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Globular glial tauopathy was associated with the strongest heritability with 40% having a suggested autosomal dominant pattern of inheritance followed by corticobasal degeneration (19%), Pick's disease (8%), and progressive supranuclear palsy (6%).<\/jats:p><\/jats:sec><jats:sec><jats:title>Discussion<\/jats:title><jats:p>Similar to clinical frontotemporal dementia syndromes, heritability varies between pathological subtypes. Further identification of a genetic link in cases with strong heritability await discovery.<\/jats:p><\/jats:sec>","DOI":"10.1016\/j.dadm.2018.12.001","type":"journal-article","created":{"date-parts":[[2019,1,27]],"date-time":"2019-01-27T07:16:28Z","timestamp":1548573388000},"page":"115-124","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":16,"title":["Heritability in frontotemporal tauopathies"],"prefix":"10.1002","volume":"11","author":[{"given":"Shelley L.","family":"Forrest","sequence":"first","affiliation":[{"name":"Faculty of Medicine and Health, Charles Perkins Centre and Discipline of Pathology University of Sydney Sydney Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Glenda M.","family":"Halliday","sequence":"additional","affiliation":[{"name":"Faculty of Medicine and Health Brain and Mind Centre and Central Clinical School, University of Sydney Sydney Australia"},{"name":"Neuroscience 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