Steve Steinberg

Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders

Melissa L. Slawecki, Gabriele Dodt, Steve Steinberg et al. · Journal of Cell Science · 1995 · 120 citations

Life Sciences, Molecular Genetics, Pathobiology +16

Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3

Brandon Itzkovitz, Sarn Jiralerspong, Graeme Nimmo et al. · Human Mutation · 2011 · 81 citations

Life Sciences, Genetics, Molecular Genetics +17

Severe Preeclampsia with Fulminant and Extreme Elevation of Aspartate Aminotransferase and Lactate Dehydrogenase Levels: High Risk for Maternal Death

Val Catanzarite, Steve Steinberg, Coleman Mosley et al. · American Journal of Perinatology · 1995 · 45 citations

Public Health, Hematology, Obstetrics +15

Genotype–phenotype correlation of contiguous gene deletions of <i><scp>SLC6A8</scp>, <scp>BCAP31</scp></i> and <scp><i>ABCD1</i></scp>

Jiddeke M. van de Kamp, Abdellatif Errami, M. Howidi et al. · Clinical Genetics · 2014 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Biochemical analysis of cultured chorionic villi for the prenatal diagnosis of peroxisomal disorders: biochemical thresholds and molecular sensitivity for maternal cell contamination detection

Steve Steinberg, Ann B. Moser, Garry R. Cutting · Journal of Medical Genetics · 2005 · 19 citations · Full text

Medicine, Genetics, Molecular Genetics +17