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Gary Steel

Johns Hopkins University School of Medicine
Johns Hopkins University

34

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2430

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Homozygous deletion in MYL9 expands the molecular basis of megacystis–microcolon–intestinal hypoperistalsis syndrome

2018 European Journal of Human Genetics
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Supplementary Material for: Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic Disorders

2016
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Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic Disorders

2016
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At least two mutant alleles of ornithine 6-aminotransferase cause gyrate atrophy of the choroid and retina in Finns (RNase A protection/polymerase chain reaction/hyperornithinemia/chorioretinal degeneration/missense mutation)

2016
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An anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia secondary to lamin B receptor (LBR) gene mutations: Further definition of the phenotypic heterogeneity of LBR-bone dysplasias

2015 American Journal of Medical Genetics Part A
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Type I hyperprolinemia: Genotype/phenotype correlations

2010 Human Mutation
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Implicates Neuregulin 3 in Schizophrenia

2009
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Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia

2009 American Journal of Human Genetics
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PRODH variants and risk for schizophrenia.

2008 Amino Acids
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Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosis

2007 Molecular and Cellular Biochemistry
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Citations (91)