Showing results (11-20 of 17) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Genome Medicine|October 19, 2021
Comprehensive multi-omics integration identifies differentially active enhancers during human brain development with clinical relevanceSoheil Yousefi, Ruizhi Deng, Kristina Lanko, et al.Cell|November 20, 2025
BRAIN-MAGNET: A functional genomics atlas for interpretation of non-coding variantsRuizhi Deng, Elena Perenthaler, Anita Nikoncuk, et al.BMC Genomics|January 27, 2018
A SNP panel for identification of DNA and RNA specimensSoheil Yousefi, Tooba Abbassi-Daloii, Thirsa Kraaijenbrink, et al.Gastroenterology|December 26, 2024
Human Enteric Glia Diversity in Health and Disease: New Avenues for the Treatment of Hirschsprung DiseaseJonathan D Windster, Naomi J M Kakiailatu, Laura E Kuil, et al.Acta Neuropathologica|April 29, 2023
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical modelRuizhi Deng, Eva Medico-Salsench, Anita Nikoncuk, et al.Acta Neuropathologica|December 11, 2019
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseasesElena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.American Journal of Human Genetics|September 9, 2025
A clinical and genotype-phenotype analysis of MACF1 variantsJordy Dekker, Rachel Schot, Kimberly A Aldinger, et al.Pageof 2