Kelly Halliday
Overview
Explore the profile of Kelly Halliday including associated specialties, affiliations and a list of published articles.
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13
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3236
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Recent Articles
1.
Dibbens L, Tarpey P, Hynes K, Bayly M, Scheffer I, Smith R, et al.
Nat Genet
. 2008 May;
40(6):776-81.
PMID: 18469813
Epilepsy and mental retardation limited to females (EFMR) is a disorder with an X-linked mode of inheritance and an unusual expression pattern. Disorders arising from mutations on the X chromosome...
2.
Tarpey P, Raymond F, Nguyen L, Rodriguez J, Hackett A, Vandeleur L, et al.
Nat Genet
. 2007 Aug;
39(9):1127-33.
PMID: 17704778
Nonsense-mediated mRNA decay (NMD) is of universal biological significance. It has emerged as an important global RNA, DNA and translation regulatory pathway. By systematically sequencing 737 genes (annotated in the...
3.
Field M, Tarpey P, Smith R, Edkins S, OMeara S, Stevens C, et al.
Am J Hum Genet
. 2007 Aug;
81(2):367-74.
PMID: 17668385
In the course of systematic screening of the X-chromosome coding sequences in 250 families with nonsyndromic X-linked mental retardation (XLMR), two families were identified with truncating mutations in BRWD3, a...
4.
Raymond F, Tarpey P, Edkins S, Tofts C, OMeara S, Teague J, et al.
Am J Hum Genet
. 2007 Apr;
80(5):982-7.
PMID: 17436253
We have identified one frameshift mutation, one splice-site mutation, and two missense mutations in highly conserved residues in ZDHHC9 at Xq26.1 in 4 of 250 families with X-linked mental retardation...
5.
Greenman C, Stephens P, Smith R, Dalgliesh G, Hunter C, Bignell G, et al.
Nature
. 2007 Mar;
446(7132):153-8.
PMID: 17344846
Cancers arise owing to mutations in a subset of genes that confer growth advantage. The availability of the human genome sequence led us to propose that systematic resequencing of cancer...
6.
Tarpey P, Raymond F, OMeara S, Edkins S, Teague J, Butler A, et al.
Am J Hum Genet
. 2007 Jan;
80(2):345-52.
PMID: 17236139
We have identified three truncating, two splice-site, and three missense variants at conserved amino acids in the CUL4B gene on Xq24 in 8 of 250 families with X-linked mental retardation...
7.
Tarpey P, Stevens C, Teague J, Edkins S, OMeara S, Avis T, et al.
Am J Hum Genet
. 2006 Dec;
79(6):1119-24.
PMID: 17186471
In a systematic sequencing screen of the coding exons of the X chromosome in 250 families with X-linked mental retardation (XLMR), we identified two nonsense mutations and one consensus splice-site...
8.
Ikediobi O, Davies H, Bignell G, Edkins S, Stevens C, OMeara S, et al.
Mol Cancer Ther
. 2006 Nov;
5(11):2606-12.
PMID: 17088437
The panel of 60 human cancer cell lines (the NCI-60) assembled by the National Cancer Institute for anticancer drug discovery is a widely used resource. The NCI-60 has been characterized...
9.
Hunter C, Smith R, Cahill D, Stephens P, Stevens C, Teague J, et al.
Cancer Res
. 2006 Apr;
66(8):3987-91.
PMID: 16618716
Malignant gliomas have a very poor prognosis. The current standard of care for these cancers consists of extended adjuvant treatment with the alkylating agent temozolomide after surgical resection and radiotherapy....
10.
Bignell G, Smith R, Hunter C, Stephens P, Davies H, Greenman C, et al.
Genes Chromosomes Cancer
. 2005 Sep;
45(1):42-6.
PMID: 16175573
The protein kinase gene family is the most frequently mutated in human cancer. Previous work has documented activating mutations in the KIT receptor tyrosine kinase in testicular germ-cell tumors (TGCT)....