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Physiological Genomics|June 4, 2009
Modulation of the allergic asthma transcriptome following resiquimod treatmentPierre Camateros, Cynthia Kanagaratham, Jennifer Henri, et al.Human Molecular Genetics|August 6, 2005
Functional promoter SNPs in cell cycle checkpoint genesHélène Bélanger, Patrick Beaulieu, Claudia Moreau, et al.BMC Genomics|February 18, 2011
The living microarray: a high-throughput platform for measuring transcription dynamics in single cellsSaravanan Rajan, Haig Djambazian, Huan Chu Pham Dang, et al.Human Mutation|January 12, 2005
Meta-analysis of gross insertions causing human genetic disease: novel mutational mechanisms and the role of replication slippageJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.Human Genetics|May 7, 2018
Pronounced maternal parent-of-origin bias for type-1 NF1 microdeletionsLisa Neuhäusler, Anna Summerer, David N Cooper, et al.Genome Research|November 18, 2011
Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited diseaseClaudio Casola, Ugne Zekonyte, Andrew D Phillips, et al.Journal of Pediatric Hematology/Oncology|May 22, 2003
Prenatal exclusion of severe factor VII deficiencyHany Ariffin, David S Millar, David N Cooper, et al.Translational Psychiatry|March 18, 2021
Prioritization of schizophrenia risk genes from GWAS results by integrating multi-omics dataDan He, Cong Fan, Mengling Qi, et al.Nucleic Acids Research|February 10, 2017
IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variantsCarolin Knecht, Matthew Mort, Olaf Junge, et al.Human Mutation|August 20, 2005
Intrachromosomal serial replication slippage in trans gives rise to diverse genomic rearrangements involving inversionsJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.Pageof 57