Murray P - Search Results

1

Gene Expression Signatures Predict First-Year Response to Somapacitan Treatment in Children With Growth Hormone Deficiency.

Garner T, Clayton P, Højby M, Murray P, Stevens A. Garner T, et al. Among authors: murray p. J Clin Endocrinol Metab. 2024 Apr 19;109(5):1214-1221. doi: 10.1210/clinem/dgad717. J Clin Endocrinol Metab. 2024. PMID: 38066644 Free PMC article. Clinical Trial.

2

Diagnosis of childhood and adolescent growth hormone deficiency using transcriptomic data.

Garner T, Wangsaputra I, Whatmore A, Clayton PE, Stevens A, Murray PG. Garner T, et al. Front Endocrinol (Lausanne). 2023 Feb 14;14:1026187. doi: 10.3389/fendo.2023.1026187. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36864831 Free PMC article.

3

Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary gland.

Murray PG, Hague C, Fafoula O, Gleeson H, Patel L, Banerjee I, Raabe AL, Hall CM, Wright NB, Amin R, Clayton PE. Murray PG, et al. Clin Endocrinol (Oxf). 2009 Aug;71(2):215-9. doi: 10.1111/j.1365-2265.2009.03554.x. Epub 2009 Feb 18. Clin Endocrinol (Oxf). 2009. PMID: 19226266

4

Growth hormone, the insulin-like growth factor axis, insulin and cancer risk.

Clayton PE, Banerjee I, Murray PG, Renehan AG. Clayton PE, et al. Nat Rev Endocrinol. 2011 Jan;7(1):11-24. doi: 10.1038/nrendo.2010.171. Epub 2010 Oct 19. Nat Rev Endocrinol. 2011. PMID: 20956999 Review.

5

Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination.

Clayton PE, Hanson D, Magee L, Murray PG, Saunders E, Abu-Amero SN, Moore GE, Black GC. Clayton PE, et al. Clin Endocrinol (Oxf). 2012 Sep;77(3):335-42. doi: 10.1111/j.1365-2265.2012.04428.x. Clin Endocrinol (Oxf). 2012. PMID: 22624670 Review.

6

Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study.

Stevens A, Murray P, Wojcik J, Raelson J, Koledova E, Chatelain P, Clayton P; PREDICT Investigator Group. Stevens A, et al. Among authors: murray p. Eur J Endocrinol. 2016 Dec;175(6):633-643. doi: 10.1530/EJE-16-0357. Epub 2016 Sep 20. Eur J Endocrinol. 2016. PMID: 27651465 Free PMC article.

7

A genetic approach to evaluation of short stature of undetermined cause.

Murray PG, Clayton PE, Chernausek SD. Murray PG, et al. Lancet Diabetes Endocrinol. 2018 Jul;6(7):564-574. doi: 10.1016/S2213-8587(18)30034-2. Epub 2018 Feb 1. Lancet Diabetes Endocrinol. 2018. PMID: 29397377 Review.

8

Transcriptomics and machine learning predict diagnosis and severity of growth hormone deficiency.

Murray PG, Stevens A, De Leonibus C, Koledova E, Chatelain P, Clayton PE. Murray PG, et al. JCI Insight. 2018 Apr 5;3(7):e93247. doi: 10.1172/jci.insight.93247. eCollection 2018 Apr 5. JCI Insight. 2018. PMID: 29618660 Free PMC article. Clinical Trial.

9

The in vitro functional analysis of single-nucleotide polymorphisms associated with growth hormone (GH) response in children with GH deficiency.

De Leonibus C, Murray P, Garner T, Hanson D, Clayton P, Stevens A. De Leonibus C, et al. Among authors: murray p. Pharmacogenomics J. 2019 Apr;19(2):200-210. doi: 10.1038/s41397-018-0026-4. Epub 2018 Jun 1. Pharmacogenomics J. 2019. PMID: 29855605

10

Gene expression signatures predict response to therapy with growth hormone.

Stevens A, Murray P, De Leonibus C, Garner T, Koledova E, Ambler G, Kapelari K, Binder G, Maghnie M, Zucchini S, Bashnina E, Skorodok J, Yeste D, Belgorosky A, Siguero JL, Coutant R, Vangsøy-Hansen E, Hagenäs L, Dahlgren J, Deal C, Chatelain P, Clayton P. Stevens A, et al. Among authors: murray p. Pharmacogenomics J. 2021 Oct;21(5):594-607. doi: 10.1038/s41397-021-00237-5. Epub 2021 May 27. Pharmacogenomics J. 2021. PMID: 34045667 Free PMC article. Clinical Trial.

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