| 1 | indelPost: harmonizing ambiguities in simple and complex indel alignments | 4.8 | 17 | Citations (PDF) |
| 2 | A <i>CTNNB1</i>‐altered medulloblastoma shows the immunophenotypic, DNA methylation and transcriptomic profiles of SHH‐activated, and not WNT‐activated, medulloblastoma | 3.2 | 3 | Citations (PDF) |
| 3 | Consensus subtypes of hepatocellular carcinoma associated with clinical outcomes and genomic phenotypes | 10.6 | 24 | Citations (PDF) |
| 4 | RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data | 10.4 | 40 | Citations (PDF) |
| 5 | Infectious Diseases/Human Immunodeficiency Virus Physician Ambassadors: Advancing Policy to Improve Health | 5.4 | 3 | Citations (PDF) |
| 6 | The Exceptional Responders Initiative: Feasibility of a National Cancer Institute Pilot Study | 4.7 | 28 | Citations (PDF) |
| 7 | The Proximal Airway Is a Reservoir for Adaptive Immunologic Memory in Idiopathic Subglottic Stenosis | 1.5 | 25 | Citations (PDF) |
| 8 | Multiomic analysis identifies natural intrapatient temporal variability and changes in response to systemic corticosteroid therapy in chronic rhinosinusitis | 2.6 | 7 | Citations (PDF) |
| 9 | Molecular Features of Cancers Exhibiting Exceptional Responses to Treatment | 38.5 | 94 | Citations (PDF) |
| 10 | DNA methylation patterns identify subgroups of pancreatic neuroendocrine tumors with clinical association | 4.4 | 41 | Citations (PDF) |
| 11 | Responses of <i>Chlamydomonas reinhardtii</i> during the transition from P‐deficient to P‐sufficient growth (the P‐overplus response): The roles of the vacuolar transport chaperones and polyphosphate synthesis | 3.0 | 38 | Citations (PDF) |
| 12 | Conservation genomics of a critically endangered brown seaweed | 3.0 | 7 | Citations (PDF) |
| 13 | Novel Anaplastic Thyroid Cancer PDXs and Cell Lines: Expanding Preclinical Models of Genetic Diversity | 4.2 | 12 | Citations (PDF) |
| 14 | A High-throughput Approach to Identify Effective Systemic Agents for the Treatment of Anaplastic Thyroid Carcinoma | 4.2 | 10 | Citations (PDF) |
| 15 | Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing | 25.6 | 177 | Citations (PDF) |
| 16 | Differences in Breast and Colorectal Cancer Screening Adherence Among Women Residing in Urban and Rural Communities in the United States | 6.8 | 67 | Citations (PDF) |
| 17 | ID/HIV Physician Ambassadors: Advancing Policy to Improve Health | 1.5 | 3 | Citations (PDF) |
| 18 | Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival | 13.9 | 75 | Citations (PDF) |
| 19 | Identification of novel fusion transcripts in meningioma | 2.6 | 10 | Citations (PDF) |
| 20 | Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples | 13.9 | 44 | Citations (PDF) |
| 21 | Accumulation of Molecular Aberrations Distinctive to Hepatocellular Carcinoma Progression | 0.6 | 26 | Citations (PDF) |
| 22 | Proteogenomic Characterization of Endometrial CarcinomaCell, 2020, 180, 729-748.e26 | 34.1 | 425 | Citations (PDF) |
| 23 | Pathway and network analysis of more than 2500 whole cancer genomes | 13.9 | 99 | Citations (PDF) |
| 24 | The repertoire of mutational signatures in human cancer | 38.7 | 3,137 | Citations (PDF) |
| 25 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes | 38.7 | 570 | Citations (PDF) |
| 26 | Telomere Maintenance Mechanisms Define Clinical Outcome in High-Risk Neuroblastoma | 0.6 | 86 | Citations (PDF) |
| 27 | An enhanced genetic model of colorectal cancer progression history | 8.2 | 43 | Citations (PDF) |
| 28 | Integrated Analysis of TP53 Gene and Pathway Alterations in The Cancer Genome Atlas | 6.4 | 552 | Citations (PDF) |
| 29 | Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design | 6.4 | 148 | Citations (PDF) |
| 30 | Integrated Proteogenomic Characterization of Clear Cell Renal Cell CarcinomaCell, 2019, 179, 964-983.e31 | 34.1 | 635 | Citations (PDF) |
| 31 | Molecular profiling predicts meningioma recurrence and reveals loss of DREAM complex repression in aggressive tumors | 7.6 | 179 | Citations (PDF) |
| 32 | Framework for microRNA variant annotation and prioritization using human population and disease datasets | 3.9 | 22 | Citations (PDF) |
| 33 | How Do You Measure Up: Quality Measurement for Improving Patient Care and Establishing the Value of Infectious Diseases Specialists | 5.4 | 6 | Citations (PDF) |
| 34 | Genetic Mechanisms of Immune Evasion in Colorectal Cancer | 25.6 | 459 | Citations (PDF) |
| 35 | Chemistry-First Approach for Nomination of Personalized Treatment in Lung CancerCell, 2018, 173, 864-878.e29 | 34.1 | 136 | Citations (PDF) |
| 36 | An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome AnalyticsCell, 2018, 173, 400-416.e11 | 34.1 | 3,192 | Citations (PDF) |
| 37 | Comprehensive Characterization of Cancer Driver Genes and MutationsCell, 2018, 173, 371-385.e18 | 34.1 | 2,053 | Citations (PDF) |
| 38 | Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of CancerCell, 2018, 173, 291-304.e6 | 34.1 | 2,264 | Citations (PDF) |
| 39 | Perspective on Oncogenic Processes at the End of the Beginning of Cancer GenomicsCell, 2018, 173, 305-320.e10 | 34.1 | 359 | Citations (PDF) |
| 40 | Machine Learning Identifies Stemness Features Associated with Oncogenic DedifferentiationCell, 2018, 173, 338-354.e15 | 34.1 | 1,951 | Citations (PDF) |
| 41 | Oncogenic Signaling Pathways in The Cancer Genome AtlasCell, 2018, 173, 321-337.e10 | 34.1 | 2,852 | Citations (PDF) |
| 42 | Pathogenic Germline Variants in 10,389 Adult CancersCell, 2018, 173, 355-370.e14 | 34.1 | 782 | Citations (PDF) |
| 43 | Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types | 6.4 | 423 | Citations (PDF) |
| 44 | Driver Fusions and Their Implications in the Development and Treatment of Human Cancers | 6.4 | 567 | Citations (PDF) |
| 45 | The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma | 6.4 | 679 | Citations (PDF) |
| 46 | Spatial Organization and Molecular Correlation of Tumor-Infiltrating Lymphocytes Using Deep Learning on Pathology Images | 6.4 | 907 | Citations (PDF) |
| 47 | The Immune Landscape of Cancer | 23.3 | 4,904 | Citations (PDF) |
| 48 | Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas | 6.4 | 145 | Citations (PDF) |
| 49 | Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas | 6.4 | 1,025 | Citations (PDF) |
| 50 | Systematic Analysis of Splice-Site-Creating Mutations in Cancer | 6.4 | 222 | Citations (PDF) |
| 51 | Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines | 5.8 | 789 | Citations (PDF) |
| 52 | Genomic and Functional Approaches to Understanding Cancer Aneuploidy | 38.5 | 1,015 | Citations (PDF) |
| 53 | A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers | 38.5 | 605 | Citations (PDF) |
| 54 | Analysis of Genomes and Transcriptomes of Hepatocellular Carcinomas Identifies Mutations and Gene Expression Changes in the Transforming Growth Factor-β Pathway | 1.0 | 127 | Citations (PDF) |
| 55 | A Pan-Cancer Analysis Reveals High-Frequency Genetic Alterations in Mediators of Signaling by the TGF-β Superfamily | 5.8 | 171 | Citations (PDF) |
| 56 | TBIO-20. CLINICAL TUMOR WHOLE EXOME SEQUENCING FOR PEDIATRIC NEURO-ONCOLOGY PATIENTS – RESULTS FROM THE BAYLOR ADVANCING SEQUENCING IN CHILDHOOD CANCER CARE (BASIC3) CLINICAL SEQUENCING STUDY | 1.1 | 0 | Citations (PDF) |
| 57 | Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer | 2.2 | 28 | Citations (PDF) |
| 58 | Integrated Molecular Characterization of Testicular Germ Cell Tumors | 6.4 | 420 | Citations (PDF) |
| 59 | SMARCA4-inactivating mutations increase sensitivity to Aurora kinase A inhibitor VX-680 in non-small cell lung cancers | 13.9 | 100 | Citations (PDF) |
| 60 | Genomic Alterations of Adamantinomatous and Papillary Craniopharyngioma | 1.8 | 58 | Citations (PDF) |
| 61 | Whole-genome landscape of pancreatic neuroendocrine tumours | 38.7 | 913 | Citations (PDF) |
| 62 | Comprehensive and Integrative Genomic Characterization of Hepatocellular CarcinomaCell, 2017, 169, 1327-1341.e23 | 34.1 | 2,193 | Citations (PDF) |
| 63 | Comprehensive Genomic Characterization of Upper Tract Urothelial Carcinoma | 2.2 | 203 | Citations (PDF) |
| 64 | Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles | 6.4 | 502 | Citations (PDF) |
| 65 | A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor | 26.1 | 339 | Citations (PDF) |
| 66 | Integrated Genomic Characterization of Pancreatic Ductal Adenocarcinoma | 38.5 | 1,824 | Citations (PDF) |
| 67 | Genomic analysis of hepatoblastoma identifies distinct molecular and prognostic subgroups | 10.6 | 234 | Citations (PDF) |
| 68 | SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads | 3.3 | 8 | Citations (PDF) |
| 69 | Non-malignant respiratory epithelial cells preferentially proliferate from resected non-small cell lung cancer specimens cultured under conditionally reprogrammed conditions | 1.7 | 23 | Citations (PDF) |
| 70 | Activating <i>MAPK1</i> (ERK2) mutation in an aggressive case of disseminated juvenile xanthogranuloma | 1.7 | 33 | Citations (PDF) |
| 71 | Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogs | 1.3 | 3 | Citations (PDF) |
| 72 | Cross-species identification of genomic drivers of squamous cell carcinoma development across preneoplastic intermediates | 13.9 | 146 | Citations (PDF) |
| 73 | Coexistence of gain-of-function JAK2 germ line mutations with JAK2V617F in polycythemia veraBlood, 2016, 128, 2266-2270 | 4.2 | 25 | Citations (PDF) |
| 74 | Mixed-phenotype acute leukemia (MPAL) exhibits frequent mutations in DNMT3A and activated signaling genes | 0.4 | 57 | Citations (PDF) |
| 75 | Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma | 38.5 | 580 | Citations (PDF) |
| 76 | Significance of <i>TP53</i> Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group | 6.9 | 99 | Citations (PDF) |
| 77 | Integrated tumor and germline whole-exome sequencing identifies mutations in MAPK and PI3K pathway genes in an adolescent with rosette-forming glioneuronal tumor of the fourth ventricle | 1.5 | 27 | Citations (PDF) |
| 78 | MuSE: accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data | 8.2 | 281 | Citations (PDF) |
| 79 | An open access pilot freely sharing cancer genomic data from participants in Texas | 5.7 | 23 | Citations (PDF) |
| 80 | Multilevel Genomics-Based Taxonomy of Renal Cell Carcinoma | 6.4 | 338 | Citations (PDF) |
| 81 | Acquired uniparental disomy of chromosome 9p in hematologic malignancies | 0.4 | 14 | Citations (PDF) |
| 82 | ITD assembler: an algorithm for internal tandem duplication discovery from short-read sequencing data | 3.0 | 18 | Citations (PDF) |
| 83 | Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors | 14.6 | 447 | Citations (PDF) |
| 84 | Mutational Strand Asymmetries in Cancer Genomes Reveal Mechanisms of DNA Damage and Repair | 34.1 | 423 | Citations (PDF) |
| 85 | Ampullary Cancers Harbor ELF3 Tumor Suppressor Gene Mutations and Exhibit Frequent WNT Dysregulation | 6.4 | 127 | Citations (PDF) |
| 86 | Clonal Dynamics In Vivo of Virus Integration Sites of T Cells Expressing a Safety Switch | 10.4 | 15 | Citations (PDF) |
| 87 | Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer | 2.2 | 34 | Citations (PDF) |
| 88 | Genomic analyses identify molecular subtypes of pancreatic cancer | 38.7 | 3,324 | Citations (PDF) |
| 89 | Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse | 0.6 | 153 | Citations (PDF) |
| 90 | Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma | 43.7 | 1,229 | Citations (PDF) |
| 91 | Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease | 10.7 | 82 | Citations (PDF) |
| 92 | Integrated Genomic Analysis of Down Syndrome Acute Lymphoblastic Leukemia Reveals Recurrent Cancer Gene Alterations and Evidence of Frequent Subclonal Driver EventsBlood, 2016, 128, 4083-4083 | 4.2 | 0 | Citations (PDF) |
| 93 | Initial testing (stage 1) of the PARP inhibitor BMN 673 by the pediatric preclinical testing program: <i>PALB2</i> mutation predicts exceptional <i>in vivo</i> response to BMN 673 | 1.4 | 73 | Citations (PDF) |
| 94 | A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing | 13.9 | 288 | Citations (PDF) |
| 95 | MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours | 13.9 | 85 | Citations (PDF) |
| 96 | Recurrent DGCR8, DROSHA, and SIX Homeodomain Mutations in Favorable Histology Wilms Tumors | 38.5 | 288 | Citations (PDF) |
| 97 | Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia | 13.9 | 317 | Citations (PDF) |
| 98 | Dnmt3a loss predisposes murine hematopoietic stem cells to malignant transformationBlood, 2015, 125, 629-638 | 4.2 | 225 | Citations (PDF) |
| 99 | Assessing structural variation in a personal genome—towards a human reference diploid genome | 3.3 | 160 | Citations (PDF) |
| 100 | Recurrent internal tandem duplications of BCOR in clear cell sarcoma of the kidney | 13.9 | 150 | Citations (PDF) |
| 101 | Genomic profiling of Sézary syndrome identifies alterations of key T cell signaling and differentiation genes | 26.1 | 311 | Citations (PDF) |
| 102 | Comparison of Positive End-Expiratory Pressure of 8 versus 5 cm H<sub>2</sub>O on Outcome After Cardiac Operations | 2.3 | 8 | Citations (PDF) |
| 103 | SubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization | 8.2 | 64 | Citations (PDF) |
| 104 | Mutational Landscape of Aggressive Cutaneous Squamous Cell Carcinoma | 6.9 | 568 | Citations (PDF) |
| 105 | Heterochromatin protein 1 expression is reduced in human thyroid malignancy | 3.3 | 9 | Citations (PDF) |
| 106 | Integrated Genomic Characterization of Papillary Thyroid Carcinoma | 34.1 | 2,761 | Citations (PDF) |
| 107 | Effects of <i><scp>TP53</scp></i> mutational status on gene expression patterns across 10 human cancer types | 5.0 | 75 | Citations (PDF) |
| 108 | Genomic Sequencing for Cancer Diagnosis and Therapy | 19.5 | 39 | Citations (PDF) |
| 109 | Trans-ancestry mutational landscape of hepatocellular carcinoma genomes | 26.1 | 732 | Citations (PDF) |
| 110 | Characterization of HPV and host genome interactions in primary head and neck cancers | 7.6 | 369 | Citations (PDF) |
| 111 | Dynamic analyses of alternative polyadenylation from RNA-seq reveal a 3′-UTR landscape across seven tumour types | 13.9 | 531 | Citations (PDF) |
| 112 | Exonuclease mutations in DNA polymerase epsilon reveal replication strand specific mutation patterns and human origins of replication | 4.6 | 276 | Citations (PDF) |
| 113 | The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma | 38.5 | 771 | Citations (PDF) |
| 114 | Squamous Cell Carcinoma of the Oral Tongue in Young Non-Smokers Is Genomically Similar to Tumors in Older Smokers | 6.9 | 136 | Citations (PDF) |
| 115 | Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesisBlood, 2014, 124, 3007-3015 | 4.2 | 404 | Citations (PDF) |
| 116 | BCOR–CCNB3 fusions are frequent in undifferentiated sarcomas of male children | 4.9 | 139 | Citations (PDF) |
| 117 | Genomic Characterization of Sinonasal Undifferentiated Carcinoma | 1.1 | 1 | Citations (PDF) |
| 118 | Mixed Phenotype Acute Leukemia (MPAL) Has a High Frequency of Mutations in Epigenetic Regulatory Genes: Results from Whole Exome SequencingBlood, 2014, 124, 3560-3560 | 4.2 | 4 | Citations (PDF) |
| 119 | Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif | 13.9 | 114 | Citations (PDF) |
| 120 | <i>MLH1</i>‐silenced and non‐silenced subgroups of hypermutated colorectal carcinomas have distinct mutational landscapes | 5.0 | 69 | Citations (PDF) |
| 121 | Combined sequence-based and genetic mapping analysis of complex traits in outbred rats | 26.1 | 185 | Citations (PDF) |
| 122 | From human genome to cancer genome: The first decade | 4.6 | 152 | Citations (PDF) |
| 123 | Integrative Genomic Characterization of Oral Squamous Cell Carcinoma Identifies Frequent Somatic Drivers | 25.6 | 530 | Citations (PDF) |
| 124 | Comparison Of Mutational Profiles Of Diagnosis and Relapsed Pediatric B-Acute Lymphoblastic Leukemia: A Report From The COG ALL Target ProjectBlood, 2013, 122, 824-824 | 4.2 | 5 | Citations (PDF) |
| 125 | Whole Exome Sequencing and Analysis Of Mutations In Sézary SyndromeBlood, 2013, 122, 2558-2558 | 4.2 | 0 | Citations (PDF) |
| 126 | Molecular Characterization Of Polycythemia Vera Based On The Relationship Of JAK2V617F and 9pUPDBlood, 2013, 122, 1607-1607 | 4.2 | 0 | Citations (PDF) |
| 127 | Dietary Determinants Of The White Blood Cell CountBlood, 2013, 122, 1705-1705 | 4.2 | 0 | Citations (PDF) |
| 128 | Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes | 38.7 | 1,915 | Citations (PDF) |
| 129 | Integrated Analyses of microRNAs Demonstrate Their Widespread Influence on Gene Expression in High-Grade Serous Ovarian Carcinoma | 2.4 | 113 | Citations (PDF) |
| 130 | Identification of Novel Somatic Mutations, Regions of Recurrent Loss of Heterozygosity (LOH) and Significant Clonal Evolution From Diagnosis to Relapse in Childhood AML Determined by Exome Capture Sequencing – an NCI/COG Target AML StudyBlood, 2012, 120, 123-123 | 4.2 | 3 | Citations (PDF) |
| 131 | Genome Wide Promoter Methylation Patterns Predict AML Subtype Outcomes and Identify Novel Pathways Characterizing Diagnostic and Relapsed Disease in ChildrenBlood, 2012, 120, 1287-1287 | 4.2 | 3 | Citations (PDF) |
| 132 | Whole Genome Sequencing of Four CD34+-Derived iPSC Polycythemia Vera Clones From a Single FemaleBlood, 2012, 120, 1755-1755 | 4.2 | 2 | Citations (PDF) |
| 133 | Whole Exome Sequencing of Polycythemia Vera Reveals Novel Recurrent Somatic and Germline VariationBlood, 2012, 120, 705-705 | 4.2 | 3 | Citations (PDF) |
| 134 | Clinically Significant Mutations, Deletions and Translocations Involving ETV6 Identified by Whole Genome and Whole Exome Sequencing; Report From NCI/COG Target AML InitiativeBlood, 2012, 120, 125-125 | 4.2 | 0 | Citations (PDF) |
| 135 | Activation of Multiple Proto-oncogenic Tyrosine Kinases in Breast Cancer via Loss of the PTPN12 Phosphatase | 34.1 | 265 | Citations (PDF) |
| 136 | Exome Sequencing of Ion Channel Genes Reveals Complex Profiles Confounding Personal Risk Assessment in EpilepsyCell, 2011, 145, 1036-1048 | 34.1 | 288 | Citations (PDF) |
| 137 | Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel | 0.6 | 14 | Citations (PDF) |
| 138 | Resequencing of<i>IRS2</i>reveals rare variants for obesity but not fasting glucose homeostasis in Hispanic children | 2.5 | 6 | Citations (PDF) |
| 139 | TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum | 26.1 | 344 | Citations (PDF) |
| 140 | A Primer on a Hepatocellular Carcinoma Bioresource Bank Using the Cancer Genome Atlas Guidelines: Practical Issues and Pitfalls | 2.8 | 4 | Citations (PDF) |
| 141 | Building a Comprehensive Genomic Program for Hepatocellular Carcinoma | 2.8 | 15 | Citations (PDF) |
| 142 | Overview of the Development of Personalized Genomic Medicine and Surgery | 2.8 | 20 | Citations (PDF) |
| 143 | Characterization of single-nucleotide variation in Indian-origin rhesus macaques (Macaca mulatta) | 3.3 | 31 | Citations (PDF) |
| 144 | Prediction of missense mutation functionality depends on both the algorithm and sequence alignment employed | 3.9 | 207 | Citations (PDF) |
| 145 | Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion | 7.6 | 216 | Citations (PDF) |
| 146 | Disruptive <i>TP53</i> Mutation Is Associated with Aggressive Disease Characteristics in an Orthotopic Murine Model of Oral Tongue Cancer | 6.9 | 103 | Citations (PDF) |
| 147 | Integrating common and rare genetic variation in diverse human populations | 38.7 | 2,916 | Citations (PDF) |
| 148 | A SNP discovery method to assess variant allele probability from next-generation resequencing data | 4.6 | 170 | Citations (PDF) |
| 149 | Deep resequencing reveals excess rare recent variants consistent with explosive population growth | 13.9 | 218 | Citations (PDF) |
| 150 | Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy | 43.7 | 724 | Citations (PDF) |
| 151 | Genome-Wide Analysis of Binding Sites and Direct Target Genes of the Orphan Nuclear Receptor NR2F1/COUP-TFI | 2.4 | 44 | Citations (PDF) |
| 152 | Common and rare variants of <i>DAOA</i> in bipolar disorder | 1.5 | 12 | Citations (PDF) |
| 153 | Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease | 6.5 | 545 | Citations (PDF) |
| 154 | Somatic mutations affect key pathways in lung adenocarcinoma | 38.7 | 2,781 | Citations (PDF) |
| 155 | Novel MicroRNA Candidates and miRNA-mRNA Pairs in Embryonic Stem (ES) Cells | 2.4 | 48 | Citations (PDF) |
| 156 | Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome | 4.6 | 187 | Citations (PDF) |
| 157 | Direct selection of human genomic loci by microarray hybridization | 25.9 | 639 | Citations (PDF) |
| 158 | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project | 38.7 | 4,877 | Citations (PDF) |
| 159 | A second generation human haplotype map of over 3.1 million SNPs | 38.7 | 4,275 | Citations (PDF) |
| 160 | Functional genomics of genes with small open reading frames (sORFs) in S. cerevisiae | 4.6 | 218 | Citations (PDF) |
| 161 | The DNA sequence of the human X chromosome | 38.7 | 1,058 | Citations (PDF) |
| 162 | SNPdetector: A Software Tool for Sensitive and Accurate SNP Detection | 3.1 | 110 | Citations (PDF) |
| 163 | Orphan Nuclear Receptor GCNF Is Required for the Repression of Pluripotency Genes during Retinoic Acid-Induced Embryonic Stem Cell Differentiation | 2.5 | 174 | Citations (PDF) |
| 164 | Comparative genome sequencing of Drosophila pseudoobscura: Chromosomal, gene, and cis-element evolution | 4.6 | 473 | Citations (PDF) |
| 165 | Orphan Nuclear Receptor LRH-1 Is Required To Maintain Oct4 Expression at the Epiblast Stage of Embryonic Development | 2.5 | 277 | Citations (PDF) |
| 166 | Once‐Daily versus Twice‐Daily Lopinavir/Ritonavir in Antiretroviral‐Naive HIV‐Positive Patients: A 48‐Week Randomized Clinical Trial | 3.8 | 114 | Citations (PDF) |
| 167 | Genomic Analysis of the Nuclear Receptor Family: New Insights Into Structure, Regulation, and Evolution From the Rat Genome | 4.6 | 194 | Citations (PDF) |
| 168 | Genome sequence of the Brown Norway rat yields insights into mammalian evolution | 38.7 | 2,026 | Citations (PDF) |
| 169 | Selecting the Right Protein‐Scoring Matrix | 3.3 | 14 | Citations (PDF) |
| 170 | Title is missing! | 12.8 | 326 | Citations (PDF) |
| 171 | The Breast Cancer Gene Database: a collaborative information resource | 6.7 | 45 | Citations (PDF) |
| 172 | Use of Streaming Video in Preclinical Lectures | 1.5 | 4 | Citations (PDF) |
| 173 | Relationship Between Basal Body Temperature and Stage of Disease in Asymptomatic HIV-Infected Men | 0.2 | 1 | Citations (PDF) |
| 174 | Management and Outcome of Pneumothoraces in Patients Infected with Human Immunodeficiency Virus | 5.4 | 21 | Citations (PDF) |
| 175 | Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene | 26.1 | 45 | Citations (PDF) |
| 176 | Phylogenetic and Structural Analyses of MMTV LTR ORF Sequences of Exogenous and Endogenous Origins | 2.3 | 80 | Citations (PDF) |
| 177 | Behavior in Light-Dark Cycles of Drosophila Mutants That Are Arrhythmic, Blind, or Both | 2.9 | 298 | Citations (PDF) |
| 178 | Artificial neural network classification of Drosophila courtship song mutants | 1.5 | 11 | Citations (PDF) |
| 179 | Behavior of period-altered circadian rhythm mutants ofDrosophila in light: Dark cycles (Diptera: Drosophilidae) | 0.8 | 172 | Citations (PDF) |
| 180 | Spectral analysis of courtship songs in behavioral mutants ofDrosophila melanogaster | 1.5 | 59 | Citations (PDF) |
| 181 | Spectral analysis ofDrosophila courtship songs:D. melanogaster, D. simulans, and their interspecific hybrid | 1.5 | 67 | Citations (PDF) |
| 182 | Germ-Line Transformation Involving DNA from the<i>period</i>Locus in<i>Drosophila melanogaster</i>: Overlapping Genomic Fragments that Restore Circadian and Ultradian Rhythmicity to<i>per<sup>0</sup></i>and<i>per<sup>−</sup></i>Mutants | 1.8 | 180 | Citations (PDF) |
| 183 | Humoral factors during South American visceral leishmaniasis | 1.2 | 5 | Citations (PDF) |
| 184 | Molecular basis of altered mouse mammary tumor virus expression in the D-2 hyperplastic alveolar nodule line of BALB/c mice | 2.3 | 13 | Citations (PDF) |
| 185 | Molecular analysis of the period locus in Drosophila melanogaster and identification of a transcript involved in biological rhythms | 34.1 | 408 | Citations (PDF) |
| 186 | P-element transformation with period locus DNA restores rhythmicity to mutant, arrhythmic drosophila melanogaster | 34.1 | 383 | Citations (PDF) |
| 187 | Gene expression profiling and immune cell-type deconvolution highlight robust disease progression and survival markers in multiple cohorts of CTCL patients | 5.5 | 28 | Citations (PDF) |
