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Roger A. Schultz

University of Texas Southwestern Medical Center
PerkinElmer

103

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23780

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44. Reevaluation of copy number variant (CNV) classifications in the clinical laboratory setting: challenges, insights, and experiences with a laboratory-initiated process

2021 Cancer Genetics and Cytogenetics
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Diagnostic Utility of Microarray Testing in Pregnancy Loss

2016 Obstetrical & Gynecological Survey
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Experience Using a Rapid Assay for Aneuploidy and Microdeletion/Microduplication Detection in over 2,900 Prenatal Specimens

2014 Fetal Diagnosis and Therapy
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Cryptic chromosome abnormalities in a patient with mixed phenotype acute leukemia.

2014 Leukemia & Lymphoma
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The use of cytogenetic microarrays in myelodysplastic syndrome characterization.

2013 Methods of Molecular Biology
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Microarray Analysis of Formalin-Fixed Paraffin-Embedded (FFPET) and Frozen (FZT) Uveal Melanoma Detects Clinically Relevant Abnormalities, Including Chromosome 3 Loss of Heterozygosity

2013 Cancer Genetics and Cytogenetics
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Characterization of a case of follicular lymphoma transformed into B-lymphoblastic leukemia

2013 Molecular Cytogenetics
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Patient with t(4;12)(q11;p13) with therapy-related MDS and known history of stage II metastatic colorectal cancer

2013 Atlas of genetics and cytogenetics in oncology and haematology
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MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways

2013 Neurogenetics
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Detection of Copy Number Alterations in DNA Repair/Repair-Related Genes for a Diversity of Hematologic Malignancies Identifies Disease-Specific Biomarkers of Potential Clinical Relevance.

2012 Blood
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