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American Journal of Human Genetics|January 9, 2008
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneMaricela Alarcón, Brett S Abrahams, Jennifer L Stone, et al.
Nature|January 24, 2024
The HIV capsid mimics karyopherin engagement of FG-nucleoporinsC F Dickson, S Hertel, A J Tuckwell, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 22, 2008
Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencingRavinesh A Kumar, Kevin A McGhee, Stephen Leach, et al.
Neuropsychology, Development, and Cognition. Section B, Aging, Neuropsychology and Cognition|March 13, 2014
Alterations in working memory networks in amnestic mild cognitive impairmentE M Migo, M Mitterschiffthaler, O O'Daly, et al.
Neuropsychology, Development, and Cognition. Section B, Aging, Neuropsychology and Cognition|August 4, 2015
Investigating virtual reality navigation in amnestic mild cognitive impairment using fMRIE M Migo, O O'Daly, M Mitterschiffthaler, et al.
Microbial Genomics|February 10, 2022
Towards comprehensive understanding of bacterial genetic diversity: large-scale amplifications in Bordetella pertussis and Mycobacterium tuberculosisJonathan S Abrahams, Michael R Weigand, Natalie Ring, et al.
American Journal of Human Genetics|January 9, 2008
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersBetul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, et al.
Plos Genetics|May 31, 2014
Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorderEsther R Berko, Masako Suzuki, Faygel Beren, et al.
Plos Genetics|June 27, 2009
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genesMaja Bucan, Brett S Abrahams, Kai Wang, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
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