Rhabdomyosarcoma With EWSR1::NF2 Gene Fusion: A Case Report Potentially Expanding Its Genetic Spectrum [0.03%]
带有EWSR1::NF2基因融合的横纹肌肉瘤病例报告——可能扩大其遗传谱系
Carla Saoud,Gunes Gundem,Dylan Domenico et al.
Carla Saoud et al.
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, presenting with heterogeneous clinical and molecular subtypes. While gene fusions are predominantly associated with alveolar RMS, spindle cell RMS, especially congen...
Structural Variant Analysis of Complex Karyotype Myelodysplastic Neoplasia Through Optical Genome Mapping [0.03%]
基于光学基因组测序的复杂染色体骨髓发育不良性肿瘤的结构变异分析
Andriana Valkama,Sandra Vorimo,Anna Tervasmäki et al.
Andriana Valkama et al.
Myelodysplastic neoplasia with complex karyotype (CK-MDS) poses significant clinical challenges and is associated with poor survival. Detection of structural variants (SVs) is crucial for diagnosis, prognostication, and treatment decision-m...
MicroRNA Expression in High-Grade B-Cell Lymphoma With 11q Aberration [0.03%]
伴有11q异常的高级别B细胞淋巴瘤中的微小核糖核酸表达状况分析
Gioia Di Stefano,Anja Fischer,Emil Chteinberg et al.
Gioia Di Stefano et al.
Mature aggressive B-cell lymphomas, such as Burkitt lymphoma (BL) and Diffuse large B-cell lymphoma (DLBCL), show variations in microRNA (miRNA) expression. The entity of High-grade B-cell lymphoma with 11q aberration (HGBCL-11q) shares sev...
Correction to "Temporal Trends and Regional Variability in BRAF and KRAS Genetic Testing in Denmark (2010-2022): Implications for Precision Medicine" [0.03%]
丹麦（2010-2022年）BRAF和KRAS基因检测的时间趋势和地区差异的修正：对精准医学的影响
Published Erratum
Genes, chromosomes & cancer. 2025 Jan;64(1):e70020. DOI:10.1002/gcc.70020 2025
Shan Chen,Yuanzhao Ding
Shan Chen
Given the high lethality of cancer, identifying its risk factors is crucial in both epidemiology and cancer research. This study employs a novel bibliometric analysis method, which uses the tidytext package and tidy tools in R. This approac...
A Clinicopathologic and Molecular Reappraisal of Myxoinflammatory Fibroblastic Sarcoma-A Controversial and Pathologically Challenging Low-Grade Sarcoma [0.03%]
炎性黏液样纤维肉瘤的临床病理和分子再评价——一种存在争议及病理上具有挑战性的低度恶性肉瘤
Takeshi Hirose,Hsin-Yi Chang,Carla Saoud et al.
Takeshi Hirose et al.
Purpose: Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare, low-grade sarcoma affecting with predilection the acral soft tissues of middle-aged adults. Clinically, MIFS is associated with a high rate of local recurre...
SMARCA4 Deficiency in Lung Cancer: From Signaling Pathway to Potential Therapeutic Targets [0.03%]
肺癌中SMARCA4缺陷：从信号通路至潜在治疗靶点
Mingzhu Zhang,Youhong Dong,Rui Meng et al.
Mingzhu Zhang et al.
SMARCA4-deficient lung cancer, including thoracic SMARCA4-deficient undifferentiated tumors and SMARCA4-deficient nonsmall-cell lung carcinomas, is a rare and aggressive disease characterized by rapid progression and poor prognosis. This ca...
The Transcriptomic and Gene Fusion Landscape of Pleomorphic Salivary Gland Adenomas [0.03%]
多形性腮腺腺瘤的转录组和基因融合谱系
Maryam Kakay Afshari,Paloma Tejera Nevado,André Fehr et al.
Maryam Kakay Afshari et al.
Pleomorphic adenoma (PA) is the most common salivary gland tumor. PAs are characterized by chromosomal rearrangements of 8q12 and 12q14-15, leading to gene fusions involving the PLAG1 and HMGA2 oncogenes. Here, we performed the first compre...
Identification of a novel SH3PXD2B::FER fusion in a case of plexiform myofibroblastic tumor and review of the literature [0.03%]
SH3PXD2B::FER新融合基因在丛状肌纤维母细胞瘤中的鉴定及文献复习
Silvia Vallese,Chantal Tancredi,Isabella Giovannoni et al.
Silvia Vallese et al.
Fibroblastic/myofibroblastic tumors encompass a wide spectrum of lesions. Among them, plexiform myofibroblastoma (PM) represents a rare and distinctive entity recently described as mostly occurring in children and with a favorable prognosis...
A Challenging Case of an Intraosseous Composite Hemangioendothelioma of the Occipital Bone With YAP1::FOXR1 Fusion [0.03%]
occipital骨内复合血管内皮瘤一例(YAP1::FOXR1融合型)
Fleur Cordier,Liesbeth Ferdinande,Siebe Loontiens et al.
Fleur Cordier et al.