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JCO Precision Oncology|May 26, 2021
NTRK Fusions Identified in Pediatric Tumors: The Frequency, Fusion Partners, and Clinical OutcomeXiaonan Zhao, Chelsea Kotch, Elizabeth Fox, et al.
The Journal of Molecular Diagnostics : JMD|December 16, 2023
Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-Designed Next-Generation Sequencing PanelFumin Lin, Kajia Cao, Fengqi Chang, et al.
Cold Spring Harbor Molecular Case Studies|March 2, 2022
A novel TP53 tandem duplication in a child with Li-Fraumeni syndromeFeng Xu, Erfan Aref-Eshghi, Jinhua Wu, et al.
Blood Advances|November 19, 2019
CAR T-cell therapy is effective for CD19-dim B-lymphoblastic leukemia but is impacted by prior blinatumomab therapyVinodh Pillai, Kavitha Muralidharan, Wenzhao Meng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2018
Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic dataKristin McDonald Gibson, Addie Nesbitt, Kajia Cao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic dataKristin McDonald Gibson, Addie Nesbitt, Kajia Cao, et al.
JAMA Oncology|August 19, 2021
Association of Combined Focal 22q11.22 Deletion and IKZF1 Alterations With Outcomes in Childhood Acute Lymphoblastic LeukemiaDavid Spencer Mangum, Julia A Meyer, Clinton C Mason, et al.
The Journal of Pediatrics|July 20, 2023
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic YieldNobuko Yamamoto, Jorune Balciuniene, Tiffiney Hartman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2018
Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing lossSarah Sheppard, Sawona Biswas, Mindy H Li, et al.
European Journal of Human Genetics : EJHG|January 5, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicingYoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth, et al.
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