Kate V. Everett
St George's University Of London
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Presacral malakoplakia presenting as foot drop: a case report.
Journal: Journal of medical case reports
Published: January 27, 2022
mGlu3 Metabotropic Glutamate Receptors as a Target for the Treatment of Absence Epilepsy: Preclinical and Human Genetics Data.
Journal: Current neuropharmacology
Published: January 13, 2022
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.
Journal: The Lancet. Neurology
Published: August 02, 2017
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.
Journal: Pediatric research
Published: June 13, 2016
The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family.
Journal: Journal of the neurological sciences
Published: November 30, 2015
Analysis of rare copy number variation in absence epilepsies.
Journal: Neurology. Genetics
Published: August 31, 2015
Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5.
Journal: Journal of human genetics
Published: February 22, 2013
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Journal: Human molecular genetics
Published: September 06, 2012
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Last Updated: 09/26/2026