Timothy Cox
@craniofacialprof.bsky.social
Aussie prof studying craniofacial conditions (cleft lip/palate, craniofacial microsomia). Genomics, mouse models, dev/cell biol.
Our newest collab paper showing an interplay between common regulatory SNVs and rare coding variants in SHROOM3 in Craniofacial Microsomia is now online ahead of print @genomeresearch.bsky.social: pubmed.ncbi.nlm.nih.gov/40234029/. Huge shoutout to Yong-Biao Zhang’s team again.
April 18, 2025 at 3:19 PM
Our newest collab paper showing an interplay between common regulatory SNVs and rare coding variants in SHROOM3 in Craniofacial Microsomia is now online ahead of print @genomeresearch.bsky.social: pubmed.ncbi.nlm.nih.gov/40234029/. Huge shoutout to Yong-Biao Zhang’s team again.
As always, very happy to have been able to contribute to another great story led by @kaustubhad.bsky.social and Andres Ruiz-Linares.
New paper!
Studying genetics of tooth dimensions isn't so common as measurement is cumbersome. But in our modest-sized study we report many new genes, with one which seems to have been inherited from Neanderthals in (some) Europeans.
authors.elsevier.com/sd/article/S...
@ugiatucl.bsky.social
Studying genetics of tooth dimensions isn't so common as measurement is cumbersome. But in our modest-sized study we report many new genes, with one which seems to have been inherited from Neanderthals in (some) Europeans.
authors.elsevier.com/sd/article/S...
@ugiatucl.bsky.social
ScienceDirect.com | Science, health and medical journals, full text articles and books.
authors.elsevier.com
December 25, 2024 at 2:03 AM
As always, very happy to have been able to contribute to another great story led by @kaustubhad.bsky.social and Andres Ruiz-Linares.
Our cool collaborative manuscript reporting haplotype of common variants impacting presentation associated with rare variants. Did reporter assays for 2 SNPs (of 30) in the LD block as they mapped within putative enhancers. Reviewer wants all other 28 tested as “shouldn’t take much effort”. Really?
November 27, 2024 at 8:03 PM
Our cool collaborative manuscript reporting haplotype of common variants impacting presentation associated with rare variants. Did reporter assays for 2 SNPs (of 30) in the LD block as they mapped within putative enhancers. Reviewer wants all other 28 tested as “shouldn’t take much effort”. Really?
Reposted by Timothy Cox
Hey friends! Little Fai’a and her family are SO close to reaching their goal of $45K to get her cleft lip surgery and out of Gaza.
Please consider donating any amount you can — what you’d spend on coffee or takeout or an impulse buy? Use it for good here ❤️❤️❤️
www.gofundme.com/f/e94a7-medi...
Please consider donating any amount you can — what you’d spend on coffee or takeout or an impulse buy? Use it for good here ❤️❤️❤️
www.gofundme.com/f/e94a7-medi...
Medical situation, organized by Amal M A Abughali
Hi, my name is Amal Abughali I would like to raise a fund for a medical situation! My relative in … Amal M A Abughali needs your support for Medical situation
www.gofundme.com
June 2, 2024 at 5:52 PM
Hey friends! Little Fai’a and her family are SO close to reaching their goal of $45K to get her cleft lip surgery and out of Gaza.
Please consider donating any amount you can — what you’d spend on coffee or takeout or an impulse buy? Use it for good here ❤️❤️❤️
www.gofundme.com/f/e94a7-medi...
Please consider donating any amount you can — what you’d spend on coffee or takeout or an impulse buy? Use it for good here ❤️❤️❤️
www.gofundme.com/f/e94a7-medi...