Mark A. Levenstien

发表

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

Yaning Yang, Jürg Ott, Mark A. Levenstien, 2003, BMC Bioinformatics.

Errors and Linkage Disequilibrium Interact Multiplicatively When Computing Sample Sizes for Genetic Case-Control Association Studies

Derek Gordon, Stephen J. Finch, Jürg Ott, 2002, Pacific Symposium on Biocomputing.

Predicting functionally important SNP classes based on negative selection

Robert J. Klein, Mark A. Levenstien, R. Klein, 2011, BMC Bioinformatics.

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

Chad Haynes, Stephen J Finch, Derek Gordon, 2005, BMC Genetics.

Genetic Analysis of a Large Family with Migraine, Vertigo, and Motion Sickness

Mark A. Levenstien, P. Kramer, R. Grewal, 2019, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

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

Mark A. Levenstien, S. Sen, R. Grewal, 2009, BMC neurology.

Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: a comparison of molecular and statistically estimated haplotypes

Mark A. Levenstien, J. Ott, D. Gordon, 2006, Pharmacogenetics and genomics.

Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics

Mark A. Levenstien, J. Ott, J. Hoh, 2001, Genetic epidemiology.

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

Mark A. Levenstien, J. Ott, D. Gordon, 2006, PLoS genetics.

Haplotype-Based Association Studies: Approaches to Current Challenges

Mark A. Levenstien, M. Levenstien, 2007 .

Association of Angiotensinogen Gene Polymorphisms with Essential Hypertension in African-Americans and Caucasians

Mark A. Levenstien, J. Ott, J. Hoh, 2005, Human Heredity.

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 frontotemporal dementia.

Mark A. Levenstien, S. Leal, A. Pestronk, 2001, Molecular genetics and metabolism.

Analysis of the interleukin-1 receptor antagonist gene variable number tandem repeats in ischemic stroke.

Mark A. Levenstien, S. Sen, R. Grewal, 2014, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14.

Mark A. Levenstien, J. Ott, S. Leal, 2000, JAMA.

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 statistics

Mark A. Levenstien, C. Haynes, D. Gordon, 2005, BMC Genetics.

Developmental Dysplasia of the Hip: Linkage Mapping and Whole Exome Sequencing Identify a Shared Variant in CX3CR1 in All Affected Members of a Large Multigeneration Family

Mark A. Levenstien, M. Devoto, J. Parvizi, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Integration of Linkage Analysis and Next-Generation Sequencing Data

Mark A. Levenstien, M. Devoto, F. Lantieri, 2012 .