 10.2215/Cjn.06550909 |
0.435 |
|
| 2009 |
Pai ASI, Mitchell P, Rochtchina E, Iyengar SK, Wang JJ. Complement Factor H and the Bilaterality of Age-Related Macular Degeneration: The Blue Mountains Eye Study Archives of Ophthalmology. 127: 1339-1344. PMID 19822851 DOI: 10.1001/Archophthalmol.2009.239 |
0.354 |
|
| 2009 |
SanGiovanni JP, Arking DE, Iyengar SK, Elashoff M, Clemons TE, Reed GF, Henning AK, Sivakumaran TA, Xu X, DeWan A, Agrón E, Rochtchina E, Sue CM, Wang JJ, Mitchell P, et al. Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration. Plos One. 4: e5508. PMID 19434233 DOI: 10.1371/Journal.Pone.0005508 |
0.332 |
|
| 2009 |
Bravo HC, Lee KE, Klein BE, Klein R, Iyengar SK, Wahba G. Examining the relative influence of familial, genetic, and environmental covariate information in flexible risk models. Proceedings of the National Academy of Sciences of the United States of America. 106: 8128-33. PMID 19420224 DOI: 10.1073/Pnas.0902906106 |
0.361 |
|
| 2009 |
Wang JJ, Rochtchina E, Smith W, Klein R, Klein BE, Joshi T, Sivakumaran TA, Iyengar S, Mitchell P. Combined effects of complement factor H genotypes, fish consumption, and inflammatory markers on long-term risk for age-related macular degeneration in a cohort. American Journal of Epidemiology. 169: 633-41. PMID 19074778 DOI: 10.1093/Aje/Kwn358 |
0.366 |
|
| 2008 |
Stein CM, Zalwango S, Malone LL, Won S, Mayanja-Kizza H, Mugerwa RD, Leontiev DV, Thompson CL, Cartier KC, Elston RC, Iyengar SK, Boom WH, Whalen CC. Genome scan of M. tuberculosis infection and disease in Ugandans. Plos One. 3: e4094. PMID 19116662 DOI: 10.1371/Journal.Pone.0004094 |
0.337 |
|
| 2008 |
Chang B, Mandal MN, Chavali VR, Hawes NL, Khan NW, Hurd RE, Smith RS, Davisson ML, Kopplin L, Klein BE, Klein R, Iyengar SK, Heckenlively JR, Ayyagari R. Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene. Human Molecular Genetics. 17: 3929-41. PMID 18805803 DOI: 10.1093/Hmg/Ddn295 |
0.343 |
|
| 2008 |
Arar NH, Freedman BI, Adler SG, Iyengar SK, Chew EY, Davis MD, Satko SG, Bowden DW, Duggirala R, Elston RC, Guo X, Hanson RL, Igo RP, Ipp E, Kimmel PL, et al. Heritability of the severity of diabetic retinopathy: the FIND-Eye study. Investigative Ophthalmology & Visual Science. 49: 3839-45. PMID 18765632 DOI: 10.1167/Iovs.07-1633 |
0.694 |
|
| 2008 |
Szczotka-Flynn L, Slaughter M, McMahon T, Barr J, Edrington T, Fink B, Lass J, Belin M, Iyengar SK. Disease severity and family history in keratoconus British Journal of Ophthalmology. 92: 1108-1111. PMID 18653604 DOI: 10.1136/Bjo.2007.130294 |
0.349 |
|
| 2008 |
Edwards AO, Chen D, Fridley BL, James KM, Wu Y, Abecasis G, Swaroop A, Othman M, Branham K, Iyengar SK, Sivakumaran TA, Klein R, Klein BE, Tosakulwong N. Toll-like receptor polymorphisms and age-related macular degeneration. Investigative Ophthalmology & Visual Science. 49: 1652-9. PMID 18385087 DOI: 10.1167/Iovs.07-1378 |
0.344 |
|
| 2008 |
Xing C, Sivakumaran TA, Wang JJ, Rochtchina E, Joshi T, Smith W, Mitchell P, Iyengar SK. Complement factor H polymorphisms, renal phenotypes and age-related macular degeneration: the Blue Mountains Eye Study. Genes and Immunity. 9: 231-9. PMID 18340363 DOI: 10.1038/Gene.2008.10 |
0.375 |
|
| 2008 |
Liew G, Mitchell P, Wong TY, Iyengar SK, Wang JJ. CKD increases the risk of age-related macular degeneration. Journal of the American Society of Nephrology : Jasn. 19: 806-11. PMID 18216312 DOI: 10.1681/Asn.2007080844 |
0.356 |
|
| 2008 |
Klein R, Meuer SM, Knudtson MD, Iyengar SK, Klein BE. The epidemiology of retinal reticular drusen. American Journal of Ophthalmology. 145: 317-326. PMID 18045568 DOI: 10.1016/J.Ajo.2007.09.008 |
0.307 |
|
| 2008 |
Schelling JR, Abboud HE, Nicholas SB, Pahl MV, Sedor JR, Adler SG, Arar NH, Bowden DW, Elston RC, Freedman BI, Goddard KA, Guo X, Hanson RL, Ipp E, Iyengar SK, et al. Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND). Diabetes. 57: 235-43. PMID 18003762 DOI: 10.2337/Db07-0313 |
0.415 |
|
| 2007 |
Cartier KC, Miscimarra L, Dazard JE, Song Y, Iyengar SK, Rao JS. Studying genetic determinants of natural variation in human gene expression using Bayesian ANOVA. Bmc Proceedings. 1: S115. PMID 18466456 DOI: 10.1186/1753-6561-1-S1-S115 |
0.363 |
|
| 2007 |
Iyengar SK, Elston RC. The genetic basis of complex traits: rare variants or "common gene, common disease"? Methods in Molecular Biology (Clifton, N.J.). 376: 71-84. PMID 17984539 DOI: 10.1007/978-1-59745-389-9_6 |
0.368 |
|
| 2007 |
Thompson CL, Klein BE, Klein R, Xu Z, Capriotti J, Joshi T, Leontiev D, Lee KE, Elston RC, Iyengar SK. Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes. Human Molecular Genetics. 16: 2135-48. PMID 17591627 DOI: 10.1093/Hmg/Ddm164 |
0.597 |
|
| 2007 |
Satko SG, Sedor JR, Iyengar SK, Freedman BI. Familial clustering of chronic kidney disease. Seminars in Dialysis. 20: 229-36. PMID 17555489 DOI: 10.1111/J.1525-139X.2007.00282.X |
0.321 |
|
| 2007 |
Rybicki BA, Sinha R, Iyengar S, Gray-McGuire C, Elston RC, Iannuzzi MC. Genetic linkage analysis of sarcoidosis phenotypes: the sarcoidosis genetic analysis (SAGA) study. Genes and Immunity. 8: 379-86. PMID 17476268 DOI: 10.1038/Sj.Gene.6364396 |
0.374 |
|
| 2007 |
Stein CM, Zalwango S, Chiunda AB, Millard C, Leontiev DV, Horvath AL, Cartier KC, Chervenak K, Boom WH, Elston RC, Mugerwa RD, Whalen CC, Iyengar SK. Linkage and association analysis of candidate genes for TB and TNFalpha cytokine expression: evidence for association with IFNGR1, IL-10, and TNF receptor 1 genes. Human Genetics. 121: 663-73. PMID 17431682 DOI: 10.1007/S00439-007-0357-8 |
0.317 |
|
| 2007 |
Iyengar SK, Adler SG. The application of the HapMap to diabetic nephropathy and other causes of chronic renal failure. Seminars in Nephrology. 27: 223-36. PMID 17418690 DOI: 10.1016/J.Semnephrol.2007.01.003 |
0.37 |
|
| 2007 |
Iyengar SK, Freedman BI, Sedor JR. Mining the genome for susceptibility to diabetic nephropathy: the role of large-scale studies and consortia. Seminars in Nephrology. 27: 208-22. PMID 17418689 DOI: 10.1016/J.Semnephrol.2007.01.004 |
0.418 |
|
| 2007 |
Iyengar SK. The quest for genes causing complex traits in ocular medicine: successes, interpretations, and challenges. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 11-8. PMID 17210847 DOI: 10.1001/Archopht.125.1.11 |
0.361 |
|
| 2006 |
Lewis BA, Shriberg LD, Freebairn LA, Hansen AJ, Stein CM, Taylor HG, Iyengar SK. The genetic bases of speech sound disorders: evidence from spoken and written language. Journal of Speech, Language, and Hearing Research : Jslhr. 49: 1294-312. PMID 17197497 DOI: 10.1044/1092-4388(2006/093) |
0.339 |
|
| 2006 |
Thompson CL, Rybicki BA, Iannuzzi MC, Elston RC, Iyengar SK, Gray-McGuire C. Reduction of sample heterogeneity through use of population substructure: an example from a population of African American families with sarcoidosis. American Journal of Human Genetics. 79: 606-13. PMID 16960797 DOI: 10.1086/507847 |
0.412 |
|
| 2006 |
Gray-McGuire C, Sinha R, Iyengar S, Millard C, Rybicki BA, Elston RC, Iannuzzi MC. Genetic characterization and fine mapping of susceptibility loci for sarcoidosis in African Americans on chromosome 5. Human Genetics. 120: 420-30. PMID 16896925 DOI: 10.1007/S00439-006-0201-6 |
0.388 |
|
| 2006 |
Stein CM, Millard C, Kluge A, Miscimarra LE, Cartier KC, Freebairn LA, Hansen AJ, Shriberg LD, Taylor HG, Lewis BA, Iyengar SK. Speech sound disorder influenced by a locus in 15q14 region. Behavior Genetics. 36: 858-68. PMID 16786424 DOI: 10.1007/S10519-006-9090-7 |
0.384 |
|
| 2005 |
Stein CM, Nshuti L, Chiunda AB, Boom WH, Elston RC, Mugerwa RD, Iyengar SK, Whalen CC. Evidence for a major gene influence on tumor necrosis factor-alpha expression in tuberculosis: path and segregation analysis. Human Heredity. 60: 109-18. PMID 16224188 DOI: 10.1159/000088913 |
0.304 |
|
| 2005 |
Jun G, Klein BEK, Klein R, Fox K, Millard C, Capriotti J, Russo K, Lee KE, Elston RC, Iyengar SK. Genome-wide analyses demonstrate novel loci that predispose to drusen formation Investigative Ophthalmology and Visual Science. 46: 3081-3088. PMID 16123405 DOI: 10.1167/Iovs.04-1360 |
0.368 |
|
| 2005 |
Fisher SA, Abecasis GR, Yashar BM, Zareparsi S, Swaroop A, Iyengar SK, Klein BE, Klein R, Lee KE, Majewski J, Schultz DW, Klein ML, Seddon JM, Santangelo SL, Weeks DE, et al. Meta-analysis of genome scans of age-related macular degeneration. Human Molecular Genetics. 14: 2257-64. PMID 15987700 DOI: 10.1093/Hmg/Ddi230 |
0.407 |
|
| 2005 |
Iannuzzi MC, Iyengar SK, Gray-McGuire C, Elston RC, Baughman RP, Donohue JF, Hirst K, Judson MA, Kavuru MS, Maliarik MJ, Moller DR, Newman LS, Rabin DL, Rose CS, Rossman MD, et al. Genome-wide search for sarcoidosis susceptibility genes in African Americans. Genes and Immunity. 6: 509-18. PMID 15951742 DOI: 10.1038/Sj.Gene.6364235 |
0.374 |
|
| 2005 |
Orloff MS, Iyengar SK, Winkler CA, Goddard KA, Dart RA, Ahuja TS, Mokrzycki M, Briggs WA, Korbet SM, Kimmel PL, Simon EE, Trachtman H, Vlahov D, Michel DM, Berns JS, et al. Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population. Physiological Genomics. 21: 212-21. PMID 15687485 DOI: 10.1152/Physiolgenomics.00201.2004 |
0.354 |
|
| 2005 |
Duggal P, Klein AP, Lee KE, Iyengar SK, Klein R, Bailey-Wilson JE, Klein BE. A genetic contribution to intraocular pressure: the beaver dam eye study. Investigative Ophthalmology & Visual Science. 46: 555-60. PMID 15671282 DOI: 10.1167/Iovs.04-0729 |
0.412 |
|
| 2005 |
Elston RC, Song D, Iyengar SK. Mathematical assumptions versus biological reality: Myths in affected sib pair linkage analysis American Journal of Human Genetics. 76: 152-156. PMID 15540158 DOI: 10.1086/426872 |
0.307 |
|
| 2004 |
Stein CM, Schick JH, Taylor HG, Shriberg LD, Millard C, Kundtz-Kluge A, Russo K, Minich N, Hansen A, Freebairn LA, Elston RC, Lewis BA, Iyengar SK. Pleiotropic Effects of a Chromosome 3 Locus on Speech-Sound Disorder and Reading American Journal of Human Genetics. 74: 283-297. PMID 14740317 DOI: 10.1086/381562 |
0.357 |
|
| 2003 |
Chattopadhyay P, Pakstis AJ, Mukherjee N, Iyengar S, 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. European Journal of Human Genetics : Ejhg. 11: 760-9. PMID 14512966 DOI: 10.1038/Sj.Ejhg.5201036 |
0.333 |
|
| 2003 |
Iyengar SK, 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. Journal of the American Society of Nephrology : Jasn. 14: S195-201. PMID 12819328 DOI: 10.1097/01.Asn.0000070078.66465.55 |
0.386 |
|
| 2003 |
Schick JH, Iyengar SK, 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. American Journal of Human Genetics. 72: 1412-24. PMID 12717633 DOI: 10.1016/J.Ajo.2003.08.024 |
0.355 |
|
| 2003 |
Hayden PS, Iyengar SK, Schelling JR, Sedor JR. Kidney disease, genotype and the pathogenesis of vasculopathy. Current Opinion in Nephrology and Hypertension. 12: 71-8. PMID 12496669 DOI: 10.1097/00041552-200301000-00012 |
0.344 |
|
| 2002 |
Rybicki BA, Iyengar SK, 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 Human Heredity. 53: 187-196. PMID 12435883 DOI: 10.1159/000066193 |
0.371 |
|
| 2002 |
Iyengar SK, Schelling JR, Sedor JR. Approaches to understanding susceptibility to nephropathy: from genetics to genomics. Kidney International. 61: S61-7. PMID 11841615 DOI: 10.1046/J.1523-1755.2002.0610S1061.X |
0.358 |
|
| 2001 |
Iyengar SK, Jacobs KB, Palmer LJ. Improved evidence for linkage on 6p and 5p with retrospective pooling of data from three asthma genome screens Genetic Epidemiology. 21. PMID 11793655 DOI: 10.1002/Gepi.2001.21.S1.S130 |
0.333 |
|
| 2001 |
Jacobs KB, Burton PR, Iyengar SK, Elston RC, Palmer LJ. Pooling data and linkage analysis in the chromosome 5q candidate region for asthma Genetic Epidemiology. 21. PMID 11793650 DOI: 10.1002/Gepi.2001.21.S1.S103 |
0.346 |
|
| 2001 |
Kaufman ES, Priori SG, Napolitano C, Schwartz PJ, Iyengar S, 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. Journal of Cardiovascular Electrophysiology. 12: 455-61. PMID 11332568 DOI: 10.1046/J.1540-8167.2001.00455.X |
0.352 |
|
| 2001 |
Covic AM, Iyengar SK, Olson JM, Sehgal AR, Constantiner M, Jedrey C, Kara M, Sabbagh E, Sedor JR, Schelling JR. A family-based strategy to identify genes for diabetic nephropathy. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 37: 638-47. PMID 11228193 DOI: 10.1053/Ajkd.2001.22094 |
0.38 |
|
| 2001 |
Schick JH, Iyengar SK, Elston RC, Fijal BA, Klein BE, Klein R. The Genetic Epidemiology of Age-Related Maculopathy International Journal of Human Genetics. 1: 11-24. DOI: 10.31901/24566330.2001/01.01.02 |
0.332 |
|
| 2000 |
Covic AM, Schelling JR, Constantiner M, Iyengar SK, Sedor JR. Serum C-peptide concentrations poorly phenotype type 2 diabetic end-stage renal disease patients. Kidney International. 58: 1742-50. PMID 11012908 DOI: 10.1046/J.1523-1755.2000.00335.X |
0.315 |
|
| 1999 |
Schelling JR, Zarif L, Sehgal A, Iyengar S, Sedor JR. Genetic susceptibility to end-stage renal disease Current Opinion in Nephrology and Hypertension. 8: 465-472. PMID 10491742 DOI: 10.1097/00041552-199907000-00011 |
0.32 |
|
| 1998 |
Iyengar S, Seaman M, Deinard AS, Rosenbaum HC, Sirugo G, Castiglione CM, Kidd JR, Kidd KK. Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms. Dna Sequence : the Journal of Dna Sequencing and Mapping. 8: 317-27. PMID 10993602 DOI: 10.3109/10425179809034076 |
0.319 |
|
| 1993 |
Ferrell RE, Iyengar S. Molecular studies of the genetics of non-insulin-dependent diabetes mellitus. American Journal of Human Biology : the Official Journal of the Human Biology Council. 5: 415-424. PMID 28548410 DOI: 10.1002/Ajhb.1310050406 |
0.312 |
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