Elaine Mardis
#62,278
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American geneticist
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Elaine Mardisbiology Degrees
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#2459
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#3896
Historical Rank
#1096
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Genetics
#224
World Rank
#271
Historical Rank
#116
USA Rank
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Biology
Why Is Elaine Mardis Influential?
(Suggest an Edit or Addition)According to Wikipedia, Elaine R. Mardis is the co-executive director of the Institute for Genomic Medicine at Nationwide Children's Hospital, where she also serves as the Nationwide Foundation Endowed Chair in Genomic Medicine. She also is professor of pediatrics at the Ohio State University College of Medicine. Mardis’s research focuses on the genomic characterization of cancer and its implications for cancer medicine. She was part of the team that reported the first next-generation-based sequencing of a whole cancer genome, and participated extensively in The Cancer Genome Atlas and the Pediatric Cancer Genome Project .
Elaine Mardis's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Initial sequencing and analysis of the human genome. (2001) (15222)
- A global reference for human genetic variation (2015) (11857)
- An obesity-associated gut microbiome with increased capacity for energy harvest (2006) (9978)
- Structure, Function and Diversity of the Healthy Human Microbiome (2012) (8630)
- Comprehensive molecular portraits of human breast tumors (2012) (7791)
- Finding the missing heritability of complex diseases (2009) (7749)
- An integrated map of genetic variation from 1,092 human genomes (2012) (7565)
- Integrated Genomic Analyses of Ovarian Carcinoma (2011) (6411)
- Comprehensive molecular characterization of human colon and rectal cancer (2012) (6141)
- Comprehensive genomic characterization defines human glioblastoma genes and core pathways (2008) (5775)
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) (5196)
- Initial sequencing and comparative analysis of the mouse genome. (2002) (4609)
- Comprehensive molecular profiling of lung adenocarcinoma (2014) (4095)
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012) (3841)
- Supervised risk predictor of breast cancer based on intrinsic subtypes. (2009) (3801)
- Integrated genomic characterization of endometrial carcinoma (2013) (3708)
- EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib. (2004) (3411)
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms (2001) (2879)
- The Immune Landscape of Cancer (2018) (2766)
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) (2640)
- Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution (2004) (2417)
- Next-generation DNA sequencing methods. (2008) (2270)
- Initial sequence of the chimpanzee genome and comparison with the human genome (2005) (2222)
- Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009) (2200)
- The impact of next-generation sequencing technology on genetics. (2008) (2165)
- A framework for human microbiome research (2012) (2113)
- The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes (2003) (2000)
- Clonal evolution in relapsed acute myeloid leukemia revealed by whole genome sequencing (2011) (1935)
- Oncogenic Signaling Pathways in The Cancer Genome Atlas (2018) (1646)
- Checkpoint Blockade Cancer Immunotherapy Targets Tumour-Specific Mutant Antigens (2014) (1612)
- The genetic basis of early T-cell precursor acute lymphoblastic leukaemia (2012) (1437)
- The Origin and Evolution of Mutations in Acute Myeloid Leukemia (2012) (1420)
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (2009) (1381)
- DNA sequencing of a cytogenetically normal acute myeloid leukemia genome (2008) (1365)
- Comprehensive Characterization of Cancer Driver Genes and Mutations (2018) (1360)
- De Novo Gene Disruptions in Children on the Autistic Spectrum (2012) (1335)
- Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer (2015) (1332)
- Somatic Histone H3 Alterations in Paediatric Diffuse Intrinsic Pontine Gliomas and Non-Brainstem Glioblastomas (2012) (1327)
- Evolutionary and Biomedical Insights from the Rhesus Macaque Genome (2007) (1309)
- Genome Remodeling in a Basal-like Breast Cancer Metastasis and Xenograft (2010) (1171)
- VarScan: variant detection in massively parallel sequencing of individual and pooled samples (2009) (1155)
- Characterizing the cancer genome in lung adenocarcinoma (2007) (1122)
- The DNA sequence of human chromosome 22 (1999) (1117)
- A high-resolution map of human evolutionary constraint using 29 mammals (2011) (1081)
- Cancer Exome Analysis Reveals a T Cell Dependent Mechanism of Cancer Immunoediting (2012) (1076)
- Age-related cancer mutations associated with clonal hematopoietic expansion (2014) (1053)
- Targetable kinase-activating lesions in Ph-like acute lymphoblastic leukemia. (2014) (1029)
- Whole Genome Analysis Informs Breast Cancer Response to Aromatase Inhibition (2012) (998)
- The Genome Sequence of Caenorhabditis briggsae: A Platform for Comparative Genomics (2003) (972)
- Genomic Landscape of Non-Small Cell Lung Cancer in Smokers and Never-Smokers (2012) (890)
- A decade’s perspective on DNA sequencing technology (2011) (880)
- A dendritic cell vaccine increases the breadth and diversity of melanoma neoantigen-specific T cells (2015) (878)
- The Next-Generation Sequencing Revolution and Its Impact on Genomics (2013) (854)
- The genome of a songbird (2010) (834)
- The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma (2014) (832)
- DNMT3A mutations in acute myeloid leukemia. (2010) (782)
- Germline Mutations in Predisposition Genes in Pediatric Cancer. (2015) (769)
- Integrated genomic and molecular characterization of cervical cancer (2017) (762)
- A physical map of the human genome (2001) (753)
- Clonal architecture of secondary acute myeloid leukemia. (2012) (747)
- Novel mutations target distinct subgroups of medulloblastoma (2012) (746)
- Genome analysis of the platypus reveals unique signatures of evolution (2008) (711)
- A Comparison of PAM50 Intrinsic Subtyping with Immunohistochemistry and Clinical Prognostic Factors in Tamoxifen-Treated Estrogen Receptor–Positive Breast Cancer (2010) (668)
- Activating HER2 mutations in HER2 gene amplification negative breast cancer. (2013) (658)
- Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas (2013) (655)
- Next-generation sequencing platforms. (2013) (621)
- MuSiC: Identifying mutational significance in cancer genomes (2012) (593)
- The genomic landscape of hypodiploid acute lymphoblastic leukemia (2013) (585)
- Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas (2017) (577)
- Identification of genes subject to positive selection in uropathogenic strains of Escherichia coli: a comparative genomics approach. (2006) (566)
- Comparative and demographic analysis of orang-utan genomes (2011) (545)
- SomaticSniper: identification of somatic point mutations in whole genome sequencing data (2012) (543)
- Endocrine-therapy-resistant ESR1 variants revealed by genomic characterization of breast-cancer-derived xenografts. (2013) (543)
- RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (2011) (530)
- Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014) (527)
- Recurrent DNMT3A Mutations in Patients with Myelodysplastic Syndromes (2011) (508)
- Pathogenic Germline Variants in 10,389 Adult Cancers (2018) (501)
- Generation and analysis of 280,000 human expressed sequence tags. (1996) (491)
- CREST maps somatic structural variation in cancer genomes with base-pair resolution (2011) (487)
- Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients (2018) (471)
- A Novel Retinoblastoma Therapy from Genomic and Epigenetic Analyses (2011) (462)
- C11orf95-RELA fusions drive oncogenic NF-κB signaling in ependymoma (2014) (450)
- Complete Khoisan and Bantu genomes from southern Africa (2010) (448)
- Whole-genome sequencing and variant discovery in C. elegans (2008) (444)
- Assuring the quality of next-generation sequencing in clinical laboratory practice (2012) (444)
- The Role of TP53 Mutations in the Origin and Evolution of Therapy-Related AML (2014) (442)
- Viral Discovery and Sequence Recovery Using DNA Microarrays (2003) (438)
- Tumor neoantigens: building a framework for personalized cancer immunotherapy. (2015) (430)
- The DNA sequence of human chromosome 7 (2003) (425)
- DGIdb - Mining the druggable genome (2013) (418)
- Convergent loss of PTEN leads to clinical resistance to a PI3Kα inhibitor (2014) (417)
- CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer (2017) (414)
- Sequence and analysis of chromosome 4 of the plant Arabidopsis thaliana (1999) (403)
- Modernizing Reference Genome Assemblies (2011) (402)
- SciClone: Inferring Clonal Architecture and Tracking the Spatial and Temporal Patterns of Tumor Evolution (2014) (381)
- Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. (2014) (377)
- Patterns of somatic structural variation in human cancer genomes (2020) (377)
- Association of age at diagnosis and genetic mutations in patients with neuroblastoma. (2012) (374)
- The landscape of somatic mutations in Infant MLL rearranged acute lymphoblastic leukemias (2015) (371)
- Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content (2010) (371)
- The landscape of somatic mutations in epigenetic regulators across 1,000 paediatric cancer genomes (2014) (345)
- Functional heterogeneity of genetically defined subclones in acute myeloid leukemia. (2014) (342)
- Development and verification of the PAM50-based Prosigna breast cancer gene signature assay (2015) (318)
- Comparative analysis of the small RNA transcriptomes of Pinus contorta and Oryza sativa. (2008) (315)
- The Pediatric Cancer Genome Project (2012) (311)
- The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage (2013) (305)
- DGIdb 2.0: mining clinically relevant drug–gene interactions (2015) (296)
- Extending assembly of short DNA sequences to handle error (2007) (295)
- The draft genome of the parasitic nematode Trichinella spiralis (2011) (292)
- Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia. (2015) (285)
- Evaluation of 16S rDNA-Based Community Profiling for Human Microbiome Research (2012) (282)
- pVAC-Seq: A genome-guided in silico approach to identifying tumor neoantigens (2016) (282)
- Clonal diversity of recurrently mutated genes in myelodysplastic syndromes (2013) (269)
- Use of whole-genome sequencing to diagnose a cryptic fusion oncogene. (2011) (267)
- The emerging clinical relevance of genomics in cancer medicine (2018) (263)
- The complete genome sequence of a chronic atrophic gastritis Helicobacter pylori strain: evolution during disease progression. (2006) (260)
- Integrated Analysis of Germline and Somatic Variants in Ovarian Cancer (2014) (259)
- Acquired copy number alterations in adult acute myeloid leukemia genomes (2009) (258)
- Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology (2016) (256)
- The $1,000 genome, the $100,000 analysis? (2010) (255)
- A Sequence Motif within Chromatin Entry Sites Directs MSL Establishment on the Drosophila X Chromosome (2008) (254)
- ChIP-seq: welcome to the new frontier (2007) (245)
- DNA sequencing technologies: 2006–2016 (2017) (239)
- A physical map of the chicken genome (2004) (232)
- Targeting oxidative stress in embryonal rhabdomyosarcoma. (2013) (228)
- Contribution of systemic and somatic factors to clinical response and resistance to PD-L1 blockade in urothelial cancer: An exploratory multi-omic analysis (2017) (225)
- Immunogenomics of Hypermutated Glioblastoma: A Patient with Germline POLE Deficiency Treated with Checkpoint Blockade Immunotherapy. (2016) (224)
- A 50-Gene Intrinsic Subtype Classifier for Prognosis and Prediction of Benefit from Adjuvant Tamoxifen (2012) (223)
- Patterns and functional implications of rare germline variants across 12 cancer types (2015) (222)
- Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome. (2007) (221)
- The Common Marmoset Genome Provides Insight into Primate Biology and Evolution (2014) (219)
- An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia. (2012) (215)
- Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma. (2008) (212)
- The functional spectrum of low-frequency coding variation (2011) (210)
- Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia. (2008) (205)
- Cancer genome sequencing: a review. (2009) (204)
- Transcriptome-Wide Identification of Novel Imprinted Genes in Neonatal Mouse Brain (2008) (204)
- Temporally Distinct PD-L1 Expression by Tumor and Host Cells Contributes to Immune Escape (2017) (204)
- Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
- Deregulation of DUX4 and ERG in acute lymphoblastic leukemia (2016) (197)
- Convergent Evolution of Chicken Z and Human X Chromosomes by Expansion and Gene Acquisition (2010) (197)
- Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approach (2006) (196)
- Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells. (2012) (195)
- The Oxytricha trifallax Macronuclear Genome: A Complex Eukaryotic Genome with 16,000 Tiny Chromosomes (2013) (192)
- Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context (2018) (188)
- Anticipating the $1,000 genome (2006) (188)
- The genomic landscape of core-binding factor acute myeloid leukemias (2016) (187)
- Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors (2017) (187)
- Optimizing cancer genome sequencing and analysis. (2015) (179)
- The Genomics Education Partnership: Successful Integration of Research into Laboratory Classes at a Diverse Group of Undergraduate Institutions (2010) (175)
- The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis (2017) (171)
- Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration (2013) (171)
- De novo genome sequence assembly of a filamentous fungus using Sanger, 454 and Illumina sequence data (2009) (170)
- Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML. (2011) (169)
- Applications of Immunogenomics to Cancer (2017) (168)
- The repetitive landscape of the chicken genome. (2004) (168)
- Clinical significance of CTNNB1 mutation and Wnt pathway activation in endometrioid endometrial carcinoma. (2014) (163)
- Analysis of next-generation genomic data in cancer: accomplishments and challenges. (2010) (157)
- DNMT 3 A mutations in acute myeloid leukemia (2016) (151)
- Challenges of sequencing human genomes (2010) (147)
- Germline Genetic Variation in ETV6 and Risk of Childhood Acute Lymphoblastic Leukemia: a Systematic Genetic Study (2015) (139)
- Next-generation sequencing identifies the natural killer cell microRNA transcriptome. (2010) (139)
- The Genomic Landscape of Childhood and Adolescent Melanoma (2014) (139)
- Genomic impact of transient low-dose decitabine treatment on primary AML cells. (2013) (135)
- A burst of segmental duplications in the genome of the African great ape ancestor (2009) (133)
- A burst of segmental duplications in the genome of the African great ape ancestor (2009) (131)
- Ancestry estimation and control of population stratification for sequence-based association studies (2014) (128)
- A Course-Based Research Experience: How Benefits Change with Increased Investment in Instructional Time (2014) (128)
- Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene (2014) (128)
- The Complete Sequence of a Heterochromatic Island from a Higher Eukaryote (2000) (127)
- Future cancer research priorities in the USA: a Lancet Oncology Commission. (2017) (125)
- In Genome analysis: A laboratory manual (1997) (125)
- A precise reconstruction of the emergence and constrained radiations of Escherichia coli O157 portrayed by backbone concatenomic analysis (2009) (123)
- An encyclopedia of mouse genes (1999) (122)
- Germline Genetic IKZF1 Variation and Predisposition to Childhood Acute Lymphoblastic Leukemia. (2018) (121)
- Genomics Education Partnership (2008) (119)
- Visualizing tumor evolution with the fishplot package for R (2016) (119)
- Clonal Architecture of Secondary Acute Myeloid Leukemia Defined by Single-Cell Sequencing (2014) (118)
- The value of avian genomics to the conservation of wildlife (2009) (117)
- Integrated RNA and DNA sequencing reveals early drivers of metastatic breast cancer (2018) (111)
- Conifers have a unique small RNA silencing signature. (2008) (110)
- Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) (2001) (106)
- Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma (2019) (106)
- TP53 Germline Variations Influence the Predisposition and Prognosis of B-Cell Acute Lymphoblastic Leukemia in Children. (2018) (106)
- TYK2 Protein-Coding Variants Protect against Rheumatoid Arthritis and Autoimmunity, with No Evidence of Major Pleiotropic Effects on Non-Autoimmune Complex Traits (2015) (105)
- Direct genomic selection (2005) (104)
- Generation and annotation of the DNA sequences of human chromosomes 2 and 4 (2005) (98)
- Identification of somatic JAK1 mutations in patients with acute myeloid leukemia. (2008) (97)
- Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression. (2011) (97)
- The 56-kilodalton major protein antigen of Rickettsia tsutsugamushi: molecular cloning and sequence analysis of the sta56 gene and precise identification of a strain-specific epitope (1990) (97)
- Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration. (2014) (96)
- Genomic landscape of pediatric adrenocortical tumors (2015) (94)
- pVACtools: A Computational Toolkit to Identify and Visualize Cancer Neoantigens (2020) (94)
- Predicting response and survival in chemotherapy-treated triple-negative breast cancer (2014) (94)
- Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases (2016) (92)
- Rapid expansion of preexisting nonleukemic hematopoietic clones frequently follows induction therapy for de novo AML. (2016) (92)
- Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer (2018) (92)
- Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia. (2007) (92)
- DoCM: a database of curated mutations in cancer (2016) (90)
- A Drosophila Model of Multiple Endocrine Neoplasia Type 2 (2005) (89)
- Identification of Therapeutic Targets in Rhabdomyosarcoma through Integrated Genomic, Epigenomic, and Proteomic Analyses. (2018) (89)
- Reduced PU.1 expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARalpha. (2005) (88)
- A Phase I Trial of BKM120 (Buparlisib) in Combination with Fulvestrant in Postmenopausal Women with Estrogen Receptor–Positive Metastatic Breast Cancer (2015) (88)
- Erratum: Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles (Cell Reports (2017) 18(11) (2780–2794) (S2211124717302140) (10.1016/j.celrep.2017.02.033)) (2017) (88)
- Finding the missing heritability of complex (2009) (87)
- New strategies and emerging technologies for massively parallel sequencing: applications in medical research (2009) (87)
- PathScan: a tool for discerning mutational significance in groups of putative cancer genes (2011) (87)
- Genome-wide diversity and selective pressure in the human rhinovirus (2007) (86)
- Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma (2013) (86)
- Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4 (2007) (85)
- RB1 gene inactivation by chromothripsis in human retinoblastoma (2014) (83)
- Clinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia. (2016) (83)
- Drosophila Muller F Elements Maintain a Distinct Set of Genomic Properties Over 40 Million Years of Evolution (2015) (82)
- PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation (2016) (81)
- The prognostic effects of somatic mutations in ER-positive breast cancer (2017) (81)
- Genome Modeling System: A Knowledge Management Platform for Genomics (2015) (80)
- Panton-Valentine Leukocidin-positive methicillin-resistant Staphylococcus aureus lung infection in patients with cystic fibrosis. (2007) (80)
- PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data. (2007) (80)
- Next-Generation Sequencing Technologies. (2018) (78)
- Complete characterization of the microRNAome in a patient with acute myeloid leukemia. (2010) (75)
- A Surprising Cross-Species Conservation in the Genomic Landscape of Mouse and Human Oral Cancer Identifies a Transcriptional Signature Predicting Metastatic Disease (2014) (74)
- PAM50 gene signatures and breast cancer prognosis with adjuvant anthracycline- and taxane-based chemotherapy: correlative analysis of C9741 (Alliance) (2016) (73)
- INTEGRATE-neo: a pipeline for personalized gene fusion neoantigen discovery (2016) (73)
- RNA Sequencing of Tumor-Associated Microglia Reveals Ccl5 as a Stromal Chemokine Critical for Neurofibromatosis-1 Glioma Growth1 (2015) (73)
- Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome. (2014) (71)
- Genome sequencing and cancer. (2012) (71)
- A pilot study of high-throughput, sequence-based mutational profiling of primary human acute myeloid leukemia cell genomes (2003) (70)
- Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children (2015) (67)
- CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data (2010) (66)
- BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data (2012) (66)
- Endogenous Neoantigen-Specific CD8 T Cells Identified in Two Glioblastoma Models Using a Cancer Immunogenomics Approach (2016) (65)
- What is finished, and why does it matter. (2002) (65)
- Genomic landscape of paediatric adrenocortical tumours (2016) (64)
- The chromosome 3p21.3-encoded gene, LIMD1, is a critical tumor suppressor involved in human lung cancer development (2008) (64)
- MYCN amplification and ATRX mutations are incompatible in neuroblastoma (2018) (63)
- Neoantigens and genome instability: impact on immunogenomic phenotypes and immunotherapy response (2019) (62)
- 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) (61)
- Long non-coding RNA RAMS11 promotes metastatic colorectal cancer progression (2020) (61)
- AACR Cancer Progress Report 2014 (2014) (60)
- Molecular refinement of gibbon genome rearrangements. (2007) (60)
- Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers (2016) (59)
- Novel venom gene discovery in the platypus (2010) (58)
- AACR Cancer Progress Report 2013 (2013) (58)
- The Dynamic Genome and Transcriptome of the Human Fungal Pathogen Blastomyces and Close Relative Emmonsia (2015) (57)
- contribution of genetically restricted, methicillin-susceptible strains to the ongoing epidemic of community-acquired Staphylococcus aureus infections. (2009) (57)
- Transcriptome analysis for Caenorhabditis elegans based on novel expressed sequence tags (2008) (56)
- The Oxytricha trifallax Mitochondrial Genome (2011) (55)
- Breast Cancer Neoantigens Can Induce CD8+ T-Cell Responses and Antitumor Immunity (2017) (55)
- Comparison of dot chromosome sequences from D. melanogaster and D. virilis reveals an enrichment of DNA transposon sequences in heterochromatic domains (2006) (55)
- Genetic risk factors for the development of osteonecrosis in children under age 10 treated for acute lymphoblastic leukemia. (2015) (53)
- Activating HER 2 Mutations in HER 2 Gene Amplifi cation Negative Breast Cancer (2012) (53)
- Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS (2015) (51)
- A Phase II Trial of Neoadjuvant MK-2206, an AKT Inhibitor, with Anastrozole in Clinical Stage II or III PIK3CA-Mutant ER-Positive and HER2-Negative Breast Cancer (2017) (51)
- A Central Support System Can Facilitate Implementation and Sustainability of a Classroom-Based Undergraduate Research Experience (CURE) in Genomics (2014) (51)
- Fourteen-Genome Comparison Identifies DNA Markers for Severe-Disease-Associated Strains of Clostridium difficile (2011) (51)
- Body Mass Index, PAM50 Subtype, and Outcomes in Node-Positive Breast Cancer: CALGB 9741 (Alliance). (2015) (50)
- Integrated Analysis of RNA and DNA from the Phase III Trial CALGB 40601 Identifies Predictors of Response to Trastuzumab-Based Neoadjuvant Chemotherapy in HER2-Positive Breast Cancer (2018) (48)
- A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data (2018) (48)
- Histidine Protects Against Zinc and Nickel Toxicity in Caenorhabditis elegans (2011) (46)
- Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome. (2004) (45)
- A vertebrate case study of the quality of assemblies derived from next-generation sequences (2011) (45)
- Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia. (2016) (42)
- F11R Is a Novel Monocyte Prognostic Biomarker for Malignant Glioma (2013) (42)
- Detection of neoantigen-specific T cells following a personalized vaccine in a patient with glioblastoma (2019) (41)
- Sex differences in oncogenic mutational processes (2019) (41)
- CTCF genetic alterations in endometrial carcinoma are pro-tumorigenic (2017) (40)
- cDNA hybrid capture improves transcriptome analysis on low-input and archived samples. (2014) (39)
- Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites. (2009) (39)
- Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival (2020) (38)
- High-throughput detergent extraction of M13 subclones for fluorescent DNA sequencing. (1994) (37)
- What is the future of electrophoresis in large‐scale genomic sequencing? (2006) (37)
- Application of a superword array in genome assembly (2006) (36)
- Accounting for proximal variants improves neoantigen prediction (2018) (36)
- Research-based PAM50 signature and long-term breast cancer survival (2019) (36)
- Applying next-generation sequencing to pancreatic cancer treatment (2012) (36)
- Evolution of a Distinct Genomic Domain in Drosophila: Comparative Analysis of the Dot Chromosome in Drosophila melanogaster and Drosophila virilis (2010) (34)
- Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS. (2017) (33)
- Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data (2012) (33)
- Immunological ignorance is an enabling feature of the oligo-clonal T cell response to melanoma neoantigens (2019) (32)
- RNA‐sequencing reveals oligodendrocyte and neuronal transcripts in microglia relevant to central nervous system disease (2015) (32)
- Cloning and DNA sequence of the Mycobacterium fortuitum var fortuitum plasmid pAL5000. (1992) (32)
- Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation (2016) (32)
- Association of Tumor Microenvironment T-cell Repertoire and Mutational Load with Clinical Outcome after Sequential Checkpoint Blockade in Melanoma (2019) (32)
- Association Between DQB1 and Cervical Cancer in Patients With Human Papillomavirus and Family Controls (2000) (32)
- Association of Somatic Mutations of ADAMTS Genes With Chemotherapy Sensitivity and Survival in High-Grade Serous Ovarian Carcinoma. (2015) (31)
- The challenges of big data (2016) (31)
- 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 (2011) (31)
- Automated methods for single-stranded DNA isolation and dideoxynucleotide DNA sequencing reactions on a robotic workstation. (1989) (31)
- The Clonal Evolution of Metastatic Osteosarcoma as Shaped by Cisplatin Treatment (2019) (31)
- A multiple myeloma-specific capture sequencing platform discovers novel translocations and frequent, risk-associated point mutations in IGLL5 (2018) (30)
- Next-generation sequencing of cancer genomes: back to the future. (2009) (30)
- The Impact of Next-Generation Sequencing on Cancer Genomics: From Discovery to Clinic. (2018) (29)
- Use of a chemically modified T7 DNA polymerase for manual and automated sequencing of supercoiled DNA. (1988) (29)
- Frontiers in cancer immunotherapy—a symposium report (2020) (29)
- Fosmid-based physical mapping of the Histoplasma capsulatum genome. (2004) (28)
- Caenorhabditis elegans glp-4 Encodes a Valyl Aminoacyl tRNA Synthetase (2015) (28)
- BreakTrans: uncovering the genomic architecture of gene fusions (2013) (26)
- Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis (2015) (26)
- Cancer genomics identifies determinants of tumor biology (2010) (25)
- Genomics of acute myeloid leukemia. (2011) (25)
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- Genomic profiling of murine mammary tumors identifies potential personalized drug targets for p53-deficient mammary cancers (2016) (22)
- Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (22)
- Cancer Immunogenomics: Computational Neoantigen Identification and Vaccine Design (2017) (22)
- Oral Cavity Squamous Cell Carcinoma Xenografts Retain Complex Genotypes and Intertumor Molecular Heterogeneity (2018) (21)
- An infrared fluorescent dATP for labeling DNA. (1995) (20)
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- Corrigendum: C11orf95–RELA fusions drive oncogenic NF-κB signalling in ependymoma (2014) (19)
- The translation of cancer genomics: time for a revolution in clinical cancer care (2014) (19)
- Genome Sequencing Technology and Algorithms (2007) (19)
- Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African Americans (2016) (19)
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- End sequence determination from large insert clones using energy transfer fluorescent primers. (1996) (19)
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- Characterization of the Genomic and Immunologic Diversity of Malignant Brain Tumors through Multisector Analysis (2021) (16)
- Recurrent DNMT3A Mutations In Patients with Myelodysplastic Syndrome (2010) (16)
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- The Role Of Early TP53 Mutations On The Evolution Of Therapy-Related AML (2013) (15)
- Detection of brain somatic variation in epilepsy‐associated developmental lesions (2021) (15)
- Somatic SLC35A2 mosaicism correlates with clinical findings in epilepsy brain tissue (2020) (14)
- Identification of somatic JAK 1 mutations in patients with acute myeloid leukemia (2008) (14)
- Tumor heterogeneity: next-generation sequencing enhances the view from the pathologist’s microscope (2014) (13)
- 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 (2011) (13)
- Abstract S6-05: A phase II trial of neoadjuvant palbociclib, a cyclin-dependent kinase (CDK) 4/6 inhibitor, in combination with anastrozole for clinical stage 2 or 3 estrogen receptor positive HER2 negative (ER+HER2-) breast cancer (BC) (2016) (13)
- Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010) (13)
- Comprehensive Genetic Variant Discovery in the Surfactant Protein B Gene (2007) (13)
- Design and implementation of a generalized laboratory data model (2007) (12)
- Infantile fibrosarcoma–like tumor driven by novel RBPMS-MET fusion consolidated with cabozantinib (2020) (12)
- Sequencing the AML genome, transcriptome, and epigenome. (2014) (12)
- Large-scale sequencing and analytical processing of ESTs. (2009) (12)
- Blinded Comparison of Repetitive-Sequence PCR and Multilocus Sequence Typing for Genotyping Methicillin-Resistant Staphylococcus aureus Isolates from a Children's Hospital in St. Louis, Missouri (2006) (12)
- A roadmap for the next decade in cancer research (2020) (12)
- Erratum: C11orf95-RELA fusions drive oncogenic NF-ΰ B signalling in ependymoma (Nature (2014) 506 (451-455 ) DOI:10.1038/nature13109) (2014) (12)
- Where Next for Genetics and Genomics? (2015) (11)
- Resistance-promoting effects of ependymoma treatment revealed through genomic analysis of multiple recurrences in a single patient (2018) (11)
- Correction to: Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma (2020) (11)
- An mRNA Gene Expression-Based Signature to Identify FGFR1-Amplified Estrogen Receptor-Positive Breast Tumors. (2017) (11)
- Comprehensive genomic studies: emerging regulatory, strategic, and quality assurance challenges for biorepositories. (2012) (11)
- CIViC: A knowledgebase for expert-crowdsourcing the clinical interpretation of variants in cancer (2016) (11)
- PTEN somatic mutations contribute to spectrum of cerebral overgrowth. (2021) (11)
- Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience (2020) (10)
- A Phase I Trial of BKM 120 ( Buparlisib ) in Combination with Fulvestrant in Postmenopausal Women with Estrogen Receptor – Positive Metastatic Breast Cancer (2016) (10)
- Brief Report: The Role of Rare Protein‐Coding Variants in Anti–Tumor Necrosis Factor Treatment Response in Rheumatoid Arthritis (2017) (10)
- YAP1-FAM118B Fusion Defines a Rare Subset of Childhood and Young Adulthood Meningiomas. (2020) (10)
- A supervised risk predictor of breast cancer based on biological subtypes (2008) (9)
- Gallus GBrowse: a unified genomic database for the chicken (2007) (9)
- Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes. (2017) (9)
- Mutational profiling in the human genome. (2003) (9)
- Molecular and Pathology Features of Colorectal Tumors and Patient Outcomes Are Associated with Fusobacterium nucleatum and Its Subspecies animalis (2021) (9)
- Genomic analysis to define molecular basis of aggressiveness in a mouse model of oral cancer (2014) (9)
- Somatic mutations in benign breast disease tissue and risk of subsequent invasive breast cancer (2018) (8)
- Expression of a bcr-1 isoform of RARalpha-PML does not affect the penetrance of acute promyelocytic leukemia or the acquisition of an interstitial deletion on mouse chromosome 2. (2007) (8)
- Acute lymphoblastic leukemia displays a distinct highly methylated genome (2022) (8)
- Abstract LB-327: Loss of PTEN leads to clinical resistance to the PI3Kα inhibitor BYL719 and provides evidence of convergent evolution under selective therapeutic pressure (2014) (8)
- Incidence of Germline Mutations in Cancer-Predisposition Genes in Children with Hematologic Malignancies: a Report from the Pediatric Cancer Genome Project (2014) (8)
- Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2022) (8)
- A luminal breast cancer genome atlas: Progress and barriers (2007) (8)
- Genome sequencing identifies somatic BRAF duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma (2018) (7)
- Causal and Candidate Gene Variants in a Large Cohort of Women with Primary Ovarian Insufficiency (2021) (7)
- pVACtools: a computational toolkit to select and visualize cancer neoantigens (2018) (7)
- A pneumatic device for rapid loading of DNA sequencing gels. (1998) (7)
- De novo primary central nervous system pure erythroid leukemia/sarcoma with t(1;16)(p31;q24) NFIA/CBFA2T3 translocation (2020) (7)
- Correction: Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases (2017) (7)
- Gastroblastoma with a novel EWSR1‐CTBP1 fusion presenting in adolescence (2021) (7)
- Abstract S5-6: Activating HER2 mutations in HER2 gene amplification negative breast cancers. (2012) (7)
- Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma. (2019) (7)
- What's different about women's health? (2014) (7)
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- Multiomics in primary and metastatic breast tumors from the AURORA US network finds microenvironment and epigenetic drivers of metastasis (2022) (6)
- Insights from Large-Scale Cancer Genome Sequencing (2018) (5)
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- Abstract P2-10-01: PAM50 gene signature is prognostic for breast cancer patients treated with adjuvant anthracycline and taxane based chemotherapy (2012) (5)
- Library Quantification Using SYBR Green-Quantitative Polymerase Chain Reaction (qPCR). (2017) (5)
- miRNAs and Long-term Breast Cancer Survival: Evidence from the WHEL Study (2019) (5)
- Novel morphologic findings in PLAG1‐rearranged soft tissue tumors (2021) (5)
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- Capillary electrophoresis platforms for DNA sequence analysis. (1999) (4)
- Revolutionizing cancer care with next-generation sequencing: an interview with Elaine Mardis (2014) (4)
- Abstract S3-06: Mutational analysis of CALGB 40601 (Alliance), a neoadjuvant phase III trial of weekly paclitaxel (T) and trastuzumab (H) with or without lapatinib (L) for HER2-positive breast cancer (2015) (4)
- Whole-Genome Sequencing: Automated, Nonindexed Library Preparation. (2017) (4)
- Advances in genome biology and technology. (2004) (4)
- No evidence that G6PD deficiency affects the efficacy or safety of daunorubicin in acute lymphoblastic leukemia induction therapy (2019) (4)
- Abstract 3995: pVAC-Seq: A genome-guidedin silicoapproach to identify tumor neoantigens for personalized immunotherapy (2016) (4)
- Abstract S3-05: Patient-derived xenograft study reveals endocrine therapy resistance of ER+ breast cancer caused by distinct ESR1 gene aberrations (2013) (4)
- Automated Library Preparation for DNA Sequencing. (2017) (4)
- Immune Activity and Response Differences of Oncolytic Viral Therapy in Recurrent Glioblastoma: Gene Expression Analyses of a Phase IB Study (2022) (4)
- Targeted Therapy in a Young Adult With a Novel Epithelioid Tumor Driven by a PRRC2B-ALK Fusion. (2021) (4)
- High early death rates, treatment resistance, and short survival of Black adolescents and young adults with AML (2022) (4)
- Automated plaque picking and arraying on a robotic system equipped with a CCD camera and a sampling device using intramedic tubing (1996) (4)
- Defining the AHR-regulated transcriptome in NK cells reveals gene expression programs relevant to development and function (2021) (4)
- Agarose Gel Size Selection for DNA Sequencing Libraries. (2017) (4)
- Salivary miRNA Expression in Children With Persistent Post-concussive Symptoms (2022) (4)
- Germline BAP1 Mutation in a Family With Multi-Generational Meningioma With Rhabdoid Features: A Case Series and Literature Review (2021) (4)
- Late-Breaking Abstract 4: The Cancer Genome Atlas (TCGA) project on endometrial carcinoma: Initial data and preliminary genomic analysis (2012) (3)
- Association of 17q22 Amplicon Via Cell-Free DNA With Platinum Chemotherapy Response in Metastatic Triple-Negative Breast Cancer (2021) (3)
- Genomic prediction of neoantigens: immunogenomics before NGS (2021) (3)
- Engineering in genomics. Technical improvements in high throughput genome sequencing (1995) (3)
- A community approach to the cancer-variant-interpretation bottleneck (2022) (3)
- Recurrent Somatic Genomic Alterations in Follicular NHL (FL) Revealed By Exome and Custom-Capture Next Generation Sequencing (2015) (3)
- Leveraging gene therapy to achieve long-term continuous or controllable expression of biotherapeutics (2022) (3)
- Samovar: Single-Sample Mosaic Single-Nucleotide Variant Calling with Linked Reads (2019) (3)
- RNA-Seq: RNA Conversion to cDNA and Amplification. (2017) (3)
- CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase (2022) (3)
- Modification of a commercially available DNA sequencer to increase sample throughput (2000) (3)
- Preparing Polymerase Chain Reaction (PCR) Products for Capillary Sequencing. (2017) (3)
- Abstract P5-13-04: A phase II neoadjuvant trial of MK-2206, an AKT inhibitor, in combination with anastrozole for clinical stage 2 or 3 PIK3CA mutant estrogen receptor positive HER2 negative (ER+HER2-) breast cancer (BC) (2016) (3)
- Germline Genetic Variation in IKZF1 and Predisposition to Childhood Acute Lymphoblastic Leukemia (2015) (3)
- Dysregulation and Recurrent Mutation Of miRNA-142 In De Novo AML (2013) (3)
- Whole-Genome Sequencing: Manual Library Preparation. (2017) (3)
- The era of precision oncogenomics (2018) (3)
- Clinical response to dabrafenib plus trametinib in a pediatric ganglioglioma with BRAF p.T599dup mutation (2021) (3)
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- Preparation of a 3-kb Mate-Pair Library for Illumina Sequencing. (2017) (3)
- Many mutations in one clinical-trial basket (2018) (3)
- Xenografts as models of clonal selection and acquired resistance to therapy. (2015) (2)
- Cancer Genomics (2015) (2)
- Library Quantification Using PicoGreen Fluorometry. (2017) (2)
- Next-generation sequencing, cancer and molecular diagnostics: an interview with Elaine Mardis (2015) (2)
- Somatic Variation as an Incidental Finding in the Pediatric Next Generation Sequencing Era. (2021) (2)
- Genomic DNA Copy Number Alterations Present in AML Bone Marrow Samples with Normal Cytogenetics. (2004) (2)
- Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas (2021) (2)
- TRIM-NHL protein, NHL-2, modulates cell fate choices in the C. elegans germ line (2022) (2)
- Preparation of an 8-kb Mate-Pair Library for Illumina Sequencing. (2017) (2)
- Multi-omic analysis of urothelial cancer patients treated with PD-L1 blockade demonstrates the contribution of both systemic and somatic factors to the biology of response and resistance (2016) (2)
- Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma (2021) (2)
- From “N of 1” to N of more (2015) (2)
- Estrogen receptor expression is high but is of lower intensity in tubular carcinoma than in well-differentiated invasive ductal carcinoma. (2014) (2)
- Complete Sequencing and Comparison of 12 Normal Karyotype M1 AML Genomes with 12 t(15;17) Positive M3-APL Genomes (2011) (2)
- Cycle-Sequencing Reactions. (2017) (2)
- 143 Identification of Neoantigen-specific CD8+ T Cells in Two Murine Orthotopic Glioblastoma Models Using Cancer Immunogenomics. (2016) (2)
- Cancer Genomics: Large-Scale Projects Translate into Therapeutic Advances (2016) (2)
- A Vaccine for Cancer? (2016) (2)
- Abstract 2547: Discovery and characterization of late-stage breast cancer estrogen receptor alpha 1 bound long non-coding RNAs (2017) (2)
- Preparing Plasmid Subclones for Capillary Sequencing. (2017) (2)
- Risk of secondary malignant neoplasms in children following proton therapy vs. photon therapy for primary CNS tumors: A systematic review and meta-analysis (2022) (2)
- New additions to the cancer precision medicine toolkit (2018) (2)
- Envisioning the next human genome reference (2021) (2)
- Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers. (2022) (1)
- Abstract S1-02: Prognostic effects of gene mutation in estrogen receptor positive breast cancer (2015) (1)
- The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage (2013) (1)
- BreakTrans: uncovering the genomic architecture of gene fusions (2013) (1)
- Abstract LB-87: Analysis of luminal-type breast cancer by massively parallel sequencing (2011) (1)
- Abstract LB-237: Vaccination increases the breadth and diversity of melanoma neoantigen-specific T cells in humans (2015) (1)
- An evaluation of MGMT promoter methylation within the methylation subclasses of glioblastoma (2020) (1)
- The translation of cancer genomics: time for a revolution in clinical cancer care (2014) (1)
- AACR Calls on Congress to Take Immediate Action Against COVID-19 and Protect Patients with Cancer During the Pandemic. (2020) (1)
- Abstract PR03: The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma (2014) (1)
- Samovar: Single-sample mosaic SNV calling with linked reads (2019) (1)
- Whole genome sequencing to characterize luminal-type breast cancer. (2012) (1)
- Abstract A001: Tumor-specific mutant antigens in cancer immunotherapy (2016) (1)
- Eliciting an immune-mediated antitumor response through oncolytic herpes simplex virus-based shared antigen expression in tumors resistant to viroimmunotherapy (2021) (1)
- Additional Sequencing of the Chicken Genome (2005) (1)
- PacBio Fusion and Long Isoform Pipeline (PB_FLIP) for Cancer Transcriptome-based Resolution of Isoform Complexity. (2022) (1)
- EGFR internal tandem duplications in fusion‐negative congenital and neonatal spindle cell tumors (2022) (1)
- Precision oncogenomics (2019) (1)
- Abstract 4870: Integrated genomic analysis of hypodiploid acute lymphoblastic leukemia (2012) (1)
- Next-generation cancer genomics (2010) (1)
- Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
- Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer (2018) (1)
- Gene expression profiles to predict outcome in breast cancer (2009) (1)
- Expanding the clinical phenotype of FGFR1 internal tandem duplication (2022) (1)
- Whole-Genome Sequencing: Automated, Indexed Library Preparation. (2017) (1)
- Abstract P6-05-03: Genomic diversity of ductal carcinoma in situ (DCIS) as a driver of invasion and metastasis (2016) (1)
- NF 1-associated pilocytic astrocytoma Somatic neurofibromatosis type 1 ( NF 1 ) inactivation characterizes Material Supplemental (2013) (1)
- Resistance heating device reduces gel mobility compressions in automated fluorescent sequencing. (1995) (1)
- LINC00355 regulates p27KIP expression by binding to MENIN to induce proliferation in late-stage relapse breast cancer (2022) (1)
- High Early Death Rates, Treatment Resistance and Short Survival of Black Adolescent and Young Adults (AYAs) with Acute Myeloid Leukemia (AML) (Alliance) (2021) (1)
- The repetitive landscape of the chicken genome Material Supplemental (2016) (1)
- Abstract P4-11-11: CADER prognostic gene signature for disease free survival in hormone receptor positive breast cancer: NCIC CTG MA.12 phase III placebo-controlled tamoxifen trial (2015) (1)
- Detection of Novel Mutations In MDS/AML by Whole Genome Sequencing (2010) (1)
- Mutations In the DNA Methyltransferase Gene DNMT3A Are Highly Recurrent In Patients with Intermediate Risk Acute Myeloid Leukemia, and Predict Poor Outcomes (2010) (1)
- Chromatin Immunoprecipitation of GFP-Tagged PML-Rara Coupled to High-Throughput Next Generation Sequencing. (2009) (1)
- Expression of an Oncogenic ERG isoform Characterizes a Distinct Subtype of B-Progenitor Acute Lymphoblastic Leukemia (2015) (1)
- LTBK-05. Outcomes of Infants and Young Children with Newly Diagnosed Localized (M0) SHH Medulloblastoma Treated on The NEXT Consortium “Head Start” 4 Protocol (2022) (1)
- Whole-Genome Sequencing: New Technologies, Approaches, and Applications (2013) (1)
- A brief history of (DNA sequencing) time (2007) (1)
- The NK Cell MicroRNA Transcriptome Defined by Next-Generation Sequencing Identifies IL-15-Signaled Alterations In Mature MiR-223 Expression, and MiR-223 as a Potential Regulator of Murine Granzyme B (2010) (1)
- Endogenous retrovirus envelope as a tumor-associated immunotherapeutic target in murine osteosarcoma (2021) (1)
- Molecular Heterogeneity in Pediatric Malignant Rhabdoid Tumors in Patients With Multi-Organ Involvement (2022) (1)
- Abstract 5221: Linking the molecular profile of colorectal tumors to germline genetic and environmental risk factors (2016) (1)
- A co-clinical phase II trial of carboplatin and docetaxel as neoadjuvant treatment for triple negative breast cancer with genomic discovery analysis. (2016) (1)
- Many mutations in one clinical-trial basket. (2018) (1)
- Supplementary Appendix for "Targetable Kinase-Activating Lesions in Ph-like Acute Lymphoblastic Leukemia" (2014) (1)
- Whole Genome Sequencing of Therapy-Related Acute Myeloid Leukemia (2012) (1)
- Sequencing an Acute Myeloid Leukemia (AML) Genome with “Next Generation” Technologies. (2007) (1)
- Association BetweenMutation Clearance After Induction Therapy andOutcomes in AcuteMyeloid Leukemia (2015) (1)
- Abstract S3-05: Integrated analysis of multidimensional genomic data on CALGB 40601 (Alliance), a randomized neoadjuvant phase III trial of weekly paclitaxel (T) and trastuzumab (H) with or without lapatinib (L) for HER2-positive breast cancer (2017) (1)
- ATIM-32. PREDICTORS OF IMPROVED SURVIVAL FOLLOWING ONCOLYTIC VIRUS TREATMENT IN PATIENTS WITH RECURRENT GLIOBLASTOMA: GENE EXPRESSION ANALYSIS FROM THE PHASE IB G207 CLINICAL TRIAL (2019) (1)
- Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data (2012) (1)
- P1-06-13: An Amplicon-Driven Aromatase Inhibitor Response (ADAIR) Signature Provides an Orthogonal Risk Classifier for ER+ Breast Cancer. (2011) (1)
- Author Correction: Comparative and demographic analysis of orang-utan genomes (2022) (1)
- The Role of Rare Protein-Coding Variants in Anti–Tumor Necrosis Factor Treatment Response in Rheumatoid Arthritis (2017) (1)
- ATIM-36. EVOLUTION OF CLONAL ARCHITECTURE AND NEOANTIGEN LANDSCAPE IN AN ULTRAMUTATED GLIOBLASTOMA TREATED WITH IMMUNOTHERAPY: A CASE REPORT OF A PATIENT WITH A GERMLINE POLE DEFICIENCY (2016) (0)
- Coming to grips with bioinformatics (2014) (0)
- Manufacture and Characterization of GMP-Compliant SARS-COV-2 Cytotoxic T Lymphocytes. (2022) (0)
- Nature 2011 NGS review (2011) (0)
- leukemia Identification of somatic JAK1 mutations in patients with acute myeloid (2013) (0)
- Abstract 11082: Exome Sequencing Implicates the Burden of Rare Potassium Channel Variants in the Risk of Drug Induced Long QT Syndrome (2013) (0)
- Robust diagnostic yield and candidate gene discovery through paired exome analysis in vascular malformation and overgrowth (2021) (0)
- A Second Generation, Multiple Myeloma-Specific, Targeted Sequencing Platform for Detecting Translocations, Copy Number Alterations, and Single Nucleotide Variants (2015) (0)
- CIViC: Crowdsourcing the Clinical Interpretation of Variants in Cancer (2015) (0)
- LGG Nat Genet Supplemental data 2013 (2013) (0)
- 6 Using Whole Genome Sequencing for Digital Analysis of Tumour Evolution (2012) (0)
- Abstract IA20: Genomics of a STAT1 knockout mouse model of human ER+ breast cancer (2016) (0)
- Abstract P1-06-06: Evidence for tumor heterogeneity and clonal evolution during invasive progression of breast cancer (2017) (0)
- Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
- Faculty Opinions recommendation of Two novel ALK mutations mediate acquired resistance to the next-generation ALK inhibitor alectinib. (2015) (0)
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- Improved oligonucleotides for microarrays (2000) (0)
- Abstract P1-05-30: Genomic and microenvironmental intra-tumor heterogeneity in DCIS (2017) (0)
- Abstract P1-07-11: Tumor genomic profiling of triple negative breast cancer during neoadjuvant chemotherapy: Results from a prospective trial of carboplatin and docetaxel (2017) (0)
- Abstract A70: Identification of pancreatic cancer neoantigens by exome and RNA sequencing analysis (2016) (0)
- Accurate diagnosis of pediatric brain cancers (2023) (0)
- MS1-3: Tumor Heterogeneity and Metastasis. (2011) (0)
- Solid Tumor Genomics (2018) (0)
- Abstract PR03: Genomic approaches for risk assessment in acute myeloid leukemia (2015) (0)
- Complete Nucleotide Sequence of Saccharomyces cerevisiae Chromosome VilI (2008) (0)
- EPEN-17. FAVORABLE OUTCOME TO INTENSIVE CHEMOTHERAPY WITHOUT IRRADIATION IN INFANTILE METASTATIC EPENDYMOMA WITH A NOVEL MOLECULAR PROFILE: A CASE REPORT (2020) (0)
- Abstract LB-232: Tumor clonality detection using next generation sequencing data. (2013) (0)
- pVAC-Seq: A genome-guided in silico approach to identifying tumor neoantigens (2016) (0)
- The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission. (2022) (0)
- Abstract LB-236: Patient derived xenografts as high-fidelity genomic models for advanced breast cancer. (2013) (0)
- The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission. (2022) (0)
- RARE-31. RECURRENT CHOROID PLEXUS CARCINOMA IN THE SETTING OF LI-FRAUMENI SYNDROME: REPORT OF TWO CHILDREN MANAGED WITH INTENSIVE RE-INDUCTION AND MARROW-ABLATIVE CONSOLIDATION CHEMOTHERAPY WITHOUT IRRADIATION FOLLOWED BY MOLECULARLY-TARGETED BIOLOGICAL THERAPY (2020) (0)
- arising in the setting of severe congenital neutropenia Distinct patterns of mutations occurring in de novo AML versus AML (2013) (0)
- 117. Clinical lessons learned from Translational Molecular Profiling of Cancer and Somatic Disease (2022) (0)
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- Clinical and Genomic Insights from Metastatic Cancers. (2018) (0)
- 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)
- Forum: Precision oncology roundtable with Mardis and Siu (2021) (0)
- Abstract PL05-04: Temporal evaluation of cancer heterogeneity. (2013) (0)
- Abstract P4-09-10: Spatial protein and RNA expression in tumor, immune and stromal cells in BRCA1/2 mutated metastatic breast cancer (2023) (0)
- Abstract PR01: Identifying clinically important somatic mutations through a knowledge-based approach (2015) (0)
- DIS3 Variants are Associated with Primary Ovarian Insufficiency: Importance of Transcription/Translation in Oogenesis. (2023) (0)
- SP7 Next-Generation Sequencing Technology: Practical Application (2007) (0)
- High Resolution Array-Based CGH and SNP Studies of AML Genomes. (2007) (0)
- Abstract 959: Aromatase inhibition shapes the clonal architecture of estrogen receptor-positive breast cancers (2015) (0)
- A glimpse at tumor genome evolution (2011) (0)
- 22. Standardization and systematization of somatic variant refinement using a standard operating procedure and deep learning (2019) (0)
- EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24) (2020) (0)
- fluorescent DNA sequencing (0)
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- Mayer-Sequence and analysis of chromosome 4 of the plant Arabidopsis thaliana-1999 (2016) (0)
- DNA Sequence of the Cancer Genome of a Patient with Therapy-Related Acute Myeloid Leukemia (2010) (0)
- Abstract 1651: Utilization of an ensemble approach for identification of driver fusions in pediatric cancer (2019) (0)
- Abstract 1159: Single molecule sequencing to detect and characterize somatic mutations in cancer genomes (2010) (0)
- Whole genome sequencing reveals enrichment of mutations in mucin gene family in breast cancer diagnosed during pregnancy (2017) (0)
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- RARE-37. NOONAN SYNDROME AND GLIONEURONAL TUMORS: A CENTRAL NERVOUS SYSTEM CANCER PREDISPOSITION ASSOCIATION? (2020) (0)
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- Pediatric cancer: case studies illustrate mechanisms to address significant challenges (2019) (0)
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- EPCT-05. Phase Ib study of unesbulin (PTC596) in children with newly diagnosed diffuse intrinsic pontine glioma (DIPG) and high-grade glioma (HGG): A report from the COllaborative Network for NEuro-Oncology Clinical Trials (CONNECT) (2022) (0)
- Neoantigens and genome instability: impact on immunogenomic phenotypes and immunotherapy response (2019) (0)
- Samples used for the formation of wedge-shaped sample wells for ultra-thin slab gels in electrophoresis (1993) (0)
- Fourteen-Genome Comparison Identifies DNA Markers for Severe-Disease-Associated Strains of Clostridium difficile (cid:1) † (2011) (0)
- Annotating Drosophila grimshawi Contig 15 By : (2012) (0)
- LGG-47. Single-cell RNA Sequencing Reveals Immunosuppressive Myeloid Cell Diversity During Malignant Progression in Glioma (2022) (0)
- Title A course-based research experience : How benefits change with increased investment in instructional time Permalink (2014) (0)
- Abstract IA02: Cancer genomics: Translational challenges (2015) (0)
- Abstract A1-06: Recurrent mutations of hormone-positive breast cancer and association with outcome (2015) (0)
- Correspondence comprehensive characterization of a brainstem aggregoma (light and heavy chain deposition disease). (2023) (0)
- Potential Of Integrating Human Genetics and Electronic Medical Records For Drug Discovery : The Example Of TYK2 and Rheumatoid Arthritis (2013) (0)
- Abstract GS2-01: Discovery and characterization of an estrogen bound LncRNA in late-Stage breast cancer (2018) (0)
- 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 Geno (2011) (0)
- Abstract IA12: Open-source, crowdsourcing-capable tools for N of 1 cancer genomics (2016) (0)
- The repetitive landscape of the chicken genome data (2004) (0)
- Tumor heterogeneity: next-generation sequencing enhances the view from the pathologist's microscope (2014) (0)
- Development and verification of the PAM50-based Prosigna breast cancer gene signature assay (2015) (0)
- Abstract IA11: Using genomics to study preexisting resistance (2015) (0)
- Abstract 3847: Oral cavity squamous cell carcinoma xenografts display conservation of primary tumor genomic heterogeneity (2017) (0)
- THE MOUSE GENOME SEQUENCING PROJECT: AN OVERVIEW (2005) (0)
- 22. Standard operating procedure for personalized cancer vaccine designs (2020) (0)
- P654: Evaluation of the ClinGen/CGC/VICC Oncogenicity Guidelines to support pediatric variant classification workflows (2023) (0)
- The human genome: genes, pseudogenes, and variation on chromosome 7. (2003) (0)
- 242 Genomics of myelodysplastic syndromes (2011) (0)
- Mutational analysis of EGFR signaling pathway genes in lung adenocarcinomas (2007) (0)
- Coordinate curation for variant knowledgebases, the CIViC approach (2017) (0)
- Comprehensivemolecularcharacterization of human colon and rectal cancer (2012) (0)
- LINC00355 regulates p27KIP expression by binding to MENIN to induce proliferation in late-stage relapse breast cancer (2022) (0)
- Decision letter: Supervised mutational signatures for obesity and other tissue-specific etiological factors in cancer (2020) (0)
- DNA Sequencing of a Murine Acute Promyelocytic Leukemia (APL) Genome Using Next Generation Technology. (2009) (0)
- An unusual case of atypical teratoid/rhabdoid tumor, initially diagnosed as atypical pituitary adenoma in a 13-year-old male patient (2022) (0)
- ATRT-21. RHABDOID PREDISPOSITION SYNDROME: REPORT OF MOLECULAR PROFILES AND TREATMENT APPROACH IN THREE CHILDREN WITH SYNCHRONOUS ATYPICAL TERATOID/RHABDOID TUMOR AND MALIGNANT RHABDOID TUMOR (2020) (0)
- Manufacture, Immunological Characterization and Clinical Response of GMP Grade Sars-COV-2 Cytotoxic T Lymphocytes (CTLs) Utilizing the Clinimacs® Cytokine Capture System (2023) (0)
- 75 Loss of PTEN leads to acquired resistance to the PI3Ka inhibitor BYL719: a case of convergent evolution under selective therapeutic pressure (2014) (0)
- Single-cell RNA Sequencing Reveals Immunosuppressive Myeloid Cell Diversity and Restricted Cytotoxic Effector Cell Trafficking and Activation During Malignant Progression in Glioma (2021) (0)
- Abstract IA3: Discovery in cancer genomics by next-generation sequencing and data analysis (2011) (0)
- Correction to: Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma (2020) (0)
- California Dreamin': the Future of Genomic Medicine (2016) (0)
- Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2023) (0)
- Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma (2019) (0)
- BIOM-49. A PILOT STUDY OF CEREBROSPINAL FLUID EXOSOMAL SMALL RNA-SEQUENCING IN PEDIATRIC MEDULLOBLASTOMA PATIENTS ON THE NEXT CONSORTIUM “HEAD START” 4 PROTOCOL (2022) (0)
- A glimpse at tumor genome evolution (2011) (0)
- 26. pVACtools: Computational selection and visualization of neoantigens for personalized cancer vaccine design (2018) (0)
- Evolution of the open-access CIViC knowledgebase is driven by the needs of the cancer variant interpretation community (2021) (0)
- Integrated genomic characterization of oesophageal carcinoma (2017) (0)
- Non-Malignant Oligoclonal Hematopoiesis Commonly Follows Cytoreductive Chemotherapy in Adult De Novo AML Patients (2015) (0)
- Abstract IA04: Genomic studies of breast cancer progression (2013) (0)
- Abstract 4873: Comprehensive analysis of 160 whole-genome sequences reveals striking telomere alteration patterns in 9 pediatric cancers (2012) (0)
- Ki-67 is a Luminal B marker that identifies a high-risk subgroup in hormone receptor positive and node negative breast cancer (2007) (0)
- Discovery of clinically relevant fusions in pediatric cancer (2021) (0)
- Brief Expression of a bcr-1 isoform of RAR (cid:1) -PML does not affect the penetrance of acute promyelocytic leukemia or the acquisition of an interstitial deletion on mouse chromosome 2 (2007) (0)
- Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
- High Early Death Rates, Treatment Resistance and Short Survival of Black Adolescent and Young Adults with Acute Myeloid Leukemia (2021) (0)
- Digital Commons@Becker Digital Commons@Becker The repetitive landscape of the chicken genome The repetitive landscape of the chicken genome (2022) (0)
- Abstract 1286: Targeted deep sequencing of colorectal tumor tissues to study associations of tumor subtypes with germline genetic, lifestyle, and environmental risk factors (2017) (0)
- Abstract 3878: A model to assess clonal evolution of metastatic colorectal cancer during chemotherapy utilizing patient derived xenografts (2015) (0)
- Solution-Phase Exome Capture. (2017) (0)
- Using Next Generation Solexa Sequencing to Identify Genes that Regulate Stem Cell Proliferation in the Caenorhabditis elegans Germline (2009) (0)
- Expanding the phenotypic spectrum of internal tandem duplications in somatic disease (2021) (0)
- Contribution of systemic and somatic factors to clinical response and resistance in urothelial cancer: an exploratory multi-omic analysis (2017) (0)
- Advances in Tumor Genetics (2016) (0)
- 32. Clin-MSI: A machine learning-based approach to MSI detection in endometrial cancers (2022) (0)
- Next-Generation Applications to Translation Research. (2010) (0)
- Visualizing tumor evolution with the fishplot package for R (2016) (0)
- Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers (2021) (0)
- Abstract PD6-02: The genomics of response to neoadjuvant trastuzumab and chemotherapy in HER2-positive breast cancer – Results from the ACOSOG Z1041 (Alliance) trial (2016) (0)
- Accounting for proximal variants improves neoantigen prediction (2018) (0)
- Temporal and Clonal Progression in a Pediatric Ependymoma Patient Through Multiple Treatments (2017) (0)
- The Importance of Research in the Undergraduate Curriculum: Explorations in Genomics (2007) (0)
- Advances in Genome Biology and Technology: 8th Annual Meeting (2007) (0)
- Characterization of the microRNAome in a patient with acute myeloid leukemia. (2010) (0)
- Genomic sequencing technologies: Video (2014) (0)
- Genomic landscape of pediatric adrenocortical tumors article available. Please share how this access benefits you. Your story matters (2015) (0)
- Resolution of a Clinical Dilemma with Whole Genome Sequencing, and Discovery of a New Mechanism for Generating PML-Rara: Insertional Fusion (2010) (0)
- O13: Clinical validation of copy number alteration using paired tumor-normal exome sequencing: Challenges and successes* (2023) (0)
- A novel transcriptional signature identifies T-cell infiltration in high-risk paediatric cancer (2022) (0)
- Single-cell RNA sequencing reveals immunosuppressive myeloid cell diversity during malignant progression in a murine model of glioma. (2023) (0)
- P070: Discerning the meaning of cancer predisposition variants in a pediatric cancer cohort (2023) (0)
- Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer (2018) (0)
- Massive parallel sequencing of an African-American basal-like breast cancer: Comparison of primary tumor, metastasis, and xenograft. (2010) (0)
- 21. Correcting neoantigens by accounting for proximal variants (2019) (0)
- Abstract S1-04: Exome sequencing of post-menopausal ER+ breast cancer (BC) treated pre-surgically with aromatase inhibitors (AIs) in the POETIC trial (CRUK/07/015) (2015) (0)
- Highlights from the literature (2016) (0)
- The prognostic effects of somatic mutations in ER-positive breast cancer (2018) (0)
- The technology tour de force of the Human Genome Project (2005) (0)
- Clinical Outcomes and Efficacy of Stereotactic Body Radiation Therapy in Children, Adolescents, and Young Adults with Metastatic Solid Tumors (2021) (0)
- Abstract A15: Improving immune recognition of shared tumor-associated antigens in pediatric tumors using a multimodal oncolytic virus (2020) (0)
- Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (0)
- Abstract P6-07-10: Luminal A vs. Basal-like Breast Cancer: time dependent changes in the risk of relapse in the absence of treatment (2012) (0)
- Genomic sequencing technologies: Slides (2014) (0)
- 26. Co-occurrence of rosette-forming glioneuronal tumors with Noonan Syndrome (2022) (0)
- microRNA transcriptome Next-generation sequencing identifies the natural killer cell Material (2016) (0)
- A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data (2018) (0)
- ANTHELMINTIC RESISTANCE IN PARASITIC NEMATODES CONSORTIUM (2010) (0)
- A multiple myeloma-specific capture sequencing platform discovers novel translocations and frequent, risk-associated point mutations in IGLL5 (2018) (0)
- Abstract ES7-1: Next Generation Sequencing for the Clinician: A Breast Cancer Study (2010) (0)
- Abstract LB176: Multiplatform analysis of matched primary and metastatic breast tumors from the AURORA US Network identifies microenvironment features as drivers of metastasis (2022) (0)
- The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission. (2022) (0)
- Outcomes of in-house rapid genome sequencing at a Children’s Hospital (2021) (0)
- Abstract 5181: Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers (2014) (0)
- Future of DNA Sequencing Technology (2011) (0)
- Abstract A1-44: Clinical cancer sequencing and integrated analysis of whole genomes, exomes and transcriptomes (2015) (0)
- SR2-1: The Genomic Mutation Landscape of Breast Cancer: A TCGA Report. (2011) (0)
- Identification of Novel, Non-Synonymous Sequence Changes in the Tyrosine Kinase Genes of Patients with Acute Myeloid Leukemia. (2007) (0)
- Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
- Comparative genomics of Oxytricha and related spirotrichous ciliates : Minimal eukaryotic genome architectures (2007) (0)
- New additions to the cancer precision medicine toolkit (2018) (0)
- The painted turtle genome: The evolution of extreme physiological (2013) (0)
- Erratum: The Pediatric Cancer Genome Project (2012) (0)
- A phase II trial of neoadjuvant MK2206, an AKT inhibitor, with anastrozole in clinical stage 2 or 3 PIK3CA mutant ER positive and HER2 negative breast cancer Estrogen receptor positive breast cancer, neoadjuvant endocrine therapy, (2017) (0)
- Myeloid cell heterogeneity in the tumor microenvironment and therapeutic implications for childhood central nervous system (CNS) tumors (2022) (0)
- Abstract B12: Complete characterization of the “microRNAome” of a human acute myeloid leukemia (2010) (0)
- Sequencing Acute Myeloid Leukemia Genomes with “Next Generation” Technologies. (2008) (0)
- Whole Genome Sequencing Reveals Novel Recurring Somatic Mutations Affecting HUWE1 and DIAPH2 Genes in Multiple Myeloma (2012) (0)
- Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer (2018) (0)
- Generating High Fidelity Sequence for the Drosophila Virilis Dot Chromosome (2006) (0)
- Clinical outcomes and efficacy of stereotactic body radiation therapy in children, Adolescents, and Young Adults with Metastatic Solid Tumors. (2022) (0)
- Abstract IA21: AML genomics: An update. (2015) (0)
- Single-nuclei transcriptomics enable detection of somatic variants in patient brain tissue (2023) (0)
- Abstract 484: Molecular profiling identifies a second malignancy in a patient with medulloblastoma (2019) (0)
- The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission. (2022) (0)
- Prognostic and Predictive Impact of Intrinsic Biological Classification by Immunohistochemistry (IHC) and QPCR for Adjuvant Tamoxifen in Pre-Menopausal Breast Cancer: Results from the NCIC CTG MA.12 Trial. (2009) (0)
- Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas (2021) (0)
- 23. Paired exome analysis in Mosaic Disease yields expanded Genotype-Phenotype Associations (2022) (0)
- Gene expression profiles to forecast the outcome in breast cancer (2009) (0)
- Advances in Cancer Research and Translational Medicine (2018) (0)
- Manufacture and Immunological Characterization of GMP-Compliant Functional Sars-COV-2 Cytotoxic T Lymphocytes (CTLs) Utilizing the Clinimacs ® Cytokine Capture System (2021) (0)
- Abstract LB-265: Patient-derived xenografts from advanced luminal-type breast cancer: insights into endocrine therapy resistance. (2013) (0)
- Abstract PR11: Genomic approaches for risk assessment in acute myeloid leukemia (2015) (0)
- Molecular and spatial heterogeneity of microglia in Rasmussen encephalitis (2022) (0)
- Comparison of key ciliate macronuclear genomes. (2013) (0)
- Use of whole genome sequencing to identify novel mutations in distinct subgroups of medulloblastoma. (2012) (0)
- HGV2009 meeting: bigger and better studies provide more answers and more questions (2010) (0)
- Highlights from the literature (2018) (0)
- Abstract LB-109: Exome sequencing identifies common somatic mutations in an adult patient with a concurrent germ cell tumor (GCT) and acute myeloid leukemia (AML) suggesting a single clonal origin (2015) (0)
- Abstract LB-423: Whole genome comparisons of pre- and post- aromatase inhibitor treatment in estrogen receptor positive breast cancer (2012) (0)
- The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission. (2022) (0)
- The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission. (2022) (0)
- Pathology innovations making cancer genomics personal (2014) (0)
- The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission. (2022) (0)
- Abstract CT091: A neoadjuvant co-clinical trial in triple-negative breast cancer patients with genomic discovery analysis (2016) (0)
- 143 Identification of Neoantigen-specific CD8+ T Cells in Two Murine Orthotopic Glioblastoma Models Using Cancer Immunogenomics. (2016) (0)
- In Vitro Decitabine Treatment Demonstrates Heterogeneous Changes in Methylation and Gene Expression in Primary AML Samples. (2012) (0)
- Next-Generation Sequencing: A Discovery Tool for Blood Disorders (2012) (0)
- Abstract LB-326: Identification of novel recurrent mutations in follicular lymphoma (2016) (0)
- Translating Basic Cancer Discoveries to the Clinic. (2020) (0)
- Title: Characterization of the Genomic and Immunological Diversity of Malignant Brain Tumors (2021) (0)
- Abstract 993: Identification of estrogen receptor alpha 1 bound lncRNAs in aggressive breast cancer (2016) (0)
- 881 Significant therapeutic effects of anti-ROR1 CAR NK against neuroblastoma by oncolytic virus armored with IL-21in-vitroandin-vivo (2022) (0)
- Abstract 1074: Tumor-associated microglia secrete paracrine factors that promote Nf1-deficient optic glial cell growth (2014) (0)
- Genome Histoplasma capsulatum Fosmid-Based Physical Mapping of the References (2004) (0)
- Abstract 4109: Clonal evolution of metastatic colorectal cancer (2015) (0)
- Abstract IA2: Genomic comparisons of coincident prostate cancer foci (2012) (0)
- 23 – The Technology of Analyzing Nucleic Acids in Cancer (2015) (0)
- "…by applying next-generation sequencing technology to resequence and characterize entire human genomes, geneticists have set the stage for a revolution in personal genomics that will ultimately progress towards the reality of personalized medicine." (2009) (0)
- Abstract 4949: Immunological ignorance is an enabling feature of the oligo-clonal T cell response to melanoma neoantigen (2019) (0)
- Detection of Microdeletions and Amplifications in Primary Human Acute Myeloid Leukemia (AML) Genomes Using Ultradense Oligomer Tiling Path Arrays and Comparative Genomic Hybridization (CGH). (2005) (0)
- Whole genome sequences of nematodes of the order Strongylida (2007) (0)
- Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma (2021) (0)
- 80: Recent advances in cancer genomics (2014) (0)
- Targeted Sequencing, Augmented with Public Resources, Identifies a Rare C3 Allele Associated with Large Risk of Age-related Macular Degeneration (2013) (0)
- 1135 Single cell resolution of immune responses to oncolytic herpes simplex virus C134 in preclinical medulloblastoma models (2022) (0)
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