Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

2 results

Filters applied: . Clear all
Page 1
Expanding the Genetic Landscape of Craniofacial Anomalies Through Transcriptome-Wide Association Studies.
Brokamp E, Scalici A, Miller-Fleming T, Wu D, Chung WK, Wojcik MH, Cox NJ, Shuey MM. Brokamp E, et al. Res Sq [Preprint]. 2025 Dec 30:rs.3.rs-8328679. doi: 10.21203/rs.3.rs-8328679/v1. Res Sq. 2025. PMID: 41502561 Free PMC article. Preprint.
Studies of craniofacial anomalies have identified several genetic causes, but focus on rare, Mendelian presentations. ...METHODS: We performed transcriptome-wide association studies that evaluated the association betw
Studies of craniofacial anomalies have identified several genetic causes, but focus on rare, Mendelian presentat
Expanding the Genetic Landscape of Craniofacial Anomalies Through Transcriptome-Wide Association Studies.
Brokamp E, Scalici A, Miller-Fleming T, Wu D, Chung WK, Wojcik MH, Cox NJ, Shuey MM. Brokamp E, et al. Res Sq [Preprint]. 2025 Oct 17:rs.3.rs-7645057. doi: 10.21203/rs.3.rs-7645057/v1. Res Sq. 2025. PMID: 41282252 Free PMC article. Preprint.
Studies of craniofacial anomalies have identified several genetic causes, but focus on rare, Mendelian presentations. ...METHODS: We performed transcriptome-wide association studies that evaluated the association betw
Studies of craniofacial anomalies have identified several genetic causes, but focus on rare, Mendelian presentat