Beverly Searle
Overview
Explore the profile of Beverly Searle including associated specialties, affiliations and a list of published articles.
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11
Citations
125
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Recent Articles
1.
Hill M, Ellard S, Fisher J, Fulop N, Knight M, Kroese M, et al.
NIHR Open Res
. 2023 Oct;
2:10.
PMID: 35935673
Background: Prenatal exome sequencing (ES) for the diagnosis of fetal anomalies was implemented nationally in England in October 2020 by the NHS Genomic Medicine Service (GMS). is the GMS is...
2.
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...
3.
Peter M, Hammond J, Sanderson S, Gurasashvili J, Hunter A, Searle B, et al.
Eur J Hum Genet
. 2022 Mar;
30(5):604-610.
PMID: 35264738
In this mixed methods study, a survey and in-depth interviews were used to explore whether decision regret and the psychological impact of receiving genome sequencing (GS) results differed between parents...
4.
Sanderson S, Lewis C, Hill M, Peter M, McEntagart M, Gale D, et al.
Genet Med
. 2021 Dec;
24(1):61-74.
PMID: 34906473
Purpose: The purpose of this study was to assess decisions, attitudes, and understanding of participants (patients, parents, relatives) having genome sequencing for rare disease diagnosis. Methods: This study involved a...
5.
Animation or leaflet: Does it make a difference when educating young people about genome sequencing?
Hammond J, Garner I, Hill M, Patch C, Hunter A, Searle B, et al.
Patient Educ Couns
. 2021 Mar;
104(10):2522-2530.
PMID: 33678496
Objective: To compare the effectiveness of an animation against two leaflets with and without images, in educating young people about genome sequencing (GS). Methods: An experimental survey with three assessment...
6.
Lewis C, Hammond J, Hill M, Searle B, Hunter A, Patch C, et al.
Eur J Med Genet
. 2020 Aug;
63(11):104043.
PMID: 32835846
Genome sequencing (GS) will have a profound impact on the diagnosis of rare and inherited diseases in children and young people. We conducted 27 semi-structured interviews with young people aged...
7.
Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study
Lewis C, Sanderson S, Hill M, Patch C, Searle B, Hunter A, et al.
Eur J Hum Genet
. 2020 Feb;
28(7):874-884.
PMID: 32001839
The 100,000 Genomes Project is a hybrid clinical and research project in which patients and parents are offered genome sequencing for cancer and rare and inherited disease diagnosis; all participants...
8.
Lewis C, Sanderson S, Hammond J, Hill M, Searle B, Hunter A, et al.
Eur J Hum Genet
. 2020 Jan;
28(7):896-906.
PMID: 31896776
Children and young people with rare and inherited diseases will be significant beneficiaries of genome sequencing. However, most educational resources are developed for adults. To address this gap in informational...
9.
Sanderson S, Hill M, Patch C, Searle B, Lewis C, Chitty L
BMJ Open
. 2019 Nov;
9(11):e029699.
PMID: 31685495
Objectives: Genome sequencing is poised to be incorporated into clinical care for diagnoses of rare diseases and some cancers in many parts of the world. Healthcare professionals are key stakeholders...
10.
Vasilevsky N, Foster E, Engelstad M, Carmody L, Might M, Chambers C, et al.
Nat Genet
. 2018 Apr;
50(4):474-476.
PMID: 29632381
No abstract available.