D. Sheer

发表

The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts.

T. Triche, O. Delattre, A. Aurias, 1994, The New England journal of medicine.

CTCF binds to sites in the major histocompatibility complex that are rapidly reconfigured in response to interferon-gamma

Muhammad A. Mumin, S. Krawetz, D. Sheer, 2012, Nucleic acids research.

New vector for transfer of yeast artificial chromosomes to mammalian cells

J. Ragoussis, W. Bodmer, J. Trowsdale, 1993, Somatic cell and molecular genetics.

Plasticity in the organization and sequences of human KIR/ILT gene families.

S. Beck, S. Milne, J. Trowsdale, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas

Heather L. Mulder, Erin K. Hedlund, Michael C. Rusch, 2013, Nature Genetics.

Rapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridisation on tumour imprints and bone marrow smears. United Kingdom Children's Cancer Study Group.

D. Sheer, N. Bown, A. Pearson, 1994, British Journal of Cancer.

Comparative genomic hybridization of breast tumors stratified by histological grade reveals new insights into the biological progression of breast cancer.

A. Hanby, D. Sheer, D. Barnes, 1999, Cancer research.

The role of nuclear organization in cancer

Denise Sheer, D. Sheer, E. Lever, 2010, The Journal of pathology.

Karyotypic analysis of the human monoblastic cell line U937.

D. Sheer, J. Shipley, D. Sheppard, 1988, Cancer genetics and cytogenetics.

Deletion of c-ets1 and T3γ loci from the 11q- chromosome in the human monoblastic cell line U937

D. Sheer, J. Shipley, 1989 .

Conditional immortalization of human thyroid epithelial cells: a tool for analysis of oncogene action

N. Lemoine, D. Sheer, J. Bond, 1990, Molecular and cellular biology.

The organization and conservation of the human Surfeit gene cluster and its localization telomeric to the c-abl and can proto-oncogenes at chromosome band 9q34.1.

D. Sheer, J. Yon, M. Fried, 1993, Human molecular genetics.

Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus.

D. Sheer, A. Goddard, T. Pihlajaniemi, 1990, American journal of human genetics.

Purification and composition of the human tumor-associated glycoprotein (TAG-72) defined by monoclonal antibodies CC49 and B72.3.

J. Schlom, D. Sheer, H. Cooper, 1988, Cancer research.

Assignment of the human and mouse LIM-kinase genes (LIMK1; Limk1) to chromosome bands 7q11.23 and 5G1, respectively, by in situ hybridization.

M. Noble, D. Sheer, N. Gutowski, 1996, Cytogenetics and Cell Genetics.

A somatic cell hybrid panel for regional mapping of human chromosome 18.

W. Bodmer, D. Sheer, D. Markie, 1992, Genomics.

The ubiquitin-homology gene PIC1: characterization of mouse (Pic1) and human (UBL1) genes and pseudogenes.

P. Freemont, D. Sheer, E. Solomon, 1998, Genomics.

A testis-expressed Zn finger gene (ZNF76) in human 6p21.3 centromeric to the MHC is closely linked to the human homolog of the t-complex gene tcp-11.

J. Ragoussis, P. Sanseau, J. Trowsdale, 1992, Genomics.

CD164, a novel sialomucin on CD34(+) and erythroid subsets, is located on human chromosome 6q21.

A. Zannettino, D. Sheer, P. Simmons, 1998, Blood.

Fine mapping of the human MHC class II region within chromosome band 6p21 and evaluation of probe ordering using interphase fluorescence in situ hybridization.

J. Ragoussis, J. Trowsdale, D. Sheer, 1993, Cytogenetics and cell genetics.

Characterisation of human thyroid epithelial cells immortalised in vitro by simian virus 40 DNA transfection.

D. Sheer, D. Wynford‐Thomas, N. Lemoine, 1989, British Journal of Cancer.

Cloning of the region between HLA-DMB and LMP2 in the human major histocompatibility complex.

P. Sanseau, J. Trowsdale, D. Sheer, 1994, Human immunology.

Nature Genetics Advance Online Publication

Heather L. Mulder, Erin K. Hedlund, R. Wilson, 2022 .

Molecular analysis of simple variant translocations in acute promyelocytic leukemia

F. Mitelman, T. Fioretos, A. Antony, 1994, Genes, chromosomes & cancer.

The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1p

M. Crumpton, D. Sheer, W. Sewell, 1987, Human Genetics.

Assignment of the human creatine transporter type 2 (SLC6A10) to chromosome band 16p11.2 by in situ hybridization.

P. Emson, D. Sheer, P. Gorman, 1997, Cytogenetics and Cell Genetics.

The human placental alkaline phosphatase gene and related sequences map to chromosome 2 band q37

J. Trowsdale, D. Sheer, N. Spurr, 1987, Annals of human genetics.

Widespread Expression of BORIS/CTCFL in Normal and Cancer Cells

Muhammad A. Mumin, D. Sheer, S. Patel, 2011, PloS one.

Microglia promote glioblastoma via mTOR‐mediated immunosuppression of the tumour microenvironment

A. Heimberger, D. Sheer, S. Brandner, 2020, The EMBO journal.

Proteasome components with reciprocal expression to that of the MHC-encoded LMP proteins

J. Trowsdale, D. Sheer, M. Belich, 1994, Current Biology.

Is prostate cancer worth diagnosing?

D. Sheer, J. Waxman, 1995, The Lancet.

Cloning and chromosome mapping of the human interleukin-1 receptor antagonist gene.

D. Sheer, P. Gorman, R. Solari, 1992, Cytokine.

The homeobox gene MEIS1 is amplified in IMR-32 and highly expressed in other neuroblastoma cell lines.

D. Nižetić, D. Sheer, T. Jones, 2000, European journal of cancer.

Establishment and characterisation of three new human ovarian carcinoma cell lines and initial evaluation of their potential in experimental chemotherapy studies

D. Sheer, B. Hill, R. Whelan, 1987, International journal of cancer.

Enzymatic degradation of RNA causes widespread protein aggregation in cell and tissue lysates

M. Barnes, G. Giovannoni, D. Sheer, 2019, bioRxiv.

The proteome of neurofilament-containing protein aggregates in blood

D. Sheer, Michael Bremang, Johan Aarum, 2018, Biochemistry and biophysics reports.

Replication Timing Profile Reflects the Distinct Functional and Genomic Features of the MHC Class II Region

S. Beck, T. Forshew, P. Sasieni, 2007, Cell cycle.

Assignment of the gene coding for the alpha-subunit of prolyl 4-hydroxylase to human chromosome region 10q21.3-23.1.

D. Sheer, K. Kivirikko, T. Pihlajaniemi, 1989, American journal of human genetics.

Biochemical and genetic analysis of the Oka blood group antigen

P. Goodfellow, S. Povey, D. Sheer, 2004, Immunogenetics.

Characterization and chromosomal assignment of a human cell surface antigen defined by the monoclonal antibody AUAI

W. Bodmer, D. Sheer, N. Spurr, 1986, International journal of cancer.

Confirmation that the Type I collagen gene on chromosome 17 is COL1A1 (α1(I)), using a human genomic probe

D. Rowe, D. Sheer, E. Solomon, 1984, Annals of human genetics.

Genetic analysis of the 15;17 chromosome translocation associated with acute promyelocytic leukemia.

J. Stephenson, S. Povey, N. Heisterkamp, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Assignment of the gene encoding the beta‐subunit of the human fibronectin receptor (β‐FNR) to chromosome 10p11.2

P. Goodfellow, P. Goodfellow, D. Sheer, 1989, Annals of human genetics.

The gene coding for the p68 calcium-binding protein is localised to bands q32–q34 of human chromosome 5, and to mouse chromosome 11

M. Crumpton, C. Kozak, D. Sheer, 1989, Human Genetics.

Regional assignment of the human gene coding for a multifunctional polypeptide (P4HB) acting as the beta-subunit of prolyl 4-hydroxylase and the enzyme protein disulfide isomerase to 17q25.

D. Sheer, A. Goddard, K. Kivirikko, 1991, Cytogenetics and cell genetics.

The human homologue of the mouse t‐complex gene, TCP1, is located on chromosome 6 but is not near the HLA region.

P. Goodfellow, J. Trowsdale, K. Willison, 1987, The EMBO journal.

cDNA cloning and chromosomal mapping of a mouse gene with homology to NTPases

A. Frischauf, D. Sheer, B. Chadwick, 1998, Mammalian Genome.

HnRNP-A1 binds directly to double-stranded DNA in vitro within a 36 bp sequence

W. Bowen, D. Sheer, R. Donev, 2004, Molecular and Cellular Biochemistry.

Regional localization of the gene coding for human brain nitric oxide synthase (NOS1) to 12q24.2-->24.31 by fluorescent in situ hybridization.

P. Emson, G. Bates, D. Sheer, 1993, Cytogenetics and cell genetics.

Tumour angiogenesis is reduced in the Tc1 mouse model of Down Syndrome

D. Nižetić, D. Sheer, R. Adams, 2010, Nature.

Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome

D. Nižetić, D. Sheer, R. Adams, 2010, Nature.

Construction of a genetic map of human chromosome 17 by use of chromosome-mediated gene transfer.

D. Sheer, P. Gorman, E. Solomon, 1988, Proceedings of the National Academy of Sciences of the United States of America.

CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli.

W. Bodmer, D. Sheer, L. Varesco, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of a continuous cell line in culture established from a Krukenberg tumour of the ovary arising from a primary gastric adenocarcinoma.

S. Povey, D. Sheer, B. Hill, 1988, European journal of cancer & clinical oncology.

Chromosomal localisation of the human envoplakin gene (EVPL) to the region of the tylosis oesophageal cancer gene (TOCG) on 17q25.

F. Watt, D. Sheer, C. Ruhrberg, 1996, Genomics.

Transformation associated p53 protein is encoded by a gene on human chromosome 17

T. Shows, G. Bruns, D. Sheer, 1985, Somatic cell and molecular genetics.

Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line

A. Rowan, I. Tomlinson, M. Noble, 1999, British Journal of Cancer.

Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.

W. Bodmer, I. Talbot, D. Sheer, 1996, American journal of human genetics.

Yeast artificial chromosomes for the molecular analysis of the familial polyposis APC gene region.

D. Sheer, E. Solomon, T. Jones, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Isolation of cDNA clones encoding the beta isozyme of human DNA topoisomerase II and localisation of the gene to chromosome 3p24.

A. Harris, D. Sheer, J. Jenkins, 1992, Nucleic acids research.

Deletion of part of the short arm of chromosome 17 in a congenital fibrosarcoma.

D. Sheer, P. Gorman, M. Malone, 1990, Cancer genetics and cytogenetics.

The CL100 gene, which encodes a dual specificity (Tyr/Thr) MAP kinase phosphatase, is highly conserved and maps to human chromosome 5q34

D. Sheer, S. Keyse, T. Jones, 1994, Human Genetics.

Localization of the Surfeit gene cluster containing the ribosomal protein gene L7a to chromosome bands 9q33‐34.

D. Sheer, J. Yon, M. Fried, 1989, Annals of human genetics.

The hypervariable gene locus PUM, which codes for the tumour associated epithelial mucins, is located on chromosome 1, within the region 1g21–24

S. Povey, J. Taylor‐Papadimitriou, D. Swallow, 1987, Annals of human genetics.

Recruitment of Heterogeneous Nuclear Ribonucleoprotein A1in Vivo to the LMP/TAP Region of the Major Histocompatibility Complex*

S. Beck, W. Bowen, R. Horton, 2003, The Journal of Biological Chemistry.

Combinatorial generation of variable fusion proteins in the Ewing family of tumours.

T. Triche, O. Delattre, A. Aurias, 1993, The EMBO journal.

Genomic structure and domain organisation of the human Bak gene.

S. Beck, J. Trowsdale, P. Barr, 1998, Gene.

Genetic relationships of the genes encoding the human proteasome beta subunits and the proteasome PA28 complex.

J. Trowsdale, D. Sheer, T. Jones, 1997, Genomics.

The human LFA-3 gene is located at the same chromosome band as the gene for its receptor CD2

M. Crumpton, D. Sheer, W. Sewell, 2004, Immunogenetics.

The Human Polycomb Group Complex Associates with Pericentromeric Heterochromatin to Form a Novel Nuclear Domain

P. Freemont, D. Sheer, A. Otte, 1998, The Journal of cell biology.

Spectral karyotyping suggests additional subsets of colorectal cancers characterized by pattern of chromosome rearrangement

P. Edwards, W. Bodmer, D. Sheer, 2001, Proceedings of the National Academy of Sciences of the United States of America.

"Junction trapping". A simple PCR-based method for the isolation of YAC-insert termini.

D. Sheer, K. Patel, G. Hampton, 1993, Genetic analysis, techniques and applications.

Molecular Characterization of a cDNA Encoding Functional Human CLK4 Kinase and Localization to Chromosome 4q35

P. Bork, J. Schultz, A. Ullrich, 2001 .

The polymorphic human DNA sequence D8S8 assigned to 8ql3‐21.1, close to the carbonic anhydrase gene cluster, by isotopic and non‐isotopic in situ hybridization and by linkage analysis

J. Attwood, S. Povey, D. Sheer, 1990, Annals of human genetics.

Localization of the oncogene c‐erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17

J. Rowley, M. L. Beau, D. Sheer, 1985, Annals of human genetics.

Localization of the gene for familial adenomatous polyposis on chromosome 5

F. C. Lucibello, P. Scambler, J. Bodmer, 1987, Nature.

Chromosomal locations of the gene coding for the CD3 (T3) γ subunit of the human and mouse CD3/T-cell antigen receptor complexes

P. Goodfellow, M. Crumpton, C. Kozak, 2004, Immunogenetics.

Type 5 acid phosphatase. Sequence, expression and chromosomal localization of a differentiation-associated protein of the human macrophage.

D. Sheer, N. Cross, M. Bevilacqua, 1990, European journal of biochemistry.

Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome

P. Goodfellow, S. Povey, M. Ferguson-Smith, 1983, Nature.

Carcinoembryonic antigen (CEA) expression in somatic cell hybrids

M. Bobrow, D. Sheer, R. Brown, 1982, Somatic cell genetics.

THE HIGH-FREQUENCY RED-CELL ANTIGEN OKA IS CARRIED ON A SERIES OF POLYPEPTIDES OF APPARENT MOLECULAR-WEIGHT RANGING FROM 35KD TO 68KD AND IS CONTROLLED BY A GENE ON CHROMOSOME-19

P. Goodfellow, S. Povey, D. Sheer, 1987 .

Molecular analysis of acute promyelocytic leukemia breakpoint cluster region on chromosome 17.

D. Sheer, A. Goddard, E. Solomon, 1990, Science.

The isolation and characterization of colorectal epithelial cell lines at different stages in malignant transformation from familial polyposis coli patients

D. Sheer, C. Paraskeva, C. Wigley, 1984, International journal of cancer.

Comparative expression analysis reveals lineage relationships between human and murine gliomas and a dominance of glial signatures during tumor propagation in vitro.

Richard G Grundy, Sebastian Brandner, Matthew Ellis, 2013, Cancer research.

High-Grade Gliomas

C. Q. Lee, David T. W. Jones, Michael D. Brooks, 2012, Oxford Medicine Online.

Molecular and Phenotypic Characterisation of Paediatric Glioma Cell Lines as Models for Preclinical Drug Development

Paul Workman, Darren Hargrave, Chris Jones, 2009, PloS one.

RAF gene fusion breakpoints in pediatric brain tumors are characterized by significant enrichment of sequence microhomology.

Jing Ma, T. Forshew, D. Ellison, 2011, Genome research.

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

Ian Tomlinson, Andrew Rowan, Susan Clark, 1999, Nature Medicine.

Subchromosomal positioning of the epidermal differentiation complex (EDC) in keratinocyte and lymphoblast interphase nuclei.

J. Ragoussis, D. Sheer, Ruth R. E. Williams, 2002, Experimental cell research.

Large-scale chromatin organization of the major histocompatibility complex and other regions of human chromosome 6 and its response to interferon in interphase nuclei.

J. Ragoussis, E. Volpi, S. Beck, 2000, Journal of cell science.

P-STAT1 mediates higher-order chromatin remodelling of the human MHC in response to IFNγ

I. Kerr, A. Bolzer, D. Sheer, 2007, Journal of Cell Science.

Mini review: Form and function in the human interphase chromosome

E. Volpi, D. Sheer, E. Chevret, 2000, Cytogenetic and Genome Research.

LIM–kinase deleted in Williams syndrome

M. Tassabehji, A. Read, D. Sheer, 1996, Nature Genetics.

Promyelocytic leukemia nuclear bodies associate with transcriptionally active genomic regions

Paul S. Freemont, Suhail A. Islam, Denise Sheer, 2004, The Journal of cell biology.

PML bodies associate specifically with the MHC gene cluster in interphase nuclei.

M J Sternberg, S A Islam, P Sasieni, 2001, Journal of cell science.

Molecular cloning and tissue expression of FAT, the human homologue of the Drosophila fat gene that is located on chromosome 4q34-q35 and encodes a putative adhesion molecule.

R. Poulsom, D. Sheer, T. Jones, 1995, Genomics.

The role of microhomology in genomic structural variation.

D. Sheer, D. Ottaviani, M. LeCain, 2014, Trends in genetics : TIG.

The human dendritic cell marker CD83 maps to chromosome 6p23

D. Sheer, G. Schuler, A. Steinkasserer, 1999, Annals of human genetics.

MYB upregulation and genetic aberrations in a subset of pediatric low-grade gliomas

S. Shurtleff, Jing Ma, T. Forshew, 2010, Acta Neuropathologica.

Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoire.

D. Ledbetter, D. Lancet, H. Lehrach, 1994, Human molecular genetics.

DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas

D. Ellison, D. Sheer, D. Ottaviani, 2016, Acta Neuropathologica Communications.

Genomic Profiling Identifies Discrete Deletions Associated with Translocations in Glioblastoma Multiforme

N. Carter, H. Fiegler, I. Tomlinson, 2006, Cell cycle.

Multiple tandem 18-kb sequences clustered in the region of the acute promyelocytic leukemia breakpoint on chromosome 17.

D. Sheer, E. Solomon, P. Hedge, 1989, Genomics.

Reconfiguration of genomic anchors upon transcriptional activation of the human major histocompatibility complex.

S. Krawetz, S. Beck, V. Rakyan, 2008, Genome research.

Generation of a genomic tiling array of the human Major Histocompatibility Complex (MHC) and its application for DNA methylation analysis

P. Coggill, M. D. Francis, C. Langford, 2008 .

A cDNA encoding a muscle-type tropomyosin cloned from a human epithelial cell line: identity with human fibroblast tropomyosin TM1.

D. Sheer, H. Cooper, G. L. Prasad, 1991, Biochemical and biophysical research communications.

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

D. Nižetić, D. Sheer, K. Pavelić, 2000, Genes, chromosomes & cancer.

Global hypo-methylation in a proportion of glioblastoma enriched for an astrocytic signature is associated with increased invasion and altered immune landscape

Michael R. Barnes, S. Nelander, D. Sheer, 2022, bioRxiv.

Comparative epigenetic analysis of tumour initiating cells and syngeneic EPSC-derived neural stem cells in glioblastoma

S. Nelander, V. Rakyan, D. Sheer, 2021, Nature Communications.

Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization.

P. Sanseau, D. Sheer, G. Senger, 1994, Cytogenetics and cell genetics.

Genetic mechanisms in carcinogenesis.

D. Sheer, E. Solomon, 1983, Progress in nucleic acid research and molecular biology.

Analysis of NotI linking clones isolated from human chromosome 3 specific libraries.

A. Protopopov, M. Lerman, E. Zabarovsky, 1999, Gene.

Released chromatin: linearized DNA for high resolution fluorescence in situ hybridization.

P. Sanseau, J. Trowsdale, D. Sheer, 1994, Human molecular genetics.

Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping.

P. Edwards, A. Scarpa, D. Sheer, 2001 .

Non‐random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping

P. Edwards, A. Scarpa, N. Lemoine, 2001, International journal of cancer.

Activation of the ERK/MAPK pathway: a signature genetic defect in posterior fossa pilocytic astrocytomas

Jing Ma, T. Forshew, D. Ellison, 2009, The Journal of pathology.

H-RYK, an Unusual Receptor Kinase: Isolation and Analysis of Expression in Ovarian Cancer

R. Poulsom, T. Ganesan, D. Sheer, 1996, Molecular medicine.

Cytogenetic analysis of four human ovarian carcinoma cell lines.

D. Sheer, B. Hill, R. Whelan, 1987, Cancer genetics and cytogenetics.

Genome-wide methylation analysis identifies genes silenced in non-seminoma cell lines

D. Sheer, J. Shipley, T. Reader, 2016, npj Genomic Medicine.

Characterization of cryptic rearrangements and variant translocations in acute promyelocytic leukemia.

P. Freemont, D. Sheer, S. Langabeer, 1997, Blood.

Cohesion, but not too close

E. Volpi, D. Sheer, F. Uhlmann, 2001, Current Biology.

MAPK pathway activation and the origins of pediatric low‐grade astrocytomas

T. Forshew, D. Ellison, D. Sheer, 2009, Journal of cellular physiology.

Chromosomal mapping of the human and mouse homologues of two new members of the AP-2 family of transcription factors.

D. Sheer, T. Williams, H. Hurst, 1996, Genomics.

c-MYC overexpression induces choroid plexus papillomas through a T-cell mediated inflammatory mechanism

D. Sheer, A. Sabò, A. Behrens, 2019, Acta Neuropathologica Communications.

Allelic loss at SMAD4 in polyps from juvenile polyposis patients and use of fluorescence in situ hybridization to demonstrate clonal origin of the epithelium.

R. Houlston, B. Leggett, R. Poulsom, 2000, Cancer research.

Fluorescence in situ hybridization techniques for the rapid detection of genetic prognostic factors in neuroblastoma

D. Sheer, J. Lunec, N. Bown, 2000, British Journal of Cancer.

Localization of the gene encoding a type I protein phosphatase catalytic subunit to human chromosome band 11q13.

E. F. da Cruz e Silva, D. Sheer, N. Spurr, 1990, Genomics.

Monosomy 7 and Ph-positive acute lymphoblastic leukaemia: cytogenetic and molecular aspects.

D. Sheer, P. Gorman, S. Eridani, 1987, Leukemia research.

Monosomy 7 and multipotential stem cell transformation

M. Greaves, M. Greaves, D. Sheer, 1985, British journal of haematology.

Localization of the oncogene c‐erbA2 to human chromosome 3

B. Vennstrom, D. Sheer, P. Gorman, 1987, Annals of human genetics.

Fine Mapping of Probes in the Adenomatous Polyposis Coli Region of Chromosome 5 by In Situ Hybridization

P. Lawson, G. Zehetner, W. Bodmer, 1991, Genes, chromosomes & cancer.

Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-κB pathways

T. Jacques, T. Forshew, D. Sheer, 2015, Acta Neuropathologica Communications.

RAF gene fusions are specific to pilocytic astrocytoma in a broad paediatric brain tumour cohort

T. Jacques, T. Forshew, D. Sheer, 2010, Acta Neuropathologica.

A role for SC35 and hnRNPA1 in the determination of amyloid precursor protein isoforms

J. Thome, D. Sheer, A. Newall, 2007, Molecular Psychiatry.

A monoclonal antibody recognizing a cell surface antigen coded for by a gene on human chromosome 17

D. Sheer, A. Tunnacliffe, L. Hiorns, 1982, Annals of human genetics.

BORIS/CTCFL is an RNA-binding protein that associates with polysomes

D. Sheer, D. Ottaviani, S. Patel, 2013, BMC Cell Biology.

BORIS/CTCFL is an RNA-binding protein that associates with polysomes

D. Sheer, D. Ottaviani, B. Ogunkolade, 2013, BMC Cell Biology.

Assignment and Ordering of Twenty-Three Unique Notl-Linking Clones Containing Expressed Genes Including the Guanosine 5′-Monophosphate Synthetase Gene to Human Chromosome 3

A. Protopopov, E. Zabarovsky, D. Sheer, 1997, European journal of human genetics : EJHG.

Molecular cloning of human lysyl oxidase and assignment of the gene to chromosome 5q23.3-31.2.

D. Sheer, K. Kivirikko, T. Pihlajaniemi, 1991, Genomics.

Satellite DNA binding and cellular localisation of RNA helicase P68

D. Sheer, R. Donev, O. Podgornaya, 2005, Journal of Cell Science.

Chromosomal localisation of the human homologues to the oncogenes erbA and B.

W. Bodmer, B. Vennstrom, D. Sheer, 1984, The EMBO journal.

DNA replication-dependent induction of gene proximity by androgen.

Yong-jie Lu, D. Sheer, B. Young, 2015, Human molecular genetics.

SR8--the establishment and characterisation of a new ovarian carcinoma cell line and xenograft model.

D. Sheer, K. Raju, A. Papadopoulos, 1996, European Journal of Cancer.

Anchoring the genome

D. Sheer, D. Ottaviani, E. Lever, 2008, Genome Biology.

The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A, maps to chromosome 17p12-p13: three eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2.

J. Hauber, D. Sheer, A. Steinkasserer, 1995, Genomics.

Molecular cloning and analysis of the fragile X region in man.

A. Monaco, B. Korn, D. Sheer, 1991, Nucleic acids research.

The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI).

D. Sheer, B. Chadwick, A. Frischauf, 1998, Genomics.

Chromosome-mediated gene thnsfer.

D. Sheer, J. Shipley, 1991, Methods in molecular biology.

Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification.

D. Bentley, C. Cole, I. Dunham, 1992, Genomics.

Isolation of probes specific to human chromosomal region 6p21 from immunoselected irradiation-fusion gene transfer hybrids.

J. Ragoussis, P. Goodfellow, J. Trowsdale, 1991, Genomics.

Clinical applications of genetic rearrangements in cancer.

D. Sheer, J. Squire, 1996, Seminars in cancer biology.

Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193.

D. Nižetić, D. Sheer, P. Gorman, 1997, Journal of medical genetics.

Diagnosis of Ewing's sarcoma and peripheral neuroectodermal tumour based on the detection of t(11;22) using fluorescence in situ hybridisation.

D. Sheer, B. D. De Stavola, T. Jones, 1993, British Journal of Cancer.

Chromosomal localization, gene structure and transcription pattern of the ORFX gene, a homologue of the MHC-linked RING3 gene.

S. Beck, J. Trowsdale, D. Sheer, 1997, Gene.

Fusion of the EWS Gene to a DNA segment from 9q22‐31 in a human myxoid chondrosarcoma

B. Gusterson, C. R. Pinkerton, D. Sheer, 1995, Genes, chromosomes & cancer.

Genetic analysis ofthe15;17 chromosome translocation associated withacutepromyelocytic leukemia

D. Sheer, 1983 .

Catalog of chromosome aberrations in cancer (5th edn): by Felix Mitelman (Bertil Johansson and Fredrik Mertens associated eds) Wiley-Liss, 1994. £345.00 $518.00 (xxi + 4252 pages; 2 volumes) ISBN 0 471 11183 X

D. Sheer, 1995 .

Gene amplification accompanied by the loss of a chromosome containing the native allele and the appearance of the amplified DNA at a new chromosomal location.

E. Heard, D. Sheer, M. Fried, 1991, Proceedings of the National Academy of Sciences of the United States of America.

The human gene for xeroderma pigmentosum complementation group G (XPG) maps to 13q33 by fluorescence in situ hybridization.

R. Wood, D. Sheer, D. Scherly, 1994, Genomics.

Localisation of the gene encoding the catalytic gamma subunit of phosphorylase kinase to human chromosome bands 7p12-q21.

E. F. da Cruz e Silva, D. Sheer, N. Spurr, 1990, Biochimica et biophysica acta.

Analysis of circulating protein aggregates as a route of investigation into neurodegenerative disorders

D. Sheer, Michael Bremang, Johan Aarum, 2021, Brain communications.

Analysis of circulating protein aggregates reveals pathological hallmarks of amyotrophic lateral sclerosis

D. Sheer, Michael Bremang, Johan Aarum, 2020, bioRxiv.

Mapping of the genes encoding human inducible and endothelial nitric oxide synthase (NOS2 and NOS3) to the pericentric region of chromosome 17 and to chromosome 7, respectively.

Ian G. Charles, I. Charles, P. Emson, 1994, Genomics.

Characterization of a t(I0; II) (pI3‐I4; qI4‐2I) in the monoblastic cell line U937

M. Dyer, B. Gusterson, L. Kearney, 1995 .

Cytogenetic analysis of primitive neuroectodermal tumors. Absence of the t(11;22) in two of three cases and a review of the literature.

D. Sheer, P. Gorman, M. Malone, 1991, Cancer genetics and cytogenetics.

Three different brain tumours evolving from a common origin

A. Waldman, T. Forshew, D. Sheer, 2013, Oncogenesis.

The human HIV-1 Rev binding-protein hRIP/Rab (HRB) maps to chromosome 2q36.

J. Hauber, D. Sheer, A. Steinkasserer, 1997, Genomics.

The small cell lung cancer antigen cluster-4 and the leukocyte antigen CD24 are allelic isoforms of the same gene (CD24) on chromosome band 6q21.

R. Stahel, D. Sheer, D. Jackson, 1995, Cytogenetics and cell genetics.

The gene coding for human deoxyhypusine synthase (DHPS) maps to chromosome 19p13.11-p13.12.

J. Hauber, D. Sheer, A. Steinkasserer, 1996, Genomics.

Cytogenetic analysis of a cell line established from a Krukenberg tumor.

D. Sheer, B. Hill, R. Whelan, 1990, Cancer Genetics and Cytogenetics.

Mapping of the human SAP1 (SRF accessory protein 1) gene and SAP2, a gene encoding a related protein, to chromosomal bands 1q32 and 12q23, respectively.

R. Treisman, D. Sheer, J. Shipley, 1994, Genomics.

DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas

D. Ellison, D. Sheer, D. Ottaviani, 2016, Acta neuropathologica communications.

Nature GeNetics ADVANCE ONLINE PUBLICATION

Heather L. Mulder, Erin K. Hedlund, Michael C. Rusch, 2013 .

Cloning and characterization of human phosphatase inhibitor-2 (IPP-2) sequences

P. Sanseau, J. Trowsdale, D. Sheer, 1994, Mammalian Genome.

Acute Promyelocytic Leukemia Characterization of Cryptic Rearrangements and Variant Translocations in

D. Sheer, S. Langabeer, P. Gorman, 2013 .

Genomic analysis of the Tapasin gene, located close to the TAP loci in the MHC

J. Sgouros, S. Humphray, P. Cresswell, 1998, European journal of immunology.

The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p.

M. MacDonald, H. Lehrach, J. Gusella, 1992, Genomics.

ANOTHER RED-CELL SURFACE-ANTIGEN, OKA, IS ENCODED BY A GENE ON CHROMOSOME-19

P. Goodfellow, S. Povey, D. Sheer, 1987 .

15/17 chromosome translocation in acute promyelocytic leukemia.

T. Lister, M. Greaves, D. Sheer, 1982, Cancer genetics and cytogenetics.

Molecular Characterization of a cDNA Encoding Functional Human CLK4 Kinase and Localization to Chromosome 4q35

P. Bork, J. Schultz, A. Ullrich, 2001 .

RFLP for the human erb-A1 gene.

D. Sheer, E. Solomon, L. Hiorns, 1986, Nucleic acids research.

Incidence of the 15q+;17q- chromosome translocation in acute promyelocytic leukaemia (APL).

T. Lister, D. Sheer, E. Solomon, 1985, British Journal of Cancer.

High grade gliomas

C. Q. Lee, David T. W. Jones, Michael D. Brooks, 2022, Progress in Brain Research.

A novel and rapid method for isolating sequences adjacent to rare cutting sites and their use in physical mapping.

D. Cox, K. Frazer, H. Lehrach, 1991, Nucleic acids research.

The genetic analysis of prostate carcinoma.

D. Sheer, N. Spurr, R. Roylance, 1997, Seminars in Cancer Biology.

Genome-wide methylation analysis identifies genes silenced in non-seminoma cell lines.

D. Sheer, J. Shipley, Christopher Tan, 2017 .

MAPK pathway activation and the origins of pediatric low‐grade astrocytomas

T. Forshew, D. Ellison, D. Sheer, 2009, Journal of cellular physiology.

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Erin K. Hedlund, Michael C. Rusch, L. Fulton, 2013 .

Genetic aspects of carcinogenesis

D. Sheer, 1985, The British journal of surgery.