Jill Kilner
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Explore the profile of Jill Kilner including associated specialties, affiliations and a list of published articles.
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11
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82
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Recent Articles
1.
Hill C, Duffy S, Kettyle L, McGlynn L, Sandholm N, Salem R, et al.
Genes (Basel)
. 2023 May;
14(5).
PMID: 37239390
Diabetic kidney disease (DKD) represents a major global health problem. Accelerated ageing is a key feature of DKD and, therefore, characteristics of accelerated ageing may provide useful biomarkers or therapeutic...
2.
Smyth L, Kerr K, Kilner J, McGill A, Maxwell A, McKnight A
Kidney Int Rep
. 2023 Feb;
8(2):330-340.
PMID: 36815102
Introduction: Kidney transplantation remains the gold standard of treatment for end-stage renal disease (ESRD), with improved patient outcomes compared with dialysis. Epigenome-Wide Association Analysis (EWAS) of DNA methylation may identify...
3.
Smyth L, Dahlstrom E, Syreeni A, Kerr K, Kilner J, Doyle R, et al.
Nat Commun
. 2022 Dec;
13(1):7891.
PMID: 36550108
Type 1 diabetes affects over nine million individuals globally, with approximately 40% developing diabetic kidney disease. Emerging evidence suggests that epigenetic alterations, such as DNA methylation, are involved in diabetic...
4.
Kerr K, McKenna C, Heggarty S, Bailie C, McMullan J, Crowe A, et al.
Genes (Basel)
. 2022 Jul;
13(7).
PMID: 35885887
Background: The UK 100,000 Genomes Project was a transformational research project which facilitated whole genome sequencing (WGS) diagnostics for rare diseases. We evaluated experiences of introducing WGS in Northern Ireland,...
5.
Balachandar S, Graves T, Shimonty A, Kerr K, Kilner J, Xiao S, et al.
Am J Med Genet A
. 2021 Dec;
188(3):959-964.
PMID: 34904380
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant multisystemic vascular dysplasia, characterized by arteriovenous malformations (AVMs), mucocutaneous telangiectasia and nosebleeds. HHT is caused by a heterozygous null allele in ACVRL1,...
6.
Smyth L, Kerr K, Duffy S, Kilner J, McKnight A
Methods Mol Biol
. 2019 Nov;
2067:205-240.
PMID: 31701455
Multiple genetic strategies are available to help improve understanding of diabetic nephropathy. This methods chapter provides an overview of phenotype considerations specific to diabetic nephropathy and biobank essentials, and provides...
7.
Smyth L, Maxwell A, Benson K, Kilner J, Mckay G, McKnight A
BMC Res Notes
. 2018 Oct;
11(1):767.
PMID: 30373632
Objectives: Altered DNA methylation and microRNA profiles are associated with diabetic kidney disease. This study compared different sequencing approaches to define the genetic and epigenetic architecture of sequences surrounding microRNAs...
8.
Benson K, Chand S, Maxwell A, Smyth L, Kilner J, Borrows R, et al.
BMC Res Notes
. 2017 Jul;
10(1):348.
PMID: 28754147
Background: Biologically active vitamin D has an important regulatory role within the genome. It binds the vitamin D receptor (VDR) in order to control the expression of a wide range...
9.
Bailie C, Kilner J, Maxwell A, McKnight A
PLoS One
. 2017 Jun;
12(6):e0178321.
PMID: 28609449
Chronic kidney disease (CKD) has a prevalence of approximately 10% in adult populations. CKD can progress to end-stage renal disease (ESRD) and this is usually fatal unless some form of...
10.
Pettigrew K, McKnight A, Patterson C, Kilner J, Sadlier D, Maxwell A
J Hum Genet
. 2010 Mar;
55(4):248-51.
PMID: 20203694
Chemokine (C-C motif) ligand 5 (CCL5) and chemokine (C-C motif) receptor 5 are implicated in the pathogenesis of diabetic nephropathy (DN). We hypothesize that variants in these genes may be...