Timothy Cheetham

Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study

Donato Iacovazzo, Richard Caswell, Benjamin Bunce et al. · Acta Neuropathologica Communications · 2016 · 131 citations · Full text

Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency

Kyriaki S. Alatzoglou, James Turton, Daniel Kelberman et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 121 citations

Catch-up growth and metabolic outcomes in adolescents born preterm

Nicholas D. Embleton, Murthy Korada, Claire Wood et al. · Archives of Disease in Childhood · 2016 · 121 citations

Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility

Alison Sutherland, Jocelyn Davies, Catherine Owen et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 113 citations · Full text

GnRH-Deficient Phenotypes in Humans and Mice with Heterozygous Variants in<i>KISS1</i>/<i>Kiss1</i>

Yee-Ming Chan, Sarabeth Broder‐Fingert, Sophia Paraschos et al. · The Journal of Clinical Endocrinology & Metabolism · 2011 · 66 citations · Full text