日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

IMS-IMWG 2025 consensus genomic staging predicts outcomes with daratumumab-based quadruplet regimens for NDMM

IMS-IMWG 2025共识基因组分期可预测基于达雷妥尤单抗的四联疗法治疗新诊断多发性骨髓瘤的疗效。

Maclachlan, Kylee H; Tan, Carlyn R; Shekarkhand, Tala; Rueda, Colin; Derkach, Andriy; Hashmi, Hamza; Hassoun, Hani; Shah, Urvi A; Hultcrantz, Malin; Lesokhin, Alexander M; Mailankody, Sham; Maura, Francesco; Merz, Maximillian; Firestone, Ross; Jurgens, Eric M; Miller, Kevin C; Rajeeve, Sridevi; Giralt, Sergio; Shah, Gunjan L; Scordo, Michael; Landau, Heather J; Zhang, Yanming; Cimera, Robert; Arcila, Maria E; Korde, Neha; Usmani, Saad Z

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

CDKN2A/B 突变和等位基因特异性改变可对 IDH 突变型星形细胞瘤的生存结果进行分层。

Hickman, Richard A; Gedvilaite, Erika; Ptashkin, Ryan; Reiner, Anne S; Cimera, Robert; Nandakumar, Subhiksha; Price, Adam; Vanderbilt, Chad; Fahy, Tara; Young, Robert J; Miller, Alexandra M; Mellinghoff, Ingo K; Rosenblum, Marc K; Ladanyi, Marc; Arcila, Maria E; Zhang, Yanming; Brannon, A Rose; Bale, Tejus A

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

局部晚期/转移性肾黏液性小管和梭形细胞癌的不良组织学特征、CDKN2A/B纯合缺失以及复杂的基因组改变

Yang, Chen; Cimera, Robert S; Aryeequaye, Ruth; Jayakumaran, Gowtham; Sarungbam, Judy; Al-Ahmadie, Hikmat A; Gopalan, Anuradha; Sirintrapun, S Joseph; Fine, Samson W; Tickoo, Satish K; Epstein, Jonathan I; Reuter, Victor E; Zhang, Yanming; Chen, Ying-Bei

Poorly differentiated chordoma with whole-genome doubling evolving from a SMARCB1-deficient conventional chordoma: A case report

由SMARCB1缺陷型常规脊索瘤演变而来的伴有全基因组加倍的低分化脊索瘤:病例报告

Curcio, Christian; Cimera, Robert; Aryeequaye, Ruth; Rao, Mamta; Fabbri, Nicola; Zhang, Yanming; Hameed, Meera

Recurrent loss of chromosome 22 and SMARCB1 deletion in extra-axial chordoma: A clinicopathological and molecular analysis

脊索瘤中22号染色体复发性丢失和SMARCB1基因缺失:临床病理及分子分析

Wen, Xiaoyun; Cimera, Robert; Aryeequaye, Ruth; Abhinta, Mohanty; Athanasian, Edward; Healey, John; Fabbri, Nicola; Boland, Patrick; Zhang, Yanming; Hameed, Meera

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

更正:全面检测复发性基因组异常:多发性骨髓瘤的靶向测序方法

Yellapantula, Venkata; Hultcrantz, Malin; Rustad, Even H; Wasserman, Ester; Londono, Dory; Cimera, Robert; Ciardiello, Amanda; Landau, Heather; Akhlaghi, Theresia; Mailankody, Sham; Patel, Minal; Medina-Martinez, Juan Santiago; Ossa, Juan Esteban Arango; Levine, Max Fine; Bolli, Niccolo; Maura, Francesco; Dogan, Ahmet; Papaemmanuil, Elli; Zhang, Yanming; Landgren, Ola

Genetic Basis of Extramedullary Plasmablastic Transformation of Multiple Myeloma

多发性骨髓瘤髓外浆母细胞转化的遗传基础

Ying Liu, Fatima Jelloul, Yanming Zhang, Tapan Bhavsar, Caleb Ho, Mamta Rao, Natasha E Lewis, Robert Cimera, Jeeyeon Baik, Allison Sigler, Filiz Sen, Mariko Yabe, Mikhail Roshal, Ola Landgren, Ahmet Dogan, Wenbin Xiao

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

全面检测复发性基因组异常:多发性骨髓瘤的靶向测序方法

Yellapantula, Venkata; Hultcrantz, Malin; Rustad, Even H; Wasserman, Ester; Londono, Dory; Cimera, Robert; Ciardiello, Amanda; Landau, Heather; Akhlaghi, Theresia; Mailankody, Sham; Patel, Minal; Medina-Martinez, Juan Santiago; Arango Ossa, Juan Esteban; Levine, Max Fine; Bolli, Niccolo; Maura, Francesco; Dogan, Ahmet; Papaemmanuil, Elli; Zhang, Yanming; Landgren, Ola

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

肾髓质癌中SMARCB1蛋白表达缺失的独特机制:20例病例的形态学和分子分析

Jia, Liwei; Carlo, Maria I; Khan, Hina; Nanjangud, Gouri J; Rana, Satshil; Cimera, Robert; Zhang, Yanming; Hakimi, A Ari; Verma, Amit K; Al-Ahmadie, Hikmat A; Fine, Samson W; Gopalan, Anuradha; Sirintrapun, S Joseph; Tickoo, Satish K; Reuter, Victor E; Gartrell, Benjamin A; Chen, Ying-Bei

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

PHF6 和 DNMT3A 突变在具有 T 细胞谱系分化的混合表型急性白血病的特定亚组中富集。

Xiao, Wenbin; Bharadwaj, Maheetha; Levine, Max; Farnhoud, Noushin; Pastore, Friederike; Getta, Bartlomiej M; Hultquist, Anne; Famulare, Christopher; Medina, Juan S; Patel, Minal A; Gao, Qi; Lewis, Natasha; Pichardo, Janine; Baik, Jeeyeon; Shaffer, Brian; Giralt, Sergio; Rampal, Raajit; Devlin, Sean; Cimera, Robert; Zhang, Yanming; E Arcila, Maria; Papaemmanuil, Elli; Levine, Ross L; Roshal, Mikhail