Genetic architecture in autism spectrum disorder von Devlin, Bernie, Scherer, Stephen W

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A copy number variation map of the human genome von Zarrei, Mehdi, MacDonald, Jeffrey R., Merico, Daniele, Scherer, Stephen W.

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Progress in the genetics of autism spectrum disorder von Woodbury‐Smith, Marc, Scherer, Stephen W

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The Database of Genomic Variants: a curated collection of structural variation in the human genome von MacDonald, Jeffrey R, Ziman, Robert, Yuen, Ryan K C, Feuk, Lars, Scherer, Stephen W

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Phase Separation as a Missing Mechanism for Interpretation of Disease Mutations von Tsang, Brian, Pritišanac, Iva, Scherer, Stephen W., Moses, Alan M., Forman-Kay, Julie D.

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What a finding of gene copy number variation can add to the diagnosis of developmental neuropsychiatric disorders von Vorstman, Jacob, Scherer, Stephen W

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Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing von Jiang, Yong-hui, Yuen, Ryan K.C., Jin, Xin, Wang, Mingbang, Chen, Nong, Wu, Xueli, Ju, Jia, Mei, Junpu, Shi, Yujian, He, Mingze, Wang, Guangbiao, Liang, Jieqin, Wang, Zhe, Cao, Dandan, Carter, Melissa T., Chrysler, Christina, Drmic, Irene E., Howe, Jennifer L., Lau, Lynette, Marshall, Christian R., Merico, Daniele, Nalpathamkalam, Thomas, Thiruvahindrapuram, Bhooma, Thompson, Ann, Uddin, Mohammed, Walker, Susan, Luo, Jun, Anagnostou, Evdokia, Zwaigenbaum, Lonnie, Ring, Robert H., Wang, Jian, Lajonchere, Clara, Wang, Jun, Shih, Andy, Szatmari, Peter, Yang, Huanming, Dawson, Geraldine, Li, Yingrui, Scherer, Stephen W.

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Identifying signatures of natural selection in Tibetan and Andean populations using dense genome scan data von Bigham, Abigail, Bauchet, Marc, Pinto, Dalila, Mao, Xianyun, Akey, Joshua M, Mei, Rui, Scherer, Stephen W, Julian, Colleen G, Wilson, Megan J, López Herráez, David, Brutsaert, Tom, Parra, Esteban J, Moore, Lorna G, Shriver, Mark D

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Single cell-derived clonal analysis of human glioblastoma links functional and genomic heterogeneity von Meyer, Mona, Reimand, Jüri, Lan, Xiaoyang, Head, Renee, Zhu, Xueming, Kushida, Michelle, Bayani, Jane, Pressey, Jessica C., Lionel, Anath C., Clarke, Ian D., Cusimano, Michael, Squire, Jeremy A., Scherer, Stephen W., Bernstein, Mark, Woodin, Melanie A., Bader, Gary D., Dirks, Peter B.

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Contribution of SHANK3 Mutations to Autism Spectrum Disorder von Moessner, Rainald, Marshall, Christian R., Sutcliffe, James S., Skaug, Jennifer, Pinto, Dalila, Vincent, John, Zwaigenbaum, Lonnie, Fernandez, Bridget, Roberts, Wendy, Szatmari, Peter, Scherer, Stephen W.

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Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling von Richter, Melanie, Murtaza, Nadeem, Scharrenberg, Robin, White, Sean H., Johanns, Ole, Walker, Susan, Yuen, Ryan K. C., Schwanke, Birgit, Bedürftig, Bianca, Henis, Melad, Scharf, Sarah, Kraus, Vanessa, Dörk, Ronja, Hellmann, Jakob, Lindenmaier, Zsuzsa, Ellegood, Jacob, Hartung, Henrike, Kwan, Vickie, Sedlacik, Jan, Fiehler, Jens, Schweizer, Michaela, Lerch, Jason P., Hanganu-Opatz, Ileana L., Morellini, Fabio, Scherer, Stephen W., Singh, Karun K., Calderon de Anda, Froylan

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ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data von Dolzhenko, Egor, Bennett, Mark F, Richmond, Phillip A, Trost, Brett, Chen, Sai, van Vugt, Joke J F A, Nguyen, Charlotte, Narzisi, Giuseppe, Gainullin, Vladimir G, Gross, Andrew M, Lajoie, Bryan R, Taft, Ryan J, Wasserman, Wyeth W, Scherer, Stephen W, Veldink, Jan H, Bentley, David R, Yuen, Ryan K C, Bahlo, Melanie, Eberle, Michael A

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Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease von Bassett, Anne S., Scherer, Stephen W., Brzustowicz, Linda M.

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Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease von Wright, Galen E.B., Collins, Jennifer A., Kay, Chris, McDonald, Cassandra, Dolzhenko, Egor, Xia, Qingwen, Bečanović, Kristina, Drögemöller, Britt I., Semaka, Alicia, Nguyen, Charlotte M., Trost, Brett, Richards, Fiona, Bijlsma, Emilia K., Squitieri, Ferdinando, Ross, Colin J.D., Scherer, Stephen W., Eberle, Michael A., Yuen, Ryan K.C., Hayden, Michael R.

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Origins and functional impact of copy number variation in the human genome von Conrad, Donald F., Pinto, Dalila, Redon, Richard, Feuk, Lars, Gokcumen, Omer, Zhang, Yujun, Aerts, Jan, Andrews, T. Daniel, Barnes, Chris, Campbell, Peter, Fitzgerald, Tomas, Hu, Min, Ihm, Chun Hwa, Kristiansson, Kati, MacArthur, Daniel G., MacDonald, Jeffrey R., Onyiah, Ifejinelo, Pang, Andy Wing Chun, Robson, Sam, Stirrups, Kathy, Valsesia, Armand, Walter, Klaudia, Wei, John, Tyler-Smith, Chris, Carter, Nigel P., Lee, Charles, Scherer, Stephen W., Hurles, Matthew E.

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Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation von Berkel, Simone, Marshall, Christian R, Weiss, Birgit, Howe, Jennifer, Roeth, Ralph, Moog, Ute, Endris, Volker, Roberts, Wendy, Szatmari, Peter, Pinto, Dalila, Bonin, Michael, Riess, Angelika, Engels, Hartmut, Sprengel, Rolf, Scherer, Stephen W, Rappold, Gudrun A

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The clinical context of copy number variation in the human genome von Lee, Charles, Scherer, Stephen W.

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Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome von Dhanraj, Santhosh, Matveev, Anna, Li, Hongbing, Lauhasurayotin, Supanun, Jardine, Lawrence, Cada, Michaela, Zlateska, Bozana, Tailor, Chetankumar S., Zhou, Joseph, Mendoza-Londono, Roberto, Vincent, Ajoy, Durie, Peter R., Scherer, Stephen W., Rommens, Johanna M., Heon, Elise, Dror, Yigal

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Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants von Martin, Joanna, BSc, Cooper, Miriam, MRCPsych, MSc, Hamshere, Marian L., PhD, Pocklington, Andrew, PhD, Scherer, Stephen W., PhD, FRSC, Kent, Lindsey, MD, PhD, Gill, Michael, MD, MRCPsych, Owen, Michael J., FRCPsych, PhD, Williams, Nigel, PhD, O'Donovan, Michael C., FRCPsych, PhD, Thapar, Anita, FRCPsych, PhD, Holmans, Peter, PhD

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Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder von Vaags, Andrea K., Lionel, Anath C., Sato, Daisuke, Goodenberger, McKinsey, Stein, Quinn P., Curran, Sarah, Ogilvie, Caroline, Ahn, Joo Wook, Drmic, Irene, Senman, Lili, Chrysler, Christina, Thompson, Ann, Russell, Carolyn, Prasad, Aparna, Walker, Susan, Pinto, Dalila, Marshall, Christian R., Stavropoulos, Dimitri J., Zwaigenbaum, Lonnie, Fernandez, Bridget A., Fombonne, Eric, Bolton, Patrick F., Collier, David A., Hodge, Jennelle C., Roberts, Wendy, Szatmari, Peter, Scherer, Stephen W.

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