Medical genetics

EP 217: Building a genomic passport for every family with Lisa Gurry of GeneDx

Genetics Wrapped: 2025 Top Advances in Genomic Medicine

Full Recording of the December 2025 ICARE Genetics Case Conference

PL3.04 - 1,000 clinical long-read genomes define a new standard for rare disease diagnostics

PL2.2 - The ticking DNA clock: lifelong somatic expansion of the disease-causing DNA repeat in Hun..

PL01 - ELPAG Award Lecture

E07.1 - Basic principles of epigenetic mechanisms and consequences for human disease

E06.1 - From topology to disease and back

Lunch Hour Lecture | Genes, Depression, and Diversity

Повторная интерпретация сырых данных NGS: когда она необходима

Re-interpretation of raw NGS data: when it is necessary

Somatic escape variants in SERPINA1 in alpha-1 antitrypsin deficiency – JR 2025

EP 214: Innovating large-scale and sustainable genomics with Slavé Petrovski of AstraZeneca

EP 210: Live from ASHG: Breaking barriers in genomics with Heidi Rehm of the Broad Institute and ...

EP 207: Decoding Parkinson’s genetics on a global scale with Andy Singleton and Sonya Dumanis of ...

EP 204: Bringing cardiovascular genetics and biobank discoveries into the clinic with Samuli Ripa...

Li-Fraumeni Syndrome: Metformin Trial and Other Updates

Épigénétique et santé humaine, par Edith Heard (Le Collège Belgique reçoit le Collège de France)

Epigenetics and human health, by Edith Heard (The Collège Belgique hosts the Collège de France)

CGC Webinar: Transforming Tumor Methylation Profiling with Oxford Nanopore Direct DNA Sequencing

Genetic Testing Finds Surprise Cryptic Mutation! ...And Something Else? | RGW Ep 133

Breast Cancer Genetic Testing in Italy: A Curated Gene Panel

EP 210: Live from ASHG: Breaking barriers in genomics with Heidi Rehm and Slavé Petrovski

Cancer Genetics with Dr. Nicole Edison | Evening Rounds: Ambulatory Lecture Series

ASHG 2025

Dr. Ashwin Dalal Explains Rare Genetic Diseases in India

Updates on RAD51C, RAD51D, and BRIP1

Optical Genome Mapping: Detecting Structural Variants Missed by Traditional Tests

Full Recording of the October 2025 ICARE Genetics Case Conference

ESHG Webinar Series Episode 6 with Serena Nik-Zainal

EP 207: Decoding Parkinson’s genetics on a global scale with Andy Singleton and Sonya Dumanis

Hereditary Breast Cancer on the Big Screen with “Love, Danielle”

Stephen Quake (4) - Edith Heard (2024-2025)

EP 205: Building hope for children with ultra-rare diseases with Terry Pirovolakis

AGBT Precision Health 2025 Meeting Recaps and Reflections

Tumor Predisposition Genes: Penetrance, Prevalence, and Estimation of Risk

EP 204: Bringing cardiovascular genetics and biobank discoveries into the clinic with Samuli Ripatti

Epigenetics Podcast #157 - Epigenetic Mechanisms in Breast Cancer with Luca Magnani

How Genomics Is Transforming Rare Disease Diagnosis in Turkey

A Closer Look at…Genetic Medicine and Artificial Intelligence

Updates on PALB2

Les USA dévoilent comment manipuler l'ADN, c'est le CHOC !

The USA reveals how to manipulate DNA, it's SHOCKING!