Lucy Loong
Overview
Explore the profile of Lucy Loong including associated specialties, affiliations and a list of published articles.
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14
Citations
107
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Recent Articles
1.
Hassan H, Rahman T, Bacon A, Knott C, Allen I, Huntley C, et al.
BMJ Oncol
. 2025 Mar;
4(1):e000574.
PMID: 40046828
Objectives: To investigate the association between bilateral salpingo-oophorectomy (BSO) and long-term health outcomes in women with a personal history of breast cancer. Methods And Analysis: We used data on women...
2.
Allen I, Hassan H, Walburga Y, Huntley C, Loong L, Rahman T, et al.
J Clin Oncol
. 2024 Oct;
43(6):651-661.
PMID: 39475295
Purpose: Second primary cancer (SPC) risks after breast cancer (BC) in pathogenic variant (PV) carriers are uncertain. We estimated relative and absolute risks using a novel linkage of genetic testing...
3.
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...
4.
Allen I, Hassan H, Joko-Fru W, Huntley C, Loong L, Rahman T, et al.
Lancet Reg Health Eur
. 2024 May;
40:100903.
PMID: 38745989
Background: Second primary cancers (SPCs) after breast cancer (BC) present an increasing public health burden, with little existing research on socio-demographic, tumour, and treatment effects. We addressed this in the...
5.
Huntley C, Loong L, Mallinson C, Bethell R, Rahman T, Alhaddad N, et al.
EClinicalMedicine
. 2024 Feb;
69:102465.
PMID: 38356732
Background: Lynch Syndrome (LS) is a cancer predisposition syndrome caused by constitutional pathogenic variants in the mismatch repair (MMR) genes. To date, fragmentation of clinical and genomic data has restricted...
6.
Allen S, Loong L, Garrett A, Torr B, Durkie M, Drummond J, et al.
J Med Genet
. 2023 Dec;
61(4):305-312.
PMID: 38154813
Background: National and international amalgamation of genomic data offers opportunity for research and audit, including analyses enabling improved classification of variants of uncertain significance. Review of individual-level data from National...
7.
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...
8.
Hanson H, Kulkarni A, Loong L, Kavanaugh G, Torr B, Allen S, et al.
J Med Genet
. 2022 Nov;
60(5):417-429.
PMID: 36411032
Germline pathogenic variants (GPVs) in the cancer predisposition genes , , , , , , , and are identified in approximately 15% of patients with ovarian cancer (OC). While there...
9.
Loong L, Tardivo A, Knaus A, Hashim M, Pagnamenta A, Alt K, et al.
Genet Med
. 2022 Nov;
25(1):37-48.
PMID: 36322149
Purpose: Biallelic PIGN variants have been described in Fryns syndrome, multiple congenital anomalies-hypotonia-seizure syndrome (MCAHS), and neurologic phenotypes. The full spectrum of clinical manifestations in relation to the genotypes is...
10.
Torr B, Jones C, Choi S, Allen S, Kavanaugh G, Hamill M, et al.
J Med Genet
. 2022 Jul;
59(12):1179-1188.
PMID: 35868849
Background: Germline genetic testing affords multiple opportunities for women with breast cancer, however, current UK NHS models for delivery of germline genetic testing are clinician-intensive and only a minority of...