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Scientific Reports|April 12, 2024
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428Anthony M Musolf, Cristina M Justice, Zeynep Erdogan-Yildirim, et al.Nature Communications|November 17, 2023
Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shapeSeppe Goovaerts, Hanne Hoskens, Ryan J Eller, et al.Investigative Ophthalmology & Visual Science|April 28, 2021
IMI 2021 Yearly DigestMonica Jong, Jost B Jonas, James S Wolffsohn, et al.General Relativity and Gravitation|December 5, 2022
Detection of early-universe gravitational-wave signatures and fundamental physicsRobert Caldwell, Yanou Cui, Huai-Ke Guo, et al.Communications Biology|January 3, 2023
Rare variant analyses across multiethnic cohorts identify novel genes for refractive errorAnthony M Musolf, Annechien E G Haarman, Robert N Luben, et al.American Journal of Human Genetics|September 27, 2016
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense VariantsNilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, et al.Nature Genetics|March 28, 2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityHye In Kim, Christopher DeBoever, Klaudia Walter, et al.Physical Review Letters|July 7, 2026
Probing Scalar-Neutrino and Scalar-Dark-Matter Interactions with PandaX-4TTao Li, Zihao Bo, Wei Chen, et al.Pageof 8