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JAMA|April 21, 2011
Use of whole-genome sequencing to diagnose a cryptic fusion oncogeneJohn S Welch, Peter Westervelt, Li Ding, et al.
NPJ Genomic Medicine|January 26, 2023
Cross center single-cell RNA sequencing study of the immune microenvironment in rapid progressing multiple myelomaWilliam Pilcher, Beena E Thomas, Swati S Bhasin, et al.
The New England Journal of Medicine|March 20, 2024
Anti-Interleukin-23 Autoantibodies in Adult-Onset ImmunodeficiencyAristine Cheng, Anuj Kashyap, Helene Salvator, et al.
Cell Reports|April 5, 2018
Driver Fusions and Their Implications in the Development and Treatment of Human CancersQingsong Gao, Wen-Wei Liang, Steven M Foltz, et al.
NPJ Breast Cancer|July 20, 2017
DNA defects, epigenetics, and gene expression in cancer-adjacent breast: a study from The Cancer Genome AtlasMelissa A Troester, Katherine A Hoadley, Monica D'Arcy, et al.
Annals of Translational Medicine|January 20, 2023
Efficacy and safety of neoadjuvant pertuzumab plus trastuzumab in combination with chemotherapy regimen in Chinese patients with HER2-positive early breast cancer: a real-world retrospective multi-center cohort studyMeirong Zhou, Shouman Wang, Nengbin Wan, et al.
Communications Biology|June 6, 2023
A Common East Asian aldehyde dehydrogenase 2*2 variant promotes ventricular arrhythmia with chronic light-to-moderate alcohol use in miceAn-Sheng Lee, Yen-Ling Sung, Szu-Hua Pan, et al.
JAMA|March 15, 2012
Association of age at diagnosis and genetic mutations in patients with neuroblastomaNai-Kong V Cheung, Jinghui Zhang, Charles Lu, et al.
Cell Stem Cell|May 1, 2012
Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cellsMargaret A Young, David E Larson, Chiao-Wang Sun, et al.
Plos Genetics|July 11, 2014
Clonal architecture of secondary acute myeloid leukemia defined by single-cell sequencingAndrew E O Hughes, Vincent Magrini, Ryan Demeter, et al.
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