Meet the author of the recent paper “Is that something that should concern me?”: a qualitative exploration of parent understanding of their child’s genomic test results".

‘Fostering Responsible Research on Ancient DNA’ lays out practical recommendations to help scientists understand and integrate ethical engagement with communities.

Meet the author of the recent paper “Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk.”

Preparing for a job in different career sectors that include academia, industry, and biotechnology.

Learn how variants discovered in human populations with African ancestry have great potential to achieve better polygenic risk score prediction across populations.

This month's presentation is on the recent AJHG paper, "Genome-Wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios".

This webinar will provide insight on how to set up meetings with members of Congress, along with communication tips and strategies during the coronavirus pandemic.

This month's presentation is on the recent AJHG paper, "Improved Detection of Chromosomal Rearrangements in Developmental Diseases".

This webinar will provide some insight into how one needs to adapt in the current world with the constant change in research and clinical environments.

This month's presentation is on the recent AJHG paper, "Allele-Specific QTL Fine Mapping with PLASMA". Attendees will have the opportunity to ask questions in a live...

Advocacy is more important than ever. Dr. Allison McCague with President and CEO of Research!America, Mary Woolley, discuss science advocacy with Dr. Lynn Jorde.

This month, attend the presentation on the AJHG paper "A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease".

Learn how to engage your community around genetics online and in person.

Join Drs. Chris Gunter, Jennifer Below, and Janina Jeff as they discuss using Twitter professionally, how to reach large audiences through Reddit, and using a podcast...

Join Drs. Kathryn North and Stephanie Devaney as they discuss population genomic studies!

The “Matchmaker Exchange” was launched in 2013 in order to facilitate the process of matching a patient with a rare disease and a candidate gene to another to identify...