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Blood|August 9, 2023
Prognostic significance of ETP phenotype and minimal residual disease in T-ALL: a Children's Oncology Group studyBrent L Wood, Meenakshi Devidas, Ryan J Summers, et al.
Nature Genetics|February 5, 2013
Relapse-specific mutations in NT5C2 in childhood acute lymphoblastic leukemiaJulia A Meyer, Jinhua Wang, Laura E Hogan, et al.
Advances in Wound Care|September 3, 2025
Multi-State Modeling of Pressure Injury Staging Transition Trajectories to Inform Next-Generation Clinical Decision SupportWenyu Song, Min-Jeoung Kang, Luwei Liu, et al.
JCI Insight|July 27, 2018
Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomesJasmine C Wong, Victoria Bryant, Tamara Lamprecht, et al.
Cell Genomics|December 3, 2025
Analysis of error profiles of indels and structural variants in deep-sequencing dataYing Shao, Quang Tran, Yuan Feng, et al.
The Canadian Journal of Cardiology|November 7, 2021
Beyond Wellness Monitoring: Continuous Multiparameter Remote Automated Monitoring of PatientsMichael H McGillion, Katherine Allan, Sara Ross-Howe, et al.
Epilepsia|February 1, 2017
Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201HSarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, et al.
Leukemia|January 21, 2014
Long-term follow-up of imatinib in pediatric Philadelphia chromosome-positive acute lymphoblastic leukemia: Children's Oncology Group study AALL0031K R Schultz, A Carroll, N A Heerema, et al.
International Journal of Radiation Oncology, Biology, Physics|November 20, 2015
MicroRNA-Related DNA Repair/Cell-Cycle Genes Independently Associated With Relapse After Radiation Therapy for Early Breast CancerHarriet E Gee, Francesca M Buffa, Adrian L Harris, et al.
Nature Medicine|July 16, 2013
BACH2 mediates negative selection and p53-dependent tumor suppression at the pre-B cell receptor checkpointSrividya Swaminathan, Chuanxin Huang, Huimin Geng, et al.
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