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Molecular and Cellular Endocrinology|October 28, 2008
Growth hormone (GH1) gene variation and the growth hormone receptor (GHR) exon 3 deletion polymorphism in a West-African populationDavid S Millar, Mark D Lewis, Martin Horan, et al.American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.Human Mutation|September 19, 2008
A gene conversion hotspot in the human growth hormone (GH1) gene promoterAndreas Wolf, David S Millar, Amke Caliebe, et al.Human Genetics|March 31, 2006
Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and strokeMartin Horan, Vicky Newsway, Yasmin, et al.Human Mutation|March 26, 2003
Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short statureDavid S Millar, Mark D Lewis, Martin Horan, et al.The Journal of Clinical Endocrinology and Metabolism|March 6, 2004
A novel dysfunctional growth hormone variant (Ile179Met) exhibits a decreased ability to activate the extracellular signal-regulated kinase pathwayMark D Lewis, Martin Horan, David S Millar, et al.Science Translational Medicine|July 10, 2020
Cyclin-dependent-like kinase 5 is required for pain signaling in human sensory neurons and mouse modelsPaolo La Montanara, Arnau Hervera, Lucas L Baltussen, et al.Pageof 4