TY - JOUR AU - Leckman, J. F. PY - 2002 DA - 2002// TI - Tourette's syndrome JO - Lancet. VL - 360 UR - https://doi.org/10.1016/S0140-6736(02)11526-1 DO - 10.1016/S0140-6736(02)11526-1 ID - Leckman2002 ER - TY - JOUR AU - Scharf, J. M. AU - Miller, L. L. AU - Gauvin, C. A. AU - Alabiso, J. AU - Mathews, C. A. AU - Ben-Shlomo, Y. PY - 2015 DA - 2015// TI - Population prevalence of Tourette syndrome: a systematic review and meta-analysis JO - Mov Disord VL - 30 UR - https://doi.org/10.1002/mds.26089 DO - 10.1002/mds.26089 ID - Scharf2015 ER - TY - JOUR AU - Swain, J. E. AU - Scahill, L. AU - Lombroso, P. J. AU - King, R. A. AU - Leckman, J. F. PY - 2007 DA - 2007// TI - Tourette syndrome and tic disorders: a decade of progress JO - J Am Acad Child Adolesc Psychiatry VL - 46 UR - https://doi.org/10.1097/chi.0b013e318068fbcc DO - 10.1097/chi.0b013e318068fbcc ID - Swain2007 ER - TY - JOUR AU - Cravedi, E. AU - Deniau, E. AU - Giannitelli, M. AU - Xavier, J. AU - Hartmann, A. AU - Cohen, D. PY - 2017 DA - 2017// TI - Tourette syndrome and other neurodevelopmental disorders: a comprehensive review JO - Child Adolesc Psychiatry Ment Health VL - 11 UR - https://doi.org/10.1186/s13034-017-0196-x DO - 10.1186/s13034-017-0196-x ID - Cravedi2017 ER - TY - JOUR AU - Hirschtritt, M. E. AU - Lee, P. C. AU - Pauls, D. L. AU - Dion, Y. AU - Grados, M. A. AU - Illmann, C. PY - 2015 DA - 2015// TI - Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome JO - JAMA Psychiatry VL - 72 UR - https://doi.org/10.1001/jamapsychiatry.2014.2650 DO - 10.1001/jamapsychiatry.2014.2650 ID - Hirschtritt2015 ER - TY - STD TI - Jankovic J. Tourette syndrome: pathogenesis, clinical features and diagnosis. Waltham, MA (Accessed on November 26, 2019): UpToDate. ID - ref6 ER - TY - JOUR AU - Qiao, Y. AU - Mercier, E. AU - Dastan, J. AU - Hurlburt, J. AU - McGillivray, B. AU - Chudley, A. E. PY - 2014 DA - 2014// TI - Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID) JO - BMC Med Genet VL - 15 UR - https://doi.org/10.1186/1471-2350-15-82 DO - 10.1186/1471-2350-15-82 ID - Qiao2014 ER - TY - JOUR AU - Zarrei, M. AU - Burton, C. L. AU - Engchuan, W. AU - Young, E. J. AU - Higginbotham, E. J. AU - MacDonald, J. R. PY - 2019 DA - 2019// TI - A large data resource of genomic copy number variation across neurodevelopmental disorders JO - NPJ Genom Med VL - 4 UR - https://doi.org/10.1038/s41525-019-0098-3 DO - 10.1038/s41525-019-0098-3 ID - Zarrei2019 ER - TY - JOUR AU - Mataix-Cols, D. AU - Isomura, K. AU - Perez-Vigil, A. AU - Chang, Z. AU - Ruck, C. AU - Larsson, K. J. PY - 2015 DA - 2015// TI - Familial risks of Tourette syndrome and chronic tic disorders JO - A Population-Based Cohort Study JAMA Psychiatry VL - 72 UR - https://doi.org/10.1001/jamapsychiatry.2015.0627 DO - 10.1001/jamapsychiatry.2015.0627 ID - Mataix-Cols2015 ER - TY - JOUR AU - Robertson, M. M. AU - Eapen, V. AU - Singer, H. S. AU - Martino, D. AU - Scharf, J. M. AU - Paschou, P. PY - 2017 DA - 2017// TI - Gilles de la Tourette syndrome JO - Nat Rev Dis Primers VL - 3 UR - https://doi.org/10.1038/nrdp.2016.97 DO - 10.1038/nrdp.2016.97 ID - Robertson2017 ER - TY - JOUR AU - Qi, Y. AU - Zheng, Y. AU - Li, Z. AU - Liu, Z. AU - Xiong, L. PY - 2011 DA - 2011// TI - Genetic studies of tic disorders and Tourette syndrome JO - Methods Mol Biol VL - 2019 ID - Qi2011 ER - TY - JOUR AU - Abelson, J. F. AU - Kwan, K. Y. AU - O'Roak, B. J. AU - Baek, D. Y. AU - Stillman, A. A. AU - Morgan, T. M. PY - 2005 DA - 2005// TI - Sequence variants in SLITRK1 are associated with Tourette's syndrome JO - Science. VL - 310 UR - https://doi.org/10.1126/science.1116502 DO - 10.1126/science.1116502 ID - Abelson2005 ER - TY - JOUR AU - Pak, C. AU - Danko, T. AU - Zhang, Y. AU - Aoto, J. AU - Anderson, G. AU - Maxeiner, S. PY - 2015 DA - 2015// TI - Human neuropsychiatric disease modeling using conditional deletion reveals synaptic transmission defects caused by heterozygous mutations in NRXN1 JO - Cell Stem Cell VL - 17 UR - https://doi.org/10.1016/j.stem.2015.07.017 DO - 10.1016/j.stem.2015.07.017 ID - Pak2015 ER - TY - JOUR AU - Oguro-Ando, A. AU - Zuko, A. AU - Kleijer, K. T. E. AU - Burbach, J. P. H. PY - 2017 DA - 2017// TI - A current view on contactin-4, −5, and −6: implications in neurodevelopmental disorders JO - Mol Cell Neurosci VL - 81 UR - https://doi.org/10.1016/j.mcn.2016.12.004 DO - 10.1016/j.mcn.2016.12.004 ID - Oguro-Ando2017 ER - TY - JOUR AU - Daalen, E. AU - Kemner, C. AU - Verbeek, N. E. AU - Zwaag, B. AU - Dijkhuizen, T. AU - Rump, P. PY - 2011 DA - 2011// TI - Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism JO - Neurogenetics. VL - 12 UR - https://doi.org/10.1007/s10048-011-0297-2 DO - 10.1007/s10048-011-0297-2 ID - Daalen2011 ER - TY - STD TI - Qi Y, Zheng Y, Li Z, Xiong L. Progress in Genetic Studies of Tourette's Syndrome. Brain Sci. 2017;7(10). ID - ref16 ER - TY - JOUR AU - Bonis, M. L. AU - Cerase, A. AU - Matarazzo, M. R. AU - Ferraro, M. AU - Strazzullo, M. AU - Hansen, R. S. PY - 2006 DA - 2006// TI - Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications JO - Hum Mol Genet VL - 15 UR - https://doi.org/10.1093/hmg/ddl027 DO - 10.1093/hmg/ddl027 ID - Bonis2006 ER - TY - JOUR AU - Matarazzo, M. R. AU - Bonis, M. L. AU - Gregory, R. I. AU - Vacca, M. AU - Hansen, R. S. AU - Mercadante, G. PY - 2002 DA - 2002// TI - Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes JO - Hum Mol Genet VL - 11 UR - https://doi.org/10.1093/hmg/11.25.3191 DO - 10.1093/hmg/11.25.3191 ID - Matarazzo2002 ER - TY - JOUR AU - Danglot, L. AU - Zylbersztejn, K. AU - Petkovic, M. AU - Gauberti, M. AU - Meziane, H. AU - Combe, R. PY - 2012 DA - 2012// TI - Absence of TI-VAMP/Vamp7 leads to increased anxiety in mice JO - J Neurosci VL - 32 UR - https://doi.org/10.1523/JNEUROSCI.4436-11.2012 DO - 10.1523/JNEUROSCI.4436-11.2012 ID - Danglot2012 ER - TY - JOUR AU - Crawford, D. C. AU - Ramirez, D. M. AU - Trauterman, B. AU - Monteggia, L. M. AU - Kavalali, E. T. PY - 2017 DA - 2017// TI - Selective molecular impairment of spontaneous neurotransmission modulates synaptic efficacy JO - Nat Commun VL - 8 UR - https://doi.org/10.1038/ncomms14436 DO - 10.1038/ncomms14436 ID - Crawford2017 ER - TY - JOUR AU - Saito, T. AU - Parsia, S. AU - Papolos, D. F. AU - Lachman, H. M. PY - 2000 DA - 2000// TI - Analysis of the pseudoautosomal X-linked gene SYBL1in bipolar affective disorder: description of a new candidate allele for psychiatric disorders JO - Am J Med Genet VL - 96 UR - https://doi.org/3.0.CO;2-R DO - 3.0.CO;2-R ID - Saito2000 ER - TY - JOUR AU - Muller, D. J. AU - Schulze, T. G. AU - Jahnes, E. AU - Cichon, S. AU - Krauss, H. AU - Kesper, K. PY - 2002 DA - 2002// TI - Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder JO - Am J Med Genet VL - 114 UR - https://doi.org/10.1002/ajmg.10115 DO - 10.1002/ajmg.10115 ID - Muller2002 ER - TY - JOUR AU - Panagiotaki, N. AU - Dajas-Bailador, F. AU - Amaya, E. AU - Papalopulu, N. AU - Dorey, K. PY - 2010 DA - 2010// TI - Characterisation of a new regulator of BDNF signalling, Sprouty3, involved in axonal morphogenesis in vivo JO - Development. VL - 137 UR - https://doi.org/10.1242/dev.053173 DO - 10.1242/dev.053173 ID - Panagiotaki2010 ER - TY - JOUR AU - Ning, Z. AU - McLellan, A. S. AU - Ball, M. AU - Wynne, F. AU - O'Neill, C. AU - Mills, W. PY - 2015 DA - 2015// TI - Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region JO - Hum Mol Genet VL - 24 UR - https://doi.org/10.1093/hmg/ddv231 DO - 10.1093/hmg/ddv231 ID - Ning2015 ER - TY - JOUR AU - Ning, Z. AU - Williams, J. M. AU - Kumari, R. AU - Baranov, P. V. AU - Moore, T. PY - 2019 DA - 2019// TI - Opposite expression patterns of Spry3 and p75NTR in cerebellar Vermis suggest a male-specific mechanism of autism pathogenesis JO - Front Psychiatry VL - 10 UR - https://doi.org/10.3389/fpsyt.2019.00416 DO - 10.3389/fpsyt.2019.00416 ID - Ning2019 ER - TY - JOUR AU - MacDonald, J. R. AU - Ziman, R. AU - Yuen, R. K. AU - Feuk, L. AU - Scherer, S. W. PY - 2014 DA - 2014// TI - The database of genomic variants: a curated collection of structural variation in the human genome JO - Nucleic Acids Res VL - 42 UR - https://doi.org/10.1093/nar/gkt958 DO - 10.1093/nar/gkt958 ID - MacDonald2014 ER - TY - JOUR AU - Firth, H. V. AU - Richards, S. M. AU - Bevan, A. P. AU - Clayton, S. AU - Corpas, M. AU - Rajan, D. PY - 2009 DA - 2009// TI - DECIPHER: database of chromosomal imbalance and phenotype in humans using Ensembl resources JO - Am J Hum Genet VL - 84 UR - https://doi.org/10.1016/j.ajhg.2009.03.010 DO - 10.1016/j.ajhg.2009.03.010 ID - Firth2009 ER - TY - JOUR AU - Rehm, H. L. AU - Berg, J. S. AU - Brooks, L. D. AU - Bustamante, C. D. AU - Evans, J. P. AU - Landrum, M. J. PY - 2015 DA - 2015// TI - ClinGen--the clinical genome resource JO - N Engl J Med VL - 372 UR - https://doi.org/10.1056/NEJMsr1406261 DO - 10.1056/NEJMsr1406261 ID - Rehm2015 ER - TY - JOUR AU - Harewood, L. AU - Fraser, P. PY - 2014 DA - 2014// TI - The impact of chromosomal rearrangements on regulation of gene expression JO - Hum Mol Genet VL - 23 UR - https://doi.org/10.1093/hmg/ddu278 DO - 10.1093/hmg/ddu278 ID - Harewood2014 ER -