Predicting functionally important SNP classes based on negative selection

Por Levenstien, Mark A, Klein, Robert J
Publicado em 2011

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

Por Levenstien, Mark A, Yang, Yaning, Ott, Jürg
Publicado em 2003

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

Por Levenstien, Mark A, Ott, Jürg, Gordon, Derek
Publicado em 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...

Por Barral, Sandra, Haynes, Chad, Levenstien, Mark A, Gordon, Derek
Publicado em 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

Por Sen Souvik, Levenstien Mark A, Dutra Ana, Peddareddygari Leema, Grewal Raji P
Publicado em 2009-07-01

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

Por Finch Stephen J, Levenstien Mark A, Haynes Chad, Edwards Brian J, Gordon Derek
Publicado em 2005-04-01

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

Por Edwards, Brian J, Haynes, Chad, Levenstien, Mark A, Finch, Stephen J, Gordon, Derek
Publicado em 2005

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

Por Peddareddygari, Leema Reddy, Dutra, Ana Virginia, Levenstien, Mark A, Sen, Souvik, Grewal, Raji P
Publicado em 2009

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

Por 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.
Publicado no 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...

Por 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.
Publicado no Mol Genet Metab (2001)