Brett S. Abrahams
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Congenital heart defects research, Genomic variations and chromosomal abnormalities, CRISPR and Genetic Engineering
Most-Cited Works
- → Functional impact of global rare copy number variation in autism spectrum disorders(2010)2,041 cited
- → Advances in autism genetics: on the threshold of a new neurobiology(2008)1,856 cited
- → Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits(2011)1,067 cited
- → Common genetic variants on 5p14.1 associate with autism spectrum disorders(2009)969 cited
- → SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)(2013)917 cited
- → Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene(2008)822 cited
- → A Functional Genetic Link between Distinct Developmental Language Disorders(2008)686 cited
- → A genome-wide scan for common alleles affecting risk for autism(2010)587 cited
- → Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders(2008)541 cited
- → Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes(2009)432 cited