A framework for the investigation of rare genetic disorders in neuropsychiatry

A framework for the investigation of rare genetic disorders in neuropsychiatry

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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...

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Main Authors: Sanders, Stephan J. (Author), Sahin, Mustafa (Author), Hostyk, Joseph (Author), Thurm, Audrey (Author), Jacquemont, Sebastien (Author), Avillach, Paul (Author), Douard, Elise (Author), Martin, Christa L. (Author), Modi, Meera E. (Author), Moreno- (Author), Raznahan, Armin (Author), Anticevic, Alan (Author), Dolmetsch, Ricardo (Author), Feng, Guoping (Author), Geschwind, Daniel H. (Author), Glahn, David C. (Author), Goldstein, David B. (Author), Ledbetter, David H. (Author), Mulle, Jennifer G. (Author), Pasca, Sergiu P. (Author), Samaco, Rodney (Author), Sebat, Jonathan (Author), Pariser, Anne (Author), Lehner, Thomas (Author), Gur, Raquel E. (Author), Bearden, Carrie E. (Author)
Other Authors: McGovern Institute for Brain Research at MIT (Contributor), Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences (Contributor)
Format: Article
Language:English
Published: Springer Science and Business Media LLC, 2021-04-23T16:04:33Z.
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