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Oncogene|February 7, 2017
Detecting intratumoral heterogeneity of EGFR activity by liposome-based in vivo transfection of a fluorescent biosensorG Weitsman, N J Mitchell, R Evans, et al.Nature Biotechnology|January 3, 2024
Characterization and visualization of tandem repeats at genome scaleEgor Dolzhenko, Adam English, Harriet Dashnow, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 13, 2019
BEECH: a dose-finding run-in followed by a randomised phase II study assessing the efficacy of AKT inhibitor capivasertib (AZD5363) combined with paclitaxel in patients with estrogen receptor-positive advanced or metastatic breast cancer, and in a PIK3CA mutant sub-populationN C Turner, E Alarcón, A C Armstrong, et al.Human Mutation|October 17, 2025
One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient MatchmakingMatthew Osmond, E Magda Price, Orion J Buske, et al.Nature Communications|May 29, 2023
Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohortWarren A Cheung, Adam F Johnson, William J Rowell, et al.Genome Biology|May 9, 2019
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenomeWarren A Cheung, Xiaojian Shao, Andréanne Morin, et al.Genome Biology|March 12, 2017
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenomeWarren A Cheung, Xiaojian Shao, Andréanne Morin, et al.Nature Communications|March 21, 2019
H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesisAshot S Harutyunyan, Brian Krug, Haifen Chen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2023
Insurance denials and diagnostic rates in a pediatric genomic research cohortTricia N Zion, Courtney D Berrios, Ana S A Cohen, et al.Nature Genetics|June 27, 2024
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locusDavid Pellerin, Giulia F Del Gobbo, Madeline Couse, et al.Pageof 24