{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,6]],"date-time":"2026-05-06T07:20:25Z","timestamp":1778052025986,"version":"3.51.4"},"reference-count":60,"publisher":"The Endocrine Society","issue":"3","license":[{"start":{"date-parts":[[2019,10,19]],"date-time":"2019-10-19T00:00:00Z","timestamp":1571443200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["P50HD028138"],"award-info":[{"award-number":["P50HD028138"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R01HD081256"],"award-info":[{"award-number":["R01HD081256"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["GM061354"],"award-info":[{"award-number":["GM061354"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["K99DE026824"],"award-info":[{"award-number":["K99DE026824"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Singapore\u2019s Agency for Science, Technology and Research"},{"name":"Desmond and Ann Heathwood MGH Research Scholar"},{"name":"Daland Fellowship of the American Philosophical Society","award":["GM061354"],"award-info":[{"award-number":["GM061354"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2020,3,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Context<\/jats:title>\n                    <jats:p>Kallmann syndrome (KS) is a rare, genetically heterogeneous Mendelian disorder. Structural defects in KS patients have helped define the genetic architecture of gonadotropin-releasing hormone (GnRH) neuronal development in this condition.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>Examine the functional role a novel structural defect affecting a long noncoding RNA (lncRNA), RMST, found in a KS patient.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design<\/jats:title>\n                    <jats:p>Whole genome sequencing, induced pluripotent stem cells and derived neural crest cells (NCC) from the KS patient were contrasted with controls.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Setting<\/jats:title>\n                    <jats:p>The Harvard Reproductive Sciences Center, Massachusetts General Hospital Center for Genomic Medicine, and Singapore Genome Institute.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Patient<\/jats:title>\n                    <jats:p>A KS patient with a unique translocation, t(7;12)(q22;q24).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interventions\/Main Outcome Measure\/Results<\/jats:title>\n                    <jats:p>A novel translocation was detected affecting the lncRNA, RMST, on chromosome 12 in the absence of any other KS mutations. Compared with controls, the patient\u2019s induced pluripotent stem cells and NCC provided functional information regarding RMST. Whereas RMST expression increased during NCC differentiation in controls, it was substantially reduced in the KS patient\u2019s NCC coincident with abrogated NCC morphological development and abnormal expression of several \u201cdownstream\u201d genes essential for GnRH ontogeny (SOX2, PAX3, CHD7, TUBB3, and MKRN3). Additionally, an intronic single nucleotide polymorphism in RMST was significantly implicated in a genome-wide association study associated with age of menarche.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>A novel deletion in RMST implicates the loss of function of a lncRNA as a unique cause of KS and suggests it plays a critical role in the ontogeny of GnRH neurons and puberty.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1210\/clinem\/dgz011","type":"journal-article","created":{"date-parts":[[2019,10,19]],"date-time":"2019-10-19T14:39:05Z","timestamp":1571495945000},"page":"e231-e244","source":"Crossref","is-referenced-by-count":29,"title":["A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator"],"prefix":"10.1210","volume":"105","author":[{"given":"Maria","family":"Stamou","sequence":"first","affiliation":[{"name":"Harvard Reproductive Endocrine Science Center, Massachusetts General Hospital, Boston"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shi-Yan","family":"Ng","sequence":"additional","affiliation":[{"name":"Institute of Molecular & Cell Biology, Singapore"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Harrison","family":"Brand","sequence":"additional","affiliation":[{"name":"Center for Genomic Medicine, Massachusetts General Hospital, Boston"},{"name":"Neurology, Psychiatry, & Pathology Departments, Massachusetts General Hospital, Boston"},{"name":"Program in Medical & Population Genetics, Broad Institute, Cambridge, MA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Harold","family":"Wang","sequence":"additional","affiliation":[{"name":"Center for Genomic Medicine, Massachusetts General Hospital, 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Singapore"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chiea Chuen","family":"Khor","sequence":"additional","affiliation":[{"name":"Genome Institute of Singapore, Singapore"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James","family":"Gusella","sequence":"additional","affiliation":[{"name":"Center for Genomic Medicine, Massachusetts General Hospital, Boston"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ravikumar","family":"Balasubramanian","sequence":"additional","affiliation":[{"name":"Harvard Reproductive Endocrine Science Center, Massachusetts General Hospital, Boston"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael","family":"Talkowski","sequence":"additional","affiliation":[{"name":"Center for Genomic Medicine, Massachusetts General Hospital, Boston"},{"name":"Neurology, Psychiatry, & Pathology Departments, Massachusetts General Hospital, Boston"},{"name":"Program in Medical & Population Genetics, 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