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The phenotype is highly heritable and hormone dependent, with androgens being the recognized critical hormonal factor. Numerous molecular genetic studies have focused on genetic variation in and around the gene that encodes the androgen receptor. More recently, however, the availability of high\u2010throughput molecular genetic methods, novel methods of data analysis and sufficiently large sample sizes have rendered possible the systematic investigation of the contribution of other components of the androgen receptor pathway or hormonal pathways beyond the androgen receptor signalling pathways. Over the past decade, genome\u2010wide association studies of increasingly large cohorts have enabled the genome\u2010wide identification of genetic risk factors for AGA, and yielded unprecedented insights into the underlying pathobiology. The present review discusses some of the most intriguing genetic findings on the relevance of (sex)hormonal signalling in AGA.<\/jats:p>","DOI":"10.1111\/exd.14130","type":"journal-article","created":{"date-parts":[[2020,6,17]],"date-time":"2020-06-17T17:24:32Z","timestamp":1592414672000},"page":"814-827","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":58,"title":["Hormonal regulation in male androgenetic alopecia\u2014Sex hormones and beyond: Evidence from recent genetic studies"],"prefix":"10.1111","volume":"29","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1057-465X","authenticated-orcid":false,"given":"Stefanie","family":"Heilmann\u2010Heimbach","sequence":"first","affiliation":[{"name":"Institute of Human Genetics School of Medicine &amp; University Hospital Bonn University of Bonn Bonn Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lara M.","family":"Hochfeld","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics School of Medicine &amp; University Hospital Bonn University of Bonn Bonn Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2953-2700","authenticated-orcid":false,"given":"Sabrina K.","family":"Henne","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics School of Medicine &amp; University Hospital Bonn University of Bonn Bonn Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8770-2464","authenticated-orcid":false,"given":"Markus M.","family":"N\u00f6then","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics School of Medicine &amp; University Hospital Bonn University of Bonn Bonn Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2020,7,3]]},"reference":[{"key":"e_1_2_15_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1749-6632.1951.tb31971.x"},{"key":"e_1_2_15_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/aja.1000710306"},{"key":"e_1_2_15_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0738-081X(00)00125-5"},{"key":"e_1_2_15_5_1","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-20-10-1309"},{"key":"e_1_2_15_6_1","doi-asserted-by":"publisher","DOI":"10.1158\/1055-9965.EPI-04-0778"},{"key":"e_1_2_15_7_1","doi-asserted-by":"publisher","DOI":"10.1086\/431425"},{"key":"e_1_2_15_8_1","doi-asserted-by":"publisher","DOI":"10.1126\/science.186.4170.1213"},{"key":"e_1_2_15_9_1","first-page":"339","volume":"15","author":"Levy\u2010Nissenbaum E.","year":"2005","journal-title":"Eur. 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