Megan Frone
@meganf1
She/her. Genetic Counselor. Bioinformatics. Research. views=own. RT ≠ endorsements.
ID: 30453539
11-04-2009 14:16:11
722 Tweet
336 Followers
208 Following
ACMG Carrier Screening Guidelines: Falling Short On Equity and Inclusion thednaexchange.com/2021/07/26/acm… via WordPress.com
Excellent article. GCs & the genetics community need to grapple with this. If you care about CMS recognition think hard about the dynamics in play to keep us from getting there. With a system like this there is no incentive. thednaexchange.com/2021/10/12/an-… via WordPress.com
Curating variants for clinical relevance is especially challenging for genes like RTEL1. Check out #NCI_ClinicalGenetics post-bacc fellow Ashley Thompson's #ASHG21 poster. #telomere Cancer Epi & Genetics
Our manuscript on the evaluation of associations of BRCA1 and BRCA2 mutations with 22 different cancers (other than breast/ovarian cancers in women) out Journal of Clinical Oncology. Analysed Data from >5000 families with mutations from CIMBA @oncoalert #gcchat CRUK Cambridge Institute ascopubs.org/doi/abs/10.120…
Inspired a bit by talking virtually at U. Tennesse with Robert W. Williams in the audience, here are 10 thoughts for human geneticists navigating conversations with each other and broader publics around ethnicity and genetics.
So folks have been comparing the weird Good Morning Britain morning show interview with the climate activist in the UK with *that* scene from #DontLookUp. So we at the The Mehdi Hasan Show put them side by side & the results are.. astounding. Reality mirroring art! Watch:
One of the best session of LFS Association #REACH22 every year. International Youth Panel. Learn something every time.
Health insurers have spent over $141 billion buying back their own shares since 2007 while premiums and deductibles have skyrocketed, by Wendell Potter open.substack.com/pub/wendellpot…