| 1 | Cerebral organoids containing an <i>AUTS2</i> missense variant model microcephalyBrain, 2023, 146, 387-404 | 8.5 | 50 | Citations (PDF) |
| 2 | Long‐read whole genome sequencing reveals HOXD13 alterations in synpolydactyly | 3.9 | 12 | Citations (PDF) |
| 3 | A deletion in the N gene of SARS-CoV-2 may reduce test sensitivity for detection of SARS-CoV-2 | 1.7 | 15 | Citations (PDF) |
| 4 | Case report and review of the literature: immune dysregulation in a large familial cohort due to a novel pathogenic<i>RELA</i>variant | 1.9 | 16 | Citations (PDF) |
| 5 | Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers | 0.6 | 11 | Citations (PDF) |
| 6 | Acute lymphoblastic leukemia displays a distinct highly methylated genome | 22.9 | 42 | Citations (PDF) |
| 7 | De novo missense variant in <i>GRIA2</i> in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy | 1.4 | 8 | Citations (PDF) |
| 8 | Detection of brain somatic variation in epilepsy‐associated developmental lesions | 4.6 | 45 | Citations (PDF) |
| 9 | Molecular Heterogeneity in Pediatric Malignant Rhabdoid Tumors in Patients With Multi-Organ Involvement | 2.7 | 7 | Citations (PDF) |
| 10 | The genome of the stable fly, Stomoxys calcitrans, reveals potential mechanisms underlying reproduction, host interactions, and novel targets for pest control | 4.0 | 31 | Citations (PDF) |
| 11 | Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma | 5.2 | 11 | Citations (PDF) |
| 12 | PTEN somatic mutations contribute to spectrum of cerebral overgrowthBrain, 2021, 144, 2971-2978 | 8.5 | 37 | Citations (PDF) |
| 13 | Hypomorphic alleles pose challenges in rare disease genomic variant interpretation | 2.1 | 5 | Citations (PDF) |
| 14 | Genomic Profiling of Lung Adenocarcinoma in Never-Smokers | 21.6 | 98 | Citations (PDF) |
| 15 | A novel sialic acid-binding adhesin present in multiple species contributes to the pathogenesis of Infective endocarditis | 4.5 | 17 | Citations (PDF) |
| 16 | YAP1-FAM118B Fusion Defines a Rare Subset of Childhood and Young Adulthood Meningiomas | 3.6 | 26 | Citations (PDF) |
| 17 | Maternal mosaicism for a missense variant in the <i>SMS</i> gene that causes Snyder–Robinson syndrome | 1.4 | 1 | Citations (PDF) |
| 18 | Discovery of clinically relevant fusions in pediatric cancer | 3.3 | 24 | Citations (PDF) |
| 19 | Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas | 5.2 | 15 | Citations (PDF) |
| 20 | Infantile fibrosarcoma–like tumor driven by novel <i>RBPMS-MET</i> fusion consolidated with cabozantinib | 1.4 | 23 | Citations (PDF) |
| 21 | Genetic Characterization of Pediatric Sarcomas by Targeted RNA Sequencing | 2.6 | 16 | Citations (PDF) |
| 22 | Sequence analysis in <i>Bos taurus</i> reveals pervasiveness of X–Y arms races in mammalian lineages | 4.6 | 42 | Citations (PDF) |
| 23 | Long non-coding RNA RAMS11 promotes metastatic colorectal cancer progression | 13.9 | 110 | Citations (PDF) |
| 24 | Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience | 1.4 | 27 | Citations (PDF) |
| 25 | Early-onset Wilson disease caused by <i>ATP7B</i> exon skipping associated with intronic variant | 1.4 | 7 | Citations (PDF) |
| 26 | The clonal evolution of metastatic colorectal cancer | 11.2 | 71 | Citations (PDF) |
| 27 | Somatic
<i>SLC35A2</i>
mosaicism correlates with clinical findings in epilepsy brain tissue | 2.4 | 36 | Citations (PDF) |
| 28 | MYCN amplification and ATRX mutations are incompatible in neuroblastoma | 13.9 | 98 | Citations (PDF) |
| 29 | The Genotypic and Phenotypic Spectrum of <i>BICD2</i> Variants in Spinal Muscular Atrophy | 6.3 | 29 | Citations (PDF) |
| 30 | <i>De novo</i> primary central nervous system pure erythroid leukemia/sarcoma with t(1;16)(p31;q24) <i>NFIA/CBFA2T3</i> translocation | 4.1 | 15 | Citations (PDF) |
| 31 | Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q | 1.2 | 13 | Citations (PDF) |
| 32 | Mutations in
<i>PLS1</i>
, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss | 3.9 | 27 | Citations (PDF) |
| 33 | Streptococcus oralis subsp.
<i>dentisani</i>
Produces Monolateral Serine-Rich Repeat Protein Fibrils, One of Which Contributes to Saliva Binding via Sialic Acid | 2.7 | 20 | Citations (PDF) |
| 34 | Expansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasia | 3.2 | 18 | Citations (PDF) |
| 35 | Exome sequencing of Finnish isolates enhances rare-variant association power | 39.5 | 189 | Citations (PDF) |
| 36 | Samovar: Single-Sample Mosaic Single-Nucleotide Variant Calling with Linked Reads | 3.7 | 9 | Citations (PDF) |
| 37 | Comparative genomic analysis of six Glossina genomes, vectors of African trypanosomes | 8.2 | 92 | Citations (PDF) |
| 38 | The Clonal Evolution of Metastatic Osteosarcoma as Shaped by Cisplatin Treatment | 3.5 | 54 | Citations (PDF) |
| 39 | Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma | 1.6 | 14 | Citations (PDF) |
| 40 | Novel in-frame <i>FLNB</i> deletion causes Larsen syndrome in a three-generation pedigree | 1.4 | 2 | Citations (PDF) |
| 41 | Association of Tumor Microenvironment T-cell Repertoire and Mutational Load with Clinical Outcome after Sequential Checkpoint Blockade in Melanoma | 4.3 | 57 | Citations (PDF) |
| 42 | Characterizing the Major Structural Variant Alleles of the Human GenomeCell, 2019, 176, 663-675.e19 | 34.4 | 440 | Citations (PDF) |
| 43 | Genome sequencing identifies somatic <i>BRAF</i> duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma | 1.4 | 9 | Citations (PDF) |
| 44 | Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (
<i>CFH</i>
) gene family | 7.8 | 59 | Citations (PDF) |
| 45 | An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome AnalyticsCell, 2018, 173, 400-416.e11 | 34.4 | 3,192 | Citations (PDF) |
| 46 | Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of CancerCell, 2018, 173, 291-304.e6 | 34.4 | 2,264 | Citations (PDF) |
| 47 | A Pan-Cancer Analysis of Enhancer Expression in Nearly 9000 Patient SamplesCell, 2018, 173, 386-399.e12 | 34.4 | 290 | Citations (PDF) |
| 48 | Perspective on Oncogenic Processes at the End of the Beginning of Cancer GenomicsCell, 2018, 173, 305-320.e10 | 34.4 | 359 | Citations (PDF) |
| 49 | Machine Learning Identifies Stemness Features Associated with Oncogenic DedifferentiationCell, 2018, 173, 338-354.e15 | 34.4 | 1,951 | Citations (PDF) |
| 50 | Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types | 6.4 | 423 | Citations (PDF) |
| 51 | Driver Fusions and Their Implications in the Development and Treatment of Human Cancers | 6.4 | 567 | Citations (PDF) |
| 52 | Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context | 6.4 | 238 | Citations (PDF) |
| 53 | Spatial Organization and Molecular Correlation of Tumor-Infiltrating Lymphocytes Using Deep Learning on Pathology Images | 6.4 | 907 | Citations (PDF) |
| 54 | Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas | 6.4 | 145 | Citations (PDF) |
| 55 | Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer Types | 6.4 | 102 | Citations (PDF) |
| 56 | Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas | 6.4 | 1,025 | Citations (PDF) |
| 57 | Molecular Characterization and Clinical Relevance of Metabolic Expression Subtypes in Human Cancers | 6.4 | 281 | Citations (PDF) |
| 58 | Systematic Analysis of Splice-Site-Creating Mutations in Cancer | 6.4 | 222 | Citations (PDF) |
| 59 | A de novo nonsense mutation in <i>ASXL3</i> shared by siblings with Bainbridge–Ropers syndrome | 1.4 | 40 | Citations (PDF) |
| 60 | Improving eukaryotic genome annotation using single molecule mRNA sequencing | 3.3 | 20 | Citations (PDF) |
| 61 | Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines | 6.0 | 789 | Citations (PDF) |
| 62 | Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas | 6.0 | 392 | Citations (PDF) |
| 63 | lncRNA Epigenetic Landscape Analysis Identifies EPIC1 as an Oncogenic lncRNA that Interacts with MYC and Promotes Cell-Cycle Progression in Cancer | 38.5 | 449 | Citations (PDF) |
| 64 | Genomic and Functional Approaches to Understanding Cancer Aneuploidy | 38.5 | 1,015 | Citations (PDF) |
| 65 | Comparative Molecular Analysis of Gastrointestinal Adenocarcinomas | 38.5 | 507 | Citations (PDF) |
| 66 | Comprehensive Molecular Characterization of the Hippo Signaling Pathway in Cancer | 6.4 | 469 | Citations (PDF) |
| 67 | Immune Escape of Relapsed AML Cells after Allogeneic Transplantation | 44.0 | 433 | Citations (PDF) |
| 68 | Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer | 13.9 | 151 | Citations (PDF) |
| 69 | The prognostic effects of somatic mutations in ER-positive breast cancer | 13.9 | 119 | Citations (PDF) |
| 70 | In-frame de novo mutation in <i>BICD2</i> in two patients with muscular atrophy and arthrogryposis | 1.4 | 18 | Citations (PDF) |
| 71 | Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients | 38.5 | 856 | Citations (PDF) |
| 72 | Structure-Guided Redesign Improves NFL HIV Env Trimer Integrity and Identifies an Inter-Protomer Disulfide Permitting Post-Expression Cleavage | 5.1 | 43 | Citations (PDF) |
| 73 | Cleavage-Independent HIV-1 Trimers From CHO Cell Lines Elicit Robust Autologous Tier 2 Neutralizing Antibodies | 5.1 | 29 | Citations (PDF) |
| 74 | Identification of Therapeutic Targets in Rhabdomyosarcoma through Integrated Genomic, Epigenomic, and Proteomic Analyses | 38.5 | 138 | Citations (PDF) |
| 75 | High-resolution comparative analysis of great ape genomes | 37.0 | 364 | Citations (PDF) |
| 76 | Long-read sequence and assembly of segmental duplications | 26.1 | 203 | Citations (PDF) |
| 77 | Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation | 8.5 | 227 | Citations (PDF) |
| 78 | Avian W and mammalian Y chromosomes convergently retained dosage-sensitive regulators | 25.9 | 179 | Citations (PDF) |
| 79 | Building and Improving Reference Genome Assemblies | 9.6 | 7 | Citations (PDF) |
| 80 | CpG Island Hypermethylation Mediated by DNMT3A Is a Consequence of AML ProgressionCell, 2017, 168, 801-816.e13 | 34.4 | 209 | Citations (PDF) |
| 81 | The evolution and population diversity of human-specific segmental duplications | 10.7 | 155 | Citations (PDF) |
| 82 | Mutational landscape and response are conserved in peripheral blood of AML and MDS patients during decitabine therapyBlood, 2017, 129, 1397-1401 | 4.2 | 28 | Citations (PDF) |
| 83 | Real-Time Electronic Tracking of Diarrheal Episodes and Laxative Therapy Enables Verification of Clostridium difficile Clinical Testing Criteria and Reduction of Clostridium difficile Infection Rates | 4.1 | 73 | Citations (PDF) |
| 84 | Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly | 4.6 | 1,103 | Citations (PDF) |
| 85 | The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis | 12.4 | 278 | Citations (PDF) |
| 86 | Whole genome analysis of a schistosomiasis-transmitting freshwater snail | 13.9 | 253 | Citations (PDF) |
| 87 | Ancient hybridization and strong adaptation to viruses across African vervet monkey populations | 25.9 | 125 | Citations (PDF) |
| 88 | Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate | 25.9 | 65 | Citations (PDF) |
| 89 | Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes | 0.4 | 10 | Citations (PDF) |
| 90 | Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue SarcomasCell, 2017, 171, 950-965.e28 | 34.4 | 957 | Citations (PDF) |
| 91 | Discovery and genotyping of structural variation from long-read haploid genome sequence data | 4.6 | 378 | Citations (PDF) |
| 92 | Glutaraldehyde Cross-linking of HIV-1 Env Trimers Skews the Antibody Subclass Response in Mice | 5.1 | 9 | Citations (PDF) |
| 93 | Acute Illness Among Surfers After Exposure to Seawater in Dry- and Wet-Weather Conditions | 3.4 | 64 | Citations (PDF) |
| 94 | The Contribution of GWAS Loci in Familial Dyslipidemias | 3.3 | 54 | Citations (PDF) |
| 95 | Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases | 8.1 | 98 | Citations (PDF) |
| 96 | Dictyocaulus viviparus genome, variome and transcriptome elucidate lungworm biology and support future intervention | 3.5 | 28 | Citations (PDF) |
| 97 | Long-read sequence assembly of the gorilla genome | 37.0 | 392 | Citations (PDF) |
| 98 | Opsin Repertoire and Expression Patterns in Horseshoe Crabs: Evidence from the Genome of<i>Limulus polyphemus</i>(Arthropoda: Chelicerata) | 2.4 | 55 | Citations (PDF) |
| 99 | DGIdb 2.0: mining clinically relevant drug–gene interactions | 15.8 | 431 | Citations (PDF) |
| 100 | Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas | 6.4 | 29 | Citations (PDF) |
| 101 | Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region | 4.6 | 41 | Citations (PDF) |
| 102 | Pangolin genomes and the evolution of mammalian scales and immunity | 4.6 | 118 | Citations (PDF) |
| 103 | Rare Variation in <i>TET2</i> Is Associated with Clinically Relevant Prostate Carcinoma in African Americans | 1.2 | 26 | Citations (PDF) |
| 104 | <i>TP53</i> and Decitabine in Acute Myeloid Leukemia and Myelodysplastic Syndromes | 44.0 | 762 | Citations (PDF) |
| 105 | Deregulation of DUX4 and ERG in acute lymphoblastic leukemia | 25.9 | 286 | Citations (PDF) |
| 106 | Genome sequence of the basal haplorrhine primate Tarsius syrichta reveals unusual insertions | 13.9 | 38 | Citations (PDF) |
| 107 | Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers | 13.9 | 75 | Citations (PDF) |
| 108 | Genomic analysis reveals hidden biodiversity within colugos, the sister group to primates | 11.2 | 80 | Citations (PDF) |
| 109 | A High-Resolution SNP Array-Based Linkage Map Anchors a New Domestic Cat Draft Genome Assembly and Provides Detailed Patterns of Recombination | 2.0 | 51 | Citations (PDF) |
| 110 | Research note: Natural environments and prescribing in England | 9.0 | 12 | Citations (PDF) |
| 111 | Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia | 0.4 | 48 | Citations (PDF) |
| 112 | Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology | 9.2 | 358 | Citations (PDF) |
| 113 | INTEGRATE: gene fusion discovery using whole genome and transcriptome data | 4.6 | 131 | Citations (PDF) |
| 114 | The<i>Physarum polycephalum</i>Genome Reveals Extensive Use of Prokaryotic Two-Component and Metazoan-Type Tyrosine Kinase Signaling | 2.4 | 96 | Citations (PDF) |
| 115 | Thermostability of Well-Ordered HIV Spikes Correlates with the Elicitation of Autologous Tier 2 Neutralizing Antibodies | 4.5 | 79 | Citations (PDF) |
| 116 | Inactivation of RASA1 promotes melanoma tumorigenesis via R-Ras activation | 1.7 | 24 | Citations (PDF) |
| 117 | Abstract 1863: Inactivation of RASA1 promotes melanoma tumorigenesis via R-Ras activation 2016, , | | 0 | Citations (PDF) |
| 118 | Rare Pre-Existing MDS Subclones Contribute to Secondary AML ProgressionBlood, 2016, 128, 959-959 | 4.2 | 12 | Citations (PDF) |
| 119 | Dynamic Changes in MDS Clonal Architecture Following Allogeneic Stem Cell TransplantBlood, 2016, 128, 5506-5506 | 4.2 | 0 | Citations (PDF) |
| 120 | Clonal Evolution of Acute Myeloid Leukemia Following Allogeneic Stem Cell TransplantationBlood, 2016, 128, 1528-1528 | 4.2 | 5 | Citations (PDF) |
| 121 | DNMT3A-Dependent DNA Methylation May Act As a Tumor Suppressor-Not a Tumor Promoter-during AML ProgressionBlood, 2016, 128, 1050-1050 | 4.2 | 3 | Citations (PDF) |
| 122 | Optimizing Cancer Genome Sequencing and Analysis | 6.0 | 191 | Citations (PDF) |
| 123 | Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemiaBlood, 2015, 126, 2484-2490 | 4.2 | 228 | Citations (PDF) |
| 124 | Genetic Heterogeneity of Induced Pluripotent Stem Cells: Results from 24 Clones Derived from a Single C57BL/6 Mouse | 2.4 | 13 | Citations (PDF) |
| 125 | Genome Modeling System: A Knowledge Management Platform for Genomics | 3.2 | 84 | Citations (PDF) |
| 126 | Whole Body Melanoma Transcriptome Response in Medaka | 2.4 | 14 | Citations (PDF) |
| 127 | Extreme selective sweeps independently targeted the X chromosomes of the great apes | 7.8 | 86 | Citations (PDF) |
| 128 | Genome of
<i>Rhodnius prolixus</i>
, an insect vector of Chagas disease, reveals unique adaptations to hematophagy and parasite infection | 7.8 | 376 | Citations (PDF) |
| 129 | Germline Mutations in Predisposition Genes in Pediatric Cancer | 44.0 | 1,184 | Citations (PDF) |
| 130 | Patterns and functional implications of rare germline variants across 12 cancer types | 13.9 | 277 | Citations (PDF) |
| 131 | The Genomic Landscape of Childhood and Adolescent Melanoma | 2.4 | 169 | Citations (PDF) |
| 132 | Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci | 6.6 | 172 | Citations (PDF) |
| 133 | Genomic landscape of paediatric adrenocortical tumours | 13.9 | 194 | Citations (PDF) |
| 134 | Cracking the nodule worm code advances knowledge of parasite biology and biotechnology to tackle major diseases of livestock | 12.0 | 24 | Citations (PDF) |
| 135 | The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias | 25.9 | 464 | Citations (PDF) |
| 136 | A global reference for human genetic variation | 39.5 | 17,885 | Citations (PDF) |
| 137 | Genome Sequence of Enterovirus D68 from St. Louis, Missouri, USA | 3.9 | 35 | Citations (PDF) |
| 138 | Genetic variation and the de novo assembly of human genomes | 46.1 | 337 | Citations (PDF) |
| 139 | Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits | 4.0 | 46 | Citations (PDF) |
| 140 | Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer | 34.4 | 1,758 | Citations (PDF) |
| 141 | Alzheimer's disease: rare variants with large effect sizes | 3.3 | 39 | Citations (PDF) |
| 142 | Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia | 17.2 | 322 | Citations (PDF) |
| 143 | The genome of the vervet (<i>Chlorocebus aethiops sabaeus</i>) | 4.6 | 125 | Citations (PDF) |
| 144 | Recurrent Somatic Genomic Alterations in Follicular NHL (FL) Revealed By Exome and Custom-Capture Next Generation SequencingBlood, 2015, 126, 574-574 | 4.2 | 3 | Citations (PDF) |
| 145 | Dynamic Changes in the Clonal Structure of MDS and AML in Response to Epigenetic TherapyBlood, 2015, 126, 610-610 | 4.2 | 3 | Citations (PDF) |
| 146 | Dynamic Changes in Clonal Clearance with Decitabine Therapy in AML and MDS PatientsBlood, 2015, 126, 689-689 | 4.2 | 1 | Citations (PDF) |
| 147 | Expression of an Oncogenic ERG isoform Characterizes a Distinct Subtype of B-Progenitor Acute Lymphoblastic LeukemiaBlood, 2015, 126, 693-693 | 4.2 | 1 | Citations (PDF) |
| 148 | Abstract A05: Identification of RASA1 as a novel melanoma tumor suppressor gene 2015, , | | 0 | Citations (PDF) |
| 149 | Abstract 3878: A model to assess clonal evolution of metastatic colorectal cancer during chemotherapy utilizing patient derived xenografts 2015, , | | 0 | Citations (PDF) |
| 150 | Abstract 169: Metastatic colorectal cancer associated long non-coding RNAs identified by transcriptome sequencing of matched primary and metastatic patient tissues 2015, , | | 0 | Citations (PDF) |
| 151 | Abstract 4792: Comprehensive molecular pathology analysis of small bowel adenocarcinoma reveals novel targets with clinical utility 2015, , | | 0 | Citations (PDF) |
| 152 | Abstract 4109: Clonal evolution of metastatic colorectal cancer 2015, , | | 0 | Citations (PDF) |
| 153 | Abstract 959: Aromatase inhibition shapes the clonal architecture of estrogen receptor-positive breast cancers 2015, , | | 0 | Citations (PDF) |
| 154 | Abstract PR03: Genomic approaches for risk assessment in acute myeloid leukemia 2015, , | | 0 | Citations (PDF) |
| 155 | Abstract PR11: Genomic approaches for risk assessment in acute myeloid leukemia 2015, , | | 0 | Citations (PDF) |
| 156 | Abstract A1-06: Recurrent mutations of hormone-positive breast cancer and association with outcome 2015, , | | 0 | Citations (PDF) |
| 157 | Abstract A1-44: Clinical cancer sequencing and integrated analysis of whole genomes, exomes and transcriptomes 2015, , | | 0 | Citations (PDF) |
| 158 | Abstract A2-25: Identification of RASA1 as a novel melanoma tumor suppressor gene 2015, , | | 0 | Citations (PDF) |
| 159 | Abstract A2-42: Identifying clinically important somatic mutations through a knowledge-based approach 2015, , | | 0 | Citations (PDF) |
| 160 | Abstract A1-13: Ultra-deep whole-genome sequencing reveals clinically relevant low-frequency subclones in an acute myeloid leukemia 2015, , | | 0 | Citations (PDF) |
| 161 | Abstract PR01: Identifying clinically important somatic mutations through a knowledge-based approach 2015, , | | 0 | Citations (PDF) |
| 162 | Detection of Clonal Hematopoiesis in Cytopenic Patients Using Targeted SequencingBlood, 2015, 126, 1654-1654 | 4.2 | 0 | Citations (PDF) |
| 163 | Non-Malignant Oligoclonal Hematopoiesis Commonly Follows Cytoreductive Chemotherapy in Adult De Novo AML PatientsBlood, 2015, 126, 686-686 | 4.2 | 0 | Citations (PDF) |
| 164 | Clonal Architectures and Driver Mutations in Metastatic Melanomas | 2.4 | 79 | Citations (PDF) |
| 165 | Abnormal B cell memory subsets dominate HIV-specific responses in infected individuals | 9.0 | 140 | Citations (PDF) |
| 166 | Genome of the house fly, Musca domestica L., a global vector of diseases with adaptations to a septic environment | 8.2 | 295 | Citations (PDF) |
| 167 | A Dominant Mutation in Hexokinase 1 (<i>HK1</i>) Causes Retinitis Pigmentosa 2014, 55, 7147 | | 59 | Citations (PDF) |
| 168 | SciClone: Inferring Clonal Architecture and Tracking the Spatial and Temporal Patterns of Tumor Evolution | 3.2 | 446 | Citations (PDF) |
| 169 | Clonal Architecture of Secondary Acute Myeloid Leukemia Defined by Single-Cell Sequencing | 3.3 | 125 | Citations (PDF) |
| 170 | Draft Genome Sequence of Acetobacter aceti Strain 1023, a Vinegar Factory Isolate | 0.7 | 5 | Citations (PDF) |
| 171 | C11ORF95-RELA FUSIONS DRIVE ONCOGENIC NF-KB SIGNALING IN EPENDYMOMA | 0.9 | 1 | Citations (PDF) |
| 172 | Comparative genomics reveals insights into avian genome evolution and adaptation | 37.0 | 1,029 | Citations (PDF) |
| 173 | Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci | 3.3 | 51 | Citations (PDF) |
| 174 | Functional Heterogeneity of Genetically Defined Subclones in Acute Myeloid Leukemia | 38.5 | 363 | Citations (PDF) |
| 175 | The landscape of somatic mutations in epigenetic regulators across 1,000 paediatric cancer genomes | 13.9 | 385 | Citations (PDF) |
| 176 | Genome of the human hookworm Necator americanus | 25.9 | 178 | Citations (PDF) |
| 177 | C11orf95–RELA fusions drive oncogenic NF-κB signalling in ependymoma | 39.5 | 639 | Citations (PDF) |
| 178 | Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders | 6.6 | 38 | Citations (PDF) |
| 179 | Subtelomeric CTCF and cohesin binding site organization using improved subtelomere assemblies and a novel annotation pipeline | 4.6 | 76 | Citations (PDF) |
| 180 | Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators | 39.5 | 642 | Citations (PDF) |
| 181 | Genome Sequence of the Tsetse Fly (
<i>Glossina morsitans</i>
): Vector of African Trypanosomiasis | 37.0 | 273 | Citations (PDF) |
| 182 | Using SomaticSniper to Detect Somatic Single Nucleotide Variants | 3.3 | 4 | Citations (PDF) |
| 183 | Reconstructing complex regions of genomes using long-read sequencing technology | 4.6 | 235 | Citations (PDF) |
| 184 | Integrated analysis of germline and somatic variants in ovarian cancer | 13.9 | 283 | Citations (PDF) |
| 185 | Elephant shark genome provides unique insights into gnathostome evolution | 39.5 | 757 | Citations (PDF) |
| 186 | Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability | 25.9 | 119 | Citations (PDF) |
| 187 | Sequencing the Mouse Y Chromosome Reveals Convergent Gene Acquisition and Amplification on Both Sex Chromosomes | 34.4 | 333 | Citations (PDF) |
| 188 | Single haplotype assembly of the human genome from a hydatidiform mole | 4.6 | 143 | Citations (PDF) |
| 189 | Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domestication | 7.8 | 331 | Citations (PDF) |
| 190 | Genomic Landscape of Ewing Sarcoma Defines an Aggressive Subtype with Co-Association of <i>STAG2</i> and <i>TP53</i> Mutations | 25.6 | 514 | Citations (PDF) |
| 191 | Age-related mutations associated with clonal hematopoietic expansion and malignancies | 40.4 | 1,791 | Citations (PDF) |
| 192 | Targetable Kinase-Activating Lesions in Ph-like Acute Lymphoblastic Leukemia | 44.0 | 1,315 | Citations (PDF) |
| 193 | Gibbon genome and the fast karyotype evolution of small apes | 39.5 | 372 | Citations (PDF) |
| 194 | Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome | 3.3 | 49 | Citations (PDF) |
| 195 | The R882H DNMT3A Mutation Associated with AML Dominantly Inhibits Wild-Type DNMT3A by Blocking Its Ability to Form Active Tetramers | 38.5 | 428 | Citations (PDF) |
| 196 | Caspase-9 is required for normal hematopoietic development and protection from alkylator-induced DNA damage in miceBlood, 2014, 124, 3887-3895 | 4.2 | 23 | Citations (PDF) |
| 197 | Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity | 3.8 | 52 | Citations (PDF) |
| 198 | Incidence of Germline Mutations in Cancer-Predisposition Genes in Children with Hematologic Malignancies: a Report from the Pediatric Cancer Genome ProjectBlood, 2014, 124, 127-127 | 4.2 | 11 | Citations (PDF) |
| 199 | Whole-Genome Bisulfite Sequencing of Primary AML Cells with the DNMT3A R882H Mutation Identifies Regions of Focal Hypomethylation That Are Associated with Open ChromatinBlood, 2014, 124, 608-608 | 4.2 | 4 | Citations (PDF) |
| 200 | RB1 gene inactivation by chromothripsis in human retinoblastoma | 1.7 | 124 | Citations (PDF) |
| 201 | Abstract 442:RASA1alteration promotes melanoma tumorigenesis 2014, , | | 0 | Citations (PDF) |
| 202 | Abstract 5181: Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers 2014, , | | 0 | Citations (PDF) |
| 203 | Abstract PR03: The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma | 0.6 | 2 | Citations (PDF) |
| 204 | Whole Genome Bisulfite Sequencing of Purified Mouse Promyelocytes Reveals Differentially Methylated Regions in Cells Expressing PML-RaraBlood, 2014, 124, 3531-3531 | 4.2 | 0 | Citations (PDF) |
| 205 | The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage | 8.2 | 289 | Citations (PDF) |
| 206 | Retrotransposition of gene transcripts leads to structural variation in mammalian genomes | 8.2 | 112 | Citations (PDF) |
| 207 | Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation | 6.6 | 265 | Citations (PDF) |
| 208 | Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection | 3.3 | 208 | Citations (PDF) |
| 209 | DGIdb: mining the druggable genome | 26.1 | 523 | Citations (PDF) |
| 210 | The Somatic Genomic Landscape of Glioblastoma | 34.4 | 4,657 | Citations (PDF) |
| 211 | Mutational landscape and significance across 12 major cancer types | 39.5 | 4,210 | Citations (PDF) |
| 212 | The Next-Generation Sequencing Revolution and Its Impact on Genomics | 34.4 | 969 | Citations (PDF) |
| 213 | Endocrine-Therapy-Resistant ESR1 Variants Revealed by Genomic Characterization of Breast-Cancer-Derived Xenografts | 6.4 | 598 | Citations (PDF) |
| 214 | Targeting Oxidative Stress in Embryonal Rhabdomyosarcoma | 38.5 | 279 | Citations (PDF) |
| 215 | Genomic Pathology of SLE-Associated Copy-Number Variation at the FCGR2C/FCGR3B/FCGR2B Locus | 6.6 | 68 | Citations (PDF) |
| 216 | Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas | 25.9 | 783 | Citations (PDF) |
| 217 | Implementing genomic medicine in the clinic: the future is here | 4.4 | 517 | Citations (PDF) |
| 218 | Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution | 25.9 | 629 | Citations (PDF) |
| 219 | The Oxytricha trifallax Macronuclear Genome: A Complex Eukaryotic Genome with 16,000 Tiny Chromosomes | 4.9 | 212 | Citations (PDF) |
| 220 | Implementing Genomic Medicine in the Clinic | 0.6 | 1 | Citations (PDF) |
| 221 | The genomic landscape of hypodiploid acute lymphoblastic leukemia | 25.9 | 654 | Citations (PDF) |
| 222 | Genomic impact of transient low-dose decitabine treatment on primary AML cellsBlood, 2013, 121, 1633-1643 | 4.2 | 146 | Citations (PDF) |
| 223 | A Lover and a Fighter: The Genome Sequence of an Entomopathogenic Nematode Heterorhabditis bacteriophora | 2.4 | 98 | Citations (PDF) |
| 224 | Subclonal “skewing” Of De Novo AML Samples After Engraftment In Immunodeficient MiceBlood, 2013, 122, 609-609 | 4.2 | 0 | Citations (PDF) |
| 225 | A non-human primate system for large-scale genetic studies of complex traits | 3.0 | 51 | Citations (PDF) |
| 226 | SomaticSniper: identification of somatic point mutations in whole genome sequencing data | 4.7 | 631 | Citations (PDF) |
| 227 | The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2 | 4.6 | 38 | Citations (PDF) |
| 228 | BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data | 4.7 | 56 | Citations (PDF) |
| 229 | An Inv(16)(p13.3q24.3)-Encoded CBFA2T3-GLIS2 Fusion Protein Defines an Aggressive Subtype of Pediatric Acute Megakaryoblastic Leukemia | 38.5 | 261 | Citations (PDF) |
| 230 | Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data | 8.2 | 34 | Citations (PDF) |
| 231 | MuSiC: Identifying mutational significance in cancer genomes | 4.6 | 650 | Citations (PDF) |
| 232 | Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas | 25.9 | 1,586 | Citations (PDF) |
| 233 | De Novo Gene Disruptions in Children on the Autistic Spectrum | 12.4 | 1,409 | Citations (PDF) |
| 234 | Background Mutations in Parental Cells Account for Most of the Genetic Heterogeneity of Induced Pluripotent Stem Cells | 17.1 | 204 | Citations (PDF) |
| 235 | Whole-genome analysis informs breast cancer response to aromatase inhibition | 39.5 | 973 | Citations (PDF) |
| 236 | Genomic Landscape of Non-Small Cell Lung Cancer in Smokers and Never-SmokersCell, 2012, 150, 1121-1134 | 34.4 | 1,103 | Citations (PDF) |
| 237 | The Pediatric Cancer Genome Project | 25.9 | 365 | Citations (PDF) |
| 238 | Clonal Architecture of Secondary Acute Myeloid Leukemia | 44.0 | 728 | Citations (PDF) |
| 239 | The genetic basis of early T-cell precursor acute lymphoblastic leukaemia | 39.5 | 1,558 | Citations (PDF) |
| 240 | A novel retinoblastoma therapy from genomic and epigenetic analyses | 39.5 | 493 | Citations (PDF) |
| 241 | Novel mutations target distinct subgroups of medulloblastoma | 39.5 | 806 | Citations (PDF) |
| 242 | VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing | 4.6 | 4,684 | Citations (PDF) |
| 243 | Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication | 34.4 | 400 | Citations (PDF) |
| 244 | Chromothripsis and Human Disease: Piecing Together the Shattering Process | 34.4 | 150 | Citations (PDF) |
| 245 | The Origin and Evolution of Mutations in Acute Myeloid Leukemia | 34.4 | 1,482 | Citations (PDF) |
| 246 | Association of Age at Diagnosis and Genetic Mutations in Patients With Neuroblastoma | 17.2 | 435 | Citations (PDF) |
| 247 | Landscape of Somatic Retrotransposition in Human Cancers | 37.0 | 699 | Citations (PDF) |
| 248 | Insights into hominid evolution from the gorilla genome sequence | 39.5 | 718 | Citations (PDF) |
| 249 | Resolving the Breakpoints of the 17q21.31 Microdeletion Syndrome with Next-Generation Sequencing | 6.6 | 23 | Citations (PDF) |
| 250 | Abstract 4869: Whole genome sequence analysis of MLL rearranged infant acute lymphoblastic leukemias reveals remarkably few somatic mutations: A Report From the St Jude Children's Research Hospital - Washington University Pediatric Cancer Genome Project 2012, , | | 4 | Citations (PDF) |
| 251 | Whole Genome Sequencing of Therapy-Related Acute Myeloid LeukemiaBlood, 2012, 120, 784-784 | 4.2 | 1 | Citations (PDF) |
| 252 | Somatic Mutations of PIK3R1 Promote Gliomagenesis | 2.4 | 57 | Citations (PDF) |
| 253 | Abstract 4873: Comprehensive analysis of 160 whole-genome sequences reveals striking telomere alteration patterns in 9 pediatric cancers 2012, , | | 0 | Citations (PDF) |
| 254 | Abstract 4867: Identification of an inv(16)-encodedCBFA2T3-GLIS2fusion protein in 34% of non-infant acute megkaryoblastic leukemias: A report from the Pediatric Cancer Genome Project 2012, , | | 0 | Citations (PDF) |
| 255 | Abstract 4870: Integrated genomic analysis of hypodiploid acute lymphoblastic leukemia 2012, , | | 1 | Citations (PDF) |
| 256 | Deep Digital Sequencing Identifies an AML Subclone with Enhanced in Vitro and in Vivo Growth Properties Associated with Disease RelapseBlood, 2012, 120, 407-407 | 4.2 | 0 | Citations (PDF) |
| 257 | Whole Genome Sequencing Reveals Novel Recurring Somatic Mutations Affecting HUWE1 and DIAPH2 Genes in Multiple MyelomaBlood, 2012, 120, 320-320 | 4.2 | 0 | Citations (PDF) |
| 258 | Next-Generation Sequencing: A Discovery Tool for Blood DisordersBlood, 2012, 120, SCI-10-SCI-10 | 4.2 | 0 | Citations (PDF) |
| 259 | CREST maps somatic structural variation in cancer genomes with base-pair resolution | 26.1 | 469 | Citations (PDF) |
| 260 | A vertebrate case study of the quality of assemblies derived from next-generation sequences | 8.2 | 33 | Citations (PDF) |
| 261 | The draft genome of the parasitic nematode Trichinella spiralis | 25.9 | 312 | Citations (PDF) |
| 262 | A high-resolution map of human evolutionary constraint using 29 mammals | 39.5 | 1,091 | Citations (PDF) |
| 263 | Demographic history and rare allele sharing among human populations | 7.8 | 653 | Citations (PDF) |
| 264 | Use of Whole-Genome Sequencing to Diagnose a Cryptic Fusion Oncogene | 17.2 | 238 | Citations (PDF) |
| 265 | Modernizing Reference Genome Assemblies | 4.9 | 567 | Citations (PDF) |
| 266 | PathScan: a tool for discerning mutational significance in groups of putative cancer genes | 4.7 | 92 | Citations (PDF) |
| 267 | Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee | 4.6 | 75 | Citations (PDF) |
| 268 | Identification of a Novel <emph type="ital">TP53</emph> Cancer Susceptibility Mutation Through Whole-Genome Sequencing of a Patient With Therapy-Related AML | 17.2 | 148 | Citations (PDF) |
| 269 | Abstract LB-87: Analysis of luminal-type breast cancer by massively parallel sequencing | 0.6 | 1 | Citations (PDF) |
| 270 | Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression | 9.0 | 91 | Citations (PDF) |
| 271 | Complete Sequencing and Comparison of 12 Normal Karyotype M1 AML Genomes with 12 t(15;17) Positive M3-APL GenomesBlood, 2011, 118, 404-404 | 4.2 | 1 | Citations (PDF) |
| 272 | Whole Genome Sequence Analysis of 22 MLL Rearranged Infant Acute Lymphoblastic Leukemias Reveals Remarkably Few Somatic Mutations: A Report From the St Jude Children‘s Research Hospital - Washington University Pediatric Cancer Genome Project | 4.2 | 6 | Citations (PDF) |
| 273 | Transcriptome Sequence Analysis of Pediatric Acute Megakaryoblastic Leukemia Identifies An Inv(16)(p13.3;q24.3)-Encoded CBFA2T3-GLIS2 Fusion Protein As a Recurrent Lesion in 39% of Non-Infant Cases: A Report From the St. Jude Children's Research Hospital – Washington University Pediatric Cancer Genome ProjectBlood, 2011, 118, 757-757 | 4.2 | 8 | Citations (PDF) |
| 274 | Discovery of Novel Recurrent Mutations in Childhood Early T-Cell Precursor Acute Lymphoblastic Leukemia by Whole Genome Sequencing - a Report From the St Jude Children's Research Hospital - Washington University Pediatric Cancer Genome Project | 4.2 | 0 | Citations (PDF) |
| 275 | Complete characterization of the microRNAome in a patient with acute myeloid leukemiaBlood, 2010, 116, 5316-5326 | 4.2 | 64 | Citations (PDF) |
| 276 | Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation | 3.3 | 51 | Citations (PDF) |
| 277 | Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA, IDH1, EGFR, and NF1 | 38.5 | 6,918 | Citations (PDF) |
| 278 | Identification of a CpG Island Methylator Phenotype that Defines a Distinct Subgroup of Glioma | 38.5 | 2,222 | Citations (PDF) |
| 279 | Comparative genomics based on massive parallel transcriptome sequencing reveals patterns of substitution and selection across 10 bird species | 3.7 | 107 | Citations (PDF) |
| 280 | International network of cancer genome projects | 39.5 | 2,301 | Citations (PDF) |
| 281 | Genome remodelling in a basal-like breast cancer metastasis and xenograft | 39.5 | 1,109 | Citations (PDF) |
| 282 | A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk | 25.9 | 97 | Citations (PDF) |
| 283 | Characterization of missing human genome sequences and copy-number polymorphic insertions | 26.1 | 142 | Citations (PDF) |
| 284 | Challenges of sequencing human genomes | 6.8 | 141 | Citations (PDF) |
| 285 | CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data | 4.7 | 60 | Citations (PDF) |
| 286 | The Genome of the Western Clawed Frog
<i>Xenopus tropicalis</i> | 37.0 | 781 | Citations (PDF) |
| 287 | A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms | 34.4 | 271 | Citations (PDF) |
| 288 | <i>DNMT3A</i>Mutations in Acute Myeloid Leukemia | 44.0 | 1,925 | Citations (PDF) |
| 289 | A Catalog of Reference Genomes from the Human Microbiome | 37.0 | 677 | Citations (PDF) |
| 290 | Novel venom gene discovery in the platypus | 8.2 | 78 | Citations (PDF) |
| 291 | Reconstructing sex chromosome evolution | 8.2 | 5 | Citations (PDF) |
| 292 | Genome Sequence of Cronobacter sakazakii BAA-894 and Comparative Genomic Hybridization Analysis with Other Cronobacter Species | 2.4 | 207 | Citations (PDF) |
| 293 | DNA Sequence of the Cancer Genome of a Patient with Therapy-Related Acute Myeloid LeukemiaBlood, 2010, 116, 580-580 | 4.2 | 0 | Citations (PDF) |
| 294 | Mutations In the DNA Methyltransferase Gene DNMT3A Are Highly Recurrent In Patients with Intermediate Risk Acute Myeloid Leukemia, and Predict Poor Outcomes | 4.2 | 9 | Citations (PDF) |
| 295 | Recurrent DNMT3A Mutations In Patients with Myelodysplastic SyndromeBlood, 2010, 116, 608-608 | 4.2 | 0 | Citations (PDF) |
| 296 | Detection of Novel Mutations In MDS/AML by Whole Genome SequencingBlood, 2010, 116, 299-299 | 4.2 | 0 | Citations (PDF) |
| 297 | Resolution of a Clinical Dilemma with Whole Genome Sequencing, and Discovery of a New Mechanism for Generating PML-Rara: Insertional FusionBlood, 2010, 116, 2755-2755 | 4.2 | 0 | Citations (PDF) |
| 298 | Sequencing human–gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites | 4.6 | 29 | Citations (PDF) |
| 299 | The Physical and Genetic Framework of the Maize B73 Genome | 3.3 | 99 | Citations (PDF) |
| 300 | Detailed Analysis of a Contiguous 22-Mb Region of the Maize Genome | 3.3 | 42 | Citations (PDF) |
| 301 | Characterizing a model human gut microbiota composed of members of its two dominant bacterial phyla | 7.8 | 679 | Citations (PDF) |
| 302 | VarScan: variant detection in massively parallel sequencing of individual and pooled samples | 4.7 | 1,340 | Citations (PDF) |
| 303 | A Phase I Study of the P-Glycoprotein Antagonist Tariquidar in Combination with Vinorelbine | 6.8 | 112 | Citations (PDF) |
| 304 | Comparative genomics of protoploid <i>Saccharomycetaceae</i> | 4.6 | 216 | Citations (PDF) |
| 305 | Molecular determinants archetypical to the phylum Nematoda | 3.3 | 11 | Citations (PDF) |
| 306 | Transcriptomic analysis of the entomopathogenic nematode Heterorhabditis bacteriophora TTO1 | 3.3 | 24 | Citations (PDF) |
| 307 | Statistical aspects of discerning indel-type structural variation via DNA sequence alignment | 3.3 | 10 | Citations (PDF) |
| 308 | The theory of discovering rare variants via DNA sequencing | 3.3 | 13 | Citations (PDF) |
| 309 | BreakDancer: an algorithm for high-resolution mapping of genomic structural variation | 26.1 | 1,442 | Citations (PDF) |
| 310 | The transcriptomes of the cattle parasitic nematode Ostertagia ostartagi | 2.0 | 12 | Citations (PDF) |
| 311 | Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome | 44.0 | 2,109 | Citations (PDF) |
| 312 | Next-Generation Sequencing of Cancer Genomes: Back to the Future | 1.4 | 28 | Citations (PDF) |
| 313 | The B73 Maize Genome: Complexity, Diversity, and Dynamics | 37.0 | 3,882 | Citations (PDF) |
| 314 | Acquired copy number alterations in adult acute myeloid leukemia genomes | 7.8 | 236 | Citations (PDF) |
| 315 | Cancer genome sequencing: a review | 3.0 | 194 | Citations (PDF) |
| 316 | Chromatin Immunoprecipitation of GFP-Tagged PML-Rara Coupled to High-Throughput Next Generation Sequencing.Blood, 2009, 114, 1276-1276 | 4.2 | 1 | Citations (PDF) |
| 317 | Platypus globin genes and flanking loci suggest a new insertional model for beta-globin evolution in birds and mammals | 4.0 | 48 | Citations (PDF) |
| 318 | Mapping and sequencing of structural variation from eight human genomes | 39.5 | 1,001 | Citations (PDF) |
| 319 | Genome analysis of the platypus reveals unique signatures of evolution | 39.5 | 683 | Citations (PDF) |
| 320 | Somatic mutations affect key pathways in lung adenocarcinoma | 39.5 | 2,781 | Citations (PDF) |
| 321 | DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome | 39.5 | 1,334 | Citations (PDF) |
| 322 | Evolutionary toggling of the MAPT 17q21.31 inversion region | 25.9 | 208 | Citations (PDF) |
| 323 | The Pristionchus pacificus genome provides a unique perspective on nematode lifestyle and parasitism | 25.9 | 330 | Citations (PDF) |
| 324 | Whole-genome sequencing and variant discovery in C. elegans | 26.1 | 389 | Citations (PDF) |
| 325 | Aspects of coverage in medical DNA sequencing | 3.0 | 27 | Citations (PDF) |
| 326 | The canine hookworm genome: Analysis and classification of Ancylostoma caninum survey sequences | 1.3 | 39 | Citations (PDF) |
| 327 | The genome of
<i>Cyanothece</i>
51142, a unicellular diazotrophic cyanobacterium important in the marine nitrogen cycle | 7.8 | 159 | Citations (PDF) |
| 328 | Haplotype sorting using human fosmid clone end-sequence pairs | 4.6 | 25 | Citations (PDF) |
| 329 | Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemiaBlood, 2008, 111, 4797-4808 | 4.2 | 213 | Citations (PDF) |
| 330 | Intestinal Transcriptomes of Nematodes: Comparison of the Parasites Ascaris suum and Haemonchus contortus with the Free-living Caenorhabditis elegans | 3.1 | 45 | Citations (PDF) |
| 331 | Molecular refinement of gibbon genome rearrangements | 4.6 | 56 | Citations (PDF) |
| 332 | Genomic and metabolic adaptations of
<i>Methanobrevibacter smithii</i>
to the human gut | 7.8 | 510 | Citations (PDF) |
| 333 | PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data | 4.6 | 76 | Citations (PDF) |
| 334 | Comprehensive Genetic Variant Discovery in the Surfactant Protein B Gene | 2.4 | 17 | Citations (PDF) |
| 335 | Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropeniaBlood, 2007, 110, 1648-1655 | 4.2 | 92 | Citations (PDF) |
| 336 | Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome | 4.6 | 187 | Citations (PDF) |
| 337 | Evolution of Symbiotic Bacteria in the Distal Human Intestine | 4.9 | 527 | Citations (PDF) |
| 338 | Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4 | 2.4 | 78 | Citations (PDF) |
| 339 | PD5-3-7: EGFR and KRAS mutations are molecular predictors of survival in resected lung adenocarcinoma | 2.2 | 0 | Citations (PDF) |
| 340 | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project | 39.5 | 4,877 | Citations (PDF) |
| 341 | A second generation human haplotype map of over 3.1 million SNPs | 39.5 | 4,275 | Citations (PDF) |
| 342 | Evolution of genes and genomes on the Drosophila phylogeny | 39.5 | 1,992 | Citations (PDF) |
| 343 | Design and implementation of a generalized laboratory data model | 3.0 | 9 | Citations (PDF) |
| 344 | Identification of Novel, Non-Synonymous Sequence Changes in the Tyrosine Kinase Genes of Patients with Acute Myeloid Leukemia.Blood, 2007, 110, 823-823 | 4.2 | 0 | Citations (PDF) |
| 345 | Use of Cigarette-Smoking History to Estimate the Likelihood of Mutations in Epidermal Growth Factor Receptor Gene Exons 19 and 21 in Lung Adenocarcinomas | 21.6 | 206 | Citations (PDF) |
| 346 | Identification and analysis of genes expressed in the adult filarial parasitic nematode Dirofilaria immitis | 2.9 | 15 | Citations (PDF) |
| 347 | Application of a superword array in genome assembly | 15.8 | 29 | Citations (PDF) |
| 348 | Physical map-assisted whole-genome shotgun sequence assemblies | 4.6 | 27 | Citations (PDF) |
| 349 | After the Duplication: Gene Loss and Adaptation in Saccharomyces Genomes | 4.2 | 86 | Citations (PDF) |
| 350 | The DNA sequence of the human X chromosome | 39.5 | 1,058 | Citations (PDF) |
| 351 | Generation and annotation of the DNA sequences of human chromosomes 2 and 4 | 39.5 | 94 | Citations (PDF) |
| 352 | A genome-wide comparison of recent chimpanzee and human segmental duplications | 39.5 | 369 | Citations (PDF) |
| 353 | Investigating hookworm genomes by comparative analysis of two Ancylostoma species | 3.3 | 47 | Citations (PDF) |
| 354 | Genome Science: A Video Tour of the Washington University Genome Sequencing Center for High School and Undergraduate Students | 0.7 | 3 | Citations (PDF) |
| 355 | Punctuated duplication seeding events during the evolution of human chromosome 2p11 | 4.6 | 32 | Citations (PDF) |
| 356 | Molecular Study of Malignant Gliomas Treated with Epidermal Growth Factor Receptor Inhibitors: Tissue Analysis from North American Brain Tumor Consortium Trials 01-03 and 00-01 | 6.8 | 245 | Citations (PDF) |
| 357 | Reduced PU.1 expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RAR | 7.8 | 82 | Citations (PDF) |
| 358 | Comparing low coverage random shotgun sequence data from Brassica oleracea and Oryza sativa genome sequence for their ability to add to the annotation of Arabidopsis thaliana | 4.6 | 27 | Citations (PDF) |
| 359 | Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes | 4.6 | 3,940 | Citations (PDF) |
| 360 | Sequence and Comparative Analysis of the Maize NB Mitochondrial Genome | 5.5 | 323 | Citations (PDF) |
| 361 | EAnnot: A genome annotation tool using experimental evidence | 4.6 | 19 | Citations (PDF) |
| 362 | The repetitive landscape of the chicken genome | 4.6 | 118 | Citations (PDF) |
| 363 | Analysis of Human mRNAs With the Reference Genome Sequence Reveals Potential Errors, Polymorphisms, and RNA Editing | 4.6 | 28 | Citations (PDF) |
| 364 | EGF receptor gene mutations are common in lung cancers from “never smokers” and are associated with sensitivity of tumors to gefitinib and erlotinib | 7.8 | 4,219 | Citations (PDF) |
| 365 | Nematode.net: a tool for navigating sequences from parasitic and free-living nematodes | 15.8 | 77 | Citations (PDF) |
| 366 | Comparison of genome degradation in Paratyphi A and Typhi, human-restricted serovars of Salmonella enterica that cause typhoid | 25.9 | 389 | Citations (PDF) |
| 367 | The structure and evolution of centromeric transition regions within the human genome | 39.5 | 188 | Citations (PDF) |
| 368 | A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms | 39.5 | 410 | Citations (PDF) |
| 369 | Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndromeBlood, 2004, 104, 3588-3590 | 4.2 | 118 | Citations (PDF) |
| 370 | Quantitative Chromatographic Estimation of α-Amino-Acids | 39.5 | 4 | Citations (PDF) |
| 371 | The DNA sequence and analysis of human chromosome 14 | 39.5 | 111 | Citations (PDF) |
| 372 | The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes | 39.5 | 2,019 | Citations (PDF) |
| 373 | The DNA sequence of human chromosome 7 | 39.5 | 247 | Citations (PDF) |
| 374 | A pilot study of high-throughput, sequence-based mutational profiling of primary human acute myeloid leukemia cell genomes | 7.8 | 55 | Citations (PDF) |
| 375 | Viral Discovery and Sequence Recovery Using DNA Microarrays | 4.9 | 401 | Citations (PDF) |
| 376 | The Genome Sequence of Caenorhabditis briggsae: A Platform for Comparative Genomics | 4.9 | 839 | Citations (PDF) |
| 377 | What is Finished, and Why Does it Matter | 4.6 | 58 | Citations (PDF) |
| 378 | Analysis of the Human Neurexin Genes: Alternative Splicing and the Generation of Protein Diversity | 2.8 | 172 | Citations (PDF) |
| 379 | Initial sequencing and comparative analysis of the mouse genome | 39.5 | 6,666 | Citations (PDF) |
| 380 | A physical map of the human genome | 39.5 | 883 | Citations (PDF) |
| 381 | The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men | 25.9 | 656 | Citations (PDF) |
| 382 | Initial sequencing and analysis of the human genome | 39.5 | 22,433 | Citations (PDF) |
| 383 | Theories and Applications for Sequencing Randomly Selected Clones | 4.6 | 9 | Citations (PDF) |
| 384 | Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes | 7.8 | 64 | Citations (PDF) |
| 385 | Association between DQB1 and cervical cancer in patients with human papillomavirus and family controls | 1.5 | 23 | Citations (PDF) |
| 386 | How the worm was won: the C. elegans genome sequencing project | 10.0 | 111 | Citations (PDF) |
| 387 | A Pneumatic Device for Rapid Loading of DNA Sequencing Gels | 4.6 | 10 | Citations (PDF) |
| 388 | Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome | 34.4 | 1,030 | Citations (PDF) |
| 389 | High Throughput Fingerprint Analysis of Large-Insert Clones | 4.6 | 406 | Citations (PDF) |
| 390 | Comparative analysis of the polycystic kidney disease 1 (PKD1) gene reveals an integral membrane glycoprotein with multiple evolutionary conserved domains | 3.0 | 146 | Citations (PDF) |
| 391 | Representation of cloned genomic sequences in two sequencing vectors: correlation of DNA sequence and subclone distribution | 15.8 | 19 | Citations (PDF) |
| 392 | A Transposon-Based Strategy for Sequencing Repetitive DNA in Eukaryotic Genomes | 4.6 | 48 | Citations (PDF) |
| 393 | Agenesis of the corpus cállosum in Turner syndrome with ring X | 3.8 | 31 | Citations (PDF) |
| 394 | Automated plaque picking and arraying on a robotic system equipped with a CCD camera and a sampling device using intramedic tubing | 0.3 | 4 | Citations (PDF) |
| 395 | Genomic structure of a cytoplasmic dynein heavy chain gene from the nematodeCaenorhabditis elegans | 4.0 | 24 | Citations (PDF) |
| 396 | The construction and analysis of M13 libraries prepared from YAC DNA | 15.8 | 25 | Citations (PDF) |
| 397 | Genetic diversity among natural populations of endophytic Lophodermium pinastri from Pinus resinosa | 2.4 | 24 | Citations (PDF) |
| 398 | DNA sequencing with dye-labeled terminators and T7 DNA polymerase: effect of dyes and dNTPs on incorporation of dye-terminators and probability analysis of termination fragments | 15.8 | 171 | Citations (PDF) |
| 399 | Nucleotide sequence analysis of 95 kb near the 3′ end of the murine T-cell receptor αδ chain locus: Strategy and methodology | 2.8 | 53 | Citations (PDF) |
| 400 | Organization, structure, and function of 95 kb of DNA spanning the murine T-cell receptor CαCδ region | 2.8 | 139 | Citations (PDF) |
| 401 | Fluorescence chemistries for automated primer-directed DNA sequencing | 2.6 | 20 | Citations (PDF) |
| 402 | Sequence and expression of a novel human T-cell receptor ?-chain variable gene segment subfamily | 3.1 | 20 | Citations (PDF) |
| 403 | Low pressure DNA shearing: a method for random DNA sequence analysis | 15.8 | 26 | Citations (PDF) |
| 404 | Development of an automated procedure for fluorescent DNA sequencing | 2.8 | 43 | Citations (PDF) |
| 405 | Structure, Organization and Polymorphism of Murine and Human T-Cell Receptor a and beta Chain Gene Families | 6.6 | 461 | Citations (PDF) |
| 406 | Nucleotide sequence ofpheW; a third gene forE. colitRNAPhe | 15.8 | 15 | Citations (PDF) |
| 407 | The AEC and the Loss of Coolant Accident | 39.5 | 1 | Citations (PDF) |
| 408 | Biallelic SEPSECS variants in two siblings with pontocerebellar hypoplasia type 2D underscore the relevance of splice-disrupting synonymous variants in disease. | 1.4 | 1 | Citations (PDF) |
| 409 | Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder | 1.4 | 9 | Citations (PDF) |
| 410 | Expanding the Clinical Phenotype of FGFR1 Internal Tandem Duplication | 1.4 | 7 | Citations (PDF) |
