{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T22:07:46Z","timestamp":1792188466206,"version":"4.4.0"},"reference-count":192,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2016,12,12]],"date-time":"2016-12-12T00:00:00Z","timestamp":1481500800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Italian Ministry of Health","award":["GR-2011-02351636"],"award-info":[{"award-number":["GR-2011-02351636"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinical Genetics"],"published-print":{"date-parts":[[2017,2]]},"abstract":"<jats:p>\n                    Primary ovarian insufficiency (\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    ) is characterized by a loss of ovarian function before the age of 40 and account for one major cause of female infertility.\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    relevance is continuously growing because of the increasing number of women desiring conception beyond 30 years of age, when\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    prevalence is &gt;1%.\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    is highly heterogeneous and can present with ovarian dysgenesis and primary amenorrhea, or with secondary amenorrhea, and it can be associated with other congenital or acquired abnormalities. In most cases\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    remains classified as idiopathic. However, the age of menopause is an inheritable trait and\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    has a strong genetic component. This is confirmed by the existence of several candidate genes, experimental and natural models. The variable expressivity of\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    defect may indicate that, this disease may frequently be considered as a multifactorial or oligogenic defect. The most common genetic contributors to\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    are the X chromosome\u2010linked defects. Here, we review the principal X\u2010linked and autosomal genes involved in syndromic and non\u2010syndromic forms of\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    with the expectation that this list will soon be upgraded, thus allowing the possibility to predict the risk of an early age at menopause in families with\n                    <jats:styled-content style=\"fixed-case\">POI<\/jats:styled-content>\n                    .\n                  <\/jats:p>","DOI":"10.1111\/cge.12921","type":"journal-article","created":{"date-parts":[[2016,11,16]],"date-time":"2016-11-16T14:40:35Z","timestamp":1479307235000},"page":"183-198","source":"Crossref","is-referenced-by-count":203,"title":["Genetics of primary ovarian insufficiency"],"prefix":"10.1111","volume":"91","author":[{"given":"R.","family":"Rossetti","sequence":"first","affiliation":[{"name":"Department of Endocrine and Metabolic Diseases IRCCS Istituto Auxologico 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