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Bioinformatics (Oxford, England)|October 23, 2009
Targeted interrogation of copy number variation using SCIMMkitTroy Zerr, Gregory M Cooper, Evan E Eichler, et al.Nature Genetics|September 9, 2008
Systematic assessment of copy number variant detection via genome-wide SNP genotypingGregory M Cooper, Troy Zerr, Jeffrey M Kidd, et al.Nature Genetics|September 5, 2007
Mutational and selective effects on copy-number variants in the human genomeGregory M Cooper, Deborah A Nickerson, Evan E EichlerGenome Research|June 10, 2009
A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive diseaseHeather C Mefford, Gregory M Cooper, Troy Zerr, et al.Genome Research|September 16, 2010
De novo rates and selection of large copy number variationAndy Itsara, Hao Wu, Joshua D Smith, et al.American Journal of Human Genetics|January 11, 2016
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNVMichael H Duyzend, Xander Nuttle, Bradley P Coe, et al.Transfusion|September 2, 2016
Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestryKeolu Fox, Jill M Johnsen, Bradley P Coe, et al.American Journal of Human Genetics|January 27, 2009
Population analysis of large copy number variants and hotspots of human genetic diseaseAndy Itsara, Gregory M Cooper, Carl Baker, et al.American Journal of Human Genetics|March 5, 2021
2020 William Allan Award introduction: Mary-Claire KingEvan E EichlerPageof 106