A framework for the investigation of rare genetic disorders in neuropsychiatry
De novo and inherited rare genetic disorders (RGDs) are a major cause of human morbidity, frequently involving neuropsychiatric symptoms. Recent advances in genomic technologies and data sharing have revolutionized the identification and diagnosis of RGDs, presenting an opportunity to elucidate the...
Similar Items
-
A framework for the investigation of rare genetic disorders in neuropsychiatry
by: Sanders, Stephan J., et al.
Published: (2022) -
Imaging of thalamocortical dysrhythmia in neuropsychiatry
by: Joshua J Schulman, et al.
Published: (2011-07-01) -
Biological and Quantitative Issues in Neuropsychiatry
by: G. E. Berrios, et al.
Published: (1990-01-01) -
Encephalitis lethargica: The challenge of structure and function in neuropsychiatry
by: David Bruce Williams
Published: (2020-01-01) -
Editorial: Neuropsychology and neuropsychiatry of neurodegenerative disorders
by: Manuel eMenéndez-González, et al.
Published: (2015-12-01)