Momentarily delurking to mention: Pattern of modern human introgression in Neanderthal genome shows signature of incipient speciation. New paper in Curr. Bio. with @DHarrisPopGen and @SarahTishkoff . https://t.co/u8YHWR2K69
Hey everyone – proud to see the published version of our work investigating genetic causes of T2D online now @CellGenomics:
https://t.co/OmXxOtMdDY
For a rundown of the major results, please see my previous thread👇
https://t.co/Q2sdnB1J5v
Our new work is out now in @medrxivpreprint!
https://t.co/BocUXts6dc We used the largest Parkinson’s
GWAS to construct and test a Polygenic Risk Score in our Latino cohort, and had an in-depth look at the
SNCA region. @doug_loesch @nachogenePD@LARGE_PD
Thank you to the lovely folks at @AJHGNews for interviewing me as part of our recent manuscript (https://t.co/qJ5T1hneMN) on Structural Variation in rare Developmental Disorders!
https://t.co/RjeeGb4UcL
Nice to kick back and think about the impact of ones work.
Proud to see our #openaccess manuscript describing hard to find, clinically relevant structural variants
@AJHGNews!
https://t.co/RE6Elv11hP
Thanks to our collaborators and OF COURSE the #DDD familes – our work would not be possible without their confidence.
An example of abusing science for profit. This company claims to use polygenic risk scores as a parental genetic testing tool to calculate the risk of having a child with 10 common, complex diseases or to select the embryos with the least risk. Don't throw away your money 1/n
Local ancestry profiles of 1000 self-described Hispanic/Latinos from our Genetics of Latin American Diversity (GLAD) Project sorted by Native American ancestry in 10s. Red is European, Blue is African, Purple is East Asian, and Yellow is Native American. Thanks @victor_snail!
This paper was a longtime coming. In no particular order, some of the interesting things to learn from the sequencing and analysis of 53,831 human genomes. 1/n
https://t.co/N5xBtfOEbw
PDF: https://t.co/DRUQlztmGt