Unique bioinformatic approach and comprehensive reanalysis improve diagnostic yield of clinical exomes von Schmitz-Abe, Klaus, Li, Qifei, Rosen, Samantha M, Nori, Neeharika, Madden, Jill A, Genetti, Casie A, Wojcik, Monica H, Ponnaluri, Sadhana, Gubbels, Cynthia S, Picker, Jonathan D, O'Donnell-Luria, Anne H, Yu, Timothy W, Bodamer, Olaf, Brownstein, Catherine A, Beggs, Alan H, Agrawal, Pankaj B

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Revising the Psychiatric Phenotype of Homocystinuria von Almuqbil, Mohamed A., Waisbren, Susan E., Levy, Harvey L., Picker, Jonathan D.

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New innovations: Therapeutic opportunities for intellectual disabilities von Picker, Jonathan D., Walsh, Christopher A.

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Advances in the Treatment of Fragile X Syndrome von Hagerman, Randi J, Berry-Kravis, Elizabeth, Kaufmann, Walter E, Ono, Michele Y, Tartaglia, Nicole, Lachiewicz, Ave, Kronk, Rebecca, Delahunty, Carol, Hessl, David, Visootsak, Jeannie, Picker, Jonathan, Gane, Louise, Tranfaglia, Michael

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Utility of Genetic Testing in Fetal Alcohol Spectrum Disorder von Jamuar, Saumya S., Picker, Jonathan D., Stoler, Joan M.

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A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene von Rodan, Lance H, Cohen, Julie, Fatemi, Ali, Gillis, Tammy, Lucente, Diane, Gusella, James, Picker, Jonathan D

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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders von Ching, Michael S.L., Shen, Yiping, Tan, Wen-Hann, Jeste, Shafali S., Morrow, Eric M., Chen, Xiaoli, Mukaddes, Nahit M., Yoo, Seung-Yun, Hanson, Ellen, Hundley, Rachel, Austin, Christina, Becker, Ronald E., Berry, Gerard T., Driscoll, Katherine, Engle, Elizabeth C., Friedman, Sandra, Gusella, James F., Hisama, Fuki M., Irons, Mira B., Lafiosca, Tina, LeClair, Elaine, Miller, David T., Neessen, Michael, Picker, Jonathan D., Rappaport, Leonard, Rooney, Cynthia M., Sarco, Dean P., Stoler, Joan M., Walsh, Christopher A., Wolff, Robert R., Zhang, Ting, Nasir, Ramzi H., Wu, Bai-Lin

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Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample von Talkowski, Michael E, Ordulu, Zehra, Pillalamarri, Vamsee, Benson, Carol B, Blumenthal, Ian, Connolly, Susan, Hanscom, Carrie, Hussain, Naveed, Pereira, Shahrin, Picker, Jonathan, Rosenfeld, Jill A, Shaffer, Lisa G, Wilkins-Haug, Louise E, Gusella, James F, Morton, Cynthia C

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Review of Salient Investigational Drugs for the Treatment of Fragile X Syndrome von Munshi, Kaizad, Pawlowski, Katherine, Gonzalez-Heydrich, Joseph, Picker, Jonathan D

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Latent Class Analysis Identifies Distinctive Behavioral Subtypes in Children with Fragile X Syndrome von Kaufmann, Walter E., Raspa, Melissa, Bann, Carla M., Gable, Julia M., Harris, Holly K., Budimirovic, Dejan B., Lozano, Reymundo

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Abnormal Mechanisms of Plasticity and Metaplasticity in Autism Spectrum Disorders and Fragile X Syndrome von Oberman, Lindsay M, Ifert-Miller, Fritz, Najib, Umer, Bashir, Shahid, Heydrich, Joseph Gonzalez, Picker, Jonathan, Rotenberg, Alexander, Pascual-Leone, Alvaro

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A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene von Rodan, Lance H, Cohen, Julie, Fatemi, Ali, Gillis, Tammy, Lucente, Diane, Gusella, James, Picker, Jonathan D

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An altered neonatal behavioral phenotype in Mecp2 mutant mice von Picker, Jonathan D, Yang, Rebecca, Ricceri, Laura, Berger-Sweeney, Joanne

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Prokaryotic Collagen-Like Proteins as Novel Biomaterials von Picker, Jonathan, Lan, Ziyang, Arora, Srishtee, Green, Mykel, Hahn, Mariah, Cosgriff-Hernandez, Elizabeth, Hook, Magnus

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EEG abnormalities and seizures in genetically diagnosed Fragile X syndrome von Heard, Takijah T., Ramgopal, Sriram, Picker, Jonathan, Lincoln, Sharyn A., Rotenberg, Alexander, Kothare, Sanjeev V.

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Expanding the phenotypic spectrum associated with OPHN1 variants von Schwartz, Talia S., Wojcik, Monica H., Pelletier, Renee C., Edward, Heather L., Picker, Jonathan D., Holm, Ingrid A., Towne, Meghan C., Beggs, Alan H., Agrawal, Pankaj B.

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Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia von Adegbola, Abidemi, Lutz, Richard, Nikkola, Elina, Strom, Samuel P., Picker, Jonathan, Wynshaw-Boris, Anthony

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Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohort von Liu, Liying, Liu, Fang, Wang, Qiuhong, Xie, Hua, Li, Zhengchang, Lu, Qian, Wang, Yangyang, Zhang, Mengna, Zhang, Yu, Picker, Jonathan, Cui, Xiaodai, Zou, Liping, Chen, Xiaoli

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Glutamate carboxypeptidase II and folate deficiencies result in reciprocal protection against cognitive and social deficits in mice: Implications for neurodevelopmental disorders von Schaevitz, Laura R., Picker, Jonathan D., Rana, Jasmine, Kolodny, Nancy H., Shane, Barry, Berger‐Sweeney, Joanne E., Coyle, Joseph T.

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Transcranial magnetic stimulation provides means to assess cortical plasticity and excitability in humans with fragile x syndrome and autism spectrum disorder von Oberman, Lindsay, Ifert-Miller, Fritz, Najib, Umer, Bashir, Shahid, Woollacott, Ione, Gonzalez-Heydrich, Joseph, Picker, Jonathan, Rotenberg, Alexander, Pascual-Leone, Alvaro

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