De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K +22 more·2012·Molecular Psychiatry
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- Modeling Psychiatric Disorders in Experimental AnimalsHolly M Moore, Trevor William Robbins · 2015 · Wiley eBooks
- Construction of an exome-wide risk score for schizophrenia based on a weighted burden testDavid Curtis · 2017 · bioRxiv (Cold Spring Harbor Laboratory)
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- Developmental Exposure to Psychostimulant Primes Activity‐dependent Gene Induction in Frontal CortexYizhou Ye, Qing Liu, Wenyu Zhang, Surjeet S. Mastwal, Kuan Hong Wang · 2018 · Developmental Neurobiology
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- Heterozygosity for neurodevelopmental disorder-associated TRIO variants yields distinct deficits in behavior, neuronal development, and synaptic transmission in miceYevheniia Ishchenko, Amanda T. Jeng, Shufang Feng, Timothy Nottoli, Cindy Manriquez-Rodriguez, Khanh K Nguyen, Melissa G Carrizales, Matthew J Vitarelli, Ellen E Corcoran, Charles A. Greer et al. · 2024 · eLife
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- Genetics of schizophreniaKimberley Marie Kendall, James TR Walters, Michael C. O’Donovan · 2020
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- Doctor of Philosophy (PhD)Meggie Biss · 2015
- The PSDAnamika Banerjee, Karin E. Borgmann‐Winter, Rubik Ray, Chang-Gyu Hahn · 2016 · Elsevier eBooks
- The 4th Schizophrenia International Research Society Conference, 5–9 April 2014, Florence, Italy: A summary of topics and trendsOlukayode Abayomi, Davide Amato, C. C. Bailey, Byron K.Y. Bitanihirwe, Lynneice Bowen, Shimon Burshtein, Alexis E. Cullen, Montserrat Fusté, Ana Paula Herrmann, Babak Khodaie et al. · 2014 · Schizophrenia Research
- A brief report: de novo copy number variants in children with attention deficit hyperactivity disorderJoanna Martin, Grace Hosking, Megan E. Wadon · 2019 · medRxiv
- NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and X. laevis modelsMayanglambam Dhruba Singh, Matthew Jensen, Micaela C. Lasser, Emily Huber, Tanzeen Yusuff, Lucilla Pizzo, Brian Lifschutz, Inshya Desai, Alexis Kubina, Sneha Yennawar et al. · 2019 · bioRxiv (Cold Spring Harbor Laboratory)
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- Setting the stage for a role of the postsynaptic proteome in inherited neurometabolic disordersÀlex Bayés · 2018 · Journal of Inherited Metabolic Disease
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- The Genetic Architecture of Autism and Related ConditionsMichael Gill, Graham P. Kenny, Richard Anney · 2013 · InTech eBooks
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