{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Mansoorshahi S"],"funding":["National Center for Advancing Translational Sciences","Turner Syndrome Society of the United States","NCATS NIH HHS"],"pagination":["112"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10929126"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["19(1)"],"pubmed_abstract":["Background
Many different clinical specialists provide care to patients with Turner syndrome (TS), who have highly variable clinical manifestations. Therefore, a national TS registry is essential to inform a cohesive approach to healthcare and research. In 2015, the Turner Syndrome Society of the United States (TSSUS) created the Turner Syndrome Research Registry (TSRR) to engage directly with community participants who voluntarily provide longitudinal data about their experiences with TS. TSRR projects are collaborative partnerships between people with TS, TSSUS, and researchers.Results
To ensure that registry workflows conform to the data privacy choices of participants, TSSUS collaborated with UTHealth Houston in 2021 to create a new version of the TSRR that completely s"],"journal":["Orphanet journal of rare diseases"],"pubmed_title":["Methodological advances in patient-centered rare disease research: the UTHealth Houston Turner Syndrome Society of the United States research registry."],"pmcid":["PMC10929126"],"funding_grant_id":["Turner Syndrome Society of the United States","UL1 TR001105","UL1 TR000445"],"pubmed_authors":["Mansoorshahi S","Scurlock C","Research Registry SABOTTSSOTUS","Prakash SK"],"additional_accession":[]},"is_claimable":false,"name":"Methodological advances in patient-centered rare disease research: the UTHealth Houston Turner Syndrome Society of the United States research registry.","description":"Background
Many different clinical specialists provide care to patients with Turner syndrome (TS), who have highly variable clinical manifestations. Therefore, a national TS registry is essential to inform a cohesive approach to healthcare and research. In 2015, the Turner Syndrome Society of the United States (TSSUS) created the Turner Syndrome Research Registry (TSRR) to engage directly with community participants who voluntarily provide longitudinal data about their experiences with TS. TSRR projects are collaborative partnerships between people with TS, TSSUS, and researchers.Results
To ensure that registry workflows conform to the data privacy choices of participants, TSSUS collaborated with UTHealth Houston in 2021 to create a new version of the TSRR that completely s","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Mar","modification":"2026-07-15T02:15:29.476Z","creation":"2025-04-04T12:59:10.299Z"},"accession":"S-EPMC10929126","cross_references":{"pubmed":["38468317"],"doi":["10.1186/s13023-024-03120-1"]}}