Richard K. Wilson
#47,477
Most Influential Person Now
American geneticist
Richard K. Wilson's AcademicInfluence.com Rankings
Richard K. Wilsonbiology Degrees
Biology
#3587
World Rank
#5463
Historical Rank
Computational Biology
#99
World Rank
#99
Historical Rank
Genetics
#464
World Rank
#535
Historical Rank
Download Badge
Biology
Richard K. Wilson's Degrees
- PhD Genetics University of California, Berkeley
- Bachelors Biology University of California, Santa Cruz
Similar Degrees You Can Earn
Why Is Richard K. Wilson Influential?
(Suggest an Edit or Addition)According to Wikipedia, Richard K. Wilson is a leading American molecular geneticist. He is the founding Executive Director of the Institute for Genomic Medicine at Nationwide Children’s Hospital and Professor of Pediatrics at the Ohio State University College of Medicine. He received his A.B. degree from Miami University in Ohio in 1981, his Ph.D. from the University of Oklahoma in 1986, and was a Research Fellow in the Division of Biology at the California Institute of Technology . In 1990, Dr. Wilson joined the faculty of Washington University School of Medicine where he co-founded the Genome Sequencing Center/McDonnell Genome Institute. At Washington University, Dr. Wilson was the Alan A. and Edith L. Wolff Distinguished Professor of Medicine, Professor of Genetics, Professor of Molecular Microbiology, and a member of the Senior Leadership Committee of the Siteman Cancer Center.
Richard K. Wilson'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)
- Structure, Function and Diversity of the Healthy Human Microbiome (2012) (8630)
- Comprehensive molecular portraits of human breast tumors (2012) (7791)
- 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)
- Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. (2010) (5816)
- 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)
- A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
- Comprehensive molecular profiling of lung adenocarcinoma (2014) (4095)
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012) (3841)
- Integrated genomic characterization of endometrial carcinoma (2013) (3708)
- The Somatic Genomic Landscape of Glioblastoma (2013) (3693)
- Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. (2005) (3639)
- The B73 Maize Genome: Complexity, Diversity, and Dynamics (2009) (3594)
- Mutational landscape and significance across 12 major cancer types (2013) (3589)
- 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)
- 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)
- 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)
- Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. (2010) (2121)
- 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)
- Evolution of genes and genomes on the Drosophila phylogeny (2007) (1992)
- Clonal evolution in relapsed acute myeloid leukemia revealed by whole genome sequencing (2011) (1935)
- Complete genome sequence of Salmonella enterica serovar Typhimurium LT2 (2001) (1840)
- International network of cancer genome projects (2010) (1839)
- Oncogenic Signaling Pathways in The Cancer Genome Atlas (2018) (1646)
- 2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans (1994) (1449)
- 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)
- Mapping and sequencing of structural variation from eight human genomes (2008) (1195)
- 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)
- The DNA sequence of the human X chromosome (2005) (1072)
- Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome (1998) (1061)
- 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)
- 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)
- Comparative genomics reveals insights into avian genome evolution and adaptation (2014) (811)
- 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)
- The Genome of the Western Clawed Frog Xenopus tropicalis (2010) (749)
- Clonal architecture of secondary acute myeloid leukemia. (2012) (747)
- Great ape genetic diversity and population history (2013) (747)
- Novel mutations target distinct subgroups of medulloblastoma (2012) (746)
- Genome analysis of the platypus reveals unique signatures of evolution (2008) (711)
- A Catalog of Reference Genomes from the Human Microbiome (2010) (683)
- The complete nucleotide sequence of the Xenopus laevis mitochondrial genome. (1985) (675)
- Insights into hominid evolution from the gorilla genome sequence (2012) (670)
- Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas (2013) (655)
- Characterizing a model human gut microbiota composed of members of its two dominant bacterial phyla (2009) (640)
- Landscape of Somatic Retrotransposition in Human Cancers (2012) (638)
- Elephant shark genome provides unique insights into gnathostome evolution (2014) (601)
- MuSiC: Identifying mutational significance in cancer genomes (2012) (593)
- Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution (2013) (591)
- The genomic landscape of hypodiploid acute lymphoblastic leukemia (2013) (585)
- TP53 and Decitabine in Acute Myeloid Leukemia and Myelodysplastic Syndromes. (2016) (582)
- Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas (2017) (577)
- Abundant gene conversion between arms of palindromes in human and ape Y chromosomes (2003) (574)
- Evolution of Symbiotic Bacteria in the Distal Human Intestine (2007) (562)
- 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)
- Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly. (2017) (541)
- RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (2011) (530)
- Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014) (527)
- The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men (2001) (520)
- 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)
- Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators (2014) (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)
- Oil palm genome sequence reveals divergence of interfertile species in old and new worlds (2013) (469)
- Implementing genomic medicine in the clinic: the future is here (2013) (463)
- The C. elegans genome sequencing project: a beginning (1992) (462)
- A Novel Retinoblastoma Therapy from Genomic and Epigenetic Analyses (2011) (462)
- C11orf95-RELA fusions drive oncogenic NF-κB signaling in ependymoma (2014) (450)
- Genomic and metabolic adaptations of Methanobrevibacter smithii to the human gut (2007) (446)
- Whole-genome sequencing and variant discovery in C. elegans (2008) (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)
- The DNA sequence of human chromosome 7 (2003) (425)
- Structure, Organization and Polymorphism of Murine and Human T‐Cell Receptor a and β Chain Gene Families (1988) (425)
- DGIdb - Mining the druggable genome (2013) (418)
- CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer (2017) (414)
- High throughput fingerprint analysis of large-insert clones. (1997) (410)
- Sequence and analysis of chromosome 4 of the plant Arabidopsis thaliana (1999) (403)
- Modernizing Reference Genome Assemblies (2011) (402)
- A genome-wide comparison of recent chimpanzee and human segmental duplications (2005) (396)
- Comparison of genome degradation in Paratyphi A and Typhi, human-restricted serovars of Salmonella enterica that cause typhoid (2004) (395)
- 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 R882H DNMT3A mutation associated with AML dominantly inhibits wild-type DNMT3A by blocking its ability to form active tetramers. (2014) (363)
- Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA , IDH 1 , EGFR , and NF 1 Citation Verhaak (2010) (362)
- 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)
- The Pristionchus pacificus genome provides a unique perspective on nematode lifestyle and parasitism (2008) (337)
- A survey of expressed genes in Caenorhabditis elegans (1992) (336)
- Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication (2012) (327)
- Genetic variation and the de novo assembly of human genomes (2015) (324)
- Long-read sequence assembly of the gorilla genome (2016) (318)
- 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)
- Characterizing the Major Structural Variant Alleles of the Human Genome (2019) (305)
- Gibbon genome and the fast karyotype evolution of small apes (2014) (303)
- DGIdb 2.0: mining clinically relevant drug–gene interactions (2015) (296)
- The draft genome of the parasitic nematode Trichinella spiralis (2011) (292)
- Human epidermal growth factor receptor cDNA is homologous to a variety of RNAs overproduced in A431 carcinoma cells (1984) (287)
- 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)
- A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms. (2004) (279)
- Discovery and genotyping of structural variation from long-read haploid genome sequence data (2017) (276)
- A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms (2010) (274)
- Clonal diversity of recurrently mutated genes in myelodysplastic syndromes (2013) (269)
- Use of whole-genome sequencing to diagnose a cryptic fusion oncogene. (2011) (267)
- Genome of Rhodnius prolixus, an insect vector of Chagas disease, reveals unique adaptations to hematophagy and parasite infection (2015) (260)
- Integrated Analysis of Germline and Somatic Variants in Ovarian Cancer (2014) (259)
- Sequence and Comparative Analysis of the Maize NB Mitochondrial Genome1[w] (2004) (258)
- 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 genome of the platyfish, Xiphophorus maculatus, provides insights into evolutionary adaptation and several complex traits (2013) (255)
- High-resolution comparative analysis of great ape genomes (2018) (250)
- Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domestication (2014) (249)
- Human Genome Ultraconserved Elements Are Ultraselected (2007) (248)
- Sequencing the Mouse Y Chromosome Reveals Convergent Gene Acquisition and Amplification on Both Sex Chromosomes (2014) (248)
- Molecular Study of Malignant Gliomas Treated with Epidermal Growth Factor Receptor Inhibitors: Tissue Analysis from North American Brain Tumor Consortium Trials 01-03 and 00-01 (2005) (241)
- Genome of the house fly, Musca domestica L., a global vector of diseases with adaptations to a septic environment (2014) (238)
- Immune Escape of Relapsed AML Cells after Allogeneic Transplantation (2018) (235)
- Genome Sequence of the Tsetse Fly (Glossina morsitans): Vector of African Trypanosomiasis (2014) (233)
- A physical map of the chicken genome (2004) (232)
- Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes (2012) (231)
- Reconstructing complex regions of genomes using long-read sequencing technology (2014) (230)
- Targeting oxidative stress in embryonal rhabdomyosarcoma. (2013) (228)
- 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)
- Comparative genomics of protoploid Saccharomycetaceae. (2009) (221)
- The Common Marmoset Genome Provides Insight into Primate Biology and Evolution (2014) (219)
- Use of cigarette-smoking history to estimate the likelihood of mutations in epidermal growth factor receptor gene exons 19 and 21 in lung adenocarcinomas. (2006) (217)
- 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)
- 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)
- Genome Sequence of Cronobacter sakazakii BAA-894 and Comparative Genomic Hybridization Analysis with Other Cronobacter Species (2010) (197)
- Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
- Convergent Evolution of Chicken Z and Human X Chromosomes by Expansion and Gene Acquisition (2010) (197)
- Deregulation of DUX4 and ERG in acute lymphoblastic leukemia (2016) (197)
- Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells. (2012) (195)
- Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation. (2013) (194)
- The Oxytricha trifallax Macronuclear Genome: A Complex Eukaryotic Genome with 16,000 Tiny Chromosomes (2013) (192)
- The structure and evolution of centromeric transition regions within the human genome (2004) (191)
- Whole genome analysis of a schistosomiasis-transmitting freshwater snail (2017) (191)
- Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context (2018) (188)
- The genomic landscape of core-binding factor acute myeloid leukemias (2016) (187)
- Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors (2017) (187)
- Evolutionary toggling of the MAPT 17q21.31 inversion region (2008) (185)
- Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee (2005) (181)
- Analysis of the human neurexin genes: alternative splicing and the generation of protein diversity. (2002) (180)
- Optimizing cancer genome sequencing and analysis. (2015) (179)
- Structure and localization of genes encoding aberrant and normal epidermal growth factor receptor RNAs from A431 human carcinoma cells (1985) (177)
- Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection (2013) (174)
- 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)
- Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2018) (171)
- Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML. (2011) (169)
- The repetitive landscape of the chicken genome. (2004) (168)
- The genome of Cyanothece 51142, a unicellular diazotrophic cyanobacterium important in the marine nitrogen cycle (2008) (163)
- Comparative analysis of the polycystic kidney disease 1 (PKD1) gene reveals an integral membrane glycoprotein with multiple evolutionary conserved domains. (1997) (161)
- CpG Island Hypermethylation Mediated by DNMT3A Is a Consequence of AML Progression (2017) (155)
- DNA sequencing with dye-labeled terminators and T7 DNA polymerase: effect of dyes and dNTPs on incorporation of dye-terminators and probability analysis of termination fragments. (1992) (155)
- Chromothripsis and Human Disease: Piecing Together the Shattering Process (2012) (154)
- Characterization of Missing Human Genome Sequences and Copy-number Polymorphic Insertions (2010) (151)
- DNMT 3 A mutations in acute myeloid leukemia (2016) (151)
- Challenges of sequencing human genomes (2010) (147)
- Independent specialization of the human and mouse X chromosomes for the male germline (2013) (146)
- Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. (2015) (139)
- The Genomic Landscape of Childhood and Adolescent Melanoma (2014) (139)
- Organization, structure, and function of 95 kb of DNA spanning the murine T-cell receptor CαCδ region (1992) (135)
- The Somatic Genomic Landscape of Glioblastoma (2014) (135)
- 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)
- The Complete Sequence of a Heterochromatic Island from a Higher Eukaryote (2000) (127)
- In Genome analysis: A laboratory manual (1997) (125)
- Avian W and mammalian Y chromosomes convergently retained dosage-sensitive regulators (2017) (123)
- Comparative genomics based on massive parallel transcriptome sequencing reveals patterns of substitution and selection across 10 bird species (2010) (122)
- Comparison of the Escherichia coli K-12 genome with sampled genomes of a Klebsiella pneumoniae and three salmonella enterica serovars, Typhimurium, Typhi and Paratyphi. (2000) (120)
- Single haplotype assembly of the human genome from a hydatidiform mole (2014) (120)
- 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)
- Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndrome. (2004) (115)
- Exome sequencing of Finnish isolates enhances rare-variant association power (2019) (113)
- Retrotransposition of gene transcripts leads to structural variation in mammalian genomes (2013) (110)
- The genome of the vervet (Chlorocebus aethiops sabaeus) (2015) (107)
- Long-read sequence and assembly of segmental duplications (2018) (107)
- Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) (2001) (106)
- The Physical and Genetic Framework of the Maize B73 Genome (2009) (102)
- INTEGRATE: gene fusion discovery using whole genome and transcriptome data (2016) (98)
- After the Duplication: Gene Loss and Adaptation in Saccharomyces Genomes (2006) (98)
- 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)
- Nematode.net: a tool for navigating sequences from parasitic and free-living nematodes (2004) (97)
- Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression. (2011) (97)
- A large, complex structural polymorphism at 16p12.1 underlies microdeletion disease risk (2010) (96)
- Sequence and analysis of chromosome 5 of the plant Arabidopsis thaliana. (2000) (94)
- Genomic landscape of pediatric adrenocortical tumors (2015) (94)
- How the worm was won. The C. elegans genome sequencing project. (1999) (93)
- Epigenomic analysis of the HOX gene loci reveals mechanisms that may control canonical expression patterns in AML and normal hematopoietic cells (2015) (93)
- Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia. (2007) (92)
- 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)
- Ancient hybridization and strong adaptation to viruses across African vervet monkey populations (2016) (91)
- DoCM: a database of curated mutations in cancer (2016) (90)
- Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes. (2000) (89)
- Identification of Therapeutic Targets in Rhabdomyosarcoma through Integrated Genomic, Epigenomic, and Proteomic Analyses. (2018) (89)
- A Lover and a Fighter: The Genome Sequence of an Entomopathogenic Nematode Heterorhabditis bacteriophora (2013) (89)
- 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)
- Reduced PU.1 expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARalpha. (2005) (88)
- PathScan: a tool for discerning mutational significance in groups of putative cancer genes (2011) (87)
- Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4 (2007) (85)
- Mapping and characterization of structural variation in 17,795 human genomes (2020) (84)
- Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability (2014) (84)
- RB1 gene inactivation by chromothripsis in human retinoblastoma (2014) (83)
- Sequence, annotation, and analysis of synteny between rice chromosome 3 and diverged grass species. (2005) (82)
- The prognostic effects of somatic mutations in ER-positive breast cancer (2017) (81)
- Genome Modeling System: A Knowledge Management Platform for Genomics (2015) (80)
- PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data. (2007) (80)
- Physical maps of the mouse and human immunoglobulin-like loci. (1989) (80)
- Dynamic Changes in the Clonal Structure of MDS and AML in Response to Epigenetic Therapy (2015) (78)
- The evolution and population diversity of human-specific segmental duplications (2017) (76)
- The DNA sequence and analysis of human chromosome 14 (2003) (76)
- Complete characterization of the microRNAome in a patient with acute myeloid leukemia. (2010) (75)
- Pangolin genomes and the evolution of mammalian scales and immunity (2016) (75)
- The Physarum polycephalum Genome Reveals Extensive Use of Prokaryotic Two-Component and Metazoan-Type Tyrosine Kinase Signaling (2015) (74)
- Clonal Architectures and Driver Mutations in Metastatic Melanomas (2014) (72)
- A pilot study of high-throughput, sequence-based mutational profiling of primary human acute myeloid leukemia cell genomes (2003) (70)
- Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee. (2011) (70)
- Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus. (2013) (69)
- 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)
- What is finished, and why does it matter. (2002) (65)
- Genomic landscape of paediatric adrenocortical tumours (2016) (64)
- Investigating hookworm genomes by comparative analysis of two Ancylostoma species (2005) (63)
- MYCN amplification and ATRX mutations are incompatible in neuroblastoma (2018) (63)
- Long non-coding RNA RAMS11 promotes metastatic colorectal cancer progression (2020) (61)
- 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)
- Molecular refinement of gibbon genome rearrangements. (2007) (60)
- Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers (2016) (59)
- Presence of the hypermodified nucleotide N6-(delta 2-isopentenyl)-2-methylthioadenosine prevents codon misreading by Escherichia coli phenylalanyl-transfer RNA. (1989) (59)
- Novel venom gene discovery in the platypus (2010) (58)
- Subtelomeric CTCF and cohesin binding site organization using improved subtelomere assemblies and a novel annotation pipeline (2014) (58)
- Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation (2010) (57)
- The evolution and population diversity of human-specific segmental duplications. (2017) (57)
- Multiple trans-splicing events are required to produce a mature nad1 transcript in a plant mitochondrion. (1991) (57)
- Sequencing, processing, and localization of the petunia CMS-associated mitochondrial protein. (1994) (56)
- DNA sequence of the Xenopus laevis mitochondrial heavy and light strand replication origins and flanking tRNA genes. (1983) (56)
- Genomic analysis reveals hidden biodiversity within colugos, the sister group to primates (2016) (56)
- Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci (2014) (55)
- Comparative genomic analysis of six Glossina genomes, vectors of African trypanosomes (2019) (52)
- Platypus globin genes and flanking loci suggest a new insertional model for beta-globin evolution in birds and mammals (2008) (52)
- A non-human primate system for large-scale genetic studies of complex traits. (2012) (50)
- Erratum: The somatic genomic landscape of glioblastoma (Cell (2013) 155 (462-477)) (2014) (49)
- Massively parallel sequencing approaches for characterization of structural variation. (2012) (49)
- Protein polymorphism generated by differential RNA editing of a plant mitochondrial rps12 gene (1996) (49)
- Somatic Mutations of PIK3R1 Promote Gliomagenesis (2012) (48)
- Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate. (2016) (48)
- A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa. (2014) (47)
- TP 53 and decitabine in acute myeloid leukemia and myelodysplastic syndromes (2016) (47)
- Development of an automated procedure for fluorescent DNA sequencing. (1990) (47)
- Detailed Analysis of a Contiguous 22-Mb Region of the Maize Genome (2009) (47)
- Clonal Evolution Revealed by Whole Genome Sequencing in a Case of Primary Myelofibrosis Transformed to Secondary Acute Myeloid Leukemia (2012) (46)
- Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits (2015) (45)
- A vertebrate case study of the quality of assemblies derived from next-generation sequences (2011) (45)
- Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome (2014) (45)
- A transposon-based strategy for sequencing repetitive DNA in eukaryotic genomes. (1997) (44)
- The Contribution of GWAS Loci in Familial Dyslipidemias (2016) (44)
- Nucleotide sequence analysis of 95 kb near the 3′ end of the murine T-cell receptor αδ chain locus: Strategy and methodology (1992) (44)
- Intestinal Transcriptomes of Nematodes: Comparison of the Parasites Ascaris suum and Haemonchus contortus with the Free-living Caenorhabditis elegans (2008) (43)
- IRF6 mutation screening in non‐syndromic orofacial clefting: analysis of 1521 families (2016) (43)
- Molecular phylogenetics and generic taxonomy of Blechnaceae ferns (2014) (42)
- Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia. (2016) (42)
- Sex differences in oncogenic mutational processes (2019) (41)
- Exome-based mapping and variant prioritization for inherited Mendelian disorders. (2014) (40)
- Opsin Repertoire and Expression Patterns in Horseshoe Crabs: Evidence from the Genome of Limulus polyphemus (Arthropoda: Chelicerata) (2016) (40)
- Fatal hepatic sarcocystosis in two polar bears (Ursus maritimus). (1997) (40)
- Optimization of asymmetric polymerase chain reaction for rapid fluorescent DNA sequencing. (1990) (39)
- Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family (2018) (39)
- Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites. (2009) (39)
- The canine hookworm genome: analysis and classification of Ancylostoma caninum survey sequences. (2008) (39)
- Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity (2014) (38)
- Automation of dideoxynucleotide DNA sequencing reactions using a robotic workstation. (1988) (37)
- Genome Sequence of Enterovirus D68 from St. Louis, Missouri, USA (2015) (37)
- Application of a superword array in genome assembly (2006) (36)
- Analysis of human mRNAs with the reference genome sequence reveals potential errors, polymorphisms, and RNA editing. (2004) (35)
- The DNA Double-Strand Break Response Is Abnormal in Myeloblasts From Patients With Therapy-Related Acute Myeloid Leukemia (2013) (35)
- A High-Resolution SNP Array-Based Linkage Map Anchors a New Domestic Cat Draft Genome Assembly and Provides Detailed Patterns of Recombination (2016) (35)
- Organization, structure, and function of 95 kb of DNA spanning the murine T-cell receptor C alpha/C delta region. (1992) (34)
- Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data (2012) (33)
- Alzheimer's disease: rare variants with large effect sizes. (2015) (33)
- Punctuated duplication seeding events during the evolution of human chromosome 2p11. (2005) (33)
- Genome sequence of the basal haplorrhine primate Tarsius syrichta reveals unusual insertions (2016) (33)
- Aspects of coverage in medical DNA sequencing (2008) (33)
- North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene (2016) (33)
- Comparing low coverage random shotgun sequence data from Brassica oleracea and Oryza sativa genome sequence for their ability to add to the annotation of Arabidopsis thaliana. (2005) (33)
- Haplotype sorting using human fosmid clone end-sequence pairs. (2008) (33)
- Association Between DQB1 and Cervical Cancer in Patients With Human Papillomavirus and Family Controls (2000) (32)
- Association of Tumor Microenvironment T-cell Repertoire and Mutational Load with Clinical Outcome after Sequential Checkpoint Blockade in Melanoma (2019) (32)
- The Clonal Evolution of Metastatic Osteosarcoma as Shaped by Cisplatin Treatment (2019) (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)
- The impact of chromosomal translocation locus and fusion oncogene coding sequence in synovial sarcomagenesis (2016) (31)
- Physical map-assisted whole-genome shotgun sequence assemblies. (2006) (30)
- The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2 (2012) (30)
- Next-generation sequencing of cancer genomes: back to the future. (2009) (30)
- Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region (2016) (29)
- High-throughput purification of M13 templates for DNA sequencing. (1993) (28)
- EAnnot: a genome annotation tool using experimental evidence. (2004) (27)
- Genomic DNA sequencing methods. (1995) (26)
- BreakTrans: uncovering the genomic architecture of gene fusions (2013) (26)
- A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge–Ropers syndrome (2018) (25)
- Mitochondrial gene organization and expression in petunia male fertile and sterile plants. (1999) (25)
- Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing. (2012) (24)
- The clonal evolution of metastatic colorectal cancer (2020) (24)
- Low pressure DNA shearing: a method for random DNA sequence analysis. (1990) (23)
- Comparison of sample sequences of the Salmonella typhi genome to the sequence of the complete Escherichia coli K-12 genome. (1998) (23)
- Transcriptomic analysis of the entomopathogenic nematode Heterorhabditis bacteriophora TTO1 (2009) (23)
- Caspase-9 is required for normal hematopoietic development and protection from alkylator-induced DNA damage in mice. (2014) (23)
- A physical map of human chromosome 14 (2001) (22)
- Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (22)
- The characterization of the Phlebotomus papatasi transcriptome (2013) (22)
- High-Quality Assembly of an Individual of Yoruban Descent (2016) (21)
- Duck liver 'malic' enzyme. Expression in Escherichia coli and characterization of the wild-type enzyme and site-directed mutants. (1992) (21)
- Dictyocaulus viviparus genome, variome and transcriptome elucidate lungworm biology and support future intervention (2016) (21)
- Inactivation of RASA1 promotes melanoma tumorigenesis via R-Ras activation (2016) (21)
- Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas. (2016) (20)
- A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease (2018) (20)
- Genomic structure of a cytoplasmic dynein heavy chain gene from the nematode Caenorhabditis elegans. (1995) (20)
- An infrared fluorescent dATP for labeling DNA. (1995) (20)
- Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss (2019) (20)
- Corrigendum: C11orf95–RELA fusions drive oncogenic NF-κB signalling in ependymoma (2014) (19)
- Comparison of Sample Sequences of the Salmonella typhiGenome to the Sequence of the Complete Escherichia coliK-12 Genome (1998) (19)
- Sequence analysis in Bos taurus reveals pervasiveness of X–Y arms races in mammalian lineages (2020) (19)
- Cracking the nodule worm code advances knowledge of parasite biology and biotechnology to tackle major diseases of livestock. (2015) (19)
- Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African Americans (2016) (19)
- Identification and analysis of genes expressed in the adult filarial parasitic nematode Dirofilaria immitis. (2006) (19)
- Theories and applications for sequencing randomly selected clones. (2001) (18)
- Representation of cloned genomic sequences in two sequencing vectors: correlation of DNA sequence and subclone distribution. (1997) (18)
- Building and Improving Reference Genome Assemblies (2017) (18)
- Mutational landscape and response are conserved in peripheral blood of AML and MDS patients during decitabine therapy. (2017) (18)
- Genomic Profiling of Lung Adenocarcinoma in Never-Smokers (2021) (17)
- The construction and analysis of M13 libraries prepared from YAC DNA. (1995) (17)
- Sequencing reactions for the applied biosystems 373A Automated DNA Sequencer. (1993) (17)
- Improving eukaryotic genome annotation using single molecule mRNA sequencing (2018) (17)
- Fluorescence chemistries for automated primer‐directed DNA sequencing (1992) (16)
- Recurrent DNMT3A Mutations In Patients with Myelodysplastic Syndrome (2010) (16)
- Genetic Heterogeneity of Induced Pluripotent Stem Cells: Results from 24 Clones Derived from a Single C57BL/6 Mouse (2015) (15)
- 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)
- The genome of the stable fly, Stomoxys calcitrans, reveals potential mechanisms underlying reproduction, host interactions, and novel targets for pest control (2021) (14)
- Molecular determinants archetypical to the phylum Nematoda (2009) (14)
- The theory of discovering rare variants via DNA sequencing (2009) (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)
- 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)
- Whole Body Melanoma Transcriptome Response in Medaka (2015) (13)
- The Genotypic and Phenotypic Spectrum of BICD2 Variants in Spinal Muscular Atrophy (2020) (13)
- Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010) (13)
- Functional genomics of the stable fly, Stomoxys calcitrans, reveals mechanisms underlying reproduction, host interactions, and novel targets for pest control (2019) (12)
- The transcriptomes of the cattle parasitic nematode Ostertagia ostartagi. (2009) (12)
- Infantile fibrosarcoma–like tumor driven by novel RBPMS-MET fusion consolidated with cabozantinib (2020) (12)
- Design and implementation of a generalized laboratory data model (2007) (12)
- Erratum: C11orf95-RELA fusions drive oncogenic NF-ΰ B signalling in ependymoma (Nature (2014) 506 (451-455 ) DOI:10.1038/nature13109) (2014) (12)
- Genome Sequence of Additional Caenorhabditis species : Enhancing the Utility of C . elegans as a Model Organism (2003) (11)
- CIViC: A knowledgebase for expert-crowdsourcing the clinical interpretation of variants in cancer (2016) (11)
- Statistical aspects of discerning indel-type structural variation via DNA sequence alignment (2009) (11)
- PTEN somatic mutations contribute to spectrum of cerebral overgrowth. (2021) (11)
- Automated fluorescent DNA sequencing of polymerase chain reaction products. (1993) (11)
- In-frame de novo mutation in BICD2 in two patients with muscular atrophy and arthrogryposis (2018) (11)
- YAP1-FAM118B Fusion Defines a Rare Subset of Childhood and Young Adulthood Meningiomas. (2020) (10)
- Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience (2020) (10)
- Sequence and expression of a novel human T-cell receptor β-chain variable gene segment subfamily (2004) (10)
- Erratum: Genome of Rhodnius prolixus, an insect vector of Chagas disease, reveals unique adaptations to hematophagy and parasite infection (Proceedings of the National Academy of Sciences of the United States of America (2015) 112 (14936-14941) DOI 10.1073/pnas.1506226112) (2016) (10)
- Streptococcus oralis subsp. dentisani Produces Monolateral Serine-Rich Repeat Protein Fibrils, One of Which Contributes to Saliva Binding via Sialic Acid (2019) (10)
- Nucleotide sequence analysis of 95 kb near the 3' end of the murine T-cell receptor alpha/delta chain locus: strategy and methodology. (1992) (9)
- Mutational profiling in the human genome. (2003) (9)
- Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes. (2017) (9)
- Cost-Effective Recruitment Strategies That Attract Underrepresented Minority Undergraduates Who Persist to STEM Doctorates (2016) (9)
- Using SomaticSniper to Detect Somatic Single Nucleotide Variants. (2014) (9)
- Sequencing reactions in microtiter plates. (1990) (8)
- Corrigendum: Whole genome analysis of a schistosomiasis-transmitting freshwater snail (2017) (8)
- Incidence of Germline Mutations in Cancer-Predisposition Genes in Children with Hematologic Malignancies: a Report from the Pediatric Cancer Genome Project (2014) (8)
- Acute lymphoblastic leukemia displays a distinct highly methylated genome (2022) (8)
- Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate (2016) (8)
- Nucleotide sequence of pheW; a third gene for E. coli tRNAPhe. (1986) (8)
- Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP). (2016) (7)
- Correction: Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases (2017) (7)
- Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome (1999) (7)
- De novo primary central nervous system pure erythroid leukemia/sarcoma with t(1;16)(p31;q24) NFIA/CBFA2T3 translocation (2020) (7)
- A pneumatic device for rapid loading of DNA sequencing gels. (1998) (7)
- Gastroblastoma with a novel EWSR1‐CTBP1 fusion presenting in adolescence (2021) (7)
- Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q (2019) (7)
- The Glossina Genome Cluster: Comparative Genomic Analysis of the Vectors of African Trypanosomes (2019) (7)
- Genome sequencing identifies somatic BRAF duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma (2018) (7)
- Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma. (2019) (7)
- Draft Genome Sequence of Acetobacter aceti Strain 1023, a Vinegar Factory Isolate (2014) (6)
- Discovery of clinically relevant fusions in pediatric cancer (2021) (6)
- A novel sialic acid-binding adhesin present in multiple species contributes to the pathogenesis of Infective endocarditis (2020) (6)
- Large-scale complementary DNA sequencing methods. (1995) (6)
- Expansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasia (2019) (6)
- Genetic Characterization of Pediatric Sarcomas by Targeted RNA Sequencing. (2020) (6)
- Genome Assemblies across the Diverse Evolutionary Spectrum of Leishmania Protozoan Parasites (2021) (6)
- Has the chimpanzee Y chromosome been sequenced? (2006) (6)
- Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data. (2018) (6)
- Cerebral organoids containing an AUTS2 missense variant model microcephaly (2022) (6)
- A deletion in the N gene of SARS-CoV-2 may reduce test sensitivity for detection of SARS-CoV-2 (2021) (5)
- Genome science: a video tour of the Washington University Genome Sequencing Center for high school and undergraduate students. (2005) (5)
- Reconstructing sex chromosome evolution (2010) (5)
- Targeted Sequencing Informs the Evaluation of Normal Karyotype Cytopenic Patients for Low-Grade Myelodysplastic Syndrome (2016) (5)
- Novel morphologic findings in PLAG1‐rearranged soft tissue tumors (2021) (5)
- Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly (2016) (4)
- Genomic landscapes and clonality of de novo AML. (2013) (4)
- Sequencing and Annotating New Mammalian Y Chromosomes A White Paper Proposal , July , 2006 (2006) (4)
- Variations on cycle sequencing. (1994) (4)
- Somatic Mutations of PIK 3 R 1 Promote Gliomagenesis (2012) (4)
- Automated plaque picking and arraying on a robotic system equipped with a CCD camera and a sampling device using intramedic tubing (1996) (4)
- Using the automated DNA sequencer. (1996) (4)
- Corrigendum: Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators (2014) (4)
- Estimation of the likelihood of epidermal growth factor receptor (EGFR) mutations based on cigarette smoking history in patients with adenocarcinoma of the lung (2005) (4)
- Molecular Study of Malignant Gliomas Treated with Epidermal Growth Factor Receptor Inhibitors : Tissue Analysis fromNorth (2005) (4)
- Modification of a commercially available DNA sequencer to increase sample throughput (2000) (3)
- The burden of deleterious variants in a non-human primate biomedical model (2019) (3)
- Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder (2022) (3)
- Recurrent Somatic Genomic Alterations in Follicular NHL (FL) Revealed By Exome and Custom-Capture Next Generation Sequencing (2015) (3)
- Early-onset Wilson disease caused by ATP7B exon skipping associated with intronic variant (2020) (3)
- Whole-Genome Bisulfite Sequencing of Primary AML Cells with the DNMT3A R882H Mutation Identifies Regions of Focal Hypomethylation That Are Associated with Open Chromatin (2014) (3)
- Exome sequencing of Finnish isolates enhances rare-variant association power (2019) (3)
- Population genomics disentangles taxonomic relationships and identifies ancient hybridization in the genus Chlorocebus (2017) (3)
- Nature GeNetics ADVANCE ONLINE PUBLICATION (2013) (3)
- Samovar: Single-Sample Mosaic Single-Nucleotide Variant Calling with Linked Reads (2019) (3)
- Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas (2021) (2)
- tyrosine kinase genes of patients with de novo acute myeloid leukemia Somatic mutations and germline sequence variants in the expressed (2013) (2)
- Corrigendum: Elephant shark genome provides unique insights into gnathostome evolution (2014) (2)
- Long‐read whole genome sequencing reveals HOXD13 alterations in synpolydactyly (2021) (2)
- Complete Sequencing and Comparison of 12 Normal Karyotype M1 AML Genomes with 12 t(15;17) Positive M3-APL Genomes (2011) (2)
- Ancient hybridization and strong adaptation to viruses across African vervet monkey populations (2017) (2)
- Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma (2021) (2)
- Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2019) (2)
- Analysis of somatic retrotransposition in human cancers (2012) (2)
- Proposal for Complete Sequencing of the Genome of a Marsupial : The Gray , Short-tailed Opossum , Monodelphis domestic a (2003) (2)
- Genomic DNA Copy Number Alterations Present in AML Bone Marrow Samples with Normal Cytogenetics. (2004) (2)
- First Complete Genome Sequence of an Entomopathogenic Nematode Goes Public (2013) (1)
- Molecular Heterogeneity in Pediatric Malignant Rhabdoid Tumors in Patients With Multi-Organ Involvement (2022) (1)
- The repetitive landscape of the chicken genome Material Supplemental (2016) (1)
- Novel in-frame FLNB deletion causes Larsen syndrome in a three-generation pedigree (2019) (1)
- Dynamic Changes in Clonal Clearance with Decitabine Therapy in AML and MDS Patients (2015) (1)
- Association BetweenMutation Clearance After Induction Therapy andOutcomes in AcuteMyeloid Leukemia (2015) (1)
- Exome sequencing identifies high-impact trait-associated alleles enriched in Finns (2018) (1)
- Retrotransposition of gene transcripts leads to structural variation in mammalian genomes (2013) (1)
- Expanding the clinical phenotype of FGFR1 internal tandem duplication (2022) (1)
- DNMT3A-Dependent DNA Methylation May Act As a Tumor Suppressor-Not a Tumor Promoter-during AML Progression (2016) (1)
- Whole Genome Sequencing of Therapy-Related Acute Myeloid Leukemia (2012) (1)
- Abstract 4176: Familial lung cancer exhibits multiple novel linked haplotypes within pedigrees (2019) (1)
- Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data (2012) (1)
- Publisher Correction: Ancient hybridization and strong adaptation to viruses across African vervet monkey populations (2018) (1)
- Whole genome sequencing to characterize luminal-type breast cancer. (2012) (1)
- The genome of the stable fly, Stomoxys calcitrans, reveals potential mechanisms underlying reproduction, host interactions, and novel targets for pest control (2021) (1)
- Genome of the house fly, Musca domestica L., a global vector of diseases with adaptations to a septic environment (2014) (1)
- Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
- Abstract 4870: Integrated genomic analysis of hypodiploid acute lymphoblastic leukemia (2012) (1)
- The evolutionary history of the genus Chlorocebus inferred from whole genome sequencing (2014) (1)
- Author Correction: Elephant shark genome provides unique insights into gnathostome evolution (2020) (1)
- Abstract LB-87: Analysis of luminal-type breast cancer by massively parallel sequencing (2011) (1)
- Chromatin Immunoprecipitation of GFP-Tagged PML-Rara Coupled to High-Throughput Next Generation Sequencing. (2009) (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)
- Author Correction: Comparative and demographic analysis of orang-utan genomes (2022) (1)
- Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer (2018) (1)
- S. cerevisiae CYP51 complexed with fluconazole in the active site (2015) (1)
- Expression of an Oncogenic ERG isoform Characterizes a Distinct Subtype of B-Progenitor Acute Lymphoblastic Leukemia (2015) (1)
- The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage (2013) (1)
- PacBio Fusion and Long Isoform Pipeline (PB_FLIP) for Cancer Transcriptome-based Resolution of Isoform Complexity. (2022) (1)
- Saccharomyces cerevisiae CYP51 complexed with the plant pathogen inhibitor R-desthio-prothioconazole (2016) (1)
- Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers. (2022) (1)
- Saccharomyces cerevisiae CYP51 complexed with the plant pathogen inhibitor Fluquinconazole (2016) (1)
- Abstract PR03: The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma (2014) (1)
- Publisher Correction: The genome of the stable fly, Stomoxys calcitrans, reveals potential mechanisms underlying reproduction, host interactions, and novel targets for pest control (2021) (1)
- Variant prioritization and linkage mapping using whole-exome sequencing data for families with autosomal dominant retinitis pigmentosa (adRP) (2013) (1)
- Downregulation of MHC Class II in Relapsed AML Cells after Allogeneic Transplantation (2017) (1)
- Samovar: Single-sample mosaic SNV calling with linked reads (2019) (1)
- Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome (2014) (1)
- Sequencing an Acute Myeloid Leukemia (AML) Genome with “Next Generation” Technologies. (2007) (1)
- De novo missense variant in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy (2022) (1)
- Abstract S1-02: Prognostic effects of gene mutation in estrogen receptor positive breast cancer (2015) (1)
- Detection of Novel Mutations In MDS/AML by Whole Genome Sequencing (2010) (1)
- BreakTrans: uncovering the genomic architecture of gene fusions (2013) (1)
- Resistance heating device reduces gel mobility compressions in automated fluorescent sequencing. (1995) (1)
- Abstract LB-236: Patient derived xenografts as high-fidelity genomic models for advanced breast cancer. (2013) (0)
- Abstract 442:RASA1alteration promotes melanoma tumorigenesis (2014) (0)
- Abstract A1-44: Clinical cancer sequencing and integrated analysis of whole genomes, exomes and transcriptomes (2015) (0)
- A proposal to sequence the genome of the platypus, ornithorhynchus anatinus (2004) (0)
- Abstract 5181: Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers (2014) (0)
- Resolution of a Clinical Dilemma with Whole Genome Sequencing, and Discovery of a New Mechanism for Generating PML-Rara: Insertional Fusion (2010) (0)
- Identification of Novel, Non-Synonymous Sequence Changes in the Tyrosine Kinase Genes of Patients with Acute Myeloid Leukemia. (2007) (0)
- Abstract 169: Metastatic colorectal cancer associated long non-coding RNAs identified by transcriptome sequencing of matched primary and metastatic patient tissues (2015) (0)
- Brief report Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndrome (2004) (0)
- Structural variant discovery among related vervet monkeys (2015) (0)
- Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer (2018) (0)
- Clonal Evolution of Acute Myeloid Leukemia Following Allogeneic Stem Cell Transplantation (2016) (0)
- Expanding the phenotypic spectrum of internal tandem duplications in somatic disease (2021) (0)
- Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
- Erratum: The Pediatric Cancer Genome Project (2012) (0)
- Whole Genome Sequencing Reveals Novel Recurring Somatic Mutations Affecting HUWE1 and DIAPH2 Genes in Multiple Myeloma (2012) (0)
- Medical News : BJC Institute of Health at WUSTL on schedule ' Masked Marvels ' : Innovative show for ' young people ' series Washington People : Cobb seeks to return critically ill patients to health (2014) (0)
- Abstract 4873: Comprehensive analysis of 160 whole-genome sequences reveals striking telomere alteration patterns in 9 pediatric cancers (2012) (0)
- Hypomorphic alleles pose challenges in rare disease genomic variant interpretation (2021) (0)
- 9 th European Cytogenetics Conference 29 June – 2 July 2013 , Dublin ‐ Ireland (2013) (0)
- Abstract LB-265: Patient-derived xenografts from advanced luminal-type breast cancer: insights into endocrine therapy resistance. (2013) (0)
- Abstract 3878: A model to assess clonal evolution of metastatic colorectal cancer during chemotherapy utilizing patient derived xenografts (2015) (0)
- A phase I dose escalation multi-centre study of crizotinib (MET inhibitor) combined with binimetinib (MEK inhibitor) in patients with advanced solid tumours (2018) (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)
- High-throughput fluorescent DNA sequence analysis: Methods and automation (1991) (0)
- Mutational profiling of the oncogenome in non-small cell lung cancer (NSCLC) (2005) (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)
- Implications of fetal fibronectin results in triplet and quadruplet pregnancies with preterm labor (2002) (0)
- Comparison of key ciliate macronuclear genomes. (2013) (0)
- Presence of the hypermodified nucleotide N 6-( A 2-isopentenyl )-2-methylthioadenosine prevents codon misreading by Escherichia coli phenylalanyl-transfer RNA ( tRNA genes / wobble hypothesis / in vitro translation ) (0)
- DNA Sequencing of a Murine Acute Promyelocytic Leukemia (APL) Genome Using Next Generation Technology. (2009) (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)
- No bull: Upholding community standards in public sharing of biological datasets (2013) (0)
- Detection of Clonal Hematopoiesis in Cytopenic Patients Using Targeted Sequencing (2015) (0)
- Corrigendum: The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2. (2017) (0)
- Abstract LB-239: Mutational and clonal analyses across TCGA cancer types using the MuSiC suite of tools. (2013) (0)
- Rapid DNA Sequence Analysis Using Fluorescent Labels (1991) (0)
- Praveen – “ Proteome-wide binding site network analysis of M . tuberculosis ” ( Panel ) (2011) (0)
- Abstract 4109: Clonal evolution of metastatic colorectal cancer (2015) (0)
- Abstract LB-326: Identification of novel recurrent mutations in follicular lymphoma (2016) (0)
- Digital Commons@Becker Digital Commons@Becker The repetitive landscape of the chicken genome The repetitive landscape of the chicken genome (2022) (0)
- Discovery of clinically relevant fusions in pediatric cancer (2021) (0)
- Abstract A05: Identification of RASA1 as a novel melanoma tumor suppressor gene (2015) (0)
- Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
- Abstract LB-053: Familial studies identify variants in the E2A transcription factor as putative risk factors for lung cancer (2019) (0)
- Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers (2021) (0)
- Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma (2021) (0)
- Visualizing tumor evolution with the fishplot package for R (2016) (0)
- Maternal mosaicism for a missense variant in the SMS gene that causes Snyder-Robinson syndrome. (2021) (0)
- Deep Digital Sequencing Identifies an AML Subclone with Enhanced in Vitro and in Vivo Growth Properties Associated with Disease Relapse (2012) (0)
- Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits (2015) (0)
- Comparison of top 20 Pfam domains in H. bacteriophora genome with those in the 10 nematode species in the study. (2013) (0)
- CIViC: Crowdsourcing the Clinical Interpretation of Variants in Cancer (2015) (0)
- Abstract IA20: Genomics of a STAT1 knockout mouse model of human ER+ breast cancer (2016) (0)
- Massive parallel sequencing of an African-American basal-like breast cancer: Comparison of primary tumor, metastasis, and xenograft. (2010) (0)
- Disease-causing mutations in a cohort of autosomal dominant RP (adRP) families without detectable mutations in known adRP genes (2015) (0)
- Novel Presentation of Hemiplegic Migraine in a Patient With Cockayne Syndrome. (2022) (0)
- Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (0)
- Robust diagnostic yield and candidate gene discovery through paired exome analysis in vascular malformation and overgrowth (2021) (0)
- Comparative genomic analysis of six Glossina genomes, vectors of African trypanosomes (2019) (0)
- The prognostic effects of somatic mutations in ER-positive breast cancer (2018) (0)
- Antepartum Dexamethasone Rescue Therapy for Pregnancies Complicated by HELLP Syndrome (2003) (0)
- Mapping and characterization of structural variation in 17,795 human genomes (2020) (0)
- 26. Co-occurrence of rosette-forming glioneuronal tumors with Noonan Syndrome (2022) (0)
- Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case‐based review (2022) (0)
- PD5-3-7: EGFR and KRAS mutations are molecular predictors of survival in resected lung adenocarcinoma (2007) (0)
- Outcomes of in-house rapid genome sequencing at a Children’s Hospital (2021) (0)
- Abstract ES7-1: Next Generation Sequencing for the Clinician: A Breast Cancer Study (2010) (0)
- Preterm labor complicating triplet pregnancies: twelve-year experience at a single institution (2002) (0)
- Case Report And Review Of The Literature: Immune Dysregulation In A Large Familial Cohort Due To A Novel Pathogenic RELA Variant. (2022) (0)
- Abstract LB-232: Tumor clonality detection using next generation sequencing data. (2013) (0)
- Biallelic SEPSECS variants in two siblings with pontocerebellar hypoplasia type 2D underscore the relevance of splice-disrupting synonymous variants in disease (2022) (0)
- Abstract PR03: Genomic approaches for risk assessment in acute myeloid leukemia (2015) (0)
- Shwachman-Diamond syndrome gene are present in most patients with SBDS Mutations of the (2011) (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)
- ANTHELMINTIC RESISTANCE IN PARASITIC NEMATODES CONSORTIUM (2010) (0)
- Subclonal “skewing” Of De Novo AML Samples After Engraftment In Immunodeficient Mice (2013) (0)
- Abstract B12: Complete characterization of the “microRNAome” of a human acute myeloid leukemia (2010) (0)
- Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer (2018) (0)
- Sequencing Acute Myeloid Leukemia Genomes with “Next Generation” Technologies. (2008) (0)
- The painted turtle genome: The evolution of extreme physiological (2013) (0)
- Abstract PR01: Identifying clinically important somatic mutations through a knowledge-based approach (2015) (0)
- Mayer-Sequence and analysis of chromosome 4 of the plant Arabidopsis thaliana-1999 (2016) (0)
- EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24) (2020) (0)
- Abstract 484: Molecular profiling identifies a second malignancy in a patient with medulloblastoma (2019) (0)
- Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas (2021) (0)
- Genome Analysis Sequence and Comparative Analysis of the Maize NB Mitochondrial Genome 1 [ w ] (2004) (0)
- Rare Pre-Existing MDS Subclones Contribute to Secondary AML Progression (2016) (0)
- Use of whole genome sequencing to identify novel mutations in distinct subgroups of medulloblastoma. (2012) (0)
- Has the chimpanzee Y chromosome been sequenced? Authors' reply (2006) (0)
- DNA Sequence of the Cancer Genome of a Patient with Therapy-Related Acute Myeloid Leukemia (2010) (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)
- Abstract LB-423: Whole genome comparisons of pre- and post- aromatase inhibitor treatment in estrogen receptor positive breast cancer (2012) (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)
- The repetitive landscape of the chicken genome data (2004) (0)
- Next-Generation Sequencing: A Discovery Tool for Blood Disorders (2012) (0)
- Mutational analysis of EGFR signaling pathway genes in lung adenocarcinomas (2007) (0)
- A framework for human microbiome research A framework for human microbiome research (2020) (0)
- Abstract A15: The landscape of somatic mutations in the core-binding factor acute myeloid leukemias (2014) (0)
- Whole genome sequences of nematodes of the order Strongylida (2007) (0)
- Dynamic Changes in MDS Clonal Architecture Following Allogeneic Stem Cell Transplant (2016) (0)
- Abstract 3170: Identification of novel genetic alterations driving melanoma tumorigenesis. (2013) (0)
- Corrigendum: Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee (2006) (0)
- Sequence-tagged connector/DNA fingerprint framework for rice genome sequencing. (2001) (0)
- Supplemental Material Interchromosomal core duplicons drive both evolutionary and disease instability of the Chromosome 8 p 23 . 1 region (2016) (0)
- The human genome: genes, pseudogenes, and variation on chromosome 7. (2003) (0)
- Presence ofthehypermodified nucleotide N6-(A2-isopentenyl)- 2-methylthioadenosine prevents codonmisreading by Escherichia coli phenylalanyl-tra (1989) (0)
- S. CEREVISIAE CYP51 I471T MUTANT COMPLEXED WITH ITRACONAZOLE (2021) (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)
- S. CEREVISIAE CYP51 Y140H mutant COMPLEXED WITH Voriconazole (2021) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) G73E mutant complexed with itraconazole (2016) (0)
- leukemia Identification of somatic JAK1 mutations in patients with acute myeloid (2013) (0)
- Complete Nucleotide Sequence of Saccharomyces cerevisiae Chromosome VilI (2008) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) G464S mutant complexed with itraconazole (2016) (0)
- LGG Nat Genet Supplemental data 2013 (2013) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) Y140F mutant complexed with itraconazole (2016) (0)
- Saccharomyces cerevisiae CYP51 Y140F mutant complexed with posaconazole in the active site (2016) (0)
- Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
- THE MOUSE GENOME SEQUENCING PROJECT: AN OVERVIEW (2005) (0)
- Improving eukaryotic genome annotation using single molecule mRNA sequencing (2018) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) G73W mutant in complex with itraconazole (2016) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) G73W mutant (2016) (0)
- Abstract 1863: Inactivation of RASA1 promotes melanoma tumorigenesis via R-Ras activation (2016) (0)
- Messenger rna for avian fatty acid synthase contains a repetitive element which is a polypyrimidine sequence (1985) (0)
- EPEN-17. FAVORABLE OUTCOME TO INTENSIVE CHEMOTHERAPY WITHOUT IRRADIATION IN INFANTILE METASTATIC EPENDYMOMA WITH A NOVEL MOLECULAR PROFILE: A CASE REPORT (2020) (0)
- Saccharomyces cerevisiae CYP51 complexed with the plant pathogen inhibitor Prochloraz (2016) (0)
- the fusion of human chromosome 2 The evolution of African great ape subtelomeric heterochromatin Material (2012) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) G73R mutant complexed with fluconazole (2016) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) T322I mutant complexed with itraconazole (2016) (0)
- Abstract 959: Aromatase inhibition shapes the clonal architecture of estrogen receptor-positive breast cancers (2015) (0)
- High Resolution Array-Based CGH and SNP Studies of AML Genomes. (2007) (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)
- Determinants of turnaround time in a rapid genome sequencing program (2021) (0)
- Abstract 1651: Utilization of an ensemble approach for identification of driver fusions in pediatric cancer (2019) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) T322I mutant structure (2016) (0)
- A tandem duplication of PRDM13 in a family with North Carolina Macular Dystrophy (MCRD1) (2016) (0)
- Abstract A1-13: Ultra-deep whole-genome sequencing reveals clinically relevant low-frequency subclones in an acute myeloid leukemia (2015) (0)
- Abstract 4551: Expression profiling-based characterization of immune cell populations in pediatric brain cancers (2019) (0)
- S. CEREVISIAE CYP51 Y140H/I471T - double mutant COMPLEXED WITH Voriconazole (2021) (0)
- Science and Technology at a High Throughput Genome Center. (2011) (0)
- Abstract A1-06: Recurrent mutations of hormone-positive breast cancer and association with outcome (2015) (0)
- Evaluating the mutational spectrum of SIN3A alterations: a case series of patients profiled by next generation sequencing (2021) (0)
- Supplementary Materials for Landscape of Somatic Retrotransposition in Human Cancers (2012) (0)
- Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) Y140H mutant complexed with itraconazole (2016) (0)
- Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power (2019) (0)
- Long-read sequence and assembly of segmental duplications (2018) (0)
This paper list is powered by the following services:
Other Resources About Richard K. Wilson
What Schools Are Affiliated With Richard K. Wilson?
Richard K. Wilson is affiliated with the following schools:
