Regina Regan
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Chromosomal and Genetic Variations, Congenital heart defects research
Most-Cited Works
- → Functional impact of global rare copy number variation in autism spectrum disorders(2010)2,041 cited
- → Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders(2014)1,019 cited
- → Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes(2008)806 cited
- → Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome(2006)664 cited
- → A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures(2008)591 cited
- → A genome-wide scan for common alleles affecting risk for autism(2010)587 cited
- → A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism(2006)470 cited
- → Subtle chromosomal rearrangements in children with unexplained mental retardation(1999)453 cited
- → Individual common variants exert weak effects on the risk for autism spectrum disorders(2012)374 cited
- → Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant(2008)346 cited