K Colclough
Overview
Explore the profile of K Colclough including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
14
Citations
782
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Reilly F, Sanchez-Lechuga B, Clinton S, Crowe G, Burke M, Ng N, et al.
Diabet Med
. 2019 Sep;
37(5):876-884.
PMID: 31562829
Aims: To examine the phenotypic features of people identified with ABCC8-maturity-onset diabetes of the young (MODY) who were included in the adult 'Mater MODY' cohort and to establish their response...
2.
Yaghootkar H, Abbasi F, Ghaemi N, Rabbani A, Wakeling M, Eshraghi P, et al.
Diabet Med
. 2019 Jul;
36(12):1694-1702.
PMID: 31276222
Aim: To examine the extent to which discriminatory testing using antibodies and Type 1 diabetes genetic risk score, validated in European populations, is applicable in a non-European population. Methods: We...
3.
Patel K, Oram R, Flanagan S, De Franco E, Colclough K, Shepherd M, et al.
Diabetes
. 2016 May;
65(7):2094-2099.
PMID: 27207547
Distinguishing patients with monogenic diabetes from those with type 1 diabetes (T1D) is important for correct diagnosis, treatment, and selection of patients for gene discovery studies. We assessed whether a...
4.
Yew T, McCreight L, Colclough K, Ellard S, Pearson E
Diabet Med
. 2015 Nov;
33(9):e21-5.
PMID: 26526202
Background: A syndrome of young-onset diabetes mellitus associated with microcephaly, epilepsy and intellectual disability caused by mutations in the tRNA methyltransferase 10 homologue A (TRMT10A) gene has recently been described....
5.
Bacon S, Kyithar M, Rizvi S, Donnelly E, McCarthy A, Burke M, et al.
Diabet Med
. 2015 Oct;
33(7):976-84.
PMID: 26479152
Aims: HNF1A gene mutations are the most common cause of maturity-onset diabetes of the young (MODY) in the UK. Persons with HNF1A-MODY display sensitivity to sulphonylurea therapy; however, the long-term...
6.
Shepherd M, Colclough K, Ellard S, Hattersley A
Clin Med (Lond)
. 2014 Apr;
14(2):117-21.
PMID: 24715120
Increasing technological advances have resulted in the recognition of a range of genetic conditions not traditionally seen by clinical genetics teams. This has implications for the education of other healthcare...
7.
Ellard S, Lango Allen H, De Franco E, Flanagan S, Hysenaj G, Colclough K, et al.
Diabetologia
. 2013 Jun;
56(9):1958-63.
PMID: 23771172
Aims/hypothesis: Current genetic tests for diagnosing monogenic diabetes rely on selection of the appropriate gene for analysis according to the patient's phenotype. Next-generation sequencing enables the simultaneous analysis of multiple...
8.
Thanabalasingham G, Kaur K, Talbot F, Colclough K, Mathews A, Taylor J, et al.
Diabet Med
. 2013 Apr;
30(8):e233-8.
PMID: 23586928
Background: Maturity-onset diabetes of the young (MODY) caused by heterozygous mutations in the glucokinase (GCK) gene typically presents with lifelong, stable, mild fasting hyperglycaemia. With the exception of pregnancy, patients...
9.
Kyithar M, Bacon S, Pannu K, Rizvi S, Colclough K, Ellard S, et al.
Diabetes Metab
. 2011 Jun;
37(6):512-9.
PMID: 21683639
Aim: The prevalence of hepatocyte nuclear factor (HNF)-1A and HNF4A mutations, and the clinical implications following the genetic diagnosis of maturity-onset diabetes of the young (MODY) in the Irish population,...
10.
McDonald T, Colclough K, Brown R, Shields B, Shepherd M, Bingley P, et al.
Diabet Med
. 2011 Mar;
28(9):1028-33.
PMID: 21395678
Aim: Maturity-onset diabetes of the young is a monogenic form of familial, young-onset diabetes. It is rare (∼1% diabetes) and may be misdiagnosed as Type 1 diabetes and inappropriately treated...