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Veronica Buckle
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The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16
European Polycystic Kidney Disease Consortium
Cell 77 (6), 881-894, 1994
7621994
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
J Flint, AOM Wilkie, VJ Buckle, RM Winter, AJ Holland, HE McDermid
Nature genetics 9 (2), 132-140, 1995
6071995
Initiating and cancer-propagating cells in TEL-AML1-associated childhood leukemia
D Hong, R Gupta, P Ancliff, A Atzberger, J Brown, S Soneji, J Green, ...
Science 319 (5861), 336-339, 2008
4882008
Structure and polymorphism of human telomere-associated DNA
WRA Brown, PJ MacKinnon, A VillasantÚ, N Spurr, VJ Buckle, MJ Dobson
Cell 63 (1), 119-132, 1990
4091990
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
JC Taylor, HC Martin, S Lise, J Broxholme, JB Cazier, A Rimmer, ...
Nature genetics 47 (7), 717-726, 2015
3452015
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter
M De Gobbi, V Viprakasit, JR Hughes, C Fisher, VJ Buckle, H Ayyub, ...
Science 312 (5777), 1215-1217, 2006
3442006
Intragenic enhancers act as alternative promoters
MS Kowalczyk, JR Hughes, D Garrick, MD Lynch, JA Sharpe, ...
Molecular cell 45 (4), 447-458, 2012
2892012
Association between active genes occurs at nuclear speckles and is modulated by chromatin environment
JM Brown, J Green, RP das Neves, HAC Wallace, AJH Smith, J Hughes, ...
The Journal of cell biology 182 (6), 1083-1097, 2008
2852008
Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes
TL McDowell, RJ Gibbons, H Sutherland, DM O’Rourke, WA Bickmore, ...
Proceedings of the National Academy of Sciences 96 (24), 13983-13988, 1999
2691999
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome
J Wolfe, SM Darling, RP Erickson, IW Craig, VJ Buckle, PWJ Rigby, ...
Journal of molecular biology 182 (4), 477-485, 1985
2651985
Alpha-particle-induced chromosomal instability in human bone marrow cells.
MA Kadhim, SA Lorimore, MD Hepburn, DT Goodhead, VJ Buckle, ...
Lancet (London, England) 344 (8928), 987-988, 1994
2521994
Coregulated human globin genes are frequently in spatial proximity when active
JM Brown, J Leach, JE Reittie, A Atzberger, J Lee-Prudhoe, WG Wood, ...
The Journal of cell biology 172 (2), 177-187, 2006
2372006
Chromosome maps of man and mouse. IV
AG Searle, J Peters, MF Lyon, JG Hall, EP Evans, JH Edwards, VJ Buckle
Annals of human genetics 53 (2), 89-140, 1989
2291989
Radiation-induced genomic instability: delayed cytogenetic aberrations and apoptosis in primary human bone marrow cells
MA Kadhim, SA Lorimore, KMS Townsend, DT Goodhead, VJ Buckle, ...
International journal of radiation biology 67 (3), 287-293, 1995
2251995
Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16
AOM Wilkie, DR Higgs, KA Rack, VJ Buckle, NK Spurr, ...
Cell 64 (3), 595-606, 1991
2001991
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data
TS Price, R Regan, R Mott, ┼ Hedman, B Honey, RJ Daniels, L Smith, ...
Nucleic acids research 33 (11), 3455-3464, 2005
1892005
Expression of α-and β-globin genes occurs within different nuclear domains in haemopoietic cells
KE Brown, S Amoils, JM Horn, VJ Buckle, DR Higgs, M Merkenschlager, ...
Nature cell biology 3 (6), 602-606, 2001
1872001
A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype
L Pritchard, JA Sloane-Stanley, JA Sharpe, R Aspinwall, W Lu, V Buckle, ...
Human Molecular Genetics 9 (18), 2617-2627, 2000
1842000
Telomere directed fragmentation of mammalian chromosomes
MA Barnett, VJ Buckle, EP Evans, ACG Porter, D Rout, AG Smith, ...
Nucleic acids research 21 (1), 27-36, 1993
1771993
Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. 1. Cases due to deletions involving chromosome band 16p13. 3
AOM Wilkie, VJ Buckle, PC Harris, J Lamb, NJ Barton, ST Reeders, ...
American journal of human genetics 46 (6), 1112, 1990
1661990
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