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Nature Genetics|August 18, 2016
Patterns of genic intolerance of rare copy number variation in 59,898 human exomesDouglas M Ruderfer, Tymor Hamamsy, Monkol Lek, et al.
Plos Genetics|March 17, 2011
Testing for an unusual distribution of rare variantsBenjamin M Neale, Manuel A Rivas, Benjamin F Voight, et al.
Schizophrenia Research|October 24, 2006
Reaction time of the Continuous Performance Test is an endophenotypic marker for schizophrenia: a study of first-episode neuroleptic-naive schizophrenia, their non-psychotic first-degree relatives and healthy population controlsQiang Wang, Raymond Chan, Jinhua Sun, et al.
Annals of Human Genetics|September 18, 2014
Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese familyJing Cheng, Xueya Zhou, Yu Lu, et al.
Frontiers in Psychiatry|July 25, 2022
Abnormal Brain Structure Morphology in Early-Onset SchizophreniaJia Cai, Wei Wei, Liansheng Zhao, et al.
Frontiers in Neuroscience|June 6, 2017
Chronic Ketamine Exposure Causes White Matter Microstructural Abnormalities in Adolescent Cynomolgus MonkeysQi Li, Lin Shi, Gang Lu, et al.
Plos One|September 21, 2016
Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot StudyAntonella Trotta, Conrad Iyegbe, Marta Di Forti, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorderAna C Parente Pereira, Andrew McQuillin, Vinay Puri, et al.
European Journal of Human Genetics : EJHG|November 6, 2014
No evidence for rare recessive and compound heterozygous disruptive variants in schizophreniaDouglas M Ruderfer, Elaine T Lim, Giulio Genovese, et al.
Sleep Medicine|May 27, 2018
Evaluation of an automated pipeline for large-scale EEG spectral analysis: the National Sleep Research ResourceSara Mariani, Leila Tarokh, Ina Djonlagic, et al.
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