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Author Details
Full Name
Charles B Epstein
Affiliation
ORCID
Career Start Year
1985
Papers
49
H Index
35
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37500887
Exposure of iPSC-derived human microglia to brain substrates enables the generation and manipulation of diverse transcriptional states in vitro.
Nat Immunol
2023
37034577
Single-cell multi-scale footprinting reveals the modular organization of DNA regulatory elements.
bioRxiv
2023
35474001
Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes.
Nature
2022
33212152
Epigenetic Alterations in Keratinocyte Carcinoma.
J Invest Dermatol
2021
33828297
Genome-wide enhancer maps link risk variants to disease genes.
Nature
2021
32728101
Detecting sample swaps in diverse NGS data types using linkage disequilibrium.
Nat Commun
2020
32728249
Expanded encyclopaedias of DNA elements in the human and mouse genomes.
Nature
2020
31263286
Enhancer signatures stratify and predict outcomes of non-functional pancreatic neuroendocrine tumors.
Nat Med
2019
31501535
Publisher Correction: Enhancer signatures stratify and predict outcomes of non-functional pancreatic neuroendocrine tumors.
Nat Med
2019
28753427
A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression.
Cell
2017
27826357
Systematic comparison of monoclonal versus polyclonal antibodies for mapping histone modifications by ChIP-seq.
Epigenetics Chromatin
2016
26229090
Detection of Enhancer-Associated Rearrangements Reveals Mechanisms of Oncogene Dysregulation in B-cell Lymphoma.
Cancer Discov
2015
25503565
Identification of nuclear hormone receptor pathways causing insulin resistance by transcriptional and epigenomic analysis.
Nat Cell Biol
2015
25363779
Genetic and epigenetic fine mapping of causal autoimmune disease variants.
Nature
2015
25533951
Dissecting neural differentiation regulatory networks through epigenetic footprinting.
Nature
2015
25693563
Integrative analysis of 111 reference human epigenomes.
Nature
2015
25164756
Comparative analysis of metazoan chromatin organization.
Nature
2014
25129075
Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci.
Nat Neurosci
2014
24598259
Impact of sequencing depth in ChIP-seq experiments.
Nucleic Acids Res
2014
23333102
Genome-wide chromatin state transitions associated with developmental and environmental cues.
Cell
2013
24076989
Recommendations for the design and analysis of epigenome-wide association studies.
Nat Methods
2013
23664763
Transcriptional and epigenetic dynamics during specification of human embryonic stem cells.
Cell
2013
22726435
DNA sequence-dependent compartmentalization and silencing of chromatin at the nuclear lamina.
Cell
2012
22955991
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia.
Genome Res
2012
22174693
Genomic distribution and inter-sample variation of non-CpG methylation across human cell types.
PLoS Genet
2011
21441907
Mapping and analysis of chromatin state dynamics in nine human cell types.
Nature
2011
22196736
Combinatorial patterning of chromatin regulators uncovered by genome-wide location analysis in human cells.
Cell
2011
20668531
PTK6 regulates IGF-1-induced anchorage-independent survival.
PLoS One
2010
20852635
Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications.
Nat Biotechnol
2010
18022394
SIT4 regulation of Mig1p-mediated catabolite repression in Saccharomyces cerevisiae.
FEBS Letters
2007
15113399
Comparing gene discovery from Affymetrix GeneChip microarrays and Clontech PCR-select cDNA subtraction: a case study.
BMC Genomics
2004
15662205
An empirical Bayesian significance test of cDNA library data.
Journal of Computational Biology
2004
12631716
Global transcription analysis of Krebs tricarboxylic acid cycle mutants reveals an alternating pattern of gene expression and effects on hypoxic and oxidative genes.
Molecular Biology of the Cell
2003
11855849
Induction of global stress response in Saccharomyces cerevisiae cells lacking telomerase.
Biochemical and Biophysical Research Communications
2002
11222779
Identification of partial loss of function p53 gene mutations utilizing a yeast-based functional assay.
Nucleic Acids Research
2001
11381609
Numerical methods for handling uncertainty in microarray data: an example analyzing perturbed mitochondrial function in yeast.
Methods in Cell Biology
2001
11742997
RTG-dependent mitochondria to nucleus signaling is negatively regulated by the seven WD-repeat protein Lst8p.
EMBO Journal
2001
11179416
Genome-wide responses to mitochondrial dysfunction.
Molecular Biology of the Cell
2001
11120686
MAD: a suite of tools for microarray data management and processing.
Bioinformatics
2000
10679339
Microarray technology - enhanced versatility, persistent challenge.
Current Opinion in Biotechnology
2000
9572492
p53 mutations isolated in yeast based on loss of transcription factor activity: similarities and differences from p53 mutations detected in human tumors.
Oncogene
1998
9131587
A genetic approach to mapping the p53 binding site in the MDM2 protein.
Mol Med
1997
15706764
Impairments of brain and behavior: the neurological effects of alcohol.
1997
8526340
The spectrum of mutations at the p53 locus. Evidence for tissue-specific mutagenesis, selection of mutant alleles, and a "gain of function" phenotype.
Ann N Y Acad Sci
1995
8114735
Genes that can bypass the CLN requirement for Saccharomyces cerevisiae cell cycle START.
Molecular and Cellular Biology
1994
1387626
CLB5: a novel B cyclin from budding yeast with a role in S phase.
Genes and Development
1992
22200474
A method for the estimation of historical sulfate concentrations in natural freshwaters.
Environmental Science & Technology
1988
17812878
Response: Acid deposition in the Western United States.
Science
1986
17777926
Acid deposition, smelter emissions, and the linearity issue in the Western United States.
Science
1985
1 - 49 of 49
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