논문
bioRxiv Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes 2020.12
Journal of Clinical Medicine The Clinical Significance of RAS, PIK3CA, and PTEN Mutations in Non-Small Cell Lung Cancer Using Cell-Free DNA 2020.08
Nature Genetics Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease 2020.10
Scientific Reports Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients 2020.10
Journal of Pathology Comprehensive genetic features of gastric mixed adenoneuroendocrine carcinomas and pure neuroendocrine carcinomas 2020.10
British Journal Of Neurosurgery IDH-wildtype secondary glioblastoma arising in IDH-mutant diffuse astrocytoma: a case report 2020.10
Annals Of Surgical Oncology Targeted Next-Generation Sequencing Analysis for Recurrence in Early-Stage Lung Adenocarcinoma 2020.11
Genes A High Quality Asian Genome Assembly Identifies Features of Common Missing Regions 2020.11
Cancers Molecular Signature of Extracellular Vesicular Small Non-Coding RNAs Derived from Cerebrospinal Fluid of Leptomeningeal Metastasis Patients: Functional Implication of miR-21 and Other Small RNAs in Cancer Malignancy 2021.01
Nature Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program 2021.02
TOP