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- 🇨🇦CA · Medicine#1105K to 30K
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2.5K to 15K🎙 Weekly cadence·107 episodes·Long inactive - Monthly Reach
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5K to 30K🇨🇦100% - Active Followers
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1.5K to 9K
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Recent episodes
Genetics in Medicine: November 2024
Nov 6, 2024
Genetics in Medicine: June 2023
Jun 8, 2023
Genetics in Medicine: May 2023
May 4, 2023
Genetics in Medicine: April 2023
Apr 6, 2023
Genetics in Medicine: March 2023
Mar 7, 2023
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| Date | Episode | Description | Length | ||||||
|---|---|---|---|---|---|---|---|---|---|
| 11/6/24 | Genetics in Medicine: November 2024 | November 2024: Branching Out in the Decision Tree | — | ||||||
| 6/8/23 | Genetics in Medicine: June 2023 | June 2023 - The clinical impact of commercial laboratories issuing conflicting classifications of genetic variants – are some clinicians unknowingly diagnosing in the dark? | — | ||||||
| 5/4/23 | Genetics in Medicine: May 2023 | May 2023: How might medical geneticists prepare for the advent of gene therapy treatments of genetic diseases? | — | ||||||
| 4/6/23 | Genetics in Medicine: April 2023 | 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 | — | ||||||
| 3/7/23 | Genetics in Medicine: March 2023 | March 2023: OXGR1 variants: novel candidate disease gene for kidney stone disease? | — | ||||||
| 2/3/23 | Genetics in Medicine: February 2023 | February 2023: Diagnosing genetic developmental and epileptic encephalopathies in Africa | — | ||||||
| 1/9/23 | Genetics in Medicine: January 2023 | January 2023: Awareness of genetic testing – results and analysis from the 2020 Health Information National Trends Survey | — | ||||||
| 12/2/22 | Genetics in Medicine: December 2022 | December 2022: Standardizing variant annotation | — | ||||||
| 11/4/22 | Genetics in Medicine: November 2022 | November 2022: Disclosure of secondary findings from genomic testing in children | — | ||||||
| 10/4/22 | Genetics in Medicine: October 2022 | October 2022: A points to consider statement of the ACMG | — | ||||||
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| 9/2/22 | Genetics in Medicine: September 2022 | September 2022: CFTR genotype analysis of Asians in international registries highlights disparities in the diagnosis and treatment of Asian patients with cystic fibrosis | — | ||||||
| 8/1/22 | Genetics in Medicine: August 2022 | August: Klinefelter Syndrome and XYY in males mostly unrecognized in a large biobank study | — | ||||||
| 7/6/22 | Genetics in Medicine: July 2022 | July: Recommendations for next generation sequencing data reanalysis of unsolved cases with suspected Mendelian disorders: A systematic review and meta-analysis | — | ||||||
| 5/27/22 | Genetics in Medicine: June 2022 | June: Harmonizing gene–disease evidence resources globally | — | ||||||
| 5/4/22 | Genetics in Medicine: May 2022 | May: The Clinical Variant Analysis Tool: a systematic way to assess genomic testing results | — | ||||||
| 4/8/22 | Genetics in Medicine: April 2022 | April: The positive economic impact of rapid genomic testing for critically ill infants and children | — | ||||||
| 3/9/22 | Genetics in Medicine: March 2022 | March: Genome sequencing holds great potential to diagnose newborns with phenotypes suggestive of a genetic disorder. However, this technology has not been widely adopted for this population, and particularly not in newborns from underserved and low-income communities. | — | ||||||
| 2/3/22 | Genetics in Medicine: February 2022 | February: Matchmaking is an increasingly important strategy to help link rare diseases to genetic variants. These tools allow clinicians and researchers to search across previously siloed databases, clinics, and laboratories and access data about the potential genetic underpinnings of undiagnosed rare diseases across international boundaries. But to date there hasn’t been much research on the user experience. | — | ||||||
| 1/3/22 | Genetics in Medicine: January 2022 | January: When it comes to breast cancer, Non-Hispanic Black women have a 40% higher mortality rate than Non-Hispanic White women. Additionally, Non-Hispanic Black women have dramatically lower rates of uptake of genetic testing and then, if testing finds variants that would warrant such actions, undergoing prophylactic preventative surgeries. | — | ||||||
| 12/1/21 | Genetics in Medicine: December 2021 | December: As cardiovascular disease has many known genetic components, a team of researchers at Baylor College of Medicine created a panel of genes associated with cardiovascular disease they call HeartCare. David Murdock, previously the assistant director of the clinical lab at Baylor College of Medicine’s Human Genome Sequencing Center and now a lab director at Invitae, states “we thought that by looking at genetic causes of cardiovascular disease in an adult population, that could really help us to push forward genetic testing in adults in general”. | — | ||||||
| 11/1/21 | Genetics in Medicine: November 2021 | November: Polygenic risk scores (PRS) can be an important tool in breast cancer patients to help stratify individuals into levels of disease risk. The clinical utility of PRS is still being evaluated, but what hasn't yet been evaluated is how to communicate such results to patients, and how they respond to their PRS scores. | — | ||||||
| 10/15/21 | Genetics in Medicine: September 2021 | September: Team of experts creates ACMG’s first evidence-based clinical guideline recommending exome or genome sequencing for pediatric patients with congenital anomalies or intellectual disability | — | ||||||
| 10/15/21 | Genetics in Medicine: August 2021 | August: Diagnosing the undiagnosed: Genetic testing identifies the underlying causes of kidney disease | — | ||||||
| 10/15/21 | Genetics in Medicine: July 2021 | July: Artificial intelligence may provide a timely diagnosis for Fragile X syndrome | — | ||||||
| 10/1/21 | Genetics in Medicine: October 2021 | October: Researchers are still laying the groundwork in the search for therapeutics that target the mechanism for genetic disorders leading to new treatments. On this month’s GenePod, authors of two recently published articles in Genetics in Medicine discuss where trials for such molecules are succeeding and where there is still more research to be done to determine the efficacy and safety of new treatments. | — | ||||||
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Chart Positions
1 placement across 1 market.
Chart Positions
1 placement across 1 market.