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

A single next generation sequencing assay for detection of driver mutations, rearrangements and copy number abnormalities in plasma cell dyscrasias

一种用于检测浆细胞疾病中驱动突变、重排和拷贝数异常的单次新一代测序检测方法

Bonolo de Campos, Cecilia; Trujillo, Daniela; Smadbeck, James; Arribas, Mariano; Tang, Hongwei; Sharma, Neeraj; Ahmann, Gregory J; Kumar, Shaji K; Stewart, A Keith; Fonseca, Rafael; Bergsagel, P Leif; Asmann, Yan W; Baughn, Linda B; Braggio, Esteban

Functional genomics identifies therapeutic options, biomarkers, and resistance mechanisms for high-grade gliomas

功能基因组学可识别高级别胶质瘤的治疗方案、生物标志物和耐药机制。

Lin, Wan-Hsin; Kosari, Farhad; Smadbeck, James B; Barrett, Michael T; Feathers, Ryan W; Hall, Jamie; Sadeghian, Dorsay; Sotiriou, Sotiris; Johnson, Sarah H; Harris, Faye R; Berry, Taylor; McCune, Alexa F; Murphy, Stephen J; Kinsella, Lindsey; Haydu, Lauren E; Moniz-Garcia, Diogo; Fortin Ensign, Shannon P; Yang, Lin; Emanuel, Angela R; Jones, Leila A; Schaefer-Klein, Janet L; Ida, Cristiane M; Salomao, Marcela A; Sherman, Wendy J; Porter, Alyx B; Rosenfeld, Steven S; Kizilbash, Sani H; Jaeckle, Kurt A; Mrugala, Maciej M; Mansfield, Aaron S; Borad, Mitesh J; Bendok, Bernard R; Burns, Terry C; Quinones-Hinojosa, Alfredo; Cheville, John C; Vasmatzis, George; Anastasiadis, Panos Z

Functional variant rs9344 at 11q13.3 regulates CCND1 expression in multiple myeloma with t(11;14)

11q13.3 处的功能性变异 rs9344 调控 t(11;14) 多发性骨髓瘤中的 CCND1 表达

Tang, Hongwei; Yan, Huihuang; Shivaram, Suganti; Lehman, Stacey; Sharma, Neeraj; Smadbeck, James; Zepeda-Mendoza, Cinthya; Tian, Shulan; Asmann, Yan; Vachon, Celine; Gaspar Maia, Alexandre; Keats, Jonathan; Bergsagel, P Leif; Fonseca, Rafael; Stewart, A Keith; Hsu, Joel-Sean; Kandasamy, Richard K; Pandey, Akhilesh; Kaddoura, Marcella A; Maura, Francesco; Mitra, Amit; Rajkumar, S Vincent; Kumar, Shaji K; Elhaik, Eran; Braggio, Esteban; Baughn, Linda B

Genomic and Immune Landscape of Pancreatic Ductal Adenocarcinoma Associated with Germline Pathogenic Variants in ATM.

与 ATM 基因种系致病变异相关的胰腺导管腺癌的基因组和免疫图谱。

Yadav Siddhartha, Bao Riyue, Graham Rondell P, Hu Chunling, Hart Steven N, Na Jie, Boddicker Nicholas, Gnanaolivu Rohan D, Smadbeck James, Ding Li, Billadeau Daniel D, Mayer Aaron T, Majumder Shounak, Morais Lyra Paulo Cilas, Lee Adrian V, Monteiro Alvaro N, Villasboas Jose C, McWilliams Robert, Couch Fergus J

Tumor ploidy determination in low-pass whole genome sequencing and allelic copy number visualization using the Constellation Plot

利用星座图进行低深度全基因组测序中的肿瘤倍性测定和等位基因拷贝数可视化。

Johnson, Sarah H; Smadbeck, James B; Zenka, Roman M; Barrett, Michael T; Gaitatzes, Athanasios; Solanki, Arnav; Florio, Angela B; Borad, Mitesh J; Cheville, John C; Vasmatzis, George

Functional impact of the hyperduplication genomophenotype in high copy number endometrial cancer.

高拷贝数子宫内膜癌中超重复基因表型的功能影响

Florio Angela, Smadbeck James, Johnson Sarah H, Lin Wan-Hsin, Sadeghian Dorsay, Sotiriou Sotiris, Salvatori Rebeca, Feathers Ryan W, Berry Taylor, Kinsella Lindsey, Harris Faye R, McCune Alexa F, Murphy Stephen J, Ali Mohamed F, Pezeshki Abdulmohammad, Barrett Michael T, Grcevich Leah, Capasso Ilaria, De Vitis Luigi Antonio, Schivardi Gabriella, Occhiali Tommaso, Larish Alyssa M, Weroha John, Borad Mitesh J, Cheville John, Anastasiadis Panos Z, Mariani Andrea, Vasmatzis George

Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome.

涉及 PITX2 的复杂平衡染色体内重排被确定为 Axenfeld-Rieger 综合征的病因

Farris Joseph, Khanna Cheryl, Smadbeck James B, Johnson Sarah H, Bothun Erick, Kaplan Tyler, Hoffman Francis, Polonis Katarzyna, Oliver Gavin, Reis Linda M, Semina Elena V, Rust Laura, Hoppman Nicole L, Vasmatzis George, Marcou Cherisse A, Schimmenti Lisa A, Klee Eric W

Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia

前瞻性评估基因组测序与急性髓系白血病常规细胞遗传学的比较

Pitel, Beth A; Zepeda-Mendoza, Cinthya; Sachs, Zohar; Tang, Hongwei; Shivaram, Suganti; Sharma, Neeraj; Smadbeck, James B; Smoley, Stephanie A; Pearce, Kathryn E; Luoma, Ivy M; Cook, Joselle; Litzow, Mark R; Hoppman, Nicole L; Viswanatha, David; Xu, Xinjie; Ketterling, Rhett P; Greipp, Patricia T; Peterson, Jess F; Baughn, Linda B

Disparity in the detection of chromosome 15 centromere in patients of African ancestry with a plasma cell neoplasm

非洲裔浆细胞肿瘤患者15号染色体着丝粒检测结果的差异

Koleilat, Alaa; Tang, Hongwei; Sharma, Neeraj; Yan, Huihuang; Tian, Shulan; Smadbeck, James; Shivaram, Suganti; Meyer, Reid; Pearce, Kathryn; Baird, Michael; Zepeda-Mendoza, Cinthya J; Xu, Xinjie; Greipp, Patricia T; Peterson, Jess F; Ketterling, Rhett P; Bergsagel, P Leif; Vachon, Celine; Rajkumar, S Vincent; Kumar, Shaji; Asmann, Yan W; Elhaik, Eran; Baughn, Linda B

EXTH-20. IDENTIFICATION OF EX VIVO THERAPEUTIC VULNERABILITIES IN DIFFUSE GLIOMAS USING A FUNCTIONAL GENOMICS APPROACH

EXTH-20. 利用功能基因组学方法鉴定弥漫性胶质瘤的体外治疗脆弱性

Krupovic, Mart; Cvirkaite-Krupovic, Virginija; Iranzo, Jaime; Prangishvili, David; Koonin, Eugene V; Lin, Wan-Hsin; Smadbeck, James; Barrett, Michael; Feathers, Ryan; Dorsay, Sadeghian; Johnson, Sarah; Karagouga, Giannoula; Harris, Faye; Murphy, Stephen; Quiñones-Hinojosa, Alfredo; Kizilbash, Sani; Burns, Terry; Jaeckle, Kurt; Mrugala, Maciej; Bendok, Bernard; Moniz-Garcia, Diogo; Fortin-Ensign, Shannon; Rosenfeld, Steven; Ida, Cristiane; Jentoft, Mark; Salomao, Marcela; Yang, Lin; Emanuel, Angela; Schaefer-Klein, Janet; Mansfield, Aaron; Borad, Mitesh; Cheville, John; Vasmatzis, George; Anastasiadis, Panos