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New Mexico State Statute (New Mexico: NMSA §24-21-1 et seq.)
The statutes contain provisions on the acquisition, collection, retention, transmission or use of genetic information. Consent requirements provide an exemption (1) if DNA, genetic information or…- state statute
- New Mexico
- employment nondiscrimination
- health insurance nondiscrimination
- genetic privacy
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Timeline of the Genetic Counseling Profession, National Society of Genetic Counselors (NSGC)
The National Society of Genetic Counselors (NSGC) offers a timeline of its 40-year history that includes genetic advances, public policies, technology, and key events.- genetic counselors
- NSGC
- genetic counselor network
- healthcare professionals
- timeline
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ELSI Publications and Products Database, National Human Genome Research Institute (NHGRI)
The ELSI Publications and Products Database is a collection of journal articles, books, and other materials that were produced with funding from the ELSI Research Program at the National Human Genome…- ELSI
- publication database
- ELSI Research Program
- Education
- Research
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Kansas 2014 State Bills (Kansas 2014 SB 367)
Prohibits school districts from collecting biometric data from a student, including a DNA sequence, unless the student, if an adult, or the parent or legal guardian of the student, if a minor,…- state bill
- bill
- bill status enacted
- Kansas
- Privacy
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Colorado 2015 State Bills (Colorado 2015 HB 1199)
This bill requires a state agency or educational institution to obtain consent from parents or eligible students prior to collecting certain data, including biometric records. Biometric records are…- state bill
- bill
- Colorado
- Data Collection
- biometric records
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California 2009 State Bills (California 2009 SB 482)
This bill states that all biological data derived from post-CLIA bioinformatics services shall be considered to contain genetic characteristics, as defined in section 1374.7 of the Health and Safety…- state bill
- bill
- Bioinformatics
- California
- biological data analysis
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Polygenic Risk Methods in Diverse Populations (PRIMED) Consortium
The Polygenic Risk Methods in Diverse Populations (PRIMED) Consortium (comprised of NIH program staff, affiliate members, investigators at 7 study sites, and a Coordinating Center) is funded by the…- Polygenic risk scores
- precision medicine
- diversity
- Genetic Risk
- multi-site