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Denise Batista

Johns Hopkins University
Kennedy Krieger Institute
Johns Hopkins University School of Medicine

51

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Genomic analysis identifies frequent deletions of Dystrophin in olfactory neuroblastoma

2018 Nature Communications
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Loss of the mismatched human leukocyte antigen haplotype in two acute myelogenous leukemia relapses after haploidentical bone marrow transplantation with post-transplantation cyclophosphamide

2016 Leukemia
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NUP98-PHF23 fusion is recurrent in acute myeloid leukemia and shares gene expression signature of leukemic stem cells

2016 Leukemia Research
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The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

2015 Case reports in genetics
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Impact of Hypomethylating Agent Therapy in Myelodysplastic Syndromes with Chromosome 3 Abnormalities

2015 Blood
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Genetic profiling by single-nucleotide polymorphism-based array analysis defines three distinct subtypes of orbital meningioma

2015 Brain Pathology
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Mutations in FARS2 and non-fatal mitochondrial dysfunction in two siblings

2015 American Journal of Medical Genetics Part A
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An atypical 0.73 MB microduplication of 22q11.21 and a novel SALL4 missense mutation associated with thumb agenesis and radioulnar synostosis

2015 American Journal of Medical Genetics Part A
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Mucoepidermoid Carcinoma Does Not Harbor Transcriptionally Active High Risk Human Papillomavirus Even in the Absence of the MAML2 Translocation

2014 Head and Neck Pathology
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Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum

2014 Developmental Medicine & Child Neurology
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