Sitao Wu

机构：Infinity (United States) · ORCID：0000-0002-4740-8885

发表论文 76 篇 · 总被引 17347 次 · h-index 29

代表论文

• De novo variants in neurodevelopmental disorders with epilepsy (2018 · Nature Genetics · 被引 320)
• Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing (2018 · JAMA Oncology · 被引 181)
• Targeting cellular heterogeneity with CXCR2 blockade for the treatment of therapy-resistant prostate cancer (2019 · Science Translational Medicine · 被引 138)
• Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes (2020 · npj Precision Oncology · 被引 87)
• Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders (2020 · Genome Medicine · 被引 74)
• Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases (2016 · Genetics in Medicine · 被引 55)