Kate V Everett
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Explore the profile of Kate V Everett including associated specialties, affiliations and a list of published articles.
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12
Citations
184
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Recent Articles
1.
Yates T, Devlin K, Arnaout A, Hurt W, Stone N, Everett K, et al.
J Med Case Rep
. 2023 Apr;
17(1):154.
PMID: 37024963
Background: Malakoplakia is a rare condition characterized by inflammatory masses with specific histological characteristics. These soft tissue masses can mimic tumors and tend to develop in association with chronic or...
2.
Everett K, Ataliotis P, Chioza B, Shaw-Smith C, Chung E
Pediatr Res
. 2016 Nov;
81(4):632-638.
PMID: 27855150
Background: The aim was to identify susceptibility alleles for infantile hypertrophic pyloric stenosis (IHPS) in a pedigree previously linked to IHPS5 on chromosome 16q24. Methods: We screened the positional and...
3.
Addis L, Rosch R, Valentin A, Makoff A, Robinson R, Everett K, et al.
Neurol Genet
. 2016 Apr;
2(2):e56.
PMID: 27123475
Objective: To identify shared genes and pathways between common absence epilepsy (AE) subtypes (childhood absence epilepsy [CAE], juvenile absence epilepsy [JAE], and unclassified absence epilepsy [UAE]) that may indicate common...
4.
Everett K, Chung E
J Hum Genet
. 2013 Feb;
58(4):236-7.
PMID: 23426030
Infantile hypertrophic pyloric stenosis (IHPS) is a multifactorial heritable condition affecting infants in the first 3 months of life. It is characterized by hypertrophy of the pylorus resulting in blockage...
5.
Steffens M, Leu C, Ruppert A, Zara F, Striano P, Robbiano A, et al.
Hum Mol Genet
. 2012 Sep;
21(24):5359-72.
PMID: 22949513
Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% and account for 20-30% of all epilepsies. Despite their high heritability of 80%, the genetic factors predisposing to GGEs remain...
6.
Leu C, de Kovel C, Zara F, Striano P, Pezzella M, Robbiano A, et al.
Epilepsia
. 2012 Jan;
53(2):308-18.
PMID: 22242659
Purpose: Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% with heritability estimates of 80%. A considerable proportion of families with siblings affected by GGEs presumably display an oligogenic...
7.
Everett K
Adv Exp Med Biol
. 2011 Feb;
704:1011-32.
PMID: 21290338
Transient receptor potential (TRP) genes have been implicated in a wide array of human disorders, from cancers to bipolar disorder. The extraordinary range of diseases in whose pathogenesis they may...
8.
Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, et al.
Epilepsy Res
. 2009 Oct;
87(2-3):247-55.
PMID: 19837565
Childhood absence epilepsy (CAE) is an idiopathic generalised epilepsy (IGE) characterised by typical absence seizures manifested by transitory loss of awareness with 2.5-4 Hz spike-wave complexes on ictal EEG. A...
9.
Everett K, Chioza B, Georgoula C, Reece A, Gardiner R, Chung E
Hum Genet
. 2009 Aug;
126(6):819-31.
PMID: 19701773
Infantile hypertrophic pyloric stenosis (IHPS) is the most common inherited form of gastrointestinal obstruction in infancy with a striking male preponderance. Infants present with vomiting due to gastric outlet obstruction...
10.
Everett K, Capon F, Georgoula C, Chioza B, Reece A, Jaswon M, et al.
Eur J Hum Genet
. 2008 May;
16(9):1151-4.
PMID: 18478043
Infantile hypertrophic pyloric stenosis (IHPS) is the most common inherited form of gastrointestinal obstruction in infancy. The disease is considered a paradigm for the sex-modified model of multifactorial inheritance and...