Michael S Jackson
Overview
Explore the profile of Michael S Jackson including associated specialties, affiliations and a list of published articles.
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34
Citations
753
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Recent Articles
1.
Gallon R, Holt G, Alfailakawi W, Husain A, Jones C, Sowter P, et al.
Clin Exp Dermatol
. 2025 Jan;
PMID: 39847610
Background: One in five sebaceous tumour (ST) patients may have Lynch syndrome (LS), a hereditary cancer predisposition. LS patients benefit from cancer surveillance and prevention programmes and immunotherapy. Whilst universal...
2.
Vromman M, Anckaert J, Bortoluzzi S, Buratin A, Chen C, Chu Q, et al.
Nat Methods
. 2025 Jan;
22(2):448.
PMID: 39825083
No abstract available.
3.
Sowter P, Gallon R, Hayes C, Phelps R, Borthwick G, Prior S, et al.
Cancers (Basel)
. 2024 Dec;
16(23).
PMID: 39682157
Mismatch repair (MMR) deficiency can be indicative of Lynch syndrome (LS) and guide treatment with immune checkpoint inhibitors. Colorectal cancers (CRCs) and endometrial cancers (ECs) are routinely screened to identify...
4.
Gallon R, Herrero-Belmonte P, Phelps R, Hayes C, Sollars E, Egan D, et al.
BJC Rep
. 2024 Jul;
2(1):48.
PMID: 38962168
Background: Lynch syndrome (LS) is under-diagnosed. UK National Institute for Health and Care Excellence guidelines recommend multistep molecular testing of all colorectal cancers (CRCs) to screen for LS. However, the...
5.
Whittle B, Izuogu O, Lowes H, Deen D, Pyle A, Coxhead J, et al.
NPJ Parkinsons Dis
. 2024 Jan;
10(1):25.
PMID: 38245550
Neurodegeneration in Parkinson's disease (PD) precedes diagnosis by years. Early neurodegeneration may be reflected in RNA levels and measurable as a biomarker. Here, we present the largest quantification of whole...
6.
Vromman M, Anckaert J, Bortoluzzi S, Buratin A, Chen C, Chu Q, et al.
Nat Methods
. 2023 Jul;
20(8):1159-1169.
PMID: 37443337
The detection of circular RNA molecules (circRNAs) is typically based on short-read RNA sequencing data processed using computational tools. Numerous such tools have been developed, but a systematic comparison with...
7.
Rasmussen M, Sowter P, Gallon R, Durhuus J, Hayes C, Andersen O, et al.
Front Oncol
. 2023 May;
13:1147591.
PMID: 37143941
Introduction: Lynch syndrome-associated cancer develops due to germline pathogenic variants in one of the mismatch repair (MMR) genes, , , or . Somatic second hits in tumors cause MMR deficiency,...
8.
Gallon R, Phelps R, Hayes C, Brugieres L, Guerrini-Rousseau L, Colas C, et al.
Gastroenterology
. 2022 Dec;
164(4):579-592.e8.
PMID: 36586540
Background & Aims: Constitutional mismatch repair deficiency (CMMRD) is a rare recessive childhood cancer predisposition syndrome caused by germline mismatch repair variants. Constitutional microsatellite instability (cMSI) is a CMMRD diagnostic...
9.
Gallon R, Phelps R, Betts L, Hayes C, Masic D, Irving J, et al.
Leuk Lymphoma
. 2022 Oct;
64(1):217-220.
PMID: 36272172
No abstract available.
10.
Ahadova A, Witt J, Haupt S, Gallon R, Huneburg R, Nattermann J, et al.
Int J Cancer
. 2022 Oct;
152(10):2024-2031.
PMID: 36214792
Lynch syndrome (LS) is the most common inherited cancer syndrome. It is inherited via a monoallelic germline variant in one of the DNA mismatch repair (MMR) genes. LS carriers have...