S. Horsley

发表

Covert preleukemia driven by MLL gene fusion

M. Greaves, E. Mejstrikova, O. Hrusak, 2009, Genes, chromosomes & cancer.

Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia.

K. Anderson, M. Greaves, M. Greaves, 2009, Blood.

Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia.

K. Anderson, M. Greaves, L. Kearney, 2009, Blood.

Translocation between chromosome 5q35 and chromosome 11q13-- an unusual cytogenetic finding in a primary refractory acute myeloid leukemia.

S. Horsley, Sung-Chao Chu, T.F. Wang, 2006, Clinical and laboratory haematology.

Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16.

J. Peden, L. Kearney, D. Higgs, 2001, Human molecular genetics.

Molecular-cytogenetic detection of a deletion of 1p36.3.

J. Flint, S. Knight, L. Kearney, 1997, Journal of medical genetics.

Specific JAK 2 mutation ( JAK 2 R 683 ) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia

K. Anderson, M. Greaves, L. Kearney, 2009 .

Chromosomal stabilisation by a subtelomeric rearrangement involving two closely related Alu elements.

L. Kearney, D. Higgs, S. Horsley, 1996, Human molecular genetics.

A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

L. Kearney, S. Hodgson, S. Horsley, 2001, Cytogenetic and Genome Research.

Rapid mapping of markers applying vectorette technology to YAC fragmentation allows easy assembly of a high-density STS bacterial clone contig spanning the markers D6S1260-D6S1918

L. Kearney, Jennifer J. Pointon, S. Horsley, 1998, Mammalian Genome.

The mouse homologue of the polycystic kidney disease gene (Pkd1) is a single-copy gene.

L. Kearney, P. Harris, S. Horsley, 1996, Genomics.

A fetus with an X;1 balanced reciprocal translocation and eye disease.

S. Horsley, A. Davies, M. Seller, 1995, Journal of medical genetics.

Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects

J. Peden, L. Kearney, D. Higgs, 2001, European Journal of Human Genetics.

Down syndrome acute lymphoblastic leukemia R 683 ) and multiple gene deletions in JAK 2 mutation ( JAK 2 Specific

K. Anderson, M. Greaves, L. Kearney, 2009 .

Characterisation of X; 17(q12;p 13) Translocation Breakpoints in a Female Patient with Hypomelanosis of Ito and Choroid Plexus Papilloma

A. Monaco, T. Kirchhoff, S. Horsley, 1997, European journal of human genetics : EJHG.

A complete set of human telomeric probes and their clinical application

D. Ledbetter, R. Regan, J. Flint, 1996, Nature Genetics.

Subtle chromosomal rearrangements in children with unexplained mental retardation

Jonathan Flint, R. Regan, P. Bolton, 1999, The Lancet.

Development and Clinical Application of an Innovative Fluorescence in situ Hybridization Technique Which Detects Submicroscopic Rearrangements Involving Telomeres

R. Regan, S. Knight, L. Kearney, 1997, European journal of human genetics : EJHG.

De novo deletion within the telomeric region flanking the human α globin locus as a cause of α thalassaemia

J. Hughes, D. Higgs, S. Horsley, 2003, British journal of haematology.

Array CGH of fusion gene–positive leukemia‐derived cell lines reveals cryptic regions of genomic gain and loss

A. Ashworth, L. Kearney, K. Fenwick, 2006, Genes, chromosomes & cancer.

Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generations.

A. Jauch, F. Speleman, N. Van Roy, 2000, American journal of medical genetics.

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

J. Flint, S. Knight, L. Kearney, 1998, Journal of medical genetics.

ATR16 Syndrome: Mechanisms Linking Monosomy to Phenotype

A. Wilkie, D. Higgs, J. Traeger-Synodinos, 2019, bioRxiv.

Molecular cytogenetics in haematological malignancy: current technology and future prospects

L. Kearney, S. Horsley, Lyndal Kearney, 2005, Chromosoma.

Genetic lesions in a preleukemic aplasia phase in a child with acute lymphoblastic leukemia

M. Greaves, L. Kearney, S. Horsley, 2008, Genes, chromosomes & cancer.

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease.

V. Torres, P. Harris, K. Hopp, 2009, Kidney international.

Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL

R. Eils, A. Jauch, K. Saracoglu, 2000, European Journal of Human Genetics.

Characterization and variation of a human inwardly‐rectifying K‐channel gene (KCNJ6): a putative ATP‐sensitive K‐channel subunit

F. Ashcroft, L. Kearney, M. Warren-Perry, 1995, FEBS letters.

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

L. Kearney, P. Njølstad, S. Twigg, 1998, American journal of human genetics.

Comparative expressed sequence hybridization studies of high‐hyperdiploid childhood acute lymphoblastic leukemia

Anthony V Moorman, Fiona M Ross, M. Greaves, 2004, Genes, chromosomes & cancer.

Sequence of Genetic Events in ETV6-RUNX1 Positive B Precursor ALL: Insights from Identical Twins with Concordant Leukaemia

M. Greaves, L. Kearney, S. Horsley, 2008 .

Corrigendum: A complete set of human telomeric probes and their clinical application

D. Ledbetter, R. Regan, J. Flint, 1996, Nature Genetics.

Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia.

M. Greaves, L. Kearney, S. Horsley, 2009, Blood.

Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia.

M. Greaves, L. Kearney, C. Eckert, 2009, Blood.

ATR-16 syndrome: mechanisms linking monosomy to phenotype

A. Wilkie, D. Higgs, J. Traeger-Synodinos, 2020, Journal of Medical Genetics.