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Author Details
Full Name
Minjie Luo
Affiliation
Children's Hospital of Philadelphia
ORCID
Career Start Year
2004
Papers
61
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37473993
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield.
J Pediatr
2023
37473993
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield.
J Pediatr
2023
37250588
Relationship between Monoclonal Gammopathy of undetermined significance and multiple myeloma via online database analysis.
Pak J Med Sci
2023
37170750
Maximizing the Detection of Copy Number Variants in the Highly Homologous Deafness-Infertility Syndrome Locus in Standard-of-care Testing.
Clin Chem
2023
37250588
Relationship between Monoclonal Gammopathy of undetermined significance and multiple myeloma via online database analysis.
Pak J Med Sci
2023
37170750
Maximizing the Detection of Copy Number Variants in the Highly Homologous Deafness-Infertility Syndrome Locus in Standard-of-care Testing.
Clin Chem
2023
35232817
A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndrome.
Cold Spring Harb Mol Case Stud
2022
35836290
Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma.
Acta Neuropathol Commun
2022
36086952
Long-read sequencing for molecular diagnostics in constitutional genetic disorders.
Hum Mutat
2022
35696422
Deletion C-terminal thioesterase abolishes melanin biosynthesis, affects metabolism and reduces the pathogenesis of Fonsecaea monophora.
PLoS Negl Trop Dis
2022
35870179
Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss.
Hum Mutat
2022
35865311
Case Report: Reversible Hyperglycemia Following Rapamycin Treatment for Atypical Choroid Plexus Papilloma in an Infant.
Front Endocrinol (Lausanne)
2022
35857506
ZMYND8 is a master regulator of 27-hydroxycholesterol that promotes tumorigenicity of breast cancer stem cells.
Sci Adv
2022
35777130
IL-1R1 blockade attenuates liver injury through inhibiting the recruitment of myeloid-derived suppressor cells in sepsis.
Biochem Biophys Res Commun
2022
35232817
A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndrome.
Cold Spring Harb Mol Case Stud
2022
35065284
Molecular Diagnostic Outcomes from 700 Cases: What Can We Learn from a Retrospective Analysis of Clinical Exome Sequencing?
J Mol Diagn
2022
35836290
Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma.
Acta Neuropathol Commun
2022
35857506
ZMYND8 is a master regulator of 27-hydroxycholesterol that promotes tumorigenicity of breast cancer stem cells.
Sci Adv
2022
35696422
Deletion C-terminal thioesterase abolishes melanin biosynthesis, affects metabolism and reduces the pathogenesis of Fonsecaea monophora.
PLoS Negl Trop Dis
2022
35777130
IL-1R1 blockade attenuates liver injury through inhibiting the recruitment of myeloid-derived suppressor cells in sepsis.
Biochem Biophys Res Commun
2022
35870179
Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss.
Hum Mutat
2022
35865311
Case Report: Reversible Hyperglycemia Following Rapamycin Treatment for Atypical Choroid Plexus Papilloma in an Infant.
Front Endocrinol (Lausanne)
2022
36086952
Long-read sequencing for molecular diagnostics in constitutional genetic disorders.
Hum Mutat
2022
35065284
Molecular Diagnostic Outcomes from 700 Cases: What Can We Learn from a Retrospective Analysis of Clinical Exome Sequencing?
J Mol Diagn
2022
32681571
Congenital tumors of the central nervous system: an institutional review of 64 cases with emphasis on tumors with unique histologic and molecular characteristics.
Brain Pathol
2021
34111299
Audiologic Phenotype and Progression in Pediatric STRC-Related Autosomal Recessive Hearing Loss.
Laryngoscope
2021
33832921
Clinical impact of genomic characterization of 15 patients with acute megakaryoblastic leukemia-related malignancies.
Cold Spring Harb Mol Case Stud
2021
33775353
Circ-SKA3 upregulates ID3 expression by decoying miR-326 to accelerate the development of medulloblastoma.
J Clin Neurosci
2021
34036219
NTRK Fusions Identified in Pediatric Tumors: The Frequency, Fusion Partners, and Clinical Outcome.
JCO Precis Oncol
2021
33496739
Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.
Blood Adv
2021
32681571
Congenital tumors of the central nervous system: an institutional review of 64 cases with emphasis on tumors with unique histologic and molecular characteristics.
Brain Pathol
2021
33398081
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing.
Eur J Hum Genet
2021
34410295
Association of Combined Focal 22q11.22 Deletion and IKZF1 Alterations With Outcomes in Childhood Acute Lymphoblastic Leukemia.
JAMA Oncol
2021
33832921
Clinical impact of genomic characterization of 15 patients with acute megakaryoblastic leukemia-related malignancies.
Cold Spring Harb Mol Case Stud
2021
33775353
Circ-SKA3 upregulates ID3 expression by decoying miR-326 to accelerate the development of medulloblastoma.
J Clin Neurosci
2021
33496739
Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.
Blood Adv
2021
34410295
Association of Combined Focal 22q11.22 Deletion and IKZF1 Alterations With Outcomes in Childhood Acute Lymphoblastic Leukemia.
JAMA Oncol
2021
34036219
NTRK Fusions Identified in Pediatric Tumors: The Frequency, Fusion Partners, and Clinical Outcome.
JCO Precis Oncol
2021
34111299
Audiologic Phenotype and Progression in Pediatric STRC-Related Autosomal Recessive Hearing Loss.
Laryngoscope
2021
33398081
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing.
Eur J Hum Genet
2021
32139434
Glanzmann thrombasthenia: genetic basis and clinical correlates.
Haematologica
2020
32203924
Copy number assessment in the genomic analysis of CNS neoplasia: An evidence-based review from the cancer genomics consortium (CGC) working group on primary CNS tumors.
Cancer Genet
2020
32139434
Glanzmann thrombasthenia: genetic basis and clinical correlates.
Haematologica
2020
31900259
HIF2-Induced Long Noncoding RNA RAB11B-AS1 Promotes Hypoxia-Mediated Angiogenesis and Breast Cancer Metastasis.
Cancer Res
2020
32302940
Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia.
Cancer Genet
2020
32000839
A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data.
Genome Med
2020
32805689
A Novel KMT2A-ARHGEF12 Fusion Gene Identified in a High-Grade B-cell Lymphoma.
Cancer Genet
2020
32738923
Patient specific circulating tumor DNA fingerprints to monitor treatment response across multiple tumors.
J Transl Med
2020
32619790
Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome.
Cancer Genet
2020
32554798
A germline <i>PALB2</i> pathogenic variant identified in a pediatric high-grade glioma.
Cold Spring Harb Mol Case Stud
2020
1 - 50 of 122
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Children's Hospital of Philadelphia
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13
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Co-authored papers
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Ian D Krantz
Children's Hospital of Philadelphia
Co-authored papers
10
Gerald Wertheim
Co-authored papers
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Elaine H Zackai
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Matthew C Dulik
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4
Xiaonan Zhao
Co-authored papers
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Mariarita Santi
Children's Hospital of Philadelphia
Co-authored papers
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Phillip B Storm
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Co-authored papers
4
Sami S Amr
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Co-authored papers
4
Vinodh Pillai
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Kristin Zelley
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Shruthi Mohan
University of North Carolina at Chapel Hill
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Kristy Lee
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