Mark A. Levenstien

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

Margaret J. Kovach, Brook Waggoner, Suzanne M. Leal et al. · Molecular Genetics and Metabolism · 2001 · 197 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +12

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

Brian J. Edwards, Chad Haynes, Mark A. Levenstien et al. · BMC Genetics · 2005 · 109 citations · Full text

ERRORS AND LINKAGE DISEQUILIBRIUM INTERACT MULTIPLICATIVELY WHEN COMPUTING SAMPLE SIZES FOR GENETIC CASE-CONTROL ASSOCIATION STUDIES

Derek Gordon, Mark A. Levenstien, Stephen J. Finch et al. · 2002 · 92 citations

Developmental Dysplasia of the Hip: Linkage Mapping and Whole Exome Sequencing Identify a Shared Variant in <i>CX</i> <i>3</i> <i>CR</i> <i>1</i> in All Affected Members of a Large Multigeneration Family

George Feldman, Javad Parvizi, Mark A. Levenstien et al. · Journal of Bone and Mineral Research · 2013 · 66 citations · Full text

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

Dmitri Proudnikov, K. Steven LaForge, Heather Hofflich et al. · Pharmacogenetics and Genomics · 2006 · 60 citations