Danielle S. Rudd
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Autism Spectrum Disorder Research, Genetics and Neurodevelopmental Disorders, Congenital heart defects research, Schizophrenia research and treatment
Most-Cited Works
- → Autism genome-wide copy number variation reveals ubiquitin and neuronal genes(2009)1,435 cited
- → Pax6 3′ deletion results in aniridia, autism and mental retardation(2008)137 cited
- → Early Detection of Subclinical Visual Damage After Blast-Mediated TBI Enables Prevention of Chronic Visual Deficit by Treatment With P7C3-S243(2014)90 cited
- → Influence of ZNF804a on Brain Structure Volumes and Symptom Severity in Individuals With Schizophrenia(2012)50 cited
- → PRICKLE1 Interaction with SYNAPSIN I Reveals a Role in Autism Spectrum Disorders(2013)44 cited
- → Genome-wide analysis of copy number variants in age-related macular degeneration(2010)41 cited
- → Novel copy number variants in children with autism and additional developmental anomalies(2009)39 cited
- → Copy Number Variations and Primary Open-Angle Glaucoma(2011)37 cited
- → Identification of chronic brain protein changes and protein targets of serum auto-antibodies after blast-mediated traumatic brain injury(2020)35 cited
- → A genome‐wide CNV analysis of schizophrenia reveals a potential role for a multiple‐hit model(2014)27 cited