Amy Hunter
Overview
Explore the profile of Amy Hunter including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
30
Citations
264
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Salmela K, Curtis L, Hunter A, Aron E
Child Adolesc Psychiatr Clin N Am
. 2025 Mar;
34(2):363-374.
PMID: 40044273
Infant and early childhood mental health (IECMH) is an important field within psychiatry and related disciplines. Historically, IECMH has been absent from mental health training and curricula. However, evidence shows...
2.
Morris S, Walton H, Simpson A, Leeson-Beevers K, Bloom L, Hunter A, et al.
Orphanet J Rare Dis
. 2024 Sep;
19(1):332.
PMID: 39252123
Background: Evidence suggests that coordination of care for people affected by rare diseases is poor. In order to improve the way that care is coordinated it is necessary to understand...
3.
Faye F, Crocione C, Anido de Pena R, Bellagambi S, Escati Penaloza L, Hunter A, et al.
Eur J Hum Genet
. 2024 May;
32(9):1116-1126.
PMID: 38755315
Timely diagnosis is one of the most serious challenges faced by people living with a rare disease (PLWRD), and this study estimates that in Europe, the average total diagnosis time...
4.
Jones J, Cruddas M, Simpson A, Meade N, Pushparajah D, Peter M, et al.
Orphanet J Rare Dis
. 2024 Feb;
19(1):77.
PMID: 38373961
Background: Although individually rare, collectively, rare conditions are common and affect a large number of people and are often chronic, life threatening and affect multiple body systems; the majority of...
5.
Walton H, Ng P, Simpson A, Bloom L, Chitty L, Fulop N, et al.
Orphanet J Rare Dis
. 2023 Nov;
18(1):364.
PMID: 37996938
Background: Poorly coordinated care can have major impacts on patients and families affected by rare conditions, with negative physical health, psychosocial and financial consequences. This study aimed to understand how...
6.
Peter M, Hammond J, Sanderson S, Gurasashvili J, Hunter A, Searle B, et al.
Eur J Hum Genet
. 2023 Oct;
31(12):1407-1413.
PMID: 37789083
We used cross-sectional surveys to compare the knowledge, attitudes, and decision regret of participants who had consented for genome sequencing (GS) for rare disease diagnosis in the 100,000 Genomes Project...
7.
Costa A, Frankova V, Robert G, Macek M, Patch C, Alexander E, et al.
J Community Genet
. 2022 Jun;
13(3):365-369.
PMID: 35773560
No abstract available.
8.
Spencer-Tansley R, Meade N, Ali F, Simpson A, Hunter A
BMC Health Serv Res
. 2022 May;
22(1):648.
PMID: 35568910
Background: Rare disease patients and carers report significant impacts on mental health but studies on UK populations have focussed on relatively few, specific conditions. Collectively rare conditions represent a substantial...
9.
Thomas R, Hunter A, Butterworth L, Feeney C, Graves T, Holmes S, et al.
J Inherit Metab Dis
. 2022 May;
45(4):796-803.
PMID: 35543492
Primary mitochondrial disorders encompass a wide range of clinical presentations and a spectrum of severity. They currently lack effective disease-modifying therapies and have a high mortality and morbidity rate. It...
10.
Costa A, Frankova V, Robert G, Macek M, Patch C, Alexander E, et al.
J Community Genet
. 2022 May;
13(3):313-327.
PMID: 35523996
The communication of genomic results to patients and families with rare diseases raise distinctive challenges. However, there is little evidence about optimal methods to communicate results to this group of...