Search Results - Picker, Jonathan D

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  1. 1
    New Innovations: Therapeutic opportunities for Intellectual disabilities

    New Innovations: Therapeutic opportunities for Intellectual disabilities by Picker, Jonathan D., Walsh, Christopher A.

    Published 2013
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  2. 2
    A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene

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

    Published 2016
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  3. 3
    A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene

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

    Published 2016
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  4. 4
    Phenotypic Characterization of Mice Heterozygous for a Null Mutation of Glutamate Carboxypeptidase II

    Phenotypic Characterization of Mice Heterozygous for a Null Mutation of Glutamate Carboxypeptidase II by Han, Liqun, Picker, Jonathan D., Schaevitz, Laura R., Tsai, Guochuan, Feng, Jiamin, Jiang, Zhichun, Chu, Hillary C., Basu, Alo C., Berger-Sweeney, Joanne, Coyle, Joseph T.

    Published 2009
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  5. 5
    Expanding the Phenotypic Spectrum Associated with OPHN1 Variants

    Expanding the Phenotypic Spectrum Associated with OPHN1 Variants by 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.

    Published 2018
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  6. 6
    Unique bioinformatic approach and comprehensive reanalysis improve diagnostic yield of clinical exomes

    Unique bioinformatic approach and comprehensive reanalysis improve diagnostic yield of clinical exomes by 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.

    Published 2019
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  7. 7
    Expanding the phenotypic spectrum of GABRG2 variants: A recurrent GABRG2 missense variant associated with a severe phenotype

    Expanding the phenotypic spectrum of GABRG2 variants: A recurrent GABRG2 missense variant associated with a severe phenotype by Zou, Fanggeng, McWalter, Kirsty, Schmidt, Lindsay, Decker, Amy, Picker, Jonathan D., Lincoln, Sharyn, Sweetser, David A., Briere, Lauren C., Chellamani, Harini, Marsh, Eric, Medne, Livija, Wang, Raymond Y, Leydiker, Karen, Mower, Andrew, Visser, Gepke, Cuppen, Inge, van Gassen, Koen L, van der Smagt, Jasper, Yousaf, Adeel, Tennison, Michael, Shanmugham, Anita, Butler, Elizabeth, Richard, Gabriele, McKnight, Dianalee

    Published 2017
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  8. 8
    Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders

    Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders by Ching, Michael SL, 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

    Published 2010
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