| Strong association of de novo copy number mutations with sporadic schizophrenia B Xu, JL Roos, S Levy, EJ Van Rensburg, JA Gogos, M Karayiorgou Nature genetics 40 (7), 880-885, 2008 | 974 | 2008 |
| Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model KL Stark, B Xu, A Bagchi, WS Lai, H Liu, R Hsu, X Wan, P Pavlidis, ... Nature genetics 40 (6), 751-760, 2008 | 681 | 2008 |
| A spectral approach integrating functional genomic annotations for coding and noncoding variants I Ionita-Laza, K McCallum, B Xu, JD Buxbaum Nature genetics 48 (2), 214-220, 2016 | 639 | 2016 |
| Exome sequencing supports a de novo mutational paradigm for schizophrenia B Xu, JL Roos, P Dexheimer, B Boone, B Plummer, S Levy, JA Gogos, ... Nature genetics 43 (9), 864-868, 2011 | 542 | 2011 |
| De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia B Xu, I Ionita-Laza, JL Roos, B Boone, S Woodrick, Y Sun, S Levy, ... Nature genetics 44 (12), 1365-1369, 2012 | 491 | 2012 |
| Deficiency of Dgcr8, a gene disrupted by the 22q11. 2 microdeletion, results in altered short-term plasticity in the prefrontal cortex K Fénelon, J Mukai, B Xu, PK Hsu, LJ Drew, M Karayiorgou, ... Proceedings of the National Academy of Sciences 108 (11), 4447-4452, 2011 | 229 | 2011 |
| Diverse types of genetic variation converge on functional gene networks involved in schizophrenia SR Gilman, J Chang, B Xu, TS Bawa, JA Gogos, M Karayiorgou, D Vitkup Nature neuroscience 15 (12), 1723-1728, 2012 | 215 | 2012 |
| Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene A Takata, B Xu, I Ionita-Laza, JL Roos, JA Gogos, M Karayiorgou Neuron 82 (4), 773-780, 2014 | 212 | 2014 |
| Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans B Xu, A Woodroffe, L Rodriguez-Murillo, JL Roos, EJ van Rensburg, ... Proceedings of the National Academy of Sciences 106 (39), 16746-16751, 2009 | 174 | 2009 |
| The 22q11. 2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders LJ Drew, GW Crabtree, S Markx, KL Stark, F Chaverneff, B Xu, J Mukai, ... International Journal of Developmental Neuroscience 29 (3), 259-281, 2011 | 163 | 2011 |
| Derepression of a neuronal inhibitor due to miRNA dysregulation in a schizophrenia-related microdeletion B Xu, PK Hsu, KL Stark, M Karayiorgou, JA Gogos Cell 152 (1), 262-275, 2013 | 159 | 2013 |
| Akt1 deficiency affects neuronal morphology and predisposes to abnormalities in prefrontal cortex functioning WS Lai, B Xu, KGC Westphal, M Paterlini, B Olivier, P Pavlidis, ... Proceedings of the National Academy of Sciences 103 (45), 16906-16911, 2006 | 159 | 2006 |
| De novo synonymous mutations in regulatory elements contribute to the genetic etiology of autism and schizophrenia A Takata, I Ionita-Laza, JA Gogos, B Xu, M Karayiorgou Neuron 89 (5), 940-947, 2016 | 145 | 2016 |
| MicroRNAs in psychiatric and neurodevelopmental disorders B Xu, M Karayiorgou, JA Gogos Brain research 1338, 78-88, 2010 | 136 | 2010 |
| The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion K Fénelon, B Xu, CS Lai, J Mukai, S Markx, KL Stark, PK Hsu, WB Gan, ... Journal of neuroscience 33 (37), 14825-14839, 2013 | 112 | 2013 |
| Recapitulation and reversal of schizophrenia-related phenotypes in Setd1a-deficient mice J Mukai, E Cannavò, GW Crabtree, Z Sun, A Diamantopoulou, P Thakur, ... Neuron 104 (3), 471-487. e12, 2019 | 106 | 2019 |
| Urinary exosome miR‐30c‐5p as a biomarker of clear cell renal cell carcinoma that inhibits progression by targeting HSPA5 S Song, M Long, G Yu, Y Cheng, Q Yang, J Liu, Y Wang, J Sheng, ... Journal of cellular and molecular medicine 23 (10), 6755-6765, 2019 | 101 | 2019 |
| MicroRNA dysregulation in neuropsychiatric disorders and cognitive dysfunction B Xu, PK Hsu, M Karayiorgou, JA Gogos Neurobiology of disease 46 (2), 291-301, 2012 | 98 | 2012 |
| Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13. 3 as a susceptibility gene for schizophrenia and autism I Ionita-Laza, B Xu, V Makarov, JD Buxbaum, JL Roos, JA Gogos, ... Proceedings of the National Academy of Sciences 111 (1), 343-348, 2014 | 86 | 2014 |
| Cortical overgrowth in a preclinical forebrain organoid model of CNTNAP2-associated autism spectrum disorder JO de Jong, C Llapashtica, M Genestine, K Strauss, F Provenzano, Y Sun, ... Nature Communications 12 (1), 4087, 2021 | 72 | 2021 |
Joseph A. Gogos MD, PhDColumbia University, Zuckerman Institute and SNF Center for Precision Psychiatry and Mental Health在 columbia.edu 的电子邮件经过验证
