Author details

Full Name

Peter Ellis

Affiliation

ORCID

Career Start Year

2000

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36849600	Author Correction: Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing.	Nat Protoc	2023
36353313	Exploring technologies to better link physical evidence and digital information for disaster victim identification.	Forensic Sciences Research	2022
34433962	The mutational landscape of human somatic and germline cells.	Nature	2021
33911282	Somatic mutation landscapes at single-molecule resolution.	Nature	2021
33990801	High-throughput full-length single-cell RNA-seq automation.	Nat Protoc	2021
33658498	Somatic mutations and single-cell transcriptomes reveal the root of malignant rhabdoid tumours.	Nat Commun	2021
33318691	Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing.	Nat Protoc	2021
32350471	The mutational landscape of normal human endometrial epithelium.	Nature	2020
30218636	A lentiviral vector-based insertional mutagenesis screen identifies mechanisms of resistance to MAPK inhibitors in melanoma.	Pigment Cell Melanoma Res	2019
31645730	The landscape of somatic mutation in normal colorectal epithelial cells.	Nature	2019
31645727	Somatic mutations and clonal dynamics in healthy and cirrhotic human liver.	Nature	2019
31616465	Evaluation of DNA Extraction Methods on Individual Helminth Egg and Larval Stages for Whole-Genome Sequencing.	Front Genet	2019
25999502	Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin.	Science	2015
25915121	G&T-seq: parallel sequencing of single-cell genomes and transcriptomes.	Nat Methods	2015
25056318	5' isomiR variation is of functional and evolutionary importance.	Nucleic Acids Research	2014
24507442	SASI-Seq: sample assurance Spike-Ins, and highly differentiating 384 barcoding for Illumina sequencing.	BMC Genomics	2014
24510098	Selective nuclear export of specific classes of mRNA from mammalian nuclei is promoted by GANP.	Nucleic Acids Res	2014
23702683	Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture.	Leukemia	2013
23912340	Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis.	Hum Mol Genet	2013
24030381	Clinical and biological implications of driver mutations in myelodysplastic syndromes.	Blood	2013
22856684	Gene expression profiles in white blood cells of volunteers exposed to a 50 Hz electromagnetic field.	Radiation Research	2012
22446964	Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles.	Nat Genet	2012
21995386	Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.	N Engl J Med	2011
21441929	Mutant nucleophosmin and cooperating pathways drive leukemia initiation and progression in mice.	Nat Genet	2011
21803864	CCR4-associated factor 1 coordinates the expression of Plasmodium falciparum egress and invasion proteins.	Eukaryotic Cell	2011
20140202	Genomic approaches uncover increasing complexities in the regulatory landscape at the human SCL (TAL1) locus.	PLoS ONE	2010
20808788	Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution.	PLoS One	2010
20947725	PiggyBac transposon mutagenesis: a tool for cancer gene discovery in mice.	Science	2010
20081834	FRT-seq: amplification-free, strand-specific transcriptome sequencing.	Nat Methods	2010
19924136	Molecular analysis of tumor-promoting CD8+ T cells in two-stage cutaneous chemical carcinogenesis.		2010
19941159	Microarray-based cytogenetic profiling reveals recurrent and subtype-associated genomic copy number aberrations in feline sarcomas.	Chromosome Res	2009
19544422	CARM1 is required in embryonic stem cells to maintain pluripotency and resist differentiation.	Stem Cells	2009
19544311	Neonates harbour highly active gammadelta T cells with selective impairments in preterm infants.	European Journal of Immunology	2009
19333554	'Putting our heads together': insights into genomic conservation between human and canine intracranial tumors.	Journal of Neuro-Oncology	2009
19228925	A HaemAtlas: characterizing gene expression in differentiated human blood cells.	Blood	2009
19845972	Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.	BMC Med	2009
18232738	A novel CpG island set identifies tissue-specific methylation at developmental gene loci.	PLoS Biol	2008
19096206	A genome assembly-integrated dog 1 Mb BAC microarray: a cytogenetic resource for canine cancer studies and comparative genomic analysis.	Cytogenet Genome Res	2008
18513384	Generation of a genomic tiling array of the human major histocompatibility complex (MHC) and its application for DNA methylation analysis.	BMC Med Genomics	2008
17571346	Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.	Nature	2007
17567991	Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes.	Genome Res	2007
17567990	The landscape of histone modifications across 1% of the human genome in five human cell lines.	Genome Res	2007
17702974	A cytogenetically characterized, genome-anchored 10-Mb BAC set and CGH array for the domestic dog.	J Hered	2007
17371987	Distinct cytokine-driven responses of activated blood gammadelta T cells: insights into unconventional T cell pleiotropy.	Journal of Immunology	2007
17901693	Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation.	Cytogenetic and Genome Research	2007
17491589	Spreading of mammalian DNA-damage response factors studied by ChIP-chip at damaged telomeres.	EMBO J	2007
17192395	Comparative gene expression profiling of in vitro differentiated megakaryocytes and erythroblasts identifies novel activatory and inhibitory platelet membrane proteins.	Blood	2007
17122085	Accurate and reliable high-throughput detection of copy number variation in the human genome.	Genome Res	2006
16221759	Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays.	Hum Mol Genet	2005
16314265	Visualization of alternative splicing in vivo.	Methods	2005