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Nucleic Acids Research|March 28, 2015
SubmiRine: assessing variants in microRNA targets using clinical genomic data setsEvan K Maxwell, Joshua D Campbell, Avrum Spira, et al.BMC Genomics|December 22, 2012
MicroRNAs and essential components of the microRNA processing machinery are not encoded in the genome of the ctenophore Mnemiopsis leidyiEvan K Maxwell, Joseph F Ryan, Christine E Schnitzler, et al.BMC Evolutionary Biology|October 5, 2014
Evolutionary profiling reveals the heterogeneous origins of classes of human disease genes: implications for modeling disease genetics in animalsEvan K Maxwell, Christine E Schnitzler, Paul Havlak, et al.Bioinformatics (Oxford, England)|September 19, 2015
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing dataJonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variantsBrenda Finucane, Matthew T Oetjens, Alicia Johns, et al.JAMA Psychiatry|July 23, 2020
Identification of Neuropsychiatric Copy Number Variants in a Health Care System PopulationChrista Lese Martin, Karen E Wain, Matthew T Oetjens, et al.Nature Genetics|September 25, 2024
Yield of genetic association signals from genomes, exomes and imputation in the UK BiobankSheila M Gaynor, Tyler Joseph, Xiaodong Bai, et al.American Journal of Human Genetics|May 5, 2018
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 ExomesJeffrey Staples, Evan K Maxwell, Nehal Gosalia, et al.Pageof 1