E Feingold - Publications

University of Pittsburgh, Pittsburgh, PA, United States 
Genetics, Statistics, Biostatistics Biology

129 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Leslie EJ, Liu H, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, et al. A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. American Journal of Human Genetics. PMID 27018472 DOI: 10.1016/j.ajhg.2016.02.014  0.72
2016 Begum F, Sharker MH, Sherman SL, Tseng GC, Feingold E. Regionally Smoothed Meta-Analysis Methods for GWAS Datasets. Genetic Epidemiology. 40: 154-60. PMID 26707090 DOI: 10.1002/gepi.21949  0.72
2015 Zeng Z, Weeks DE, Chen W, Mukhopadhyay N, Feingold E. A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information. Genetic Epidemiology. PMID 26709242 DOI: 10.1002/gepi.21948  0.72
2015 Özbek U, Feingold E, Weeks DE. Efficient Identification of Null-Allele Single Nucleotide Polymorphism Markers. Human Heredity. 80: 79-89. PMID 26613255 DOI: 10.1159/000441279  0.72
2015 Demirci FY, Wang X, Kelly JA, Morris DL, Barmada MM, Feingold E, Kao AH, Sivils KL, Bernatsky S, Pineau C, Clarke A, Ramsey-Goldman R, Vyse TJ, Gaffney PM, Manzi S, et al. Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry. Arthritis & Rheumatology (Hoboken, N.J.). PMID 26316170 DOI: 10.1002/art.39403  0.72
2015 Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. G3 (Bethesda, Md.). 5: 1961-71. PMID 26194203 DOI: 10.1534/g3.115.019943  0.72
2015 Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E. Genome-wide copy-number variation study of psychosis in Alzheimer's disease. Translational Psychiatry. 5: e574. PMID 26035058 DOI: 10.1038/tp.2015.64  0.72
2015 Weinreb NJ, Finegold DN, Feingold E, Zeng Z, Rosenbloom BE, Shankar SP, Amato D. Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3). Orphanet Journal of Rare Diseases. 10: 64. PMID 25994334 DOI: 10.1186/s13023-015-0280-3  0.72
2015 Wolf ZT, Brand HA, Shaffer JR, Leslie EJ, Arzi B, Willet CE, Cox TC, McHenry T, Narayan N, Feingold E, Wang X, Sliskovic S, Karmi N, Safra N, Sanchez C, et al. Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. Plos Genetics. 11: e1005059. PMID 25798845 DOI: 10.1371/journal.pgen.1005059  0.72
2015 Wang X, Lopez O, Sweet RA, Becker JT, DeKosky ST, Barmada MM, Feingold E, Demirci FY, Kamboh MI. Genetic Determinants of Survival in Patientswith Alzheimer’s Disease. Journal of Alzheimer's Disease : Jad. 45: 651-8. PMID 25649651 DOI: 10.3233/JAD-142442  0.72
2015 Shaffer JR, Carlson JC, Stanley BO, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, et al. Effects of enamel matrix genes on dental caries are moderated by fluoride exposures. Human Genetics. 134: 159-67. PMID 25373699 DOI: 10.1007/s00439-014-1504-7  0.72
2015 Shaffer JR, Leslie EJ, Feingold E, Govil M, McNeil DW, Crout RJ, Weyant RJ, Marazita ML. Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia International Journal of Dentistry. 2015. DOI: 10.1155/2015/938213  0.72
2014 Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E. A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease. Plos One. 9: e111462. PMID 25379732 DOI: 10.1371/journal.pone.0111462  0.72
2014 Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SL. An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction. Plos One. 9: e99560. PMID 24926858 DOI: 10.1371/journal.pone.0099560  0.72
2014 Stanley BO, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML, Shaffer JR. Genetic Association of MPPED2 and ACTN2 with Dental Caries. Journal of Dental Research. 93: 626-632. PMID 24810274 DOI: 10.1177/0022034514534688  0.72
2014 Zeng Z, Feingold E, Wang X, Weeks DE, Lee M, Cuenco DT, Broffitt B, Weyant RJ, Crout R, McNeil DW, Levy SM, Marazita ML, Shaffer JR. Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries. Caries Research. 48: 330-8. PMID 24556642 DOI: 10.1159/000356299  0.72
2014 Qutub K, Lacomis D, Albert SM, Feingold E. Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 15: 292-7. PMID 24555470 DOI: 10.3109/21678421.2014.886699  0.72
2014 Shaffer JR, Polk DE, Wang X, Feingold E, Weeks DE, Lee MK, Cuenco KT, Weyant RJ, Crout RJ, McNeil DW, Marazita ML. Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. G3 (Bethesda, Md.). 4: 307-14. PMID 24347629 DOI: 10.1534/g3.113.008755  0.72
2014 Middlebrooks CD, Mukhopadhyay N, Tinker SW, Allen EG, Bean LJ, Begum F, Chowdhury R, Cheung V, Doheny K, Adams M, Feingold E, Sherman SL. Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. Human Molecular Genetics. 23: 408-17. PMID 24014426 DOI: 10.1093/hmg/ddt433  0.72
2013 Wang Q, Jia P, Cuenco KT, Feingold E, Marazita ML, Wang L, Zhao Z. Multi-dimensional prioritization of dental caries candidate genes and its enriched dense network modules. Plos One. 8: e76666. PMID 24146904 DOI: 10.1371/journal.pone.0076666  0.72
2013 Wang Q, Jia P, Cuenco KT, Zeng Z, Feingold E, Marazita ML, Wang L, Zhao Z. Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies. Plos One. 8: e72653. PMID 23967329 DOI: 10.1371/journal.pone.0072653  0.72
2013 Zeng Z, Shaffer JR, Wang X, Feingold E, Weeks DE, Lee M, Cuenco KT, Wendell SK, Weyant RJ, Crout R, McNeil DW, Marazita ML. Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition. Journal of Dental Research. 92: 432-7. PMID 23470693 DOI: 10.1177/0022034513481976  0.72
2013 Shaffer JR, Polk DE, Feingold E, Wang X, Cuenco KT, Weeks DE, DeSensi RS, Weyant RJ, Crout R, McNeil DW, Marazita ML. Demographic, socioeconomic, and behavioral factors affecting patterns of tooth decay in the permanent dentition: principal components and factor analyses. Community Dentistry and Oral Epidemiology. 41: 364-73. PMID 23106439 DOI: 10.1111/cdoe.12016  0.72
2013 Shaffer JR, Feingold E, Wang X, Lee M, Tcuenco K, Weeks DE, Weyant RJ, Crout R, McNeil DW, Marazita ML. GWAS of dental caries patterns in the permanent dentition. Journal of Dental Research. 92: 38-44. PMID 23064961 DOI: 10.1177/0022034512463579  0.72
2013 Shaffer JR, Feingold E, Wang X, Weeks DE, Weyant RJ, Crout R, McNeil DW, Marazita ML. Clustering tooth surfaces into biologically informative caries outcomes. Journal of Dental Research. 92: 32-7. PMID 23064960 DOI: 10.1177/0022034512463241  0.72
2012 Wang X, Shaffer JR, Zeng Z, Begum F, Vieira AR, Noel J, Anjomshoaa I, Cuenco KT, Lee MK, Beck J, Boerwinkle E, Cornelis MC, Hu FB, Crosslin DR, Laurie CC, ... ... Feingold E, et al. Genome-wide association scan of dental caries in the permanent dentition. Bmc Oral Health. 12: 57. PMID 23259602 DOI: 10.1186/1472-6831-12-57  0.72
2012 Polk DE, Wang X, Feingold E, Shaffer JR, Weeks DE, Weyant RJ, Crout RJ, McNeil DW, Marazita ML. Effects of smoking and genotype on the PSR index of periodontal disease in adults aged 18-49. International Journal of Environmental Research and Public Health. 9: 2839-50. PMID 23066400 DOI: 10.3390/ijerph9082839  0.72
2012 Ackerman C, Locke AE, Feingold E, Reshey B, Espana K, Thusberg J, Mooney S, Bean LJ, Dooley KJ, Cua CL, Reeves RH, Sherman SL, Maslen CL. An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. American Journal of Human Genetics. 91: 646-59. PMID 23040494 DOI: 10.1016/j.ajhg.2012.08.017  0.72
2012 Ghosh P, Bhaumik P, Ghosh S, Ozbek U, Feingold E, Maslen C, Sarkar B, Pramanik V, Biswas P, Bandyopadhyay B, Dey SK. Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect. American Journal of Medical Genetics. Part A. 158: 2843-8. PMID 22987595 DOI: 10.1002/ajmg.a.35626  0.72
2012 Alleman BW, Myking S, Ryckman KK, Myhre R, Feingold E, Feenstra B, Geller F, Boyd HA, Shaffer JR, Zhang Q, Begum F, Crosslin D, Doheny K, Pugh E, Pay ASD, et al. No observed association for mitochondrial SNPs with preterm delivery and related outcomes Pediatric Research. 72: 539-544. PMID 22902432 DOI: 10.1038/pr.2012.112  0.72
2012 Kamboh MI, Demirci FY, Wang X, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Jun G, Baldwin C, Logue MW, Buros J, Farrer L, Pericak-Vance MA, ... ... Feingold E, et al. Genome-wide association study of Alzheimer's disease. Translational Psychiatry. 2: e117. PMID 22832961 DOI: 10.1038/tp.2012.45  0.72
2012 Zheng X, Shaffer JR, McHugh CP, Laurie CC, Feenstra B, Melbye M, Murray JC, Marazita ML, Feingold E. Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies. Genetic Epidemiology. 36: 253-62. PMID 22714937 DOI: 10.1002/gepi.21618  0.72
2012 Shaffer JR, Feingold E, Marazita ML. Genome-wide association studies: prospects and challenges for oral health. Journal of Dental Research. 91: 637-41. PMID 22562461 DOI: 10.1177/0022034512446968  0.72
2012 Laurie CC, Laurie CA, Rice K, Doheny KF, Zelnick LR, McHugh CP, Ling H, Hetrick KN, Pugh EW, Amos C, Wei Q, Wang LE, Lee JE, Barnes KC, Hansel NN, ... ... Feingold E, et al. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature Genetics. 44: 642-50. PMID 22561516 DOI: 10.1038/ng.2271  0.72
2012 Shaffer JR, Feingold E, Wang X, Tcuenco KT, Weeks DE, DeSensi RS, Polk DE, Wendell S, Weyant RJ, Crout R, McNeil DW, Marazita ML. Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses. Bmc Oral Health. 12: 7. PMID 22405185 DOI: 10.1186/1472-6831-12-7  0.72
2012 Finegold DN, Baty CJ, Knickelbein KZ, Perschke S, Noon SE, Campbell D, Karlsson JM, Huang D, Kimak MA, Lawrence EC, Feingold E, Meriney SD, Brufsky AM, Ferrell RE. Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 18: 2382-90. PMID 22351697 DOI: 10.1158/1078-0432.CCR-11-2303  0.72
2012 Tseng GC, Ghosh D, Feingold E. Comprehensive literature review and statistical considerations for microarray meta-analysis. Nucleic Acids Research. 40: 3785-99. PMID 22262733 DOI: 10.1093/nar/gkr1265  0.72
2012 Begum F, Ghosh D, Tseng GC, Feingold E. Comprehensive literature review and statistical considerations for GWAS meta-analysis. Nucleic Acids Research. 40: 3777-84. PMID 22241776 DOI: 10.1093/nar/gkr1255  0.72
2012 Oliver TR, Tinker SW, Allen EG, Hollis N, Locke AE, Bean LJ, Chowdhury R, Begum F, Marazita M, Cheung V, Feingold E, Sherman SL. Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. Human Genetics. 131: 1039-46. PMID 22160426 DOI: 10.1007/s00439-011-1121-7  0.72
2012 Kamboh MI, Barmada MM, Demirci FY, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Sweet RA, Feingold E, DeKosky ST, Lopez OL. Genome-wide association analysis of age-at-onset in Alzheimer's disease. Molecular Psychiatry. 17: 1340-6. PMID 22005931 DOI: 10.1038/mp.2011.135  0.72
2012 Ryckman KK, Feenstra B, Shaffer JR, Bream EN, Geller F, Feingold E, Weeks DE, Gadow E, Cosentino V, Saleme C, Simhan HN, Merrill D, Fong CT, Busch T, Berends SK, et al. Replication of a genome-wide association study of birth weight in preterm neonates. The Journal of Pediatrics. 160: 19-24.e4. PMID 21885063 DOI: 10.1016/j.jpeds.2011.07.038  0.72
2011 Ghosh S, Hong CS, Feingold E, Ghosh P, Ghosh P, Bhaumik P, Dey SK. Epidemiology of Down syndrome: new insight into the multidimensional interactions among genetic and environmental risk factors in the oocyte. American Journal of Epidemiology. 174: 1009-16. PMID 21957181 DOI: 10.1093/aje/kwr240  0.72
2011 Shaffer JR, Wang X, Feingold E, Lee M, Begum F, Weeks DE, Cuenco KT, Barmada MM, Wendell SK, Crosslin DR, Laurie CC, Doheny KF, Pugh EW, Zhang Q, Feenstra B, et al. Genome-wide association scan for childhood caries implicates novel genes. Journal of Dental Research. 90: 1457-62. PMID 21940522 DOI: 10.1177/0022034511422910  0.72
2011 Nielsen SM, Rubinstein WS, Thull DL, Armstrong MJ, Feingold E, Yip L, Tisherman SA, Carty SE. Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A. Familial Cancer. 10: 701-7. PMID 21713522 DOI: 10.1007/s10689-011-9465-7  0.72
2011 Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, Cunningham JM, de Andrade M, Feenstra B, Feingold E, Hayes MG, Hill WG, Landi MT, Alonso A, Lettre G, Lin P, et al. Genome partitioning of genetic variation for complex traits using common SNPs. Nature Genetics. 43: 519-25. PMID 21552263 DOI: 10.1038/ng.823  0.72
2011 Nielsen SM, Rubinstein WS, Thull DL, Armstrong MJ, Feingold E, Stang MT, Gnarra JR, Carty SE. Genotype-phenotype correlations of pheochromocytoma in two large von Hippel-Lindau (VHL) type 2A kindreds with different missense mutations. American Journal of Medical Genetics. Part A. 155: 168-73. PMID 21204227 DOI: 10.1002/ajmg.a.33760  0.72
2011 Zheng X, Morrison AC, Feingold E, Turner ST, Ferrell RE. Association between NEDD4L gene and sodium lithium countertransport. American Journal of Hypertension. 24: 145-8. PMID 21088674 DOI: 10.1038/ajh.2010.222  0.72
2010 Locke AE, Dooley KJ, Tinker SW, Cheong SY, Feingold E, Allen EG, Freeman SB, Torfs CP, Cua CL, Epstein MP, Wu MC, Lin X, Capone G, Sherman SL, Bean LJ. Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genetic Epidemiology. 34: 613-23. PMID 20718043 DOI: 10.1002/gepi.20518  0.72
2010 Ferrell RE, Baty CJ, Kimak MA, Karlsson JM, Lawrence EC, Franke-Snyder M, Meriney SD, Feingold E, Finegold DN. GJC2 missense mutations cause human lymphedema. American Journal of Human Genetics. 86: 943-8. PMID 20537300 DOI: 10.1016/j.ajhg.2010.04.010  0.72
2010 Diergaarde B, Brand R, Lamb J, Cheong SY, Stello K, Barmada MM, Feingold E, Whitcomb DC. Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis. Pancreatology : Official Journal of the International Association of Pancreatology (Iap) ... [Et Al.]. 10: 194-200. PMID 20484958 DOI: 10.1159/000236023  0.72
2010 Cheung VG, Sherman SL, Feingold E. Genetics. Genetic control of hotspots. Science (New York, N.Y.). 327: 791-2. PMID 20150474 DOI: 10.1126/science.1187155  0.72
2010 Cornelis MC, Agrawal A, Cole JW, Hansel NN, Barnes KC, Beaty TH, Bennett SN, Bierut LJ, Boerwinkle E, Doheny KF, Feenstra B, Feingold E, Fornage M, Haiman CA, Harris EL, et al. The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genetic Epidemiology. 34: 364-72. PMID 20091798 DOI: 10.1002/gepi.20492  0.72
2010 D'Angelo GM, Kamboh MI, Feingold E. A Likelihood-Based Approach for Missing Genotype Data. Human Heredity. 69: 171-83. PMID 20068333 DOI: 10.1159/000273732  0.72
2010 Ghosh S, Feingold E, Chakraborty S, Dey SK. Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth. Human Genetics. 127: 403-9. PMID 20063167 DOI: 10.1007/s00439-009-0785-8  0.72
2010 Kuo CL, Feingold E. What's the best statistic for a simple test of genetic association in a case-control study? Genetic Epidemiology. 34: 246-53. PMID 20025064 DOI: 10.1002/gepi.20455  0.72
2010 Mukhopadhyay I, Feingold E, Weeks DE, Thalamuthu A. Association tests using kernel-based measures of multi-locus genotype similarity between individuals. Genetic Epidemiology. 34: 213-21. PMID 19697357 DOI: 10.1002/gepi.20451  0.72
2010 Kuo CL, Feingold E. Letter to the Editor Genetic Epidemiology. 34: 772-772. DOI: 10.1002/gepi.20524  0.72
2009 Chowdhury R, Bois PR, Feingold E, Sherman SL, Cheung VG. Genetic analysis of variation in human meiotic recombination. Plos Genetics. 5: e1000648. PMID 19763160 DOI: 10.1371/journal.pgen.1000648  0.72
2009 Oliver TR, Bhise A, Feingold E, Tinker S, Masse N, Sherman SL. Investigation of factors associated with paternal nondisjunction of chromosome 21. American Journal of Medical Genetics. Part A. 149: 1685-90. PMID 19606484 DOI: 10.1002/ajmg.a.32942  0.72
2009 Ghosh S, Feingold E, Dey SK. Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations. American Journal of Medical Genetics. Part A. 149: 1415-20. PMID 19533770 DOI: 10.1002/ajmg.a.32932  0.72
2009 Iuliano AD, Feingold E, Wahed AS, Kleiner DE, Belle SH, Conjeevaram HS, Zmuda J, Liang TJ, Yee LJ. Host genetics, steatosis and insulin resistance among African Americans and Caucasian Americans with hepatitis C virus genotype-1 infection. Intervirology. 52: 49-56. PMID 19401628 DOI: 10.1159/000214380  0.72
2009 Henson BJ, Bhattacharjee S, O'Dee DM, Feingold E, Gollin SM. Decreased expression of miR-125b and miR-100 in oral cancer cells contributes to malignancy. Genes, Chromosomes & Cancer. 48: 569-82. PMID 19396866 DOI: 10.1002/gcc.20666  0.72
2009 Wang X, Kammerer CM, Anderson S, Lu J, Feingold E. A comparison of principal component analysis and factor analysis strategies for uncovering pleiotropic factors. Genetic Epidemiology. 33: 325-31. PMID 19048641 DOI: 10.1002/gepi.20384  0.72
2008 Lin Y, Tseng GC, Cheong SY, Bean LJ, Sherman SL, Feingold E. Smarter clustering methods for SNP genotype calling. Bioinformatics (Oxford, England). 24: 2665-71. PMID 18826959 DOI: 10.1093/bioinformatics/btn509  0.72
2008 Oliver TR, Feingold E, Yu K, Cheung V, Tinker S, Yadav-Shah M, Masse N, Sherman SL. New insights into human nondisjunction of chromosome 21 in oocytes. Plos Genetics. 4: e1000033. PMID 18369452 DOI: 10.1371/journal.pgen.1000033  0.72
2008 Bhattacharjee S, Kuo CL, Mukhopadhyay N, Brock GN, Weeks DE, Feingold E. Robust score statistics for QTL linkage analysis. American Journal of Human Genetics. 82: 567-82. PMID 18304491 DOI: 10.1016/j.ajhg.2007.11.012  0.72
2008 Irie J, Reck B, Wu Y, Wicker LS, Howlett S, Rainbow D, Feingold E, Ridgway WM. Genome-wide microarray expression analysis of CD4+ T Cells from nonobese diabetic congenic mice identifies Cd55 (Daf1) and Acadl as candidate genes for type 1 diabetes. Journal of Immunology (Baltimore, Md. : 1950). 180: 1071-9. PMID 18178847  0.72
2007 Benos PV, Corcoran DL, Feingold E. Web-based identification of evolutionary conserved DNA cis-regulatory elements. Methods in Molecular Biology (Clifton, N.J.). 395: 425-36. PMID 17993689 DOI: 10.1385/1-59745-514-8:425  0.72
2007 Hall HE, Surti U, Hoffner L, Shirley S, Feingold E, Hassold T. The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction. American Journal of Medical Genetics. Part A. 143: 2249-55. PMID 17705154 DOI: 10.1002/ajmg.a.31918  0.72
2007 Brock GN, Weeks DE, Sobel E, Feingold E. A hierarchical model for estimating significance levels of non-parametric linkage statistics for large pedigrees. Genetic Epidemiology. 31: 417-30. PMID 17508354 DOI: 10.1002/gepi.20222  0.72
2007 Mahony S, Corcoran DL, Feingold E, Benos PV. Regulatory conservation of protein coding and microRNA genes in vertebrates: lessons from the opossum genome. Genome Biology. 8: R84. PMID 17506886 DOI: 10.1186/gb-2007-8-5-r84  0.72
2007 Baca JT, Taormina CR, Feingold E, Finegold DN, Grabowski JJ, Asher SA. Mass spectral determination of fasting tear glucose concentrations in nondiabetic volunteers. Clinical Chemistry. 53: 1370-2. PMID 17495022 DOI: 10.1373/clinchem.2006.078543  0.72
2007 Reshmi SC, Roychoudhury S, Yu Z, Feingold E, Potter D, Saunders WS, Gollin SM. Inverted duplication pattern in anaphase bridges confirms the breakage-fusion-bridge (BFB) cycle model for 11q13 amplification. Cytogenetic and Genome Research. 116: 46-52. PMID 17268177 DOI: 10.1159/000097425  0.72
2007 Sengul H, Bhattacharjee S, Feingold E, Weeks DE. The elusive goal of pedigree weights. Genetic Epidemiology. 31: 51-65. PMID 17086515 DOI: 10.1002/gepi.20188  0.72
2007 Sundar PD, Feingold E, Minster RL, DeKosky ST, Kamboh MI. Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease. Neurobiology of Aging. 28: 856-62. PMID 16725228 DOI: 10.1016/j.neurobiolaging.2006.04.005  0.72
2006 O'Neill SM, Peters JA, Vogel VG, Feingold E, Rubinstein WS. Referral to cancer genetic counseling: are there stages of readiness? American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 142: 221-31. PMID 17068804 DOI: 10.1002/ajmg.c.30109  0.72
2006 Mukhopadhyay I, Feingold E, Wang T, Elston RC, Weeks DE. Treatment of uninformative families in mean allele sharing tests for linkage. Statistical Applications in Genetics and Molecular Biology. 5: Article13. PMID 17049024 DOI: 10.2202/1544-6115.1206  0.72
2006 Jung J, Weeks DE, Feingold E. Gene-dropping vs. empirical variance estimation for allele-sharing linkage statistics. Genetic Epidemiology. 30: 652-65. PMID 16917920 DOI: 10.1002/gepi.20177  0.72
2006 Sherman SL, Lamb NE, Feingold E. Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21. Biochemical Society Transactions. 34: 578-80. PMID 16856865 DOI: 10.1042/BST0340578  0.72
2006 Schaefer TM, Fuller CL, Basu S, Fallert BA, Poveda SL, Sanghavi SK, Choi YK, Kirschner DE, Feingold E, Reinhart TA. Increased expression of interferon-inducible genes in macaque lung tissues during simian immunodeficiency virus infection. Microbes and Infection / Institut Pasteur. 8: 1839-50. PMID 16822691 DOI: 10.1016/j.micinf.2006.02.022  0.72
2006 Kamboh MI, Minster RL, Feingold E, DeKosky ST. Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures. Molecular Psychiatry. 11: 273-9. PMID 16302009 DOI: 10.1038/sj.mp.4001775  0.72
2005 Moffett SP, Feingold E, Barmada MM, Damcott CM, Marshall JA, Hamman RF, Ferrell RE. The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated receptor gamma. Metabolism: Clinical and Experimental. 54: 1552-6. PMID 16253648 DOI: 10.1016/j.metabol.2005.05.025  0.72
2005 Corcoran DL, Feingold E, Benos PV. FOOTER: a web tool for finding mammalian DNA regulatory regions using phylogenetic footprinting. Nucleic Acids Research. 33: W442-6. PMID 15980508 DOI: 10.1093/nar/gki420  0.72
2005 Corcoran DL, Feingold E, Dominick J, Wright M, Harnaha J, Trucco M, Giannoukakis N, Benos PV. Footer: a quantitative comparative genomics method for efficient recognition of cis-regulatory elements. Genome Research. 15: 840-7. PMID 15930494 DOI: 10.1101/gr.2952005  0.72
2005 Katsiaras A, Newman AB, Kriska A, Brach J, Krishnaswami S, Feingold E, Kritchevsky SB, Li R, Harris TB, Schwartz A, Goodpaster BH. Skeletal muscle fatigue, strength, and quality in the elderly: the Health ABC Study. Journal of Applied Physiology (Bethesda, Md. : 1985). 99: 210-6. PMID 15718402 DOI: 10.1152/japplphysiol.01276.2004  0.72
2005 Szatkiewicz JP, Feingold E. QTL mapping with discordant and concordant sibling pairs: new statistics and new design strategies. Genetic Epidemiology. 28: 326-40. PMID 15662636 DOI: 10.1002/gepi.20065  0.72
2005 Lamb NE, Yu K, Shaffer J, Feingold E, Sherman SL. Association between maternal age and meiotic recombination for trisomy 21 American Journal of Human Genetics. 76: 91-99. PMID 15551222 DOI: 10.1086/427266  0.72
2004 Broman KW, Feingold E. SNPs made routine. Nature Methods. 1: 104-5. PMID 15782170 DOI: 10.1038/nmeth1104-104  0.72
2004 Kerstann KF, Feingold E, Freeman SB, Bean LJ, Pyatt R, Tinker S, Jewel AH, Capone G, Sherman SL. Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome. Genetic Epidemiology. 27: 240-51. PMID 15389927 DOI: 10.1002/gepi.20019  0.72
2004 Szatkiewicz JP, Feingold E. A powerful and robust new linkage statistic for discordant sibling pairs. American Journal of Human Genetics. 75: 906-9. PMID 15368196 DOI: 10.1086/425523  0.72
2004 Damcott CM, Feingold E, Moffett SP, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females. Metabolism: Clinical and Experimental. 53: 458-64. PMID 15045692 DOI: 10.1016/j.metabol.2003.11.019  0.72
2004 Damcott CM, Moffett SP, Feingold E, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males. Metabolism: Clinical and Experimental. 53: 303-9. PMID 15015141 DOI: 10.1016/j.metabol.2003.10.010  0.72
2004 Xu Z, Kerstann KF, Sherman SL, Chakravarti A, Feingold E. A trisomic transmission disequilibrium test. Genetic Epidemiology. 26: 125-31. PMID 14748012 DOI: 10.1002/gepi.10302  0.72
2004 Song KK, Weeks DE, Sobel E, Feingold E. Efficient Simulation of P Values for Linkage Analysis Genetic Epidemiology. 26: 88-96. PMID 14748008 DOI: 10.1002/gepi.10296  0.72
2003 T Cuenco K, Szatkiewicz JP, Feingold E. Recent advances in human quantitative-trait-locus mapping: comparison of methods for selected sibling pairs. American Journal of Human Genetics. 73: 863-73. PMID 12970847 DOI: 10.1086/378589  0.72
2003 Szatkiewicz JP, T Cuenco K, Feingold E. Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs. American Journal of Human Genetics. 73: 874-85. PMID 12970846 DOI: 10.1086/378590  0.72
2003 Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN. Age of onset in hereditary lymphedema. The Journal of Pediatrics. 142: 704-8. PMID 12838201 DOI: 10.1067/mpd.2003.235  0.72
2003 Damcott CM, Feingold E, Moffett SP, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels. Human Genetics. 112: 610-6. PMID 12634920 DOI: 10.1007/s00439-003-0937-1  0.72
2003 Zhang Y, Syed R, Uygar C, Pallos D, Gorry MC, Firatli E, Cortelli JR, VanDyke TE, Hart PS, Feingold E, Hart TC. Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients Genes and Immunity. 4: 22-29. PMID 12595898 DOI: 10.1038/sj.gene.6363900  0.72
2002 Jiang Z, Feingold E, Kochanek S, Clemens PR. Systemic delivery of a high-capacity adenoviral vector expressing mouse CTLA4Ig improves skeletal muscle gene therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 6: 369-76. PMID 12231173 DOI: 10.1006/mthe.2002.0676  0.72
2002 Feingold E. Regression-based quantitative-trait-locus mapping in the 21st century American Journal of Human Genetics. 71: 217-222. PMID 12154779 DOI: 10.1086/341964  0.72
2002 Yu K, Feingold E. Methods for analyzing the spatial distribution of chiasmata during meiosis based on recombination data Biometrics. 58: 369-377. PMID 12071410  0.72
2002 Song KK, Feingold E, Weeks DE. Statistics for nonparametric linkage analysis of X-linked traits in general pedigrees American Journal of Human Genetics. 70: 181-191. PMID 11719901 DOI: 10.1086/338308  0.72
2001 Feingold E. Methods for linkage analysis of quantitative trait loci in humans Theoretical Population Biology. 60: 167-180. PMID 11855951 DOI: 10.1006/tpbi.2001.1545  0.72
2001 Yu K, Feingold E. Estimating the frequency distribution of crossovers during meiosis from recombination data Biometrics. 57: 427-434. PMID 11414566  0.72
2001 Jiang ZL, Reay D, Kreppel F, Gambotto A, Feingold E, Kochanek S, McCarthy SA, Clemens PR. Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle. Molecular Therapy : the Journal of the American Society of Gene Therapy. 3: 892-900. PMID 11407903 DOI: 10.1006/mthe.2001.0331  0.72
2001 Sengul H, Weeks DE, Feingold E. A survey of affected-sibship statistics for nonparametric linkage analysis American Journal of Human Genetics. 69: 179-190. PMID 11404816 DOI: 10.1086/321264  0.72
2001 Peters DG, Kassam AB, Feingold E, Heidrich-O'Hare E, Yonas H, Ferrell RE, Brufsky A. Molecular anatomy of an intracranial aneurysm: coordinated expression of genes involved in wound healing and tissue remodeling. Stroke; a Journal of Cerebral Circulation. 32: 1036-42. PMID 11283408  0.72
2000 Kahsar-Miller M, Azziz R, Feingold E, Witchel SF. A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome Fertility and Sterility. 74: 1237-1240. PMID 11119758 DOI: 10.1016/S0015-0282(00)01620-4  0.72
2000 Feingold E, Song KK, Weeks DE. Comparison of allele-sharing statistics for general pedigrees Genetic Epidemiology. 19. PMID 11055376 DOI: 10.1002/1098-2272(2000)19:1+<::AID-GEPI14>3.0.CO;2-4  0.72
2000 Estop AM, Cieply K, Munne S, Surti U, Wakim A, Feingold E. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies Human Genetics. 106: 517-524. PMID 10914681  0.72
2000 Forrest WF, Feingold E. Composite statistics for QTL mapping with moderately discordant sibling pairs American Journal of Human Genetics. 66: 1642-1660. PMID 10762549 DOI: 10.1086/302897  0.72
2000 Feingold E, Brown AS, Sherman SL. Multipoint estimation of genetic maps for human trisomies with one parent or other partial data. American Journal of Human Genetics. 66: 958-68. PMID 10712210 DOI: 10.1086/302799  0.72
2000 Brown AS, Feingold E, Broman KW, Sherman SL. Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21. Human Molecular Genetics. 9: 515-23. PMID 10699174  0.72
1999 Barmada MM, Aston CE, Feingold E. A simple allele sharing statistic for multiple locus systems Genetic Epidemiology. 17. PMID 10597482  0.72
1999 Estop AM, Cieply KM, Munne S, Feingold E. Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11) Human Genetics. 104: 412-417. PMID 10394934 DOI: 10.1007/s004390050977  0.72
1998 Estop AM, Cieply KM, Wakim A, Feingold E. Meiotic products of two reciprocal translocations studied by multicolor fluorescence in situ hybridization Cytogenetics and Cell Genetics. 83: 193-198. PMID 10072576  0.72
1998 Sun F, Ashley-Koch AE, Durham LK, Feingold E, Halloran ME, Manatunga AK, Sherman SL. Testing for contributions of mitochondrial DNA mutations to complex diseases Genetic Epidemiology. 15: 451-469. PMID 9728889 DOI: 10.1002/(SICI)1098-2272(1998)15:5<451::AID-GEPI2>3.0.CO;2-3  0.72
1997 Cope TC, Sokoloff AJ, Dacko SM, Huot R, Feingold E. Stability of motor-unit force thresholds in the decerebrate cat. Journal of Neurophysiology. 78: 3077-82. PMID 9405527  0.72
1997 Durham LK, Feingold E. Genome scanning for segments shared identical by descent among distant relatives in isolated populations American Journal of Human Genetics. 61: 830-842. PMID 9382093  0.72
1997 Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, et al. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21 Human Molecular Genetics. 6: 1391-1399. PMID 9285774 DOI: 10.1093/hmg/6.9.1391  0.72
1997 Lamb NE, Feingold E, Sherman SL. Estimating meiotic exchange patterns from recombination data: An application to humans Genetics. 146: 1011-1017. PMID 9215904  0.72
1997 Feingold E, Siegmund DO. Strategies for mapping heterogeneous recessive traits by allele-sharing methods American Journal of Human Genetics. 60: 965-978. PMID 9106544  0.72
1996 Nolin SL, Lewis FA, Ye LL, Houck GE, Glicksman AE, Limprasert P, Li SY, Zhong N, Ashley AE, Feingold E, Sherman SL, Ted Brown W. Familial transmission of the FMR1 CGG repeat American Journal of Human Genetics. 59: 1252-1261. PMID 8940270  0.72
1996 Griffin DK, Abruzzo MA, Millie EA, Feingold E, Hassold TJ. Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome. American Journal of Human Genetics. 59: 1108-13. PMID 8900240  0.72
1996 Lamb NE, Feingold E, Sherman SL. Statistical models for trisomic phenotypes American Journal of Human Genetics. 58: 201-212. PMID 8554057  0.72
1995 Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ. Non-disjunction in human sperm: Evidence for an effect of increasing paternal age Human Molecular Genetics. 4: 2227-2232. PMID 8634691 DOI: 10.1093/hmg/4.12.2227  0.72
1995 Feingold E, Lamb NE, Sherman SL. Methods for genetic linkage analysis using trisomies American Journal of Human Genetics. 56: 475-483. PMID 7847384  0.72
1993 Feingold E, Brown PO, Siegmund D. Gaussian models for genetic linkage analysis using complete high- resolution maps of identity by descent American Journal of Human Genetics. 53: 234-251. PMID 8317489  0.72
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