Brian Shand
Overview
Explore the profile of Brian Shand including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
87
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0
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Recent Articles
1.
Loong L, Huntley C, Pethick J, McRonald F, Santaniello F, Shand B, et al.
J Med Genet
. 2024 Oct;
61(12):1080-1088.
PMID: 39433398
Background: For female patients with Lynch syndrome (LS), endometrial cancer (EC) is often their first cancer diagnosis. A testing pathway of somatic tumour testing triage followed by germline mismatch repair...
2.
McRonald F, Pethick J, Santaniello F, Shand B, Tyson A, Tulloch O, et al.
Eur J Hum Genet
. 2024 Feb;
32(5):529-538.
PMID: 38355963
It is believed that >95% of people with Lynch syndrome (LS) remain undiagnosed. Within the National Health Service (NHS) in England, formal guidelines issued in 2017 state that all colorectal...
3.
Loong L, Huntley C, McRonald F, Santaniello F, Pethick J, Torr B, et al.
J Med Genet
. 2022 Dec;
60(7):669-678.
PMID: 36572524
Objective: To describe national patterns of National Health Service (NHS) analysis of mismatch repair (MMR) genes in England using individual-level data submitted to the National Disease Registration Service (NDRS) by...
4.
Henson K, Brock R, Shand B, Coupland V, Elliss-Brookes L, Lyratzopoulos G, et al.
BMJ Open
. 2018 Jul;
8(7):e020980.
PMID: 29991628
Purpose: The linked prescriptions cancer registry data resource was set up to extend our understanding of the pathway for patients with cancer past secondary care into the community, to ultimately...
5.
Swann R, McPhail S, Witt J, Shand B, Abel G, Hiom S, et al.
Br J Gen Pract
. 2017 Dec;
68(666):e63-e72.
PMID: 29255111
Background: Continual improvements in diagnostic processes are needed to minimise the proportion of patients with cancer who experience diagnostic delays. Clinical audit is a means of achieving this. Aim: To...