Andrew Whatmore
Overview
Explore the profile of Andrew Whatmore including associated specialties, affiliations and a list of published articles.
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13
Citations
130
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Recent Articles
1.
Morris T, Whatmore A, Hamilton L, Hird B, Kilpatrick E, Tetlow L, et al.
Endocr Connect
. 2024 Jan;
13(2).
PMID: 38165389
Children with salt-wasting adrenal insufficiency are managed with glucocorticoid and mineralocorticoid replacement. Measurement of renin activity or concentration alongside blood electrolyte levels is used to monitor the adequacy of mineralocorticoid...
2.
Garner T, Wangsaputra I, Whatmore A, Clayton P, Stevens A, Murray P
Front Endocrinol (Lausanne)
. 2023 Mar;
14:1026187.
PMID: 36864831
Background: Gene expression (GE) data have shown promise as a novel tool to aid in the diagnosis of childhood growth hormone deficiency (GHD) when comparing GHD children to normal children....
3.
Khan S, Whatmore A, Perchard R, Khan A, Vyas A, Dua J, et al.
Front Pediatr
. 2022 Aug;
10:900404.
PMID: 35928679
Importance: The links between maternal and offspring adiposity and metabolic status are well established. There is much less evidence for the impact of these relationships combined with ethnic background on...
4.
Role of Genotype and Expression in Growth and Response to Recombinant Human Growth Hormone Treatment
Parsons S, Stevens A, Whatmore A, Clayton P, Murray P
J Endocr Soc
. 2022 Feb;
6(3):bvac006.
PMID: 35178492
Context: Single-nucleotide polymorphisms (SNPs) in have been associated with idiopathic short stature (ISS) and adult height. Objective: This study sought to (a) characterize the phenotype of ISS patients and their...
5.
Perchard R, Murray P, Payton A, Highton G, Whatmore A, Clayton P
J Endocr Soc
. 2020 Sep;
4(10):bvaa105.
PMID: 32939436
Background: Children with short stature of undefined aetiology (SS-UA) may have undiagnosed genetic conditions. Purpose: To identify mutations causing short stature (SS) and genes related to SS, using candidate gene...
6.
Murray P, Butcher I, Dunn W, Stevens A, Perchard R, Hanson D, et al.
Pediatr Res
. 2016 Apr;
80(2):299-305.
PMID: 27057740
Background: Later life metabolic dysfunction is a well-recognized consequence of being born small for gestational age (SGA). This study has applied metabolomics to identify whether there are changes in these...
7.
Wilcock A, Begley P, Stevens A, Whatmore A, Victor S
J Matern Fetal Neonatal Med
. 2015 Mar;
29(5):758-62.
PMID: 25786474
Objective: No single diagnostic investigation is currently available for necrotising enterocolitis (NEC). We implemented a novel, untargeted, exploratory study to determine whether metabolomics can reveal early biomarker(s) of NEC. The...
8.
Patel L, Whatmore A, Davies J, Bansal N, Vyas A, Gemmell I, et al.
Horm Res Paediatr
. 2013 Nov;
81(2):109-17.
PMID: 24281388
Aims: To study the effect of the insulin-like growth factor (IGF) system on growth, adiposity and systolic blood pressure (SBP) in early life in British-born South Asian (SA) and White...
9.
Stevens A, De Leonibus C, Hanson D, Whatmore A, Murray P, Donn R, et al.
Pharmacogenomics
. 2013 Nov;
14(15):1889-905.
PMID: 24236488
The advances in high-throughput genomic technologies have improved the understanding of disease pathophysiology and have allowed a better characterization of drug response and toxicity based on individual genetic make up....
10.
Stevens A, Hanson D, Whatmore A, Destenaves B, Chatelain P, Clayton P
BMC Genomics
. 2013 Aug;
14:547.
PMID: 23941278
Background: A co-ordinated tissue-independent gene expression profile associated with growth is present in rodent models and this is hypothesised to extend to all mammals. Growth in humans has similarities to...