Publications by authors named "Janet Perry"

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Multidrug-Resistant pESI-Harboring Salmonella enterica Serovar Muenchen Sequence Type 82 in Poultry and Humans, Israel, 2020-2023.
Janet Perry, Tal Rakler, Katya Arnold, Anat Wiseman, Cinthia Satuchne

Emerg Infect Dis· October 2025

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Accumulation of resistance genes in Typhimurium transmitted between poultry and dairy farms increases the risk to public health.
Janet Perry, Katya Arnold, Cinthia Satuchne, Ori Koren, Gaby Kenigswald

Appl Environ Microbiol· June 2024

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Identification of gene expression-based prognostic markers in the hematopoietic stem cells of patients with myelodysplastic syndromes.
Andrea Pellagatti, Axel Benner, Ken I Mills, Mario Cazzola, Aristoteles Giagounidis, Janet Perry

J Clin Oncol· October 2013

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Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome.
Andrea Pellagatti, Mario Cazzola, Aristoteles Giagounidis, Janet Perry, Luca Malcovati

Br J Haematol· October 2011

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Haploinsufficiency of RPS14 in 5q- syndrome is associated with deregulation of ribosomal- and translation-related genes.
Andrea Pellagatti, Eva Hellström-Lindberg, Aristoteles Giagounidis, Janet Perry, Luca Malcovati

Br J Haematol· July 2008

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Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution.
Graham R Bignell, Thomas Santarius, Jessica C M Pole, Adam P Butler, Janet Perry

Genome Res· September 2007

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Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
Patrick S Tarpey, F Lucy Raymond, Lam S Nguyen, Jayson Rodriguez, Anna Hackett, Janet Perry

Nat Genet· September 2007

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Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.
Michael Field, Patrick S Tarpey, Raffaella Smith, Sarah Edkins, Sarah O'Meara, Janet Perry

Am J Hum Genet· August 2007

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Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.
F Lucy Raymond, Patrick S Tarpey, Sarah Edkins, Calli Tofts, Sarah O'Meara, Janet Perry

Am J Hum Genet· May 2007

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Patterns of somatic mutation in human cancer genomes.
Christopher Greenman, Philip Stephens, Raffaella Smith, Gillian L Dalgliesh, Christopher Hunter, Janet Perry

Nature· March 2007

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Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
Patrick S Tarpey, F Lucy Raymond, Sarah O'Meara, Sarah Edkins, Jon Teague, Janet Perry

Am J Hum Genet· February 2007

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Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.
Patrick S Tarpey, Claire Stevens, Jon Teague, Sarah Edkins, Sarah O'Meara, Janet Perry

Am J Hum Genet· December 2006

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Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.
Ogechi N Ikediobi, Helen Davies, Graham Bignell, Sarah Edkins, Claire Stevens, Janet Perry

Mol Cancer Ther· November 2006

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A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy.
Chris Hunter, Raffaella Smith, Daniel P Cahill, Philip Stephens, Claire Stevens, Janet Perry

Cancer Res· April 2006

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Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults.
Graham Bignell, Raffaella Smith, Chris Hunter, Philip Stephens, Helen Davies, Janet Perry

Genes Chromosomes Cancer· January 2006

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Somatic mutations of the protein kinase gene family in human lung cancer.
Helen Davies, Chris Hunter, Raffaella Smith, Philip Stephens, Chris Greenman, Janet Perry

Cancer Res· September 2005

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A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer.
Philip Stephens, Sarah Edkins, Helen Davies, Chris Greenman, Charles Cox, Janet Perry

Nat Genet· June 2005

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Lung cancer: intragenic ERBB2 kinase mutations in tumours.
Philip Stephens, Chris Hunter, Graham Bignell, Sarah Edkins, Helen Davies, Janet Perry

Nature· September 2004

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