Kelly A. Frazer
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Biology
Kelly A. Frazer's Degrees
- PhD Genetics Stanford University
- Masters Bioinformatics Stanford University
- Bachelors Biology University of California, San Diego
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Why Is Kelly A. Frazer Influential?
(Suggest an Edit or Addition)According to Wikipedia, Kelly A Frazer is a Professor of Pediatrics in the Medical School at the University of California, San Diego, Chief of the Division of Genome Information Sciences and Director of the Institute for Genomic Medicine.
Kelly A. Frazer'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
- A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
- VISTA: computational tools for comparative genomics (2004) (1964)
- PipMaker--a web server for aligning two genomic DNA sequences. (2000) (1258)
- Whole-Genome Patterns of Common DNA Variation in Three Human Populations (2005) (1218)
- Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 (2001) (1178)
- Human genetic variation and its contribution to complex traits (2009) (1074)
- VISTA : visualizing global DNA sequence alignments of arbitrary length (2000) (967)
- Identification of a coordinate regulator of interleukins 4, 13, and 5 by cross-species sequence comparisons. (2000) (846)
- PI3Kγ is a molecular switch that controls immune suppression (2016) (770)
- Common Sequence Polymorphisms Shaping Genetic Diversity in Arabidopsis thaliana (2007) (744)
- Common vs. rare allele hypotheses for complex diseases. (2009) (671)
- Evaluation of next generation sequencing platforms for population targeted sequencing studies (2009) (647)
- Genomewide SNP variation reveals relationships among landraces and modern varieties of rice (2009) (604)
- High-resolution whole-genome association study of Parkinson disease. (2005) (535)
- 9p21 DNA variants associated with Coronary Artery Disease impair IFNγ signaling response (2011) (521)
- Implementing genomic medicine in the clinic: the future is here (2013) (463)
- A sequence-based variation map of 8.27 million SNPs in inbred mouse strains (2007) (431)
- Common deletions and SNPs are in linkage disequilibrium in the human genome (2006) (390)
- Identification of Liver Cancer Progenitors Whose Malignant Progression Depends on Autocrine IL-6 Signaling (2013) (387)
- Active conservation of noncoding sequences revealed by three-way species comparisons. (2000) (344)
- Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides (2008) (334)
- New models of collaboration in genome-wide association studies: the Genetic Association Information Network (2007) (313)
- Fine-scale recombination patterns differ between chimpanzees and humans (2005) (288)
- Cross-species sequence comparisons: a review of methods and available resources. (2003) (275)
- Corrigendum: Microdroplet-based PCR enrichment for large-scale targeted sequencing (2010) (239)
- Microdroplet-based PCR amplification for large scale targeted sequencing (2009) (234)
- Transcriptome Sequencing Reveals Potential Mechanism of Cryptic 3’ Splice Site Selection in SF3B1-mutated Cancers (2015) (181)
- A Pan-BCL2 inhibitor renders bone-marrow-resident human leukemia stem cells sensitive to tyrosine kinase inhibition. (2013) (166)
- ADAR1 Activation Drives Leukemia Stem Cell Self-Renewal by Impairing Let-7 Biogenesis. (2016) (160)
- Analysis of allelic differential expression in human white blood cells. (2006) (153)
- ADAR1 promotes malignant progenitor reprogramming in chronic myeloid leukemia (2012) (141)
- Large-Scale Profiling Reveals the Influence of Genetic Variation on Gene Expression in Human Induced Pluripotent Stem Cells. (2017) (137)
- Computational and biological analysis of 680 kb of DNA sequence from the human 5q31 cytokine gene cluster region. (1997) (135)
- miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1. (2014) (125)
- Accurate detection and genotyping of SNPs utilizing population sequencing data. (2010) (120)
- The apolipoprotein(a) gene is regulated by sex hormones and acute–phase inducers in YAC transgenic mice (1995) (119)
- Enrichment of sequencing targets from the human genome by solution hybridization (2009) (115)
- Whole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlanders. (2013) (110)
- Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. (2019) (107)
- Experimental selection of hypoxia-tolerant Drosophila melanogaster (2011) (105)
- Fine Mapping in 94 Inbred Mouse Strains Using a High-Density Haplotype Resource (2010) (102)
- Effective filtering strategies to improve data quality from population-based whole exome sequencing studies (2014) (101)
- Evolutionarily conserved sequences on human chromosome 21. (2001) (100)
- Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing (2011) (99)
- Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates. (2003) (98)
- A Covering Method for Detecting Genetic Associations between Rare Variants and Common Phenotypes (2010) (97)
- Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin (2014) (96)
- Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens (2012) (96)
- High-level ROR1 associates with accelerated disease progression in chronic lymphocytic leukemia. (2016) (93)
- Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional. (2004) (91)
- Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome. (2004) (90)
- Subtle changes in chromatin loop contact propensity are associated with differential gene regulation and expression (2019) (87)
- PTEN regulates glioblastoma oncogenesis through chromatin-associated complexes of DAXX and histone H3.3 (2017) (86)
- Allele-Specific KRT1 Expression Is a Complex Trait (2006) (82)
- Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes (2014) (80)
- The genomics gold rush. (2007) (80)
- iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types (2017) (78)
- A genome-wide approach to identifying novel-imprinted genes (2007) (76)
- BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma (2015) (76)
- Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors. (1992) (74)
- Method for improving sequence coverage uniformity of targeted genomic intervals amplified by LR-PCR using Illumina GA sequencing-by-synthesis technology. (2009) (72)
- Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants (2020) (72)
- Brief Report: Oxidative Stress Mediates Cardiomyocyte Apoptosis in a Human Model of Danon Disease and Heart Failure (2015) (71)
- Functional screening of an asthma QTL in YAC transgenic mice (1999) (68)
- Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes (2019) (66)
- Systematic transcriptome analysis reveals tumor-specific isoforms for ovarian cancer diagnosis and therapy (2015) (65)
- Sensitive gene fusion detection using ambiguously mapping RNA-Seq read pairs (2011) (64)
- Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk (2018) (64)
- Insights into the Mutational Burden of Human Induced Pluripotent Stem Cells from an Integrative Multi-Omics Approach. (2018) (60)
- Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels (2004) (56)
- Systematic analysis of binding of transcription factors to noncoding variants (2021) (56)
- The resequencing imperative (2007) (54)
- Glioblastoma cellular cross-talk converges on NF-κB to attenuate EGFR inhibitor sensitivity (2017) (50)
- Properties of structural variants and short tandem repeats associated with gene expression and complex traits (2020) (50)
- Properties of structural variants and short tandem repeats associated with gene expression and complex traits (2020) (50)
- iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types. (2017) (47)
- Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy (2005) (47)
- An RNA editing fingerprint of cancer stem cell reprogramming (2015) (47)
- Decoding the human genome (2012) (44)
- Isolation and characterization of a laminin-binding protein from rat and chick muscle (1988) (43)
- Genomic interval engineering of mice identifies a novel modulator of triglyceride production. (2000) (43)
- Photoreceptor localization of the KIF3A and KIF3B subunits of the heterotrimeric microtubule motor kinesin II in vertebrate retina. (1999) (43)
- Enhancer release and retargeting activates disease-susceptibility genes (2021) (43)
- Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level (2010) (41)
- In Vitro Human Keratinocyte Migration Rates Are Associated with SNPs in the KRT1 Interval (2007) (39)
- Genetic determinants of phenotypic diversity in humans (2008) (37)
- Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics (2021) (37)
- Association of Human iPSC Gene Signatures and X Chromosome Dosage with Two Distinct Cardiac Differentiation Trajectories (2019) (34)
- Reversion to an embryonic alternative splicing program enhances leukemia stem cell self-renewal (2015) (34)
- Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells (2020) (33)
- Mutations in topoisomerase IIβ result in a B cell immunodeficiency (2019) (33)
- Ancient DNA Reveals Key Stages in the Formation of Central European Mitochondrial Genetic Diversity (2013) (33)
- Corrigendum: PI3Kγ is a molecular switch that controls immune suppression (2016) (31)
- Joint effects of cancer and variants in the factor 5 gene on the risk of venous thromboembolism (2016) (31)
- Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell development (2015) (31)
- High-Throughput and Cost-Effective Characterization of Induced Pluripotent Stem Cells (2017) (30)
- Cell-Surface Marker Signature for Enrichment of Ventricular Cardiomyocytes Derived from Human Embryonic Stem Cells (2018) (30)
- Biased estimates of clonal evolution and subclonal heterogeneity can arise from PCR duplicates in deep sequencing experiments (2014) (29)
- Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing. (2016) (29)
- Aberrant DNA Methylation in Human iPSCs Associates with MYC-Binding Motifs in a Clone-Specific Manner Independent of Genetics. (2017) (28)
- Human iPSC-Derived Retinal Pigment Epithelium: A Model System for Prioritizing and Functionally Characterizing Causal Variants at AMD Risk Loci (2019) (28)
- Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing (2013) (28)
- Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
- Pgltools: a genomic arithmetic tool suite for manipulation of Hi-C peak and other chromatin interaction data (2017) (26)
- High-Resolution Mutational Profiling Suggests the Genetic Validity of Glioblastoma Patient-Derived Pre-Clinical Models (2013) (26)
- Multi-species sequence comparison: the next frontier in genome annotation (2003) (26)
- Systematic genetic analysis of the MHC region reveals mechanistic underpinnings of HLA type associations with disease (2019) (26)
- Kataegis Expression Signature in Breast Cancer Is Associated with Late Onset, Better Prognosis, and Higher HER2 Levels. (2016) (25)
- High-Throughput and Cost-Effective Characterization of Induced Pluripotent Stem Cells. (2017) (24)
- Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits (2019) (23)
- A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus. (1992) (23)
- Discovery of novel plasma biomarkers for future incident venous thromboembolism by untargeted synchronous precursor selection mass spectrometry proteomics (2018) (23)
- Elucidating the role of 8q24 in colorectal cancer (2009) (22)
- Faithful Expression of the Human 5q31 Cytokine Cluster in Transgenic Mice1 (2000) (22)
- Identification of Common and Rare Genetic Variation Associated With Plasma Protein Levels Using Whole-Exome Sequencing and Mass Spectrometry (2018) (20)
- Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats (2019) (20)
- Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancer (2017) (19)
- A Network of microRNAs Acts to Promote Cell Cycle Exit and Differentiation of Human Pancreatic Endocrine Cells (2019) (18)
- Hinds , in Three Human Populations Whole-Genome Patterns of Common DNA Variation (2008) (18)
- Associations Between Common and Rare Exonic Genetic Variants and Serum Levels of 20 Cardiovascular-Related Proteins (2016) (17)
- A novel and rapid method for isolating sequences adjacent to rare cutting sites and their use in physical mapping. (1991) (15)
- A large‐scale exome array analysis of venous thromboembolism (2019) (15)
- Evaluation of the SNP tagging approach in an independent population sample—array-based SNP discovery in Sami (2007) (15)
- Evaluation of ultra-deep targeted sequencing for personalized breast cancer care (2013) (15)
- SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues (2021) (15)
- IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis (2018) (15)
- Mutational Profiling Can Establish Clonal or Independent Origin in Synchronous Bilateral Breast and Other Tumors (2015) (14)
- Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree (2017) (13)
- Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia. (2019) (12)
- Whole Transcriptome Sequencing Enables Discovery and Analysis of Viruses in Archived Primary Central Nervous System Lymphomas (2013) (12)
- Systematic assessment of regulatory effects of human disease variants in pluripotent cells (2019) (11)
- Cycling Toward Leukemia Stem Cell Elimination Wtih a Selective Sonic Hedgehog Antagonist (2011) (11)
- Network-based analysis identifies epigenetic biomarkers of esophageal squamous cell carcinoma progression (2014) (11)
- A mutation in IFT43 causes non-syndromic recessive retinal degeneration (2017) (10)
- Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD (2014) (10)
- Genetic ancestry of participants in the National Children’s Study (2014) (10)
- Ultra‐Sharp Nanowire Arrays Natively Permeate, Record, and Stimulate Intracellular Activity in Neuronal and Cardiac Networks (2021) (10)
- Transcriptome Sequencing of Tumor Subpopulations Reveals a Spectrum of Therapeutic Options for Squamous Cell Lung Cancer (2013) (9)
- Homozygous GNAS 393C-Allele Carriers with Locally Advanced Esophageal Cancer Fail to Benefit from Platinum-Based Preoperative Chemoradiotherapy (2014) (8)
- In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms (2022) (8)
- Cellular deconvolution of GTEx tissues powers eQTL studies to discover thousands of novel disease and cell-type associated regulatory variants (2019) (8)
- Human Genome Variation (2007) (8)
- Efficient Prioritization of Multiple Causal eQTL Variants via Sparse Polygenic Modeling (2017) (8)
- Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolism (2019) (7)
- Corrigendum: Fine-scale recombination patterns differ between chimpanzees and humans (2005) (7)
- Revealing sequence variation patterns in rice with machine learning methods (2008) (7)
- Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke. The Tromsø Study (2019) (7)
- Combination Targeted Therapy to Impair Self-Renewal Capacity of Human Blast Crisis Leukemia Stem Cells (2011) (7)
- In vitro Differentiation of Human iPSC-derived Retinal Pigment Epithelium Cells (iPSC-RPE). (2019) (5)
- leukemia by regulating expression of GAB1 and FOXP1 miR-150 influences B-cell receptor signaling in chronic lymphocytic (2014) (5)
- Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program (2020) (5)
- Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis (2021) (5)
- Allele-specific NKX2-5 binding underlies multiple genetic associations with human EKG traits (2018) (4)
- Effective filtering strategies to improve data quality from population-based whole exome sequencing studies (2014) (4)
- Pgltools: a genomic arithmetic tool suite for manipulation of Hi-C peak and other chromatin interaction data (2017) (4)
- Integration of phased Hi-C and molecular phenotype data to study genetic and epigenetic effects on chromatin looping (2018) (4)
- BCL2 Splice Isoform Switching Promotes Leukemia Stem Cell Survival and Sensitivity to a Novel Pan BCL2 Inhibitor (2011) (3)
- The nature, pattern and function of human sequence variation (2004) (3)
- Structural variant classes and short tandem repeats differentially impact gene expression and complex traits (2019) (3)
- Glioblastomas derived from genetically modified pluripotent stem cells recapitulate pathobiology (2019) (3)
- FOXP1 genes chronic lymphocytic leukemia by regulating expression of GAB1 and MicroRNA-150 contributes to the proficiency of B-cell receptor signaling in (2014) (3)
- Publisher Correction: PTEN regulates glioblastoma oncogenesis through chromatin-associated complexes of DAXX and histone H3.3 (2018) (3)
- Chromatin co-accessibility is highly structured, spans entire chromosomes, and mediates long range regulatory genetic effects (2019) (3)
- Genomic properties of structural variants and short tandem repeats that impact gene expression and complex traits in humans (2019) (3)
- Correction: Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin (2014) (3)
- Systems genomics in age-related macular degeneration (2022) (2)
- Human iPSC gene signatures and X chromosome dosage impact response to WNT inhibition and cardiac differentiation fate (2019) (2)
- ROR1 Negative Chronic Lymphocytic Leukemia (CLL) Have a Distinctive Gene Expression Signature and May Represent an Indolent-Disease Subtype (2015) (2)
- In heart failure reactivation of RNA-binding proteins drives the transcriptome into a fetal state (2021) (2)
- Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease (2021) (2)
- Type 1 diabetes risk genes mediate pancreatic beta cell survival in response to proinflammatory cytokines (2021) (2)
- Insights into genetic factors contributing to variability in SARS-CoV-2 susceptibility and COVID-19 disease severity (2021) (2)
- SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues (2022) (2)
- In vitro Differentiation of Human iPSC-derived Cardiovascular Progenitor Cells (iPSC-CVPCs). (2020) (2)
- Human iPSC-derived retinal pigment epithelium: a model system for identifying and functionally characterizing causal variants at AMD risk loci (2018) (2)
- Linking disease associations with regulatory information in the (2012) (2)
- Insights into the mutational burden of human induced pluripotent stem cells using an integrative omics approach (2018) (1)
- Database searches for binding sites. (2000) (1)
- Abstract 219: Splicing inhibitors reduce human AML CD34+ cell survival and self-renewal during MDS/AML evolution in a leukemia stem cell supportive niche assay. (2013) (1)
- Genomics Links Inflammation with Neurocognitive Impairment in Children Living with Human Immunodeficiency Virus type-1. (2020) (1)
- VISTA: computational toolsfor comparative genomics (2004) (1)
- Abstract 5191: Genome-wide mutational analysis reveals core signaling pathways in mucinous neoplasms of the appendix (2014) (1)
- Subtle changes in chromatin loop contact propensity are associated with differential gene regulation and expression (2019) (1)
- Detection and validation of novel mutations in MERTK in a simplex case of retinal degeneration using WGS and hiPSC–RPEs model (2020) (1)
- MiningABs: mining associated biomarkers across multi-connected gene expression datasets (2014) (1)
- Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats (2020) (1)
- Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats (2020) (1)
- Author Correction: Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants (2020) (1)
- Regulatory variants active in iPSC-derived pancreatic progenitor cells are associated with Type 2 Diabetes in adults (2021) (1)
- Malignant Reprogramming of Progenitors into Leukemia Stem Cells Is Enhanced By Upregulation of CD44 Transcript Variant 3 in Malignant Microenvironments (2014) (1)
- iPSC-derived pancreatic progenitors are an optimal model system to study T2D regulatory variants active during fetal development of the pancreas (2021) (1)
- Affinity-optimizing variants within cardiac enhancers disrupt heart development and contribute to cardiac traits (2022) (1)
- Genetic ancestry of participants in the National Children’s Study (2014) (1)
- Abstract P2-06-01: Breast-to-breast metastasis can cause hormone-receptor positive/triple negative bilateral synchronous tumors (2012) (1)
- MiningABs: mining associated biomarkers across multi-connected gene expression datasets (2014) (1)
- Properties of structural variants and short tandem repeats associated with gene expression and complex traits (2020) (1)
- Sabutoclax, a Novel Pan BCL2 Family Inhibitor, Sensitizes Dormant Blast Crisis Chronic Myeloid Leukemia Stem Cells to Dasatinib (2012) (1)
- Properties of structural variants and short tandem repeats associated with gene expression and complex traits (2020) (1)
- Low-Power 256-Channel Nanowire Electrode-on-Chip Neural Interface for Intracellular Electrophysiology (2021) (1)
- MutaScope: a high-sensitivity variant caller dedicated to high-throughput PCR amplicons sequencing (2012) (1)
- Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
- Abstract 4798: The niche specific role of CD44 splice isoform expression in blast crisis leukemia stem cell generation (2014) (1)
- Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants (2020) (0)
- Abstract 5217: RNA editing enzyme ADAR1 drives leukemia stem cell differentiation and self-renewal in chronic myeloid leukemia (2012) (0)
- Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells (2020) (0)
- Evaluation of ultra-deep targeted sequencing for personalized breast cancer care (2013) (0)
- Revealing Instability: Genetic Variation Underlies Variability in mESC Pluripotency. (2020) (0)
- Olmec Pottery Production and Export in Ancient Mexico Determined Through Elemental Analysis (2005) (0)
- Inhibition Of Inflammation Driven Leukemia Stem Cell Self-Renewal With a Selective JAK2 Antagonist (2013) (0)
- The RNA Editase ADAR1 Promotes Malignant Progenitor Reprogramming in Chronic Myeloid Leukemia. (2012) (0)
- Erratum: Elucidating the role of 8q24 in colorectal cancer (2009) (0)
- The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. (2023) (0)
- The Oryzasnp Project - Genome - Wide Snps Discovered in Diverse Rice (2008) (0)
- Stem Cell Reports Resource Cell-Surface Marker Signature for Enrichment of Ventricular Cardiomyocytes Derived from Human Embryonic Stem Cells (0)
- 374 IDENTIFYING AND CHARACTERIZING RISK LOCI FOR CARDIOVASCULAR DISEASES (2012) (0)
- Faculty Opinions recommendation of Genetic dissection of transcriptional regulation in budding yeast. (2002) (0)
- The impact of FGG rs2066865 and pre-cancer fibrinogen concentration on cancer-related venous thromboembolism (VTE) (2018) (0)
- Faculty Opinions recommendation of Utility and distribution of conserved noncoding sequences in the grasses. (2002) (0)
- Author Correction: Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells (2020) (0)
- Genomic Analysis of Serial Chronic Lymphocytic Leukemia Samples Suggests That Epigenetic Changes, Rather Than Clonal Evolution, May Drive the Progression of This Leukemia (2012) (0)
- Cover, Volume 42, Issue 2 (2021) (0)
- Abstract 375: A novel diagnostic assay for detection of primate-specific RNA editing events in leukemia stem cells (2014) (0)
- Faculty Opinions recommendation of Great ape DNA sequences reveal a reduced diversity and an expansion in humans. (2001) (0)
- Cancer avatars derived from genetically engineered pluripotent stem cells allow for longitudinal assessment of tumor development (2019) (0)
- Detection and validation of the involvement of novel mutations in MERTK in recessive retinal degeneration using WGS and hiPSC-RPEs. (2019) (0)
- Abstract 4826: Identification of low prevalence somatic mutations in heterogeneous tumor samples (2011) (0)
- Joint effects of GP6 rs1613662 and pre-cancer platelet count on the risk of venous thromboembolism in cancer (2018) (0)
- Abstract 4115: Transcription factor 7-like-2 polymorphisms and risk of Type 2 Diabetes in Indian Asians and Northern Europeans (2006) (0)
- TMOD-42. CRISPR/Cas9-EDITED HUMAN NEURAL STEM CELLS GIVE RISE TO BRAIN TUMORS RESEMBLING GLIOBLASTOMAS (2017) (0)
- inefficient for lncRNAs predominantly co-transcriptional in the human genome but Deep sequencing of subcellular RNA fractions shows splicing to be (2013) (0)
- IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis (2018) (0)
- Faculty Opinions recommendation of Computational identification of noncoding RNAs in E. coli by comparative genomics. (2001) (0)
- Deciphering the genetic basis of common diseases by integrated functional annotation of common and rare variants (2010) (0)
- FunctionalSIM 2 in the Noncoding Sequences Conserved in a Limited Number of Mammals data (2004) (0)
- Deciphering the genetic architecture of IRD by integrated analysis of 425 whole genomes (2018) (0)
- In-depth genetic analysis of 6p21.3 reveals insights into associations between HLA types and complex traits and disease (2019) (0)
- Faculty Opinions recommendation of Insights into imprinting from parent-of-origin phased methylomes and transcriptomes. (2018) (0)
- Author Correction: Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells (2020) (0)
- 295-OR: Identification of Type 1 Diabetes Genes and Regulatory Processes Mediating Pancreatic Beta-Cell Survival in Response to Proinflammatory Cytokines (2022) (0)
- Mutations in the novel gene IFT88 are involved in causing non-syndromic inherited retinal degeneration (IRD) (2018) (0)
- MicroRNA miR-150 contributes to the disease aggressiveness and regulation of B-cell receptor signalling (BCR) in CLL (2013) (0)
- The Role Of CD44 Isoform Expression In Niche Resident Chronic Myeloid Leukemia Stem Cell Evolution (2013) (0)
- Cytokine Cluster in Transgenic Mice Faithful Expression of the Human 5q31 (2000) (0)
- Biased estimates of clonal evolution and subclonal heterogeneity can arise from PCR duplicates in deep sequencing experiments (2014) (0)
- Using deep whole genome sequence, transcriptome and epigenome data to characterize the mutational burden of induced pluripotent stem cells (2018) (0)
- Allele-Specific KRT1 Expression Is a Complex (2006) (0)
- Erratum to: Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin (2014) (0)
- Correction: Gustafson et al., Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes 2017, 8, 210 (2017) (0)
- BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma (2015) (0)
- Analysis ofChromosome22Deletions inNeurofibromatosi s Type2-related Tumors (1992) (0)
- Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancer (2017) (0)
- LYMPHOID NEOPLASIA miR-150 in fl uences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1 (2014) (0)
- Combined JAK/STAT5A and BCR-ABL Inhibition Impairs Blast Crisis Chronic Myeloid Leukemia Stem Cell Self-Renewal (2012) (0)
- A targeted 450 KB deletion in mouse chromosome 11 ideentifies a novel gene that dramatically impacts on triglyceride production (1999) (0)
- Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes (2014) (0)
- Disease-associated regulatory variation often displays plasticity or temporal-specificity in fetal pancreas (2023) (0)
- Identification of a novel SDCCAG8 gene variant in a family with retinitis pigmentosa and kidney failure (2017) (0)
- Protein Blots and Assays for 12 ~ l-Laminin-binding and LBP Antigen (2002) (0)
- Population sequencing of genomic intervals to identify variants underlying complex traits (2010) (0)
- LYMPHOID NEOPLASIA High-level ROR1 associates with accelerated disease progression in chronic lymphocytic leukemia (2016) (0)
- Identification of pathogenic mutations in patients with inherited retinal dystrophies using whole genome sequencing (2017) (0)
- Title Base-Resolution Methylome of Retinal Pigment Epithelial Cells Used in the First Trial of Human Induced Pluripotent Stem Cell-Based Autologous Transplantation (2019) (0)
- Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk (2019) (0)
- Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits (2019) (0)
- An RNA editing fingerprint of cancer stem cell reprogramming (2015) (0)
- A homozygous mutation in the novel gene ARFGAP2 is associated with non-syndromic recessive inherited retinal degeneration (IRD). (2018) (0)
- Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin (2014) (0)
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