PHF6 and DNMT3A mutations are enriched in distinct subgroups of mixed phenotype acute leukemia with T-lineage differentiation

Wenbin Xiao, Maheetha Bharadwaj, Max F. Levine, +21

Blood Advances

Distinctive mechanisms underlie the loss of SMARCB1 protein expression in renal medullary carcinoma: morphologic and molecular analysis of 20 cases

Liwei Jia, Maria I. Carlo, Hina Khan, +14

Modern Pathology

UrologyGenitourinary CancerRenal Medullary CarcinomaMedicineRenal Pathology +8

Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma

Venkata D. Yellapantula, Malin Hultcrantz, Even H. Rustad, +17

Blood Cancer Journal

Genetic Basis of Extramedullary Plasmablastic Transformation of Multiple Myeloma

Ying Liu, Fatima Zahra Jelloul, Yanming Zhang, +13

The American Journal of Surgical Pathology

Hematological MalignancyMedicineMixed-phenotype Acute LeukemiaMalignant Blood DisorderImmunology +8

Identification of NTRK3 Fusions in Childhood Melanocytic Neoplasms

Lu Wang, Klaus J. Busam, Ryma Benayed, +9

Journal of Molecular Diagnostics

Cancer ResearchPathologyMedicineNtrk3 FusionsTumor Biology +1

Chromosome 20q Amplification Defines a Subtype of Microsatellite Stable, Left-Sided Colon Cancers with Wild-type RAS/RAF and Better Overall Survival

Ryan Ptashkin, Carlos Pagan, Rona Yaeger, +12

Molecular Cancer Research

Adverse histology, homozygous loss of CDKN2A/B, and complex genomic alterations in locally advanced/metastatic renal mucinous tubular and spindle cell carcinoma

Chen Yang, Robert Cimera, Ruth Aryeequaye, +11

Modern Pathology

UrologyAdverse HistologyCancer PathologyGenitourinary CancerMedicine +8

CDKN2A/B mutations and allele-specific alterations stratify survival outcomes in IDH-mutant astrocytomas

Richard A. Hickman, Erika Gedvilaite, Ryan Ptashkin, +15

Acta Neuropathologica

Neuro-oncologySomatic VariantGliomaTumor HeterogeneityGenetic Disorder +9

Recurrent loss of chromosome 22 and <scp><i>SMARCB1</i></scp> deletion in extra‐axial chordoma: A clinicopathological and molecular analysis

Xiaoyun Wen, Robert Cimera, Ruth Aryeequaye, +7

Genes Chromosomes and Cancer

Tumoral PathologyExtra‐axial ChordomaConventional ChordomaMedicineGenetics +7

Poorly differentiated chordoma with whole‐genome doubling evolving from a <scp><i>SMARCB1</i></scp>‐deficient conventional chordoma: A case report

Christian Curcio, Robert Cimera, Ruth Aryeequaye, +4

Genes Chromosomes and Cancer

Conventional ChordomaSomatic VariantConventional Chordoma AccountingTumor HeterogeneityGenetic Disorder +9