Skip to main content
Premium Trial:

Request an Annual Quote

NHGRI Launches Web Resource on Genetic Laws, Policies

NEW YORK, July 22 (GenomeWeb News) - The National Human Genome Research Institute this week unveiled a new Web site that provides researchers, health professionals and the general public with information on laws and policies related to genetic issues.

 

The site offers free and searchable information on genetic testing and counseling; insurance and employment discrimination; newborn screening; privacy of genetic information and confidentiality; informed consent; and commercialization and patenting.

 

The resource has an interactive map of the US, enabling users to view state legislation and laws for all 50 states and the District of Columbia. In addition to the federal and state laws, the database contains information from the Department of Health and Human Services, the Department of Health, Education, and Welfare, the Equal Employment Opportunity Commission, the US Patent and Trademark Office, the Secretary's Advisory Committee on Genetics, Health, and Society, and the President's Council on Bioethics.

The Scan

UK Pilot Study Suggests Digital Pathway May Expand BRCA Testing in Breast Cancer

A randomized pilot study in the Journal of Medical Genetics points to similar outcomes for breast cancer patients receiving germline BRCA testing through fully digital or partially digital testing pathways.

Survey Sees Genetic Literacy on the Rise, Though Further Education Needed

Survey participants appear to have higher genetic familiarity, knowledge, and skills compared to 2013, though 'room for improvement' remains, an AJHG paper finds.

Study Reveals Molecular, Clinical Features in Colorectal Cancer Cases Involving Multiple Primary Tumors

Researchers compare mismatch repair, microsatellite instability, and tumor mutation burden patterns in synchronous multiple- or single primary colorectal cancers.

FarGen Phase One Sequences Exomes of Nearly 500 From Faroe Islands

The analysis in the European Journal of Human Genetics finds few rare variants and limited geographic structure among Faroese individuals.