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European Journal of Human Genetics : EJHG|May 7, 2021
Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomesAnne-Mai Ilumäe, Helen Post, Rodrigo Flores, et al.European Journal of Human Genetics : EJHG|July 27, 2020
Differences in local population history at the finest level: the case of the Estonian populationVasili Pankratov, Francesco Montinaro, Alena Kushniarevich, et al.Journal of Neurotrauma|September 12, 2024
Exploring Synaptic Pathways in Traumatic Brain Injury: A Cross-Phenotype Genomics ApproachSavvina Prapiadou, Ernst Mayerhofer, Marios K Georgakis, et al.European Journal of Human Genetics : EJHG|October 3, 2022
Lessons learned during the process of reporting individual genomic results to participants of a population-based biobankLiis Leitsalu, Anu Reigo, Marili Palover, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 2, 2018
Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from EstoniaMaris Alver, Marili Palover, Aet Saar, et al.Ebiomedicine|March 18, 2022
A genome-wide association study of outcome from traumatic brain injuryMart Kals, Kevin Kunzmann, Livia Parodi, et al.BMC Genomics|October 6, 2014
Genetic and epigenetic regulation of gene expression in fetal and adult human liversMarc Jan Bonder, Silva Kasela, Mart Kals, et al.Frontiers in Genetics|August 8, 2022
Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical SettingHannes Jürgens, Laura Roht, Liis Leitsalu, et al.Proceedings of the National Academy of Sciences of the United States of America|December 30, 2016
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanismsMichael H Guo, Satish K Nandakumar, Jacob C Ulirsch, et al.Nature Communications|November 5, 2024
High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 geneFedik Rahimov, Pekka Nieminen, Priyanka Kumari, et al.Pageof 7