Margaret G. Ehm - Publications

North Carolina State University, Raleigh, NC 
Biostatistics Biology, Pathology

39 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
2015 Lo Y, Kang HM, Nelson MR, Othman MI, Chissoe SL, Ehm MG, Abecasis GR, Zöllner S. Comparing variant calling algorithms for target-exon sequencing in a large sample. Bmc Bioinformatics. 16: 75. PMID 25884587 DOI: 10.1186/s12859-015-0489-0  0.52
2015 Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, Dauriz M, Hivert MF, Raghavan S, Lipovich L, Hidalgo B, Fox K, Huffman JE, An P, Lu Y, ... ... Ehm MG, et al. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications. 6: 5897. PMID 25631608 DOI: 10.1038/ncomms6897  0.52
2014 Waterworth DM, Li L, Scott R, Warren L, Gillson C, Aponte J, Sarov-Blat L, Sprecher D, Dupuis J, Reiner A, Psaty BM, Tracy RP, Lin H, McPherson R, Chissoe S, ... ... Ehm MG, et al. A low-frequency variant in MAPK14 provides mechanistic evidence of a link with myeloperoxidase: a prognostic cardiovascular risk marker. Journal of the American Heart Association. 3. PMID 25164947 DOI: 10.1161/JAHA.114.001074  0.52
2014 Zawistowski M, Reppell M, Wegmann D, St Jean PL, Ehm MG, Nelson MR, Novembre J, Zöllner S. Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests. European Journal of Human Genetics : Ejhg. 22: 1137-44. PMID 24398795 DOI: 10.1038/ejhg.2013.297  0.52
2014 Zheng X, Shen J, Cox C, Wakefield JC, Ehm MG, Nelson MR, Weir BS. HIBAG--HLA genotype imputation with attribute bagging. The Pharmacogenomics Journal. 14: 192-200. PMID 23712092 DOI: 10.1038/tpj.2013.18  0.52
2013 Schaibley VM, Zawistowski M, Wegmann D, Ehm MG, Nelson MR, St Jean PL, Abecasis GR, Novembre J, Zöllner S, Li JZ. The influence of genomic context on mutation patterns in the human genome inferred from rare variants. Genome Research. 23: 1974-84. PMID 23990608 DOI: 10.1101/gr.154971.113  0.52
2013 Hu Y, Li L, Ehm MG, Bing N, Song K, Nelson MR, Talmud PJ, Hingorani AD, Kumari M, Kivimäki M, Xu CF, Waterworth DM, Whittaker JC, Abecasis GR, Spino C, et al. The benefits of using genetic information to design prevention trials. American Journal of Human Genetics. 92: 547-57. PMID 23541341 DOI: 10.1016/j.ajhg.2013.03.003  0.52
2012 Nelson MR, Wegmann D, Ehm MG, Kessner D, St Jean P, Verzilli C, Shen J, Tang Z, Bacanu SA, Fraser D, Warren L, Aponte J, Zawistowski M, Liu X, Zhang H, et al. An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science (New York, N.Y.). 337: 100-4. PMID 22604722 DOI: 10.1126/science.1217876  0.52
2012 Rubio JP, Topp S, Warren L, St Jean PL, Wegmann D, Kessner D, Novembre J, Shen J, Fraser D, Aponte J, Nangle K, Cardon LR, Ehm MG, Chissoe SL, Whittaker JC, et al. Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe. Human Mutation. 33: 1087-98. PMID 22415848 DOI: 10.1002/humu.22075  0.52
2012 Warren LL, Li L, Nelson MR, Ehm MG, Shen J, Fraser DJ, Aponte JL, Nangle KL, Slater AJ, Woollard PM, Hall MD, Topp SD, Yuan X, Cardon LR, Chissoe SL, et al. Deep resequencing unveils genetic architecture of ADIPOQ and identifies a novel low-frequency variant strongly associated with adiponectin variation. Diabetes. 61: 1297-301. PMID 22403302 DOI: 10.2337/db11-0985  0.52
2012 Cruchaga C, Haller G, Chakraverty S, Mayo K, Vallania FL, Mitra RD, Faber K, Williamson J, Bird T, Diaz-Arrastia R, Foroud TM, Boeve BF, Graff-Radford NR, St Jean P, Lawson M, ... Ehm MG, et al. Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families. Plos One. 7: e31039. PMID 22312439 DOI: 10.1371/journal.pone.0031039  0.52
2011 Li L, Li Y, Browning SR, Browning BL, Slater AJ, Kong X, Aponte JL, Mooser VE, Chissoe SL, Whittaker JC, Nelson MR, Ehm MG. Performance of genotype imputation for rare variants identified in exons and flanking regions of genes Plos One. 6. PMID 21949800 DOI: 10.1371/journal.pone.0024945  0.52
2009 Nelson MR, Bacanu SA, Mosteller M, Li L, Bowman CE, Roses AD, Lai EH, Ehm MG. Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions. The Pharmacogenomics Journal. 9: 23-33. PMID 18301416 DOI: 10.1038/tpj.2008.4  0.52
2008 Nelson MR, Bryc K, King KS, Indap A, Boyko AR, Novembre J, Briley LP, Maruyama Y, Waterworth DM, Waeber G, Vollenweider P, Oksenberg JR, Hauser SL, Stirnadel HA, Kooner JS, ... ... Ehm MG, et al. The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research. American Journal of Human Genetics. 83: 347-58. PMID 18760391 DOI: 10.1016/j.ajhg.2008.08.005  0.52
2008 Bacanu SA, Nelson MR, Ehm MG. Comparison of association methods for dense marker data. Genetic Epidemiology. 32: 791-9. PMID 18551558 DOI: 10.1002/gepi.20347  0.52
2008 Li H, Wetten S, Li L, St Jean PL, Upmanyu R, Surh L, Hosford D, Barnes MR, Briley JD, Borrie M, Coletta N, Delisle R, Dhalla D, Ehm MG, Feldman HH, et al. Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. Archives of Neurology. 65: 45-53. PMID 17998437 DOI: 10.1001/archneurol.2007.3  0.52
2007 Roses AD, St Jean PL, Ehm MG. Use of whole-genome association scans in disease gene identification, drug discovery and development. Idrugs : the Investigational Drugs Journal. 10: 797-804. PMID 17968762  0.52
2006 Zaykin DV, Meng Z, Ehm MG. Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping method. American Journal of Human Genetics. 78: 737-46. PMID 16642430 DOI: 10.1086/503710  0.52
2006 Stankovich J, Cox CJ, Tan RB, Montgomery DS, Huxtable SJ, Rubio JP, Ehm MG, Johnson L, Butzkueven H, Kilpatrick TJ, Speed TP, Roses AD, Bahlo M, Foote SJ. On the utility of data from the International HapMap Project for Australian association studies. Human Genetics. 119: 220-2. PMID 16404587 DOI: 10.1007/s00439-005-0120-y  0.52
2005 Ehm MG, Nelson MR, Spurr NK. Guidelines for conducting and reporting whole genome/large-scale association studies. Human Molecular Genetics. 14: 2485-8. PMID 16037068 DOI: 10.1093/hmg/ddi252  0.52
2005 Browning SR, Briley JD, Briley LP, Chandra G, Charnecki JH, Ehm MG, Johansson KA, Jones BJ, Karter AJ, Yarnall DP, Wagner MJ. Case-control single-marker and haplotypic association analysis of pedigree data. Genetic Epidemiology. 28: 110-22. PMID 15578751 DOI: 10.1002/gepi.20051  0.52
2004 Browning BL, Brashear DL, Butler AA, Cyr DD, Harris EC, Nelsen AJ, Yarnall DP, Ehm MG, Wagner MJ. Linkage analysis using single nucleotide polymorphisms. Human Heredity. 57: 220-7. PMID 15583428 DOI: 10.1159/000081449  0.52
2004 Nielsen DM, Ehm MG, Zaykin DV, Weir BS. Effect of two- and three-locus linkage disequilibrium on the power to detect marker/phenotype associations. Genetics. 168: 1029-40. PMID 15514073 DOI: 10.1534/genetics.103.022335  0.52
2003 Meng Z, Zaykin DV, Xu CF, Wagner M, Ehm MG. Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes. American Journal of Human Genetics. 73: 115-30. PMID 12796855 DOI: 10.1086/376561  0.52
2003 Hsueh WC, St Jean PL, Mitchell BD, Pollin TI, Knowler WC, Ehm MG, Bell CJ, Sakul H, Wagner MJ, Burns DK, Shuldiner AR. Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24. Diabetes. 52: 550-7. PMID 12540634 DOI: 10.2337/diabetes.52.2.550  0.52
2002 Hosking LK, Boyd PR, Xu CF, Nissum M, Cantone K, Purvis IJ, Khakhar R, Barnes MR, Liberwirth U, Hagen-Mann K, Ehm MG, Riley JH. Linkage disequilibrium mapping identifies a 390 kb region associated with CYP2D6 poor drug metabolising activity Pharmacogenomics Journal. 2: 165-175. PMID 12082588 DOI: 10.1038/sj.tpj.6500096  0.52
2002 Zaykin DV, Westfall PH, Young SS, Karnoub MA, Wagner MJ, Ehm MG. Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals. Human Heredity. 53: 79-91. PMID 12037407 DOI: 10.1159/000057986  0.52
2001 Meng Z, Zaykin DV, Karnoub MC, Sreekumar GP, St Jean PL, Ehm MG. Identifying susceptibility genes using linkage and linkage disequilibrium analysis in large pedigrees. Genetic Epidemiology. 21: S453-8. PMID 11793718  0.52
2001 Jones KW, Ehm MG, Pericak-Vance MA, Haines JL, Boyd PR, Peroutka SJ. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus. Genomics. 78: 150-4. PMID 11735221 DOI: 10.1006/geno.2001.6665  0.52
2001 Hsueh WC, Mitchell BD, Schneider JL, St Jean PL, Pollin TI, Ehm MG, Wagner MJ, Burns DK, Sakul H, Bell CJ, Shuldiner AR. Genome-wide scan of obesity in the Old Order Amish. The Journal of Clinical Endocrinology and Metabolism. 86: 1199-205. PMID 11238509 DOI: 10.1210/jcem.86.3.7358  0.52
2000 Hsueh WC, Mitchell BD, Aburomia R, Pollin T, Sakul H, Gelder Ehm M, Michelsen BK, Wagner MJ, St Jean PL, Knowler WC, Burns DK, Bell CJ, Shuldiner AR. Diabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study. Diabetes Care. 23: 595-601. PMID 10834415  0.52
2000 Ehm MG, Karnoub MC, Sakul H, Gottschalk K, Holt DC, Weber JL, Vaske D, Briley D, Briley L, Kopf J, McMillen P, Nguyen Q, Reisman M, Lai EH, Joslyn G, et al. Genomewide search for type 2 diabetes susceptibility genes in four American populations. American Journal of Human Genetics. 66: 1871-81. PMID 10793009 DOI: 10.1086/302950  0.52
1999 Ehm MG, Karnoub MC, St. Jean P. Search for susceptibility genes, gene(x)gene interactions, and gene(x)environment interactions utilizing nonparametric linkage analysis Genetic Epidemiology. 17. PMID 10597489  0.52
1998 Nielsen DM, Ehm MG, Weir BS. Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus. American Journal of Human Genetics. 63: 1531-40. PMID 9867708 DOI: 10.1086/302114  0.52
1998 Hanson RL, Ehm MG, Pettitt DJ, Prochazka M, Thompson DB, Timberlake D, Foroud T, Kobes S, Baier L, Burns DK, Almasy L, Blangero J, Garvey WT, Bennett PH, Knowler WC. An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians. American Journal of Human Genetics. 63: 1130-8. PMID 9758619 DOI: 10.1086/302061  0.52
1998 Pratley RE, Thompson DB, Prochazka M, Baier L, Mott D, Ravussin E, Sakul H, Ehm MG, Burns DK, Foroud T, Garvey WT, Hanson RL, Knowler WC, Bennett PH, Bogardus C. An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians. The Journal of Clinical Investigation. 101: 1757-64. PMID 9541507 DOI: 10.1172/JCI1850  0.52
1998 Norman RA, Tataranni PA, Pratley R, Thompson DB, Hanson RL, Prochazka M, Baier L, Ehm MG, Sakul H, Foroud T, Garvey WT, Burns D, Knowler WC, Bennett PH, Bogardus C, et al. Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians American Journal of Human Genetics. 62: 659-668. PMID 9497255 DOI: 10.1086/301758  0.52
1998 Ehm MG, Wagner M. A test statistic to detect errors in sib-pair relationships American Journal of Human Genetics. 62: 181-188. PMID 9443861 DOI: 10.1086/301668  0.52
1996 Ehm MG, Kimmel M, Cottingham RW. Error detection for genetic data, using likelihood methods American Journal of Human Genetics. 58: 225-234. PMID 8554060  0.52
Show low-probability matches.