| 1 | Integrated multi-omics analyses identify anti-viral host factors and pathways controlling SARS-CoV-2 infection | 14.1 | 5 | Citations (PDF) |
| 2 | Ex Vivo Expanded Cord Blood Natural Killer Cells Combined with Rituximab and High-Dose Chemotherapy and Autologous Stem Cell Transplantation for B Cell Non-Hodgkin Lymphoma | 1.6 | 3 | Citations (PDF) |
| 3 | Safety, efficacy and determinants of response of allogeneic CD19-specific CAR-NK cells in CD19+ B cell tumors: a phase 1/2 trial | 25.6 | 110 | Citations (PDF) |
| 4 | Estrogen Receptor Mutations as Novel Targets for Immunotherapy in Metastatic Estrogen Receptor–positive Breast Cancer | 3.0 | 3 | Citations (PDF) |
| 5 | Label-aware distance mitigates temporal and spatial variability for clustering and visualization of single-cell gene expression data | 4.5 | 1 | Citations (PDF) |
| 6 | Forecasting acute kidney injury and resource utilization in ICU patients using longitudinal, multimodal models | 4.8 | 1 | Citations (PDF) |
| 7 | CD28 Costimulation Augments CAR Signaling in NK Cells via the LCK/CD3ζ/ZAP70 Signaling Axis | 26.4 | 6 | Citations (PDF) |
| 8 | Phase II study of talazoparib in advanced cancers with BRCA1/2, DNA repair, and PTEN alterations | 6.9 | 2 | Citations (PDF) |
| 9 | BATF is a major driver of NK cell epigenetic reprogramming and dysfunction in AML | 13.1 | 0 | Citations (PDF) |
| 10 | Targeting the Epidermal Growth Factor Receptor Pathway in Chemotherapy-Resistant Triple-Negative Breast Cancer: A Phase II Study | 3.0 | 3 | Citations (PDF) |
| 11 | A spatially resolved single-cell genomic atlas of the adult human breast | 40.1 | 66 | Citations (PDF) |
| 12 | Integrative Prognostic Machine Learning Models in Mantle Cell Lymphoma | 3.0 | 1 | Citations (PDF) |
| 13 | Actionability classification of variants of unknown significance correlates with functional effect | 6.9 | 4 | Citations (PDF) |
| 14 | Single-cell chromatin accessibility profiling of acute myeloid leukemia reveals heterogeneous lineage composition upon therapy-resistance | 4.5 | 6 | Citations (PDF) |
| 15 | Loss of metabolic fitness drives tumor resistance after CAR-NK cell therapy and can be overcome by cytokine engineering | 11.3 | 38 | Citations (PDF) |
| 16 | Single-nucleotide variant calling in single-cell sequencing data with Monopogen | 18.1 | 8 | Citations (PDF) |
| 17 | Characterizing cancer metabolism from bulk and single-cell RNA-seq data using METAFlux | 14.1 | 25 | Citations (PDF) |
| 18 | Pathway centric analysis for single-cell RNA-seq and spatial transcriptomics data with GSDensity | 14.1 | 3 | Citations (PDF) |
| 19 | Sensei: how many samples to tell a change in cell type abundance? | 3.3 | 3 | Citations (PDF) |
| 20 | Clinical and Molecular Characterization of<i>POLE</i>Mutations as Predictive Biomarkers of Response to Immune Checkpoint Inhibitors in Advanced Cancers | 2.1 | 53 | Citations (PDF) |
| 21 | Blinatumomab maintenance after allogeneic hematopoietic cell transplantation for B-lineage acute lymphoblastic leukemiaBlood, 2022, 139, 1908-1919 | 1.0 | 48 | Citations (PDF) |
| 22 | Spatially resolved transcriptomics of high-grade serous ovarian carcinoma | 3.8 | 36 | Citations (PDF) |
| 23 | Spatial charting of single-cell transcriptomes in tissues | 18.1 | 102 | Citations (PDF) |
| 24 | Molecular Correlates of Venous Thromboembolism (VTE) in Ovarian Cancer | 4.0 | 15 | Citations (PDF) |
| 25 | In-depth analysis of SARS-CoV-2–specific T cells reveals diverse differentiation hierarchies in vaccinated individuals | 5.5 | 14 | Citations (PDF) |
| 26 | BHLHE40 Regulates the T-Cell Effector Function Required for Tumor Microenvironment Remodeling and Immune Checkpoint Therapy Efficacy | 3.7 | 17 | Citations (PDF) |
| 27 | Bi-order multimodal integration of single-cell data | 8.4 | 25 | Citations (PDF) |
| 28 | Occult polyclonality of preclinical pancreatic cancer models drives in vitro evolution | 14.1 | 16 | Citations (PDF) |
| 29 | Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer | 16.3 | 102 | Citations (PDF) |
| 30 | A phase two study of high dose blinatumomab in Richter’s syndrome | 8.1 | 19 | Citations (PDF) |
| 31 | KIR-based inhibitory CARs overcome CAR-NK cell trogocytosis-mediated fratricide and tumor escape | 25.6 | 90 | Citations (PDF) |
| 32 | Direct CD32 T-cell cytotoxicity: implications for breast cancer prognosis and treatment | 2.7 | 2 | Citations (PDF) |
| 33 | Ab initio spillover compensation in mass cytometry data | 2.7 | 10 | Citations (PDF) |
| 34 | Targeting a cytokine checkpoint enhances the fitness of armored cord blood CAR-NK cellsBlood, 2021, 137, 624-636 | 1.0 | 188 | Citations (PDF) |
| 35 | Stratified Test Accurately Identifies Differentially Expressed Genes Under Batch Effects in Single-Cell Data | 3.7 | 4 | Citations (PDF) |
| 36 | MEDALT: single-cell copy number lineage tracing enabling gene discovery | 8.4 | 21 | Citations (PDF) |
| 37 | Single-cell RNA-seq analysis reveals compartment-specific heterogeneity and plasticity of microglia | 3.8 | 40 | Citations (PDF) |
| 38 | Genomic, Transcriptomic, and Proteomic Profiling of Metastatic Breast Cancer | 6.4 | 17 | Citations (PDF) |
| 39 | Spatially interacting phosphorylation sites and mutations in cancer | 14.1 | 11 | Citations (PDF) |
| 40 | Combining AFM13, a Bispecific CD30/CD16 Antibody, with Cytokine-Activated Blood and Cord Blood–Derived NK Cells Facilitates CAR-like Responses Against CD30+ Malignancies | 6.4 | 90 | Citations (PDF) |
| 41 | Metabolic Reprogramming of GMP Grade Cord Tissue Derived Mesenchymal Stem Cells Enhances Their Suppressive Potential in GVHD | 5.0 | 15 | Citations (PDF) |
| 42 | Single-cell manifold-preserving feature selection for detecting rare cell populations | 7.3 | 24 | Citations (PDF) |
| 43 | Extended live-cell barcoding approach for multiplexed mass cytometry | 3.7 | 11 | Citations (PDF) |
| 44 | Uncoupling of gene expression from copy number presents therapeutic opportunities in aneuploid cancers | 7.3 | 5 | Citations (PDF) |
| 45 | Targeting the αv integrin/TGF-β axis improves natural killer cell function against glioblastoma stem cells | 9.1 | 147 | Citations (PDF) |
| 46 | Generation of glucocorticoid-resistant SARS-CoV-2 T cells for adoptive cell therapy | 6.4 | 26 | Citations (PDF) |
| 47 | Decoupling Lineage-Associated Genes in Acute Myeloid Leukemia Reveals Inflammatory and Metabolic Signatures Associated With Outcomes | 2.7 | 9 | Citations (PDF) |
| 48 | Oxidative Phosphorylation Is a Metabolic Vulnerability in Chemotherapy-Resistant Triple-Negative Breast Cancer | 0.6 | 82 | Citations (PDF) |
| 49 | Delineating copy number and clonal substructure in human tumors from single-cell transcriptomes | 18.1 | 353 | Citations (PDF) |
| 50 | Single-cell dissection of intratumoral heterogeneity and lineage diversity in metastatic gastric adenocarcinoma | 25.6 | 150 | Citations (PDF) |
| 51 | Targeting Polo-like Kinase 4 Triggers Polyploidy and Apoptotic Cell Death in TP53-Mutant Acute Myeloid LeukemiaBlood, 2021, 138, 1167-1167 | 1.0 | 4 | Citations (PDF) |
| 52 | A robust benchmark for detection of germline large deletions and insertions | 18.1 | 198 | Citations (PDF) |
| 53 | Relative Abundance of SARS-CoV-2 Entry Genes in the Enterocytes of the Lower Gastrointestinal Tract | 2.7 | 56 | Citations (PDF) |
| 54 | Latent periodic process inference from single-cell RNA-seq data | 14.1 | 18 | Citations (PDF) |
| 55 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition | 16.3 | 257 | Citations (PDF) |
| 56 | Stratified Test Alleviates Batch Effects in Single-Cell Data | 0.0 | 1 | Citations (PDF) |
| 57 | Hybrid oncocytic/chromophobe renal tumors are molecularly distinct from oncocytoma and chromophobe renal cell carcinoma | 5.0 | 37 | Citations (PDF) |
| 58 | SiCloneFit: Bayesian inference of population structure, genotype, and phylogeny of tumor clones from single-cell genome sequencing data | 4.6 | 71 | Citations (PDF) |
| 59 | Elevated Endogenous SDHA Drives Pathological Metabolism in Highly Metastatic Uveal Melanoma 2019, 60, 4187 | | 28 | Citations (PDF) |
| 60 | SCMarker: Ab initio marker selection for single cell transcriptome profiling | 3.3 | 24 | Citations (PDF) |
| 61 | Comments on the model parameters in “SiFit: inferring tumor trees from single-cell sequencing data under finite-sites models” | 8.4 | 0 | Citations (PDF) |
| 62 | Multi-platform discovery of haplotype-resolved structural variation in human genomes | 14.1 | 544 | Citations (PDF) |
| 63 | Comparison of different functional prediction scores using a gene-based permutation model for identifying cancer driver genes | 1.8 | 7 | Citations (PDF) |
| 64 | Integrated transcriptomic–genomic tool Texomer profiles cancer tissues | 14.5 | 6 | Citations (PDF) |
| 65 | Prospective Clinical Sequencing of Adult Glioma | 1.7 | 14 | Citations (PDF) |
| 66 | A novel immature natural killer cell subpopulation predicts relapse after cord blood transplantation | 5.3 | 25 | Citations (PDF) |
| 67 | Expanded Analysis of Secondary Germline Findings From Matched Tumor/Normal Sequencing Identifies Additional Clinically Significant Mutations | 2.1 | 12 | Citations (PDF) |
| 68 | Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profiling | 14.1 | 82 | Citations (PDF) |
| 69 | Distinct Biological Types of Ocular Adnexal Sebaceous Carcinoma: HPV-Driven and Virus-Negative Tumors Arise through Nonoverlapping Molecular-Genetic Alterations | 6.4 | 44 | Citations (PDF) |
| 70 | Untying the gordion knot of targeting MET in cancer | 10.1 | 19 | Citations (PDF) |
| 71 | Computational approaches for inferring tumor evolution from single-cell genomic data | 1.9 | 20 | Citations (PDF) |
| 72 | Survival Outcomes by <i>TP53</i> Mutation Status in Metastatic Breast Cancer | 2.1 | 48 | Citations (PDF) |
| 73 | Hypervirulent group A Streptococcus emergence in an acaspular background is associated with marked remodeling of the bacterial cell surface | 2.5 | 13 | Citations (PDF) |
| 74 | Genetic biomarkers of sensitivity and resistance to venetoclax monotherapy in patients with relapsed acute myeloid leukemia | 6.3 | 120 | Citations (PDF) |
| 75 | Structural Variant Breakpoint Detection with novoBreak | 0.0 | 2 | Citations (PDF) |
| 76 | In vivo screening identifies GATAD2B as a metastasis driver in KRAS-driven lung cancer | 14.1 | 34 | Citations (PDF) |
| 77 | Metachronous Medulloblastoma in a Child With Successfully Treated Neuroblastoma: Case Report and Novel Findings of DNA Sequencing | 16.1 | 2 | Citations (PDF) |
| 78 | Targeted next generation sequencing of well-differentiated/dedifferentiated liposarcoma reveals novel gene amplifications and mutations | 1.7 | 27 | Citations (PDF) |
| 79 | HySA: a Hybrid Structural variant Assembly approach using next-generation and single-molecule sequencing technologies | 4.6 | 22 | Citations (PDF) |
| 80 | Active Disclosure of Secondary Germline Findings to Deceased Research Participants’ Personal Representatives: Process and Outcomes | 2.1 | 4 | Citations (PDF) |
| 81 | A feasibility study of returning clinically actionable somatic genomic alterations identified in a research laboratory | 1.7 | 13 | Citations (PDF) |
| 82 | Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms | 14.1 | 67 | Citations (PDF) |
| 83 | Ploidy-Seq: inferring mutational chronology by sequencing polyploid tumor subpopulations | 9.9 | 6 | Citations (PDF) |
| 84 | A Decision Support Framework for Genomically Informed Investigational Cancer Therapy | 5.1 | 162 | Citations (PDF) |
| 85 | Towards accurate characterization of clonal heterogeneity based on structural variation | 3.3 | 9 | Citations (PDF) |
| 86 | A survey of intragenic breakpoints in glioblastoma identifies a distinct subset associated with poor survival | 4.8 | 62 | Citations (PDF) |
| 87 | Background Mutations in Parental Cells Account for Most of the Genetic Heterogeneity of Induced Pluripotent Stem Cells | 17.2 | 175 | Citations (PDF) |
| 88 | Clonal Architecture of Secondary Acute Myeloid Leukemia | 25.5 | 662 | Citations (PDF) |
| 89 | Use of Whole-Genome Sequencing to Diagnose a Cryptic Fusion Oncogene | 13.7 | 210 | Citations (PDF) |
| 90 | Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression | 9.1 | 83 | Citations (PDF) |
| 91 | CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data | 5.0 | 52 | Citations (PDF) |
| 92 | PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data | 4.6 | 65 | Citations (PDF) |
| 93 | An automatic prosody labeling system using ANN-based syntactic-prosodic model and GMM-based acoustic-prosodic model 0, , | | 40 | Citations (PDF) |
| 94 | Computational Prediction of Genetic Drivers in Cancer 0, , 1-16 | | 3 | Citations (PDF) |
