Maria T. Acosta
National Institutes of Health(US)Children's National(US)National Human Genome Research Institute(US)Office of the Director(US)Université Bourgogne Franche-Comté(FR)National Institutes of Health Clinical Center(US)
Publications by Year
Research Areas
Neurofibromatosis and Schwannoma Cases, Genetics and Neurodevelopmental Disorders, Lysosomal Storage Disorders Research, Genomics and Rare Diseases, Attention Deficit Hyperactivity Disorder
Most-Cited Works
- → A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication(2010)291 cited
- → Young adult outcomes in the follow‐up of the multimodal treatment study of attention‐deficit/hyperactivity disorder: symptom persistence, source discrepancy, and height suppression(2017)283 cited
- → Clinical spectrum of succinic semialdehyde dehydrogenase deficiency(2003)209 cited
- → Symptomatology of autism spectrum disorder in a population with neurofibromatosis type 1(2012)133 cited
- → Succinic semialdehyde dehydrogenase deficiency in children and adults(2003)131 cited
- → Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1(2016)122 cited