D. Sheer

Global hypo-methylation in a proportion of glioblastoma enriched for an astrocytic signature is associated with increased invasion and altered immune landscape
20228 citationsauthor #9
LGG-44. Multi-omic analysis reveals integrated signalling networks in paediatric low-grade glioma
20220 citationsauthor #11
Comparative epigenetic analysis of tumour initiating cells and syngeneic EPSC-derived neural stem cells in glioblastoma
202124 citationsauthor #21
Analysis of circulating protein aggregates as a route of investigation into neurodegenerative disorders
202114 citationsauthor #8
Microglia promote glioblastoma via mTOR‐mediated immunosuppression of the tumour microenvironment
2020117 citationsauthor #9
Analysis of circulating protein aggregates reveals pathological hallmarks of amyotrophic lateral sclerosis
20200 citationsauthor #8
LGG-57. SIGNALLING MECHANISMS IN PAEDIATRIC LOW-GRADE GLIOMA
20200 citationsauthor #9
Choroid plexus papillomas are induced by c-Myc overexpression in the choroid plexus via a T-cell inflammatory mechanism
20190 citationsauthor #12
c-MYC overexpression induces choroid plexus papillomas through a T-cell mediated inflammatory mechanism
201911 citationsauthor #14
298 Defective DNA Repair and Chromosomal Instability in RDEB
20190 citationsauthor #7
Enzymatic degradation of RNA causes widespread protein aggregation in cell and tissue lysates
201933 citationsauthor #9
The proteome of neurofilament-containing protein aggregates in blood
201823 citationsauthor #6
Genome-wide methylation analysis identifies genes silenced in non-seminoma cell lines.
20170 citationsauthor #13
DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas
201618 citationsauthor #16
Genome-wide methylation analysis identifies genes silenced in non-seminoma cell lines
20167 citationsauthor #12
PO77EXPRESSION OF THE ONCOGENIC SPLICE VARIANT OF CYCLIN D1, CCND1B, IN PAEDIATRIC LOW GRADE GLIOMAS.
20150 citationsauthor #7
Additional file 1: Table S1. of Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-ÎşB pathways
20150 citationsauthor #13
DNA replication-dependent induction of gene proximity by androgen.
201511 citationsauthor #4
Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-κB pathways
201542 citationsauthor #13
The role of microhomology in genomic structural variation.
2014171 citationsauthor #3
OP17MICRORNA PROFILING USING SMALL RNA-SEQ IN PAEDIATRIC LOW GRADE GLIOMAS
20140 citationsauthor #6
Acute Promyelocytic Leukemia Characterization of Cryptic Rearrangements and Variant Translocations in
20130 citationsauthor #1
BORIS/CTCFL is an RNA-binding protein that associates with polysomes
201312 citationsauthor #11
BORIS/CTCFL is an RNA-binding protein that associates with polysomes
20131 citationsauthor #11
Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas
2013728 citationsauthor #42
Comparative expression analysis reveals lineage relationships between human and murine gliomas and a dominance of glial signatures during tumor propagation in vitro.
201333 citationsauthor #10
LGG Nat Genet Supplemental data 2013
20130 citationsauthor #40
Three different brain tumours evolving from a common origin
20139 citationsauthor #7
Abstracts from the 2012 BNOS Conference
20121 citationsauthor #52
CTCF binds to sites in the major histocompatibility complex that are rapidly reconfigured in response to interferon-gamma
201215 citationsauthor #12
MICRORNA SIGNATURES IN A BROAD COHORT OF PAEDIATRIC BRAIN TUMOURS
20120 citationsauthor #12
Widespread Expression of BORIS/CTCFL in Normal and Cancer Cells
201125 citationsauthor #8
MICRORNA EXPRESSION IN PAEDIATRIC BRAIN TUMOURS
20110 citationsauthor #7
8711 POSTER Addition of Erlotinib Changes Gene Expression in Glioblastoma Cell Lines Treated With Vorinostat
20112 citationsauthor #6
RAF gene fusion breakpoints in pediatric brain tumors are characterized by significant enrichment of sequence microhomology.
201167 citationsauthor #11
MYB upregulation and genetic aberrations in a subset of pediatric low-grade gliomas
201065 citationsauthor #12
RAF gene fusions are specific to pilocytic astrocytoma in a broad paediatric brain tumour cohort
201051 citationsauthor #6
PRECLINICAL EXPERIMENTAL THERAPEUTICS AND PHARMACOLOGY
20100 citationsauthor #142
Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome
201063 citationsauthor #12
Tumour angiogenesis is reduced in the Tc1 mouse model of Down Syndrome
201085 citationsauthor #12
The role of nuclear organization in cancer
201091 citationsauthor #2
Activation of the ERK/MAPK pathway: a signature genetic defect in posterior fossa pilocytic astrocytomas
2009285 citationsauthor #17
American Association of Neuropathologists, Inc.: Abstracts of the 85th Annual Meeting June 11-14, 2009 San Antonio, Texas
20091 citationsauthor #11
MAPK pathway activation and the origins of pediatric low‐grade astrocytomas
200996 citationsauthor #6
Molecular and Phenotypic Characterisation of Paediatric Glioma Cell Lines as Models for Preclinical Drug Development
2009125 citationsauthor #12
Generation of a genomic tiling array of the human Major Histocompatibility Complex (MHC) and its application for DNA methylation analysis
200832 citationsauthor #13
Anchoring the genome
200864 citationsauthor #4
Reconfiguration of genomic anchors upon transcriptional activation of the human major histocompatibility complex.
200831 citationsauthor #13
MOLECULAR GENETIC AND EPIGENETIC ANALYSIS OF PEDIATRIC LOW-GRADE ASTROCYTIC GLIOMAS
20080 citationsauthor #5
A role for SC35 and hnRNPA1 in the determination of amyloid precursor protein isoforms
200784 citationsauthor #4
P-STAT1 mediates higher-order chromatin remodelling of the human MHC in response to IFNγ
200787 citationsauthor #8
Replication Timing Profile Reflects the Distinct Functional and Genomic Features of the MHC Class II Region
20076 citationsauthor #13
Satellite DNA binding and cellular localisation of RNA helicase P68
200529 citationsauthor #3
Abstracts for the Tenth International Conference on Brain Tumour Research and Therapy
20050 citationsauthor #419
Contents, Vol. 56, 1991
20040 citationsauthor #42
Chromosomal locations of the gene coding for the CD3 (T3) γ subunit of the human and mouse CD3/T-cell antigen receptor complexes
200411 citationsauthor #5
Biochemical and genetic analysis of the Oka blood group antigen
200437 citationsauthor #4
The human LFA-3 gene is located at the same chromosome band as the gene for its receptor CD2
200415 citationsauthor #4
Promyelocytic leukemia nuclear bodies associate with transcriptionally active genomic regions
2004240 citationsauthor #7
HnRNP-A1 binds directly to double-stranded DNA in vitro within a 36 bp sequence
200420 citationsauthor #4
Recruitment of Heterogeneous Nuclear Ribonucleoprotein A1in Vivo to the LMP/TAP Region of the Major Histocompatibility Complex*
200331 citationsauthor #7
Subchromosomal positioning of the epidermal differentiation complex (EDC) in keratinocyte and lymphoblast interphase nuclei.
2002221 citationsauthor #3
Molecular characterization of a cDNA encoding functional human CLK4 kinase and localization to chromosome 5q35 [correction of 4q35].
20013 citationsauthor #4
Non‐random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping
200132 citationsauthor #5
Human Chromosomes (4th Edition)
20015 citationsauthor #1
Expression and association of the human trithorax and polycomb group of proteins
20010 citationsauthor #3
Molecular Characterization of a cDNA Encoding Functional Human CLK4 Kinase and Localization to Chromosome 4q35
200111 citationsauthor #4
Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping.
200124 citationsauthor #5
Spectral Karyotyping reveals a new subset of colorectal cancers characterized by balanced translocations
20010 citationsauthor #5
Cohesion, but not too close.
200115 citationsauthor #2
Large-Scale chromatin structure and function in the Major Histocompatibility Complex
20010 citationsauthor #1
Spectral karyotyping suggests additional subsets of colorectal cancers characterized by pattern of chromosome rearrangement
2001182 citationsauthor #5
The 36th American Cytogenetics Conference
20000 citationsauthor #3
Large-scale chromatin organization of the major histocompatibility complex and other regions of human chromosome 6 and its response to interferon in interphase nuclei.
2000490 citationsauthor #12
Mini review: Form and function in the human interphase chromosome
200047 citationsauthor #3
Narrowing of the region of allelic loss in 21q11‐21 in squamous non‐small cell lung carcinoma and cloning of a novel ubiquitin‐specific protease gene from the deleted segment
200013 citationsauthor #6
Allelic loss at SMAD4 in polyps from juvenile polyposis patients and use of fluorescence in situ hybridization to demonstrate clonal origin of the epithelium.
2000112 citationsauthor #12
Plasticity in the organization and sequences of human KIR/ILT gene families.
2000678 citationsauthor #6
Fluorescence in situ hybridization techniques for the rapid detection of genetic prognostic factors in neuroblastoma
200021 citationsauthor #7
Analysis of NotI linking clones isolated from human chromosome 3 specific libraries.
199938 citationsauthor #19
The human dendritic cell marker CD83 maps to chromosome 6p23
199916 citationsauthor #4
The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis
1999410 citationsauthor #13
Comparative genomic hybridization of breast tumors stratified by histological grade reveals new insights into the biological progression of breast cancer.
1999267 citationsauthor #7
Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line
19998 citationsauthor #10
Genomic analysis of the Tapasin gene, located close to the TAP loci in the MHC
199887 citationsauthor #6
Genomic structure and domain organisation of the human Bak gene.
199828 citationsauthor #5
The Human Polycomb Group Complex Associates with Pericentromeric Heterochromatin to Form a Novel Nuclear Domain
1998290 citationsauthor #6
cDNA cloning and chromosomal mapping of a mouse gene with homology to NTPases
19982 citationsauthor #3
The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI).
199819 citationsauthor #6
The ubiquitin-homology gene PIC1: characterization of mouse (Pic1) and human (UBL1) genes and pseudogenes.
199823 citationsauthor #4
The genetic analysis of prostate carcinoma.
199714 citationsauthor #3
The human HIV-1 Rev binding-protein hRIP/Rab (HRB) maps to chromosome 2q36.
19975 citationsauthor #2
Genetic relationships of the genes encoding the human proteasome beta subunits and the proteasome PA28 complex.
199717 citationsauthor #3
Chromosomal localization, gene structure and transcription pattern of the ORFX gene, a homologue of the MHC-linked RING3 gene.
199738 citationsauthor #4
Structural organization of chromosome 6 in interphase.
19970 citationsauthor #7
The sialomicin CD164, a negative regulator of haemopoiesis, is expressed by CD34 + and erythroid subsets and is located on chromosome 6q21
19970 citationsauthor #10
Genetics of Human Neoplasia. Volume 3 of Advances in Genome Biology. Edited by Ram S. Verma. JAI Press, London. 1995. 2 Vols: Pp. 232 & Pp. 248. £125.00 (US$195.00). ISBN: 1 55938 835 8.
19970 citationsauthor #1
Assignment of the human creatine transporter type 2 (SLC6A10) to chromosome band 16p11.2 by in situ hybridization.
199713 citationsauthor #4
Characterization of cryptic rearrangements and variant translocations in acute promyelocytic leukemia.
1997145 citationsauthor #14
Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.
199684 citationsauthor #10

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