Meet the author of recent paper “BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control...

Join us for an hourlong conversation with Dr. Mike Bamshad, Editor-In-Chief of Human Genetics and Genomics Advances (HGG Advances), ASHG’s open-access journal.

Meet the author of recent paper “Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms."

Speakers will discuss the clinical benefits and system impacts of population-based screening for CPS genes, across the age spectrum from newborn screening to adult...

This webinar will present findings and analysis from an ASHG Board commissioned report on the economic and functional impact of human genetics and genomics research.

Discover how researchers evaluate the functional effect of genomic variants and guide clinicians in their interpretation of patients’ sequencing results.

Attend the Human Genetics Scholars Initiative Virtual Interest Session to learn more about the program and all its benefits.

Meet the author of the recent paper “Human ancient DNA analyses reveal the high burden of tuberculosis in Europeans over the last 2,000 years."

Learn how to engage your community on the current state of the COVID-19 vaccine and ways to debunk anti-vaccine information with scientific facts and reasoning

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...