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Journal of Morphology|October 22, 2013
Ectocranial suture fusion in primates: pattern and phylogenyJames Cray, Gregory M Cooper, Mark P Mooney, et al.Journal of Medical Primatology|October 4, 2012
Ectocranial suture fusion in primates: as related to cranial volume and dental eruptionJames Cray, Gregory M Cooper, Mark P Mooney, et al.Nucleic Acids Research|October 30, 2018
CADD: predicting the deleteriousness of variants throughout the human genomePhilipp Rentzsch, Daniela Witten, Gregory M Cooper, et al.Biorxiv : the Preprint Server for Biology|February 8, 2024
Patient derived model of UBA5-associated encephalopathy identifies defects in neurodevelopment and highlights potential therapiesHelen Chen, Yong-Dong Wang, Aidan W Blan, et al.Genome Research|May 3, 2003
Quantitative estimates of sequence divergence for comparative analyses of mammalian genomesGregory M Cooper, Michael Brudno, , et al.Epigenetics & Chromatin|November 28, 2013
Mapping genome-wide transcription factor binding sites in frozen tissuesDaniel Savic, Jason Gertz, Preti Jain, et al.Neurology|July 31, 2015
Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombinationHeather C Mefford, Matthew Zemel, Eileen Geraghty, et al.American Journal of Human Genetics|August 21, 2024
Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of biasColin A Ellis, Karen L Oliver, Rebekah V Harris, et al.Nature Genetics|August 17, 2010
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndromeSarah B Ng, Abigail W Bigham, Kati J Buckingham, et al.Epilepsia|May 13, 2024
Familial aggregation of seizure outcomes in four familial epilepsy cohortsColin A Ellis, Danni Tu, Karen L Oliver, et al.Pageof 38