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Stuart Schwartz

Case Western Reserve University
University of Maryland, Baltimore
Research Triangle Park

219

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12227

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Clinical significance and mechanisms associated with segmental UPD.

2021 Molecular Cytogenetics
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Partnering with patients to get better outcomes with chimeric antigen receptor T-cell therapy: towards engagement of patients in early phase trials

2020 Research Involvement and Engagement
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Whole genome SNP arrays for best practice for detection of diagnostic, prognostic and therapy related copy number changes and copy neutral-loss of heterozygosity across solid tumors and hematologic malignancies.

2020 Journal of Clinical Oncology
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Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastoma

2020
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Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant NIPT results.

2020 American Journal of Medical Genetics Part A
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43. Considerations for implementation of the new ASCO/CAP guidelines for HER2 testing in the clinical laboratory

2019 Cancer Genetics and Cytogenetics
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Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN

2018 American Journal of Medical Genetics Part A
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80: Chromosomal microarray analysis of over 45,000 prenatal patients: Significance and efficacy as a first tier diagnostic test

2018 American Journal of Obstetrics and Gynecology
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Clinical experience of laboratory follow‐up with noninvasive prenatal testing using cell‐free DNA and positive microdeletion results in 349 cases

2018 Prenatal Diagnosis
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35. Runs of homozygosity (ROH) reveal that segmental-UPD is associated with the repair of genomic imbalance

2018 Cancer Genetics and Cytogenetics
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