Publications by authors named "Kate Everett"

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A randomized controlled trial of a trauma-informed smartphone application in reducing firefighters' mental health symptoms.
Tracey Varker, Olivia Metcalf, Yee Foong Mok, Karen E Lamb, Julia Fredrickson, Kate Everett

NPJ Digit Med· November 2025

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Workplace mental health screening for first responders: cluster-randomised control trial.
Aimee Gayed, Karen Krakue, Jessica Strudwick, Andrew Mackinnon, Alison Donohoe, Kate Everett

Br J Psychiatry· August 2025

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Presacral malakoplakia presenting as foot drop: a case report.
Tom A Yates, Katie Devlin, Abed Arnaout, William Hurt, Neil Stone, Kate V Everett

J Med Case Rep· April 2023

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Rare coding variants in genes encoding GABA receptors in genetic generalised epilepsies: an exome-based case-control study.
Patrick May, Simon Girard, Merle Harrer, Dheeraj R Bobbili, Julian Schubert, Kate Everett

Lancet Neurol· August 2018

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A novel missense mutation in the transcription factor FOXF1 cosegregating with infantile hypertrophic pyloric stenosis in the extended pedigree linked to IHPS5 on chromosome 16q24.
Kate V Everett, Paris Ataliotis, Barry A Chioza, Charles Shaw-Smith, Eddie M K Chung

Pediatr Res· April 2017

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The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family.
Nuha Alrayes, Hussein Sheikh Ali Mohamoud, Saleem Ahmed, Mona Mohammad Almramhi, Taghreed Mohammad Shuaib, Kate Everett

J Neurol Sci· April 2016

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Analysis of rare copy number variation in absence epilepsies.
Laura Addis, Richard E Rosch, Antonio Valentin, Andrew Makoff, Robert Robinson, Kate V Everett

Neurol Genet· April 2016

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Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5.
Kate V Everett, Eddie M K Chung

J Hum Genet· April 2013

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Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Hum Mol Genet· December 2012

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Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.

Epilepsia· February 2012

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Transient receptor potential genes and human inherited disease.
Kate V Everett

Adv Exp Med Biol· July 2011

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Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing.
Kate V Everett, Barry A Chioza, Christina Georgoula, Ashley Reece, R Mark Gardiner

Hum Genet· December 2009

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Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.
Barry A Chioza, Jean Aicardi, Harald Aschauer, Oebele Brouwer, Petra Callenbach, Kate V Everett

Epilepsy Res· December 2009

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Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24.
Kate V Everett, Francesca Capon, Christina Georgoula, Barry A Chioza, Ashley Reece

Eur J Hum Genet· September 2008

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Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23.
Kate V Everett, Barry A Chioza, Christina Georgoula, Ashley Reece, Francesca Capon

Am J Hum Genet· March 2008

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Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
Kate Everett, Barry Chioza, Jean Aicardi, Harald Aschauer, Oebele Brouwer

Epilepsy Res· July 2007

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Linkage and association analysis of CACNG3 in childhood absence epilepsy.
Kate V Everett, Barry Chioza, Jean Aicardi, Harald Aschauer, Oebele Brouwer

Eur J Hum Genet· April 2007

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Evaluation of CACNA1H in European patients with childhood absence epilepsy.
Barry Chioza, Kate Everett, Harald Aschauer, Oebele Brouwer, Petra Callenbach

Epilepsy Res· May 2006

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