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by Okbay, Aysu and Beauchamp, Jonathan and Fontana, M.A and Lee, James J and Pers, Tune and Rietveld, C.A and Turley, Patrick and Chen, G.-B and Emilsson, Valur and Meddens, S.F.W and Oskarsson, S and Pickrell, J.K and Thom, K and Timshel, P and Vlaming, Ronald and Abdellaoui, Abdel and Ahluwalia, Tarunveer Singh and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, G and Brandsma, Johan and Pina Concas, M and Derringer, J and Furlotte, N.A and Galesloot, Tessel and Girotto, S and Gupta, R and Hall, Leanne M and Harris, Sarah and Hofer, E and Horikoshi, M and Huffman, Jennifer E and Kaasik, K and Kalafati, Ioanna-Panagiota and Karlsson, Robert and Kong, Augustine and Lahti, Jari and Lee, Sven and Deleeuw, C and Lind, Penelope and Lindgren, K.-O and Liu, T and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Mike and Most, Peter and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter and Qian, Y and Raitakari, Olli and Rueedi, R and Salvi, E and Schmidt, B and Schraut, K.E and Shi, J and Smith, Albert Vernon and Poot, Raymond and St Pourcain, Beate and Teumer, Alexander and Thorleifsson, Gudmar and Verweij, Niek and Vuckovic, gana and Wellmann, J and Westra, Harm-Jan and Yang, J and Zhao, W and Zhu, Z and Alizadeh, Behrooz and Amin, Najaf and Bakshi, A and Baumeister, Sebastian and Biino, G and Bønnelykke, Klaus and Boyle, Patricia and Campbell, Harry and Cappuccio, F.P and Davies, Gail and Neve, Jan-Emmanuel and Deloukas, Panagiotis and Demuth, Ilja and Ding, J and Eibich, P and Eisele, L and Eklund, Niina and Evans, David and Faul, Jessica D and Feitosa, Mary Furlan and Forstner, Aneas and Gandin, Ilaria and Gunnarsson, B and Halldorsson, Bjarni and Harris, Tamara and Holliday, Elizabeth and Heath, Anew C and Hocking, L.J and Homuth, Georg and Horan, Mike and ... and LifeLines Cohort Study and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 05/2016, Volume 533, Issue 7604, pp. 539 - 542
Journal Article
Molecular Syndromology, ISSN 1661-8769, 02/2015, Volume 6, Issue 1, pp. 7 - 22
Based on genomic rearrangements and copy number variations, the contactin-associated protein-like 2 gene (CNTNAP2) has been implicated in neurodevelopmental... 
Review Article | Autism | CNTNAP2 | Epilepsy | DNA methylation | Schizophrenia | Specific language impairment | CNV | SNV | Neurodevelopmental disorders | Intellectual delay | Multigenic networks | Review
Journal Article
by Lee, James J and Wedow, Robbee and Okbay, Aysu and Kong, Edward and Maghzian, Omeed and Zacher, Meghan and Nguyen-Viet, Tuan Anh and Bowers, Peter and Sidorenko, Julia and Karlsson Linnér, Richard and Fontana, Mark Alan and Kundu, Tushar and Lee, Chanwook and Li, Hui and Li, Ruoxi and Royer, Rebecca and Timshel, Pascal N and Walters, Raymond K and Willoughby, Emily A and Yengo, Loïc and Agee, Michelle and Alipanahi, Babak and Auton, Adam and Bell, Robert K and Bryc, Katarzyna and Elson, Sarah L and Fontanillas, Pierre and Hinds, David A and McCreight, Jennifer C and Huber, Karen E and Litterman, Nadia K and McIntyre, Matthew H and Mountain, Joanna L and Noblin, Elizabeth S and Northover, Carrie A. M and Pitts, Steven J and Sathirapongsasuti, J. Fah and Sazonova, Olga V and Shelton, Janie F and Shringarpure, Suyash and Tian, Chao and Vacic, Vladimir and Wilson, Catherine H and Okbay, Aysu and Beauchamp, Jonathan P and Fontana, Mark Alan and Lee, James J and Pers, Tune H and Rietveld, Cornelius A and Turley, Patrick and Chen, Guo-Bo and Emilsson, Valur and Meddens, S. Fleur W and Oskarsson, Sven and Pickrell, Joseph K and Thom, Kevin and Timshel, Pascal and Vlaming, Ronald de and Abdellaoui, Abdel and Ahluwalia, Tarunveer S and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, Gyda and Brandsma, Johannes H and Concas, Maria Pina and Derringer, Jaime and Furlotte, Nicholas A and Galesloot, Tessel E and Girotto, Giorgia and Gupta, Richa and Hall, Leanne M and Harris, Sarah E and Hofer, Edith and Horikoshi, Momoko and Huffman, Jennifer E and Kaasik, Kadri and Kalafati, Ioanna P and Karlsson, Robert and Kong, Augustine and Lahti, Jari and van der Lee, Sven J and Leeuw, Christiaan de and Lind, Penelope A and Lindgren, Karl-Oskar and Liu, Tian and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Michael B and van der Most, Peter J and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter J and Qian, Yong and Raitakari, Olli and Rueedi, Rico and Salvi, Erika and Schmidt, Börge and Schraut, Katharina E and ... and 23Me Res Team and Social Sci Genetic Assoc Consortiu and COGENT Cognitive Genomics Consorti and 23andMe Research Team and COGENT (Cognitive Genomics Consortium) and Social Science Genetic Association Consortium and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 08/2018, Volume 50, Issue 8, pp. 1112 - 1121
Journal Article
Molecular Syndromology, ISSN 1661-8769, 08/2019
Journal Article
by Steinberg, S and Jong, S. de and Mattheisen, M and Costas, J and Demontis, D and Jamain, S and Pietilainen, O.P.H and Lin, K and Papiol, S and Huttenlocher, J and Sigurdsson, E and Vassos, E and Giegling, I and Breuer, R and Fraser, G and Walker, N and Melle, I and Djurovic, S and Agartz, I and Tuulio-Henriksson, A and Suvisaari, J and Lonnqvist, J and Paunio, T and Olsen, L and Hansen, T and Ingason, A and Pirinen, M and Strengman, E and Group and Hougaard, D.M and Orntoft, T and Diiksen, M and Hollegaard, M.V and Nordentoft, M and Abramova, L and Kaleda, V and Arrojo, M and Sanjuan, J and Arango, C and Etain, B and Bellivier, F and Meary, A and Schurhoff, F and Szoke, A and Ribolsi, M and Magni, V and Siracusano, A and Sperling, S and Rossner, M and Christiansen, C and Kiemeney, L.A.L.M and Franke, B and Berg, L.H. van den and Veldink, J and Curran, S and Bolton, P and Poot, M and Staal, W and Rehnstrom, K and Kilpinen, H and Freitag, C.M and Meyer, J and Magnusson, P and Saemundsen, E and Martsenkovsky, I and Bikshaieva, I and Martsenkovska, I and Vashchenko, O and Raleva, M and Paketchieva, K and Stefanovski, B and Durmishi, N and Milovancevic, M. Pejovic and Tosevski, D. Lecic and Silagadze, T and Naneishvili, N and Mikeladze, N and Surguladze, S and Vincent, J.B and Farmer, A and Mitchell, P.B and Wright, A and Schofield, P.R and Fullerton, J.M and Montgomery, G.W and Martin, N.G and Rubino, I.A and Winkel, R. van and Kenis, G and Hert, M. de and Rethelyi, J.M and Bitter, I and Terenius, L and Jonsson, E.G and Bakker, S and Os, J. van and Jablensky, A and Leboyer, M and Bramon, E and Wellcome Trust Case Control Consor and GROUP and Wellcome Trust Case Control Consortium 2
Molecular Psychiatry, ISSN 1359-4184, 2014, Volume 19, Issue 1, pp. 108 - 114
Journal Article
Molecular Syndromology, ISSN 1661-8769, 05/2017, Volume 8, Issue 3, pp. 118 - 130
Intragenic deletions of the contactin-associated protein-like 2 gene ( ) have been found in patients with Gilles de la Tourette syndrome, intellectual... 
Neurodevelopmental disorders | CNTNAP2 | Intragenic deletions | Review
Journal Article
Molecular Syndromology, ISSN 1661-8769, 01/2019, Volume 9, Issue 6, pp. 275 - 278
Journal Article
Molecular Syndromology, ISSN 1661-8769, 01/2019, Volume 9, Issue 5, pp. 225 - 227
Journal Article
Molecular Syndromology, ISSN 1661-8769, 08/2014, Volume 5, Issue 5, pp. 229 - 235
Although autism spectrum disorder (ASD) shows a high degree of heritability, only a few mutated genes and mostly de novo copy number variations (CNVs) with a... 
Original Article | Autism | CNTNAP2 | Copy number variation | CNTN5 | CNTN6 | Candidate gene association study | Contactin gene family | Original
Journal Article
Molecular Syndromology, ISSN 1661-8769, 07/2018, Volume 9, Issue 4, pp. 171 - 174
Journal Article
Molecular Syndromology, ISSN 1661-8769, 05/2017, Volume 8, Issue 3, pp. 115 - 117
Journal Article
Molecular Syndromology, ISSN 1661-8769, 05/2018, Volume 9, Issue 3, pp. 119 - 121
Journal Article
Molecular Syndromology, ISSN 1661-8769, 12/2017, Volume 9, Issue 1, pp. 1 - 4
Journal Article