Identification of a Coordinate Regulator of Interleukins 4, 13, and 5 by Cross-Species Sequence ComparisonsExperimental selection of hypoxia-tolerant Drosophila melanogasterHigh-resolution whole-genome association study of Parkinson disease.Whole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlandersMulti-species sequence comparison: the next frontier in genome annotationVariation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy.Photoreceptor localization of the KIF3A and KIF3B subunits of the heterotrimeric microtubule motor kinesin II in vertebrate retinamiR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1Genetic ancestry of participants in the National Children's StudyGenomic interval engineering of mice identifies a novel modulator of triglyceride productionConsanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCDVISTA: computational tools for comparative genomicsHuman genetic variation and its contribution to complex traitsWhole-genome patterns of common DNA variation in three human populationsBAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma.Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.PTEN regulates glioblastoma oncogenesis through chromatin-associated complexes of DAXX and histone H3.3.Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genesGenome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin.MiningABs: mining associated biomarkers across multi-connected gene expression datasetsPI3Kγ is a molecular switch that controls immune suppressionBiased estimates of clonal evolution and subclonal heterogeneity can arise from PCR duplicates in deep sequencing experiments.An RNA editing fingerprint of cancer stem cell reprogramming.Transcriptome sequencing reveals potential mechanism of cryptic 3' splice site selection in SF3B1-mutated cancersGenetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell developmentSystematic transcriptome analysis reveals tumor-specific isoforms for ovarian cancer diagnosis and therapyMutational Profiling Can Establish Clonal or Independent Origin in Synchronous Bilateral Breast and Other Tumors.Decoding the human genomePgltools: a genomic arithmetic tool suite for manipulation of Hi-C peak and other chromatin interaction data.Reversion to an embryonic alternative splicing program enhances leukemia stem cell self-renewal.ADAR1 promotes malignant progenitor reprogramming in chronic myeloid leukemia.Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing.Associations Between Common and Rare Exonic Genetic Variants and Serum Levels of 20 Cardiovascular-Related Proteins: The Tromsø Study.Joint effects of cancer and variants in the factor 5 gene on the risk of venous thromboembolism.High-level ROR1 associates with accelerated disease progression in chronic lymphocytic leukemia.Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree.High-Throughput and Cost-Effective Characterization of Induced Pluripotent Stem Cells.Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing.Kataegis Expression Signature in Breast Cancer Is Associated with Late Onset, Better Prognosis, and Higher HER2 Levels.ADAR1 Activation Drives Leukemia Stem Cell Self-Renewal by Impairing Let-7 Biogenesis.
P50
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P50
description
researcher
@en
name
Frazer KA
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Kelly A. Frazer
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Frazer KA
@nl
Kelly A. Frazer
@en
altLabel
Frazer KA
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Frazer KA
@nl
Kelly A. Frazer
@en
P106
P21
P31
P496
0000-0002-6060-8902