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Nucleic Acids Research|June 20, 2007
oPOSSUM: integrated tools for analysis of regulatory motif over-representationShannan J Ho Sui, Debra L Fulton, David J Arenillas, et al.
Plos Computational Biology|May 10, 2006
SAGE2Splice: unmapped SAGE tags reveal novel splice junctionsByron Yu-Lin Kuo, Ying Chen, Slavita Bohacec, et al.
Genome Biology|August 19, 2006
Transcriptional and structural impact of TATA-initiation site spacing in mammalian core promotersJasmina Ponjavic, Boris Lenhard, Chikatoshi Kai, et al.
Pediatric Neurology|September 8, 2019
Strabismus in Children With Intellectual Disability: Part of a Broader Motor Control Phenotype?Xin Cynthia Ye, Robin van der Lee, Wyeth W Wasserman, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 23, 2010
Laboratory Animal Management Assistant (LAMA): a LIMS for active research coloniesMarko Milisavljevic, Taryn Hearty, Tony Y T Wong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disordersMaja Tarailo-Graovac, Jing Yun Alice Zhu, Allison Matthews, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Knowledge base and mini-expert platform for the diagnosis of inborn errors of metabolismJessica J Y Lee, Wyeth W Wasserman, Georg F Hoffmann, et al.
BMC Medical Genomics|December 4, 2014
FLAGS, frequently mutated genes in public exomesCasper Shyr, Maja Tarailo-Graovac, Michael Gottlieb, et al.
BMC Genomics|June 11, 2010
Transcriptional regulation of gene expression clusters in motor neurons following spinal cord injuryJesper Ryge, Ole Winther, Jacob Wienecke, et al.
Human Mutation|December 28, 2020
GeneBreaker: Variant simulation to improve the diagnosis of Mendelian rare genetic diseasesPhillip A Richmond, Tamar V Av-Shalom, Oriol Fornes, et al.
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