| 1 | Subset of retinoblastoma tumours is associated with
<i>BRCA1/2</i>
mutations | 3.9 | 1 | Citations (PDF) |
| 2 | Unraveling the role of the mitochondrial one-carbon pathway in undifferentiated thyroid cancer by multi-omics analyses | 14.2 | 25 | Citations (PDF) |
| 3 | Quantitative and qualitative mutational impact of ionizing radiation on normal cells | 6.3 | 23 | Citations (PDF) |
| 4 | Whole-genome sequences reveal zygotic composition in chimeric twins | 1.9 | 0 | Citations (PDF) |
| 5 | Mitochondrial DNA mosaicism in normal human somatic cells | 26.1 | 30 | Citations (PDF) |
| 6 | Low-level brain somatic mutations in exonic regions are collectively implicated in autism with germline mutations in autism risk genes | 11.6 | 2 | Citations (PDF) |
| 7 | A male mouse model for metabolic dysfunction-associated steatotic liver disease and hepatocellular carcinoma | 14.2 | 29 | Citations (PDF) |
| 8 | Clinical application of whole-genome sequencing of solid tumors for precision oncology | 11.6 | 16 | Citations (PDF) |
| 9 | Single Cell Analysis of Human Thyroid Reveals the Transcriptional Signatures of Aging | 2.7 | 10 | Citations (PDF) |
| 10 | Widespread somatic L1 retrotransposition in normal colorectal epithelium | 34.3 | 47 | Citations (PDF) |
| 11 | Somatic evolution of marine transmissible leukemias in the common cockle, Cerastoderma edule | 22.8 | 16 | Citations (PDF) |
| 12 | Patient‐derived organoids as a preclinical platform for precision medicine in colorectal cancer | 4.2 | 36 | Citations (PDF) |
| 13 | Asymmetric Contribution of Blastomere Lineages of First Division of the Zygote to Entire Human Body Using Post-Zygotic Variants | 3.8 | 2 | Citations (PDF) |
| 14 | Weight-bearing activity impairs nuclear membrane and genome integrity via YAP activation in plantar melanoma | 14.2 | 30 | Citations (PDF) |
| 15 | p57Kip2 imposes the reserve stem cell state of gastric chief cells | 12.4 | 36 | Citations (PDF) |
| 16 | Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations | 3.7 | 3 | Citations (PDF) |
| 17 | Adenosine Deaminase 2 Deficiency Caused by Biallele Variants Including Splicing Variant: The First Case in Korea | 2.4 | 2 | Citations (PDF) |
| 18 | Spatial genomics maps the structure, nature and evolution of cancer clones | 34.3 | 138 | Citations (PDF) |
| 19 | Estimation of intrafamilial DNA contamination in family trio genome sequencing using deviation from Mendelian inheritance | 4.7 | 7 | Citations (PDF) |
| 20 | Tumor hypoxia represses γδ T cell-mediated antitumor immunity against brain tumors | 24.9 | 120 | Citations (PDF) |
| 21 | Implication of CD69<sup>+</sup>CD103<sup>+</sup> tissue‐resident‐like CD8<sup>+</sup> T cells as a potential immunotherapeutic target for cholangiocarcinoma | 4.2 | 37 | Citations (PDF) |
| 22 | Cerebral Cavernous Malformation 1 Determines YAP/TAZ Signaling-Dependent Metastatic Hallmarks of Prostate Cancer Cells | 4.1 | 5 | Citations (PDF) |
| 23 | A large-scale snapshot of intratumor heterogeneity in human cancer | 23.8 | 5 | Citations (PDF) |
| 24 | Experimental Models for SARS-CoV-2 Infection | 5.0 | 10 | Citations (PDF) |
| 25 | Nasal ciliated cells are primary targets for SARS-CoV-2 replication in the early stage of COVID-19 | 9.1 | 258 | Citations (PDF) |
| 26 | Single-cell transcriptome of bronchoalveolar lavage fluid reveals sequential change of macrophages during SARS-CoV-2 infection in ferrets | 14.2 | 60 | Citations (PDF) |
| 27 | Acquired Resistance to Third-Generation EGFR Tyrosine Kinase Inhibitors in Patients With De Novo EGFRT790M-Mutant NSCLC | 1.1 | 24 | Citations (PDF) |
| 28 | Mutational spectrum of SARS-CoV-2 during the global pandemic | 11.6 | 47 | Citations (PDF) |
| 29 | Clonal dynamics in early human embryogenesis inferred from somatic mutation | 34.3 | 116 | Citations (PDF) |
| 30 | Dissecting single-cell genomes through the clonal organoid technique | 11.6 | 15 | Citations (PDF) |
| 31 | 4‐1BB Delineates Distinct Activation Status of Exhausted Tumor‐Infiltrating CD8+ T Cells in Hepatocellular Carcinoma | 10.0 | 86 | Citations (PDF) |
| 32 | PRMT1 Is Required for the Maintenance of Mature β-Cell Identity | 0.5 | 30 | Citations (PDF) |
| 33 | Germline gain-of-function mutation of STAT1 rescued by somatic mosaicism in immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like disorder | 2.6 | 12 | Citations (PDF) |
| 34 | Three-Dimensional Human Alveolar Stem Cell Culture Models Reveal Infection Response to SARS-CoV-2 | 12.4 | 249 | Citations (PDF) |
| 35 | Dll4 Suppresses Transcytosis for Arterial Blood-Retinal Barrier Homeostasis | 11.3 | 51 | Citations (PDF) |
| 36 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition | 26.1 | 415 | Citations (PDF) |
| 37 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing | 26.1 | 629 | Citations (PDF) |
| 38 | The genome-wide landscape of C:G > T:A polymorphism at the CpG contexts in the human population | 3.3 | 30 | Citations (PDF) |
| 39 | A fusion of CD63–BCAR4 identified in lung adenocarcinoma promotes tumorigenicity and metastasis | 5.8 | 7 | Citations (PDF) |
| 40 | Comprehensive molecular characterization of mitochondrial genomes in human cancers | 26.1 | 390 | Citations (PDF) |
| 41 | Tracing Oncogene Rearrangements in the Mutational History of Lung AdenocarcinomaCell, 2019, 177, 1842-1857.e21 | 28.6 | 205 | Citations (PDF) |
| 42 | Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC MutagenesisCell, 2019, 176, 1282-1294.e20 | 28.6 | 407 | Citations (PDF) |
| 43 | Identification of a quadruple mutation that confers tenofovir resistance in chronic hepatitis B patients | 2.9 | 126 | Citations (PDF) |
| 44 | FIREVAT: finding reliable variants without artifacts in human cancer samples using etiologically relevant mutational signatures | 10.1 | 11 | Citations (PDF) |
| 45 | Alterations in the Rho pathway contribute to Epstein-Barr virus–induced lymphomagenesis in immunosuppressed environmentsBlood, 2018, 131, 1931-1941 | 1.0 | 12 | Citations (PDF) |
| 46 | Sox7 promotes high-grade glioma by increasing VEGFR2-mediated vascular abnormality | 8.1 | 42 | Citations (PDF) |
| 47 | Serotonin signals through a gut-liver axis to regulate hepatic steatosis | 14.2 | 138 | Citations (PDF) |
| 48 | Association Between Expression Level of PD1 by Tumor-Infiltrating CD8+ T Cells and Features of Hepatocellular Carcinoma | 1.0 | 244 | Citations (PDF) |
| 49 | Mutalisk: a web-based somatic MUTation AnaLyIS toolKit for genomic, transcriptional and epigenomic signatures | 16.3 | 95 | Citations (PDF) |
| 50 | Human glioblastoma arises from subventricular zone cells with low-level driver mutations | 34.3 | 566 | Citations (PDF) |
| 51 | Patterns and mechanisms of structural variations in human cancer | 11.6 | 90 | Citations (PDF) |
| 52 | Genomic and Immune Profiles of Multiple Myeloma Revealed By Whole Genome and Transcriptome SequencingBlood, 2018, 132, 4493-4493 | 1.0 | 2 | Citations (PDF) |
| 53 | Somatic mutations reveal asymmetric cellular dynamics in the early human embryo | 34.3 | 274 | Citations (PDF) |
| 54 | Clonal History and Genetic Predictors of Transformation Into Small-Cell Carcinomas From Lung Adenocarcinomas | 14.2 | 450 | Citations (PDF) |
| 55 | The mutational signatures and molecular alterations of bladder cancer | 1.3 | 7 | Citations (PDF) |
| 56 | BRAF V600E Kinase Domain Duplication Identified in Therapy-Refractory Melanoma Patient-Derived Xenografts | 6.2 | 73 | Citations (PDF) |
| 57 | Landscape of somatic mutations in 560 breast cancer whole-genome sequences | 34.3 | 2,051 | Citations (PDF) |
| 58 | Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer | 6.2 | 45 | Citations (PDF) |
| 59 | Intracellular mitochondrial DNA transfers to the nucleus in human cancer cells | 3.5 | 7 | Citations (PDF) |
| 60 | Recurrent fusion transcripts detected by whole‐transcriptome sequencing of 120 primary breast cancer samples | 3.4 | 45 | Citations (PDF) |
| 61 | Subclonal diversification of primary breast cancer revealed by multiregion sequencing | 36.5 | 782 | Citations (PDF) |
| 62 | Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells | 4.7 | 92 | Citations (PDF) |
| 63 | Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes | 19.5 | 404 | Citations (PDF) |
| 64 | Abstract 4322: The landscape of mitochondrial DNA mutations in human cancer | 0.6 | 3 | Citations (PDF) |
| 65 | Fine-scale mapping of meiotic recombination in Asians | 2.8 | 17 | Citations (PDF) |
| 66 | Combined linkage and association analyses identify a novel locus for obesity near <i>PROX1</i>
in Asians | 4.3 | 21 | Citations (PDF) |
| 67 | Diagnostic method for the detection of KIF5B-RET transformation in lung adenocarcinoma | 2.0 | 49 | Citations (PDF) |
| 68 | TIARA genome database: update 2013 | 3.0 | 6 | Citations (PDF) |
| 69 | A family-based association study after genome-wide linkage analysis identified two genetic loci for renal function in a Mongolian population | 5.3 | 13 | Citations (PDF) |
| 70 | Comprehensive genomic analyses associate<i>UGT8</i>variants with musical ability in a Mongolian population | 3.7 | 50 | Citations (PDF) |
| 71 | FX: an RNA-Seq analysis tool on the cloud | 5.0 | 67 | Citations (PDF) |
| 72 | The transcriptional landscape and mutational profile of lung adenocarcinoma | 4.7 | 561 | Citations (PDF) |
| 73 | A transforming <i>KIF5B</i> and <i>RET</i> gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing | 4.7 | 459 | Citations (PDF) |
| 74 | Abstract LB-402: New fusion genes in lung adenocarcinoma revealed from next generation RNA-seq 2012, , | | 0 | Citations (PDF) |
| 75 | Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals | 26.1 | 123 | Citations (PDF) |
| 76 | TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology | 16.3 | 15 | Citations (PDF) |
| 77 | Gene mapping study for constitutive skin color in an isolated Mongolian population | 11.6 | 8 | Citations (PDF) |
| 78 | Linkage and association scan for tanning ability in an isolated Mongolian population | 3.1 | 8 | Citations (PDF) |
| 79 | Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing | 26.1 | 179 | Citations (PDF) |
| 80 | Reference-unbiased copy number variant analysis using CGH microarrays | 16.3 | 22 | Citations (PDF) |
| 81 | Higher mitochondrial DNA copy number is associated with lower prevalence of microalbuminuria | 11.6 | 36 | Citations (PDF) |
| 82 | A highly annotated whole-genome sequence of a Korean individual | 34.3 | 301 | Citations (PDF) |
| 83 | A genome-wide Asian genetic map and ethnic comparison: The GENDISCAN study | 3.3 | 25 | Citations (PDF) |
| 84 | Heritability and linkage study on heart rates in a Mongolian population | 11.6 | 7 | Citations (PDF) |
| 85 | Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer | 1.6 | 382 | Citations (PDF) |
