I was interviewed for the article @agrawalpb_lab, so timely and important! Quick genetic test offers hope for sick, undiagnosed kids. But few insurers offer to pay. https://t.co/HEhqRF4WMH via @CBSNews
Agree with all of this!! Stay away from predatory labs and mentors that don’t truly invest in your success.
It’s worth waiting for the right place and team to launch you. Great advice below!
Excited to share the review article we just published, thanks @alissadgama.
Role of genomic medicine and implementing equitable access for critically ill infants in neonatal intensive care un… https://t.co/aUEQHxvcqY
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy
Congrats @HTChaoLab, @AgrawalPB_lab, and all co-authors!
https://t.co/hdH50wcBgR
Newborns with #hypotonia, or low muscle tone, frequently undergo multiple diagnostic tests and families sometimes must wait months for an answer. But a recent review in @JAMANeuro argues in favor of comprehensive DNA sequencing up front. https://t.co/S3PXEOXm30
Genomic Newborn Screening Studies Around the World Begin to Take Baby Steps! Fortunate to be an investigator of the Babyseq project, from inception to completion!
https://t.co/RIOqviIgxf
Our paper describing how we have successfully integrated rapid exome sequencing into NICU clinical care after a pilot research study! Congratulations @alissadgama@hereatmonica
https://t.co/rJwATyY2ww
Very interesting paper we wrote on how early genetic diagnosis can have major ethical implications and what we learn from the experience "Ethical implications of early genetic diagnosis in an infant with Lesch-Nyhan syndrome https://t.co/vdmqjNdWAI
A very extensive paper describing ATP1A3 related phenotypes. Thanks Drs. Verzyroglou and Balasubramanian for including us!
The Phenotypic Continuum of ATPLA3-Related Disorders https://t.co/n4xgOsVk53