Suchergebnisse - "Leitsalu, Liis"
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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu
ISSN: 1464-3685, 1464-3685Veröffentlicht: England 01.08.2015Veröffentlicht in International journal of epidemiology (01.08.2015)“… The Estonian Biobank cohort is a volunteer-based sample of the Estonian resident adult population (aged ≥18 years). The current number of participants-close to …”
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Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants
ISSN: 1018-4813, 1476-5438, 1476-5438Veröffentlicht: England Nature Publishing Group 01.03.2021Veröffentlicht in European journal of human genetics : EJHG (01.03.2021)“… Genotype-first approach allows to systematically identify carriers of pathogenic variants in BRCA1/2 genes conferring a high risk of familial breast and …”
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Copy number variations and cognitive phenotypes in unselected populations
ISSN: 1538-3598, 1538-3598Veröffentlicht: United States 26.05.2015Veröffentlicht in JAMA : the journal of the American Medical Association (26.05.2015)“… The association of copy number variations (CNVs), differing numbers of copies of genetic sequence at locations in the genome, with phenotypes such as …”
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Data in question: A survey of European biobank professionals on ethical, legal and societal challenges of biobank research
ISSN: 1932-6203, 1932-6203Veröffentlicht: United States Public Library of Science 18.09.2019Veröffentlicht in PloS one (18.09.2019)“… Biobanks have evolved, and their governance procedures have undergone important transformations. Our paper examines this issue by focusing on the perspective …”
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Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia
ISSN: 1664-8021, 1664-8021Veröffentlicht: Frontiers Media S.A 19.07.2022Veröffentlicht in Frontiers in genetics (19.07.2022)“… Recall-by-genotype (RbG) studies conducted with population-based biobank data remain urgently needed, and follow-up RbG studies, which add substance to this …”
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Correction: Data in question: A survey of European biobank professionals on ethical, legal and societal challenges of biobank research
ISSN: 1932-6203, 1932-6203Veröffentlicht: United States Public Library of Science 02.12.2019Veröffentlicht in PloS one (02.12.2019)“… [This corrects the article DOI: 10.1371/journal.pone.0221496.] …”
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Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting
ISSN: 1664-8021, 1664-8021Veröffentlicht: Switzerland Frontiers Media S.A 22.07.2022Veröffentlicht in Frontiers in genetics (22.07.2022)“… Although hereditary breast cancer screening and management are well accepted and established in clinical settings, these efforts result in the detection of …”
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MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies
ISSN: 1932-6203, 1932-6203Veröffentlicht: United States Public Library of Science 20.01.2017Veröffentlicht in PloS one (20.01.2017)“… Ancestry information at the individual level can be a valuable resource for personalized medicine, medical, demographical and history research, as well as for …”
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Country Reports
ISSN: 1073-1105, 1748-720XVeröffentlicht: Cambridge University Press (CUP) 01.01.2019Veröffentlicht in Journal of Law, Medicine & Ethics (01.01.2019)Volltext
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Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank
ISSN: 1018-4813, 1476-5438, 1476-5438Veröffentlicht: England Nature Publishing Group 01.09.2023Veröffentlicht in European journal of human genetics : EJHG (01.09.2023)“… The return of individual genomic results (ROR) to research participants is still in its early phase, and insight on how individuals respond to ROR is scarce …”
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Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia
ISSN: 1098-3600, 1530-0366, 1530-0366Veröffentlicht: New York Nature Publishing Group US 01.05.2019Veröffentlicht in Genetics in medicine (01.05.2019)“… Purpose Large-scale, population-based biobanks integrating health records and genomic profiles may provide a platform to identify individuals with …”
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Clinical Implementation Study of Genetic Risk-Based Breast Cancer Screening
ISSN: 1526-8209, 1938-0666, 1938-0666Veröffentlicht: United States Elsevier Inc 2025Veröffentlicht in Clinical breast cancer (2025)“… •Evaluated a genetic risk-based personalized breast cancer screening service model.•Utilized telemedicine, home-based testing, and questionnaire-based …”
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Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example
ISSN: 2075-4426, 2075-4426Veröffentlicht: Switzerland MDPI AG 29.04.2021Veröffentlicht in Journal of personalized medicine (29.04.2021)“… The current paradigm of personalized medicine envisages the use of genomic data to provide predictive information on the health course of an individual with …”
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Genetic counselling legislation and practice in cancer in EU Member States
ISSN: 1101-1262, 1464-360X, 1464-360XVeröffentlicht: England Oxford University Press 01.08.2024Veröffentlicht in European journal of public health (01.08.2024)“… Background Somatic and germline genetic alterations are significant drivers of cancer. Increasing integration of new technologies which profile these …”
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A Cluster-Randomized Trial on Personalized Feedback on Genetic Risks: Effects on Treatment Compliance of Patients with Hypertension
ISSN: 0001-5652, 1423-0062Veröffentlicht: Basel S. Karger AG 01.06.2018Veröffentlicht in Human heredity (01.06.2018)“… There is controversial evidence on the potential effects of personalized risk prediction in general practice. To study various aspects of applicability of the …”
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The role of a bioresource research impact factor as an incentive to share human bioresources
ISSN: 1061-4036, 1546-1718, 1546-1718Veröffentlicht: New York Nature Publishing Group US 01.06.2011Veröffentlicht in Nature genetics (01.06.2011)“… Bioresources need to be easily accessible to facilitate advancement of research. Besides technical and ethical aspects, a major obstacle for sharing them is …”
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Giving and Withholding of Information following Genomic Screening: Challenges Identified in a Study of Primary Care Physicians in Estonia
ISSN: 1059-7700, 1573-3599, 1573-3599Veröffentlicht: Boston Springer US 01.08.2012Veröffentlicht in Journal of genetic counseling (01.08.2012)“… The use of predictive genomic information to improve medical care remains a contentious topic. However, it is generally agreed that the potential of genomics …”
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Country Reports
ISSN: 1073-1105, 1748-720X, 1748-720XVeröffentlicht: Los Angeles, CA SAGE Publications 01.12.2019Veröffentlicht in The Journal of law, medicine & ethics (01.12.2019)“… Any proposed DTP genomic research would need to comply with the specific requirements of Chapter 3.3 to be satisfactorily addressed for ethical approval. 1.2 …”
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Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants
ISSN: 1741-0541, 1744-828X, 1744-828XVeröffentlicht: England 01.07.2016Veröffentlicht in Personalized medicine (01.07.2016)“… Procedural guidelines for disclosure of incidental genomic information are lacking. We introduce a method and evaluated the impact of returning results to …”
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Counseling for complex disease: Incorporating predictive genetic testing into the national health care system of Estonia
ISBN: 9781124031170, 1124031170Veröffentlicht: ProQuest Dissertations & Theses 01.01.2010“… Education of health care providers is crucial for effective translation of genomic information into health care practice. The project aims to facilitate the …”
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Dissertation

