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BMC Genetics|November 29, 2008
Intergenic DNA sequences from the human X chromosome reveal high rates of global gene flowMurray P Cox, August E Woerner, Jeffrey D Wall, et al.Molecular Biology and Evolution|November 5, 2003
High-resolution SNPs and microsatellite haplotypes point to a single, recent entry of Native American Y chromosomes into the AmericasStephen L Zegura, Tatiana M Karafet, Lev A Zhivotovsky, et al.Epilepsia|December 25, 2016
Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndromeAtsushi Ishii, Joseph C Watkins, Debbie Chen, et al.Molecular Biology and Evolution|August 17, 2018
The Role of Phylogenetically Conserved Elements in Shaping Patterns of Human Genomic DiversityAugust E Woerner, Krishna R Veeramah, Joseph C Watkins, et al.Epilepsia|November 18, 2024
Patients carrying pathogenic SCN8A variants with loss- and gain-of-function effects can be classified into five subgroups exhibiting varying developmental and epileptic components of encephalopathyJoshua B Hack, Joseph C Watkins, John M Schreiber, et al.Epilepsia|July 24, 2019
Influence of age at seizure onset on the acquisition of neurodevelopmental skills in an SCN8A cohortAlejandra C Encinas, Ida Ki M Moore, Joseph C Watkins, et al.Genetics|July 16, 2005
The extent of linkage disequilibrium caused by selection on G6PD in humansMatthew A Saunders, Montgomery Slatkin, Chad Garner, et al.Scientific Reports|July 7, 2018
Modeling SNP array ascertainment with Approximate Bayesian Computation for demographic inferenceConsuelo D Quinto-Cortés, August E Woerner, Joseph C Watkins, et al.Genetics|April 9, 2015
Reconstructing Past Admixture Processes from Local Genomic Ancestry Using Wavelet TransformationJean Sanderson, Herawati Sudoyo, Tatiana M Karafet, et al.Genetics|August 22, 2003
Human population structure and its effects on sampling Y chromosome sequence variationMichael F Hammer, Felisa Blackmer, Dan Garrigan, et al.Pageof 14