Joseph Glessner
Children's Hospital of Philadelphia(US)University of Pennsylvania(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetic Associations and Epidemiology, Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research
Most-Cited Works
- → Functional impact of global rare copy number variation in autism spectrum disorders(2010)2,041 cited
- → PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data(2007)1,892 cited
- → Autism genome-wide copy number variation reveals ubiquitin and neuronal genes(2009)1,435 cited
- → Common genetic variants on 5p14.1 associate with autism spectrum disorders(2009)969 cited
- → De novo mutations in histone-modifying genes in congenital heart disease(2013)953 cited
- → Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains(2023)703 cited
- → A genome-wide scan for common alleles affecting risk for autism