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

Deletion of 9p drives B-ALL through heterozygous inactivation of Pax5 and Cd72 in preleukemic cells

9p缺失通过白血病前期细胞中Pax5和Cd72的杂合失活驱动B细胞急性淋巴细胞白血病(B-ALL)的发生。

Ruiz-Corzo, Belén; Casado-García, Ana; Oak, Ninad; Somoza-Cotillas, Paula; López-Álvarez de Neyra, Andrea; Martínez-Cano, Jorge; Pérez-Pons, Alba; Sánchez, Elena G; Blanco, Oscar; Alonso-López, Diego; De Las Rivas, Javier; Riesco, Susana; Prieto-Matos, Pablo; García Criado, Francisco Javier; García Cenador, María Begoña; Orfao, Alberto; Ramírez-Orellana, Manuel; Cobaleda, César; Vicente-Dueñas, Carolina; Nichols, Kim E; Sánchez-García, Isidro

Fear of Cancer Recurrence Among Parents of Children with Cancer Who Underwent Germline Genetic Testing

接受生殖系基因检测的癌症患儿父母对癌症复发的担忧

Flesher, Emily A; Armstrong, Gabrielle M; Flynn, Jessica S; Sachner, Leila; Blake, Alise; Jones, Anna M; Webster, Rachel; Humphrey, Carolyn E; Jurbergs, Niki; Hsu, Chia-Wei; Pan, Haitao; Nichols, Kim E; Mandrell, Belinda N; Howard Sharp, Katianne M

The moderating role of parental cognitive perceptions in the link between children's cancer predisposition genetic testing results and parent psychological adjustment

父母认知感知在儿童癌症易感基因检测结果与父母心理适应之间的调节作用

Sachner, Leila; Flynn, Jessica S; Hsu, Chia-Wei; Pan, Haitao; Jurbergs, Niki; Blake, Alise; McGee, Rose B; Harrison, Lynn; Robinson, Missy; Adanri, Tolulope; Nichols, Kim E; Howard Sharp, Katianne M

Telomere length of both parents contribute to heritable POT1 cancer-predisposition syndrome

父母双方的端粒长度均与遗传性POT1癌症易感综合征有关。

Martin, Annika; Lu, Robert; Blake, Alise; Nichols, Kim E; Sanchez, Santiago E; Artandi, Steven E; Sharma, Richa; Hockemeyer, Dirk

Investigation of DNA Damage Response Genes Validates the Role of DNA Repair in Pediatric Cancer Risk and Identifies SMARCAL1 as a Novel Osteosarcoma Predisposition Gene

对DNA损伤反应基因的研究证实了DNA修复在儿童癌症风险中的作用,并鉴定出SMARCAL1是一种新的骨肉瘤易感基因

Oak, Ninad; Chen, Wenan; Blake, Alise; Harrison, Lynn; O'Brien, Martha; Previti, Christopher; Balasubramanian, Gnanaprakash; Maass, Kendra; Hirsch, Steffen; Penkert, Judith; Jones, Barbara C; Schramm, Kathrin; Nathrath, Michaela; Pajtler, Kristian W; Jones, David T W; Witt, Olaf; Dirksen, Uta; Li, Jiaming; Sapkota, Yadav; Ness, Kirsten K; Guenther, Lillian M; Pfister, Stefan M; Kratz, Christian; Wang, Zhaoming; Armstrong, Greg T; Hudson, Melissa M; Wu, Gang; Autry, Robert J; Nichols, Kim E; Sharma, Richa

Peripheral blood DNA methylation predicts the early onset of primary tumor in TP53 mutation carriers

外周血DNA甲基化可预测TP53突变携带者原发肿瘤的早期发生

Subasri, Vallijah; Brew, Benjamin; Laverty, Brianne; Erdman, Lauren; Guha, Tanya; Hansford, Jordan R; Cairney, Elizabeth; Portwine, Carol; Elser, Christine; Finlay, Jonathan L; Nichols, Kim E; Anson, Jo; Kohlmann, Wendy; Gong, Haifan; Lees, Jodi; Alon, Noa; Brunga, Ledia; Villani, Anita; de Andrade, Kelvin C; Khincha, Payal P; Savage, Sharon A; Schiffman, Joshua D; Pugh, Trevor J; Malkin, David; Goldenberg, Anna

Clinical experience of using integrated whole genome and transcriptome sequencing as a framework for pediatric and adolescent acute myeloid leukemia diagnosis and risk assessment

利用整合全基因组和转录组测序作为框架进行儿童和青少年急性髓系白血病诊断和风险评估的临床经验

Voss, Rebecca K; Pastor Loyola, Victor B; Cardenas, Maria F; Kumar, Priya; Maciaszek, Jamie L; Namwanje, Maria; Ma, Jing; Neary, Jennifer L; Jin, Meiling; Umeda, Masayuki; Wilkinson, Mark R; Payne-Turner, Debbie; Eldomery, Mohammad K; Ma, Jingqun; Gu, Jiali; Dalton, Jim; Melton, Samantha; Liu, Yen-Chun; Foy, Scott; Rusch, Michael; Wheeler, David A; Zhang, Jinghui; Nichols, Kim E; Karol, Seth E; Inaba, Hiroto; Ribeiro, Raul; Rubnitz, Jeffrey E; Klco, Jeffery M; Wang, Lu

Insights into germline predisposition to pediatric lymphoid malignancies

对儿童淋巴恶性肿瘤生殖系易感性的深入了解

Thapa, Roshina; Nichols, Kim E; Sharma, Richa

Pediatric Cancer Predisposition and Surveillance Update: Summary Perspective and Future Directions

儿童癌症易感性和监测最新进展:总结、展望和未来方向

Brodeur, Garrett M; Diller, Lisa R; Nichols, Kim E; Plon, Sharon E; Porter, Christopher C; Malkin, David

Histiocyte Society blueprint for hemophagocytic lymphohistiocytosis research: deciphering underlying disease mechanisms to optimize diagnosis and therapy

组织细胞学会制定噬血细胞性淋巴组织细胞增生症研究蓝图:揭示潜在疾病机制以优化诊断和治疗

Meyer, Lauren K; Lee, Jerry C; Rocco, Joseph M; Nichols, Kim E