Helena Kääriäinen
Biographic Data
| ID | 7619724 |
|---|---|
| NAME | Helena Kääriäinen |
| GIVEN NAMES | Helena |
| FAMILY NAME | Kääriäinen |
| SIGNATURE | KAARIAINEN H |
| AFFILIATIONS | Finnish Institute for Health and Welfare |
| VERIFIED | No |
| TOTAL WORKS | 9 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 9 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2009 |
| LATEST PUBLICATION YEAR | 2022 |
| H-INDEX | 0 |
Simulating the Genetics Clinic of the Future — whether undergoing whole-genome sequencing shapes professional attitudes
Whole-genome sequencing (WGS) can provide valuable health insight for research participants or patients. Opportunities to be sequenced are increasing as direct-to-consumer (DTC) testing becomes more prevalent, but it is still fairly unusual to have been sequenced. We offered WGS to fourteen professionals with pre-existing familiarity with an interest in human genetics - healthcare, science, policy and art. Participants received a hard drive conta…
Rare diseases
Genetics in an isolated population like Finland
A unique genetic background in an isolated population like that of Finland offers special opportunities for genetic research as well as for applying the genetic developments to the health care. On the other hand, the different genetic background may require local attempts to develop diagnostics and treatment as the selection of diseases and mutations differs from that in the other populations. In this review, we describe the experiences of resear…
Genetic causal beliefs about morbidity
Despite increased public discussion of genomics, the relative proportion of those who endorse genetic factors as the most important cause of morbidity has remained low. However, within this group beliefs about benefits of health behavior changes have become more positive. This could indicate that increase in genomic health information does not lead to more negative appraisals of efficacy of lifestyle changes
Definitions of genetic testing in European legal documents
Community genetics. Its definition 2010
This paper presents a definition of the medical field of community genetics. It starts with a brief historical overview, defines the requirements for an adequate definition, presents the definition, and discusses the constituent parts of the definition
Points to consider in assessing and appraising predictive genetic tests
The use of predictive genetic tests is expanding rapidly. Given limited health care budgets and few national coverage decisions specifically for genetic tests, evidence of benefits and harms is a key requirement in decision making; however, assessing the benefits and harms of genetic tests raises a number of challenging issues. Frequently, evidence of medical benefits and harms is limited due to practical and ethical limitations of conducting mea…
Scope of definitions of genetic testing
Expertise, empathy and ethical awareness
Along with the increase in genetic testing, it has become ever more important to assess the meanings attributed to genetic information in healthcare and in society. The objectives of this article are: (1) to review international guidelines pertaining to genetic counseling; (2) to analyze how genetic information is constructed in these documents; and (3) to summarize how these constructions affect the ideals and practice of genetic counseling. Gui…
No prominent works on this page.
Expertise, empathy and ethical awareness
Along with the increase in genetic testing, it has become ever more important to assess the meanings attributed to genetic information in healthcare and in society. The objectives of this article are: (1) to review international guidelines pertaining to genetic counseling; (2) to analyze how genetic information is constructed in these documents; and (3) to summarize how these constructions affect the ideals and practice of genetic counseling. Gui…
Community genetics. Its definition 2010
This paper presents a definition of the medical field of community genetics. It starts with a brief historical overview, defines the requirements for an adequate definition, presents the definition, and discusses the constituent parts of the definition
Points to consider in assessing and appraising predictive genetic tests
The use of predictive genetic tests is expanding rapidly. Given limited health care budgets and few national coverage decisions specifically for genetic tests, evidence of benefits and harms is a key requirement in decision making; however, assessing the benefits and harms of genetic tests raises a number of challenging issues. Frequently, evidence of medical benefits and harms is limited due to practical and ethical limitations of conducting mea…
Scope of definitions of genetic testing
Definitions of genetic testing in European legal documents
Genetic causal beliefs about morbidity
Despite increased public discussion of genomics, the relative proportion of those who endorse genetic factors as the most important cause of morbidity has remained low. However, within this group beliefs about benefits of health behavior changes have become more positive. This could indicate that increase in genomic health information does not lead to more negative appraisals of efficacy of lifestyle changes
Genetics in an isolated population like Finland
A unique genetic background in an isolated population like that of Finland offers special opportunities for genetic research as well as for applying the genetic developments to the health care. On the other hand, the different genetic background may require local attempts to develop diagnostics and treatment as the selection of diseases and mutations differs from that in the other populations. In this review, we describe the experiences of resear…
Rare diseases
Simulating the Genetics Clinic of the Future — whether undergoing whole-genome sequencing shapes professional attitudes
Whole-genome sequencing (WGS) can provide valuable health insight for research participants or patients. Opportunities to be sequenced are increasing as direct-to-consumer (DTC) testing becomes more prevalent, but it is still fairly unusual to have been sequenced. We offered WGS to fourteen professionals with pre-existing familiarity with an interest in human genetics - healthcare, science, policy and art. Participants received a hard drive conta…
BRCA gene mutations in cancer (8 works) · Medicine (8 works) · Public health (6 works) · Biology (5 works) · Genetics (5 works) · Computer Science (4 works) · Genetic testing (4 works) · Genomics and Rare Diseases (4 works) · Pathology (4 works) · Environmental health (3 works)