Amanda Moore
Overview
Explore the profile of Amanda Moore including associated specialties, affiliations and a list of published articles.
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42
Citations
482
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Recent Articles
1.
Jarvis J, Chertavian E, Buessing M, Renteria T, Tu L, Hoffer L, et al.
Orphanet J Rare Dis
. 2025 Feb;
20(1):82.
PMID: 39985061
Background: Angelman syndrome (AS) is a rare neurogenetic disorder characterized by persistent cognitive and functional impairments that necessitate lifelong care. Caring for individuals with AS leads to substantial household costs,...
2.
Gomes A, Moore A, Cross M, Hardesty C, David K, Sampedro M, et al.
Am J Med Genet A
. 2024 Dec;
197(4):e63961.
PMID: 39679858
Angelman syndrome (AS) is a severe genetic neurodevelopmental disorder with an estimated prevalence of 1:20,000. Life expectancy appears to be normal, however, data regarding lifespan in AS are scarce. Until...
3.
Palmer S, Amorim Adegboye A, Hooper G, Khan A, Leech C, Moore A, et al.
AEM Educ Train
. 2024 Nov;
8(6):e11047.
PMID: 39583083
Background: Emergency medicine (EM) is a uniquely stressful environment in which leadership training could improve individual and team performance, patient outcomes, well-being, and EM career intentions. The primary aim was...
4.
Goering M, Moore A, Barker-Kamps M, Patki A, Tiwari H, Mrug S
Dev Psychol
. 2024 Nov;
PMID: 39531697
Prosocial behavior during adolescence has been associated with better physical health, including slower epigenetic aging. However, little is known about the specific role of empathy in epigenetic aging and the...
5.
Arganbright J, Crowley T, Tracy M, Noel-MacDonnell J, Gaiser K, Yaktine L, et al.
Laryngoscope
. 2024 Sep;
135(2):929-934.
PMID: 39305214
Objectives: Hearing loss is considered common in children with 22q11.2 deletion syndrome (22q11.2DS), with a few prior studies reporting a 32%-78% prevalence; mild-moderate conductive hearing loss has been reported most...
6.
Kneafsey R, Moore A, Palmer S, Szczepura A, Hooper G, Leech C, et al.
Emerg Med J
. 2024 Jul;
41(9):543-550.
PMID: 39009425
Background: Emergency medicine (EM) consultants are expected to provide leadership to facilitate optimal clinical results, effective teamwork and learning. To foster leadership skills, the Emergency Medicine Leadership Programme (EMLeaders) was...
7.
Moore T, Lancaster A, Nelson J, Sanders J, Johnson M, Moore A, et al.
MMWR Morb Mortal Wkly Rep
. 2024 Jun;
73(25):581-582.
PMID: 38935566
No abstract available.
8.
Potter S, Reynolds E, Okoniewski K, Edwards A, Gable J, Hill C, et al.
Ther Adv Rare Dis
. 2024 May;
5:26330040241254122.
PMID: 38808315
Angelman syndrome (AS) and duplication 15q (dup15q) syndrome are rare neurogenetic conditions arising from a common locus on the long arm of chromosome 15. Individuals with both conditions share some...
9.
Wheeler A, Gantz M, Cope H, Strong T, Bohonowych J, Moore A, et al.
J Neurodev Disord
. 2023 Nov;
15(1):37.
PMID: 37936142
Objective: The objective of this study was to identify the age of diagnosis for children with one of three neurogenetic conditions resulting from changes in chromosome 15 (Angelman syndrome [AS],...
10.
Wang K, Moore A, Grayson C, Mailloux R
Free Radic Biol Med
. 2023 May;
204:287-300.
PMID: 37225107
Pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase (KGDH) are vital sources of hydrogen peroxide (HO) and key sites for redox regulation. Here, we report KGDH is more sensitive to inhibition by...