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ABOUT THIS PODCAST 🔗

Update frequency:
monthly
Average audio length:
7 minutes
English
United States
106 episodes
since Oct. 1, 2021
episodic

LATEST EPISODE 🔗

April 2023: Use of a PreEMPT model found that universal genetic screening for hypertrophic cardiomyopathy at birth would save lives but was unlikely to be cost-effective

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PREVIOUS EPISODES

March 2023: OXGR1 variants: novel candidate disease gene for kidney stone disease?
February 2023: Diagnosing genetic developmental and epileptic encephalopathies in Africa
February 2023: Diagnosing genetic developmental and epileptic encephalopathies in Africa
January 2023: Awareness of genetic testing – results and analysis from the 2020 Health Information National Trends Survey
December 2022: Standardizing variant annotation
November 2022: Disclosure of secondary findings from genomic testing in children
October 2022: A points to consider statement of the ACMG
September 2022: CFTR genotype analysis of Asians in international registries highlights disparities in the diagnosis and treatment of Asian patients with cystic fibrosis
August: Klinefelter Syndrome and XYY in males mostly unrecognized in a large biobank study
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