Margaret G. Ehm

North Carolina State University, Raleigh, NC 
Biostatistics Biology, Pathology
"Margaret Ehm"
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Lo Y, Kang HM, Nelson MR, et al. (2015) Comparing variant calling algorithms for target-exon sequencing in a large sample. Bmc Bioinformatics. 16: 75
Wessel J, Chu AY, Willems SM, et al. (2015) Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications. 6: 5897
Waterworth DM, Li L, Scott R, et al. (2014) 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
Zawistowski M, Reppell M, Wegmann D, et al. (2014) Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests. European Journal of Human Genetics : Ejhg. 22: 1137-44
Zheng X, Shen J, Cox C, et al. (2014) HIBAG--HLA genotype imputation with attribute bagging. The Pharmacogenomics Journal. 14: 192-200
Schaibley VM, Zawistowski M, Wegmann D, et al. (2013) The influence of genomic context on mutation patterns in the human genome inferred from rare variants. Genome Research. 23: 1974-84
Hu Y, Li L, Ehm MG, et al. (2013) The benefits of using genetic information to design prevention trials. American Journal of Human Genetics. 92: 547-57
Nelson MR, Wegmann D, Ehm MG, et al. (2012) An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science (New York, N.Y.). 337: 100-4
Rubio JP, Topp S, Warren L, et al. (2012) 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
Warren LL, Li L, Nelson MR, et al. (2012) Deep resequencing unveils genetic architecture of ADIPOQ and identifies a novel low-frequency variant strongly associated with adiponectin variation. Diabetes. 61: 1297-301
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