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Our understanding of the genetic control of pubertal timing has advanced thanks to active investigation in this field over the last two decades, but it remains in large part a fascinating and mysterious conundrum. The phenotype of delayed puberty is associated with adult health risks and common etiologies, and there is evidence for polygenic control of pubertal timing in the general population, sex-specificity, and epigenetic modulation. Moreover, much has been learned from comprehension of monogenic and digenic etiologies of pubertal delay and associated disorders and, in recent years, knowledge of oligogenic inheritance in conditions of GnRH deficiency. Recently there have been several novel discoveries in the field of self-limited delayed puberty, encompassing exciting developments linking this condition to both GnRH neuronal biology and metabolism and body mass. These data together highlight the fascinating heterogeneity of disorders underlying this phenotype and point to areas of future research where impactful developments can be made.<\/jats:p>","DOI":"10.1210\/er.2018-00248","type":"journal-article","created":{"date-parts":[[2019,4,9]],"date-time":"2019-04-09T09:01:36Z","timestamp":1554800496000},"page":"1285-1317","source":"Crossref","is-referenced-by-count":101,"title":["Delayed Puberty\u2014Phenotypic Diversity, Molecular Genetic Mechanisms, and Recent Discoveries"],"prefix":"10.1210","volume":"40","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6698-903X","authenticated-orcid":false,"given":"Sasha R","family":"Howard","sequence":"first","affiliation":[{"name":"Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, United 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