Predicting functionally important SNP classes based on negative selection

由 Levenstien, Mark A, Klein, Robert J
出版 2011

Statistical significance for hierarchical clustering in genetic association and microarray expression studies

由 Levenstien, Mark A, Yang, Yaning, Ott, Jürg
出版 2003

Are Molecular Haplotypes Worth the Time and Expense? A Cost-Effective Method for Applying Molecular Haplotypes

由 Levenstien, Mark A, Ott, Jürg, Gordon, Derek
出版 2006

Precision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae sta...

由 Barral, Sandra, Haynes, Chad, Levenstien, Mark A, Gordon, Derek
出版 2005

An analysis of <it>Methylenetetrahydrofolate reductase </it>and <it>Glutathione S-transferase omega-1 genes </it>as modifiers of the cerebral response to ischemia

由 Sen Souvik, Levenstien Mark A, Dutra Ana, Peddareddygari Leema, Grewal Raji P
出版 2009-07-01

Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies

由 Finch Stephen J, Levenstien Mark A, Haynes Chad, Edwards Brian J, Gordon Derek
出版 2005-04-01

Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies

由 Edwards, Brian J, Haynes, Chad, Levenstien, Mark A, Finch, Stephen J, Gordon, Derek
出版 2005

An analysis of Methylenetetrahydrofolate reductase and Glutathione S-transferase omega-1 genes as modifiers of the cerebral response to ischemia

由 Peddareddygari, Leema Reddy, Dutra, Ana Virginia, Levenstien, Mark A, Sen, Souvik, Grewal, Raji P
出版 2009

Mapping of a Gene for Severe Pediatric Gastroesophageal Reflux to Chromosome 13q14

由 Hu, Fen Ze, Preston, Robert A., Post, J. Christopher, White, Gregory J., Kikuchi, Lee W., Wang, Xue, Leal, Suzanne M., Levenstien, Mark A., Ott, Jurg, Self, Thomas W., Allen, Gregory, Stiffler, Richelle S., McGraw, Caroline, Pulsifer-Anderson, Elizabeth A., Ehrlich, Garth D.
發表在 JAMA (2000)

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Fronto...

由 Kovach, Margaret J., Waggoner, Brook, Leal, Suzanne M., Gelber, David, Khardori, Romesh, Levenstien, Mark A., Shanks, Christy A., Gregg, Gregory, Al-Lozi, Muhammad T., Miller, Timothy, Rakowicz, Wojtek, Lopate, Glenn, Florence, Juliane, Glosser, Guila, Simmons, Zachary, Morris, John C., Whyte, Michael P., Pestronk, Alan, Kimonis, Virginia E.
發表在 Mol Genet Metab (2001)