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Psychological Medicine|February 22, 2021
Genetic architecture of Tourette syndrome: our current understandingLaura Domènech, Carolina Cappi, Matt HalvorsenGenetics in Medicine : Official Journal of the American College of Medical Genetics|December 31, 2015
Mosaic mutations in early-onset genetic diseasesMatt Halvorsen, Slavé Petrovski, Renée Shellhaas, et al.Molecular Genetics and Metabolism|September 16, 2011
A novel application of pattern recognition for accurate SNP and indel discovery from high-throughput data: targeted resequencing of the glucocorticoid receptor co-chaperone FKBP5 in a Caucasian populationLinda L Pelleymounter, Irene Moon, Julie A Johnson, et al.Plos Genetics|September 3, 2015
The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage SensitivitySlavé Petrovski, Ayal B Gussow, Quanli Wang, et al.Ebiomedicine|February 9, 2017
Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary EmbolismMatt Halvorsen, Ying Lin, Barbara A Sampson, et al.Nature Communications|August 11, 2017
Annotating pathogenic non-coding variants in genic regionsSahar Gelfman, Quanli Wang, K Melodi McSweeney, et al.Epilepsia|January 23, 2016
Differential gene expression in dentate granule cells in mesial temporal lobe epilepsy with and without hippocampal sclerosisNicole G Griffin, Yu Wang, Christine M Hulette, et al.Blood|May 28, 2020
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic diseaseKarl C Desch, Ayse B Ozel, Matt Halvorsen, et al.Plos Computational Biology|October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arraysSahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.Pageof 1