Daniel D. Kinnamon, Ph.D. - Publications
Affiliations: | 2013 | Human Genetics and Genomes | University of Miami, Coral Gables, FL |
Area:
Genetics, Biostatistics Biology, Epidemiology, Bioinformatics BiologyYear | Citation | Score | |||
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2017 | Chung RH, Kinnamon DD, Martin ER. Single Marker Family-Based Association Analysis Conditional on Parental Information. Methods in Molecular Biology (Clifton, N.J.). 1666: 391-407. PMID 28980256 DOI: 10.1007/978-1-4939-7274-6_19 | 0.435 | |||
2014 | Kinnamon DD, Martin ER. Valid Monte Carlo permutation tests for genetic case-control studies with missing genotypes. Genetic Epidemiology. 38: 325-44. PMID 24723341 DOI: 10.1002/Gepi.21805 | 0.484 | |||
2013 | Nuytemans K, Bademci G, Inchausti V, Dressen A, Kinnamon DD, Mehta A, Wang L, Züchner S, Beecham GW, Martin ER, Scott WK, Vance JM. Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease. Neurology. 80: 982-9. PMID 23408866 DOI: 10.1212/Wnl.0B013E31828727D4 | 0.385 | |||
2012 | Kinnamon DD, Hershberger RE, Martin ER. Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants. Plos One. 7: e30238. PMID 22363423 DOI: 10.1371/Journal.Pone.0030238 | 0.511 | |||
2010 | Martin ER, Kinnamon DD, Schmidt MA, Powell EH, Zuchner S, Morris RW. SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies. Bioinformatics (Oxford, England). 26: 2803-10. PMID 20861027 DOI: 10.1093/Bioinformatics/Btq526 | 0.427 | |||
2010 | Rampersaud E, Kinnamon DD, Hamilton K, Khuri S, Hershberger RE, Martin ER. Common susceptibility variants examined for association with dilated cardiomyopathy. Annals of Human Genetics. 74: 110-6. PMID 20201937 DOI: 10.1111/J.1469-1809.2010.00566.X | 0.486 | |||
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