受强制性开放获取政策约束的文章 - BIN XU了解详情
可在其他位置公开访问的文章：41 篇
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
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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
强制性开放获取政策： US National Institutes of Health
MicroRNAs in psychiatric and neurodevelopmental disorders
B Xu, M Karayiorgou, JA Gogos
Brain research 1338, 78-88, 2010
强制性开放获取政策： US National Institutes of Health
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
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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
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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
强制性开放获取政策： 国家自然科学基金委员会
MicroRNA dysregulation in neuropsychiatric disorders and cognitive dysfunction
B Xu, PK Hsu, M Karayiorgou, JA Gogos
Neurobiology of disease 46 (2), 291-301, 2012
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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
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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
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Alteration of neuronal excitability and short-term synaptic plasticity in the prefrontal cortex of a mouse model of mental illness
GW Crabtree, Z Sun, M Kvajo, JAC Broek, K Fénelon, H McKellar, L Xiao, ...
Journal of Neuroscience 37 (15), 4158-4180, 2017
强制性开放获取政策： US National Institutes of Health
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