The Italian Twin Registry
Initiatives
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A valuable resource for genetic epidemiological research.
- Start Year
- 2001
- Funding
- Italian Ministry of Health
Visit ITR
Investigators | Contacts |
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Design
- Study design
- Population cohort
- Follow Up
- Ability to perform record linkages between personal twin data and disease data from registers held in clinical centers in order to identify twins affected by a certain disease in a multicenter study setting. It depends on the study, but usually information is obtained using self-administered standardized questionnaires through regular mail. Recently, a web-based platform was implemented. In specific studies regarding outpatients’ examinations, health information and clinical measurements are collected by trained physicians in selected hospitals.
Marker Paper
Fagnani C, Brescianini S, Cotichini R, D'Ippolito C, Dukic T, Giannantonio L, Medda E, Nisticò L, Patriarca V, Pulciani S, Rotondi D, Toccaceli V, Stazi MA. The Italian Twin Register: new cohorts and tools, current projects and future perspectives of a developing resource. Twin Res Hum Genet. 2006 Dec;9(6):799-805. doi: 10.1375/183242706779462624.
PUBMED 17254411
Recruitment
- Sources of Recruitment
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- Families
Number of participants
- Number of participants
- 9,000
- Number of participants with biosamples
- Supplementary Information
- Twin pairs
Access
Availability of data and biosamples
Data | |
Biosamples | |
Other |