Distinct Dose-Dependent Cortical Neuronal Migration and Neurite Extension Defects in Lis1 and Ndel1 Mutant Mice

Por Youn, Yong Ha, Pramparo, Tiziano, Hirotsune, Shinji, Wynshaw-Boris, Anthony
Publicado em 2009

Lissencephaly: Mechanistic insights from animal models and potential therapeutic strategies

Por Wynshaw-Boris, Anthony, Pramparo, Tiziano, Youn, Yong Ha, Hirotsune, Shinji
Publicado em 2010

Novel Embryonic Neuronal Migration and Proliferation Defects in Dcx Mutant Mice Are Exacerbated by Lis1 Reduction

Por Pramparo, Tiziano, Youn, Yong Ha, Yingling, Jessica, Hirotsune, Shinji, Wynshaw-Boris, Anthony
Publicado em 2010

Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division

Por Yingling, Jessica, Youn, Yong Ha, Darling, Dawn, Toyo-oka, Kazuhito, Pramparo, Tiziano, Hirotsune, Shinji, Wynshaw-Boris, Anthony
Publicado em 2008

Global Developmental Gene Expression and Pathway Analysis of Normal Brain Development and Mouse Models of Human Neuronal Migration Defects

Por Pramparo, Tiziano, Libiger, Ondrej, Jain, Sonia, Li, Hong, Youn, Yong Ha, Hirotsune, Shinji, Schork, Nicholas J., Wynshaw-Boris, Anthony
Publicado em 2011

PERP regulates enamel formation via effects on cell–cell adhesion and gene expression

Por Jheon, Andrew H., Mostowfi, Pasha, Snead, Malcolm L., Ihrie, Rebecca A., Sone, Eli, Pramparo, Tiziano, Attardi, Laura D., Klein, Ophir D.
Publicado em 2011

Cell cycle networks link gene expression dysregulation, mutation, and brain maldevelopment in autistic toddlers

Por Pramparo, Tiziano, Lombardo, Michael V, Campbell, Kathleen, Barnes, Cynthia Carter, Marinero, Steven, Solso, Stephanie, Young, Julia, Mayo, Maisi, Dale, Anders, Ahrens‐Barbeau, Clelia, Murray, Sarah S, Lopez, Linda, Lewis, Nathan, Pierce, Karen, Courchesne, Eric
Publicado no Mol Syst Biol (2015)

Age-Dependent Brain Gene Expression and Copy Number Anomalies in Autism Suggest Distinct Pathological Processes at Young Versus Mature Ages

Por Chow, Maggie L., Pramparo, Tiziano, Winn, Mary E., Barnes, Cynthia Carter, Li, Hai-Ri, Weiss, Lauren, Fan, Jian-Bing, Murray, Sarah, April, Craig, Belinson, Haim, Fu, Xiang-Dong, Wynshaw-Boris, Anthony, Schork, Nicholas J., Courchesne, Eric
Publicado em 2012

Altered proliferation and networks in neural cells derived from idiopathic autistic individuals

Por Marchetto, Maria C., Belinson, Haim, Tian, Yuan, Freitas, Beatriz C., Fu, Chen, Vadodaria, Krishna, Beltrao-Braga, Patricia, Trujillo, Cleber A., Mendes, Ana P.D., Padmanabhan, Krishnan, Nunez, Yanelli, Ou, Jing, Ghosh, Himanish, Wright, Rebecca, Brennand, Kristen, Pierce, Karen, Eichenfield, Lawrence, Pramparo, Tiziano, Eyler, Lisa, Barnes, Cynthia C., Courchesne, Eric, Geschwind, Daniel H., Gage, Fred H., Wynshaw-Boris, Anthony, Muotri, Alysson R.
Publicado no Mol Psychiatry (2016)

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

Por van Bon, Bregje W M, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Moloney, Susan, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA
Publicado em 2010

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

Por van Bon, Bregje WM, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA
Publicado em 2010

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

Por van Bon, Bregje WM, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA
Publicado em 2010

Targeted sequencing identifies 91 neurodevelopmental disorder risk genes with autism and developmental disability biases

Por Stessman, Holly A. F., Xiong, Bo, Coe, Bradley P., Wang, Tianyun, Hoekzema, Kendra, Fenckova, Michaela, Kvarnung, Malin, Gerdts, Jennifer, Trinh, Sandy, Cosemans, Nele, Vives, Laura, Lin, Janice, Turner, Tychele N., Santen, Gijs, Ruivenkamp, Claudia, Kriek, Marjolein, van Haeringen, Arie, Aten, Emmelien, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Haan, Eric, Shaw, Marie, Gecz, Jozef, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Schwartz, Charles, Kooy, R. Frank, Vandeweyer, Geert, Helsmoortel, Celine, Romano, Corrado, Alberti, Antonino, Vinci, Mirella, Avola, Emanuela, Giusto, Stefania, Courchesne, Eric, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Amaral, David, Scheffer, Ingrid E., Delatycki, Martin B., Lockhart, Paul J., Hormozdiari, Fereydoun, Harich, Benjamin, Castells-Nobau, Anna, Xia, Kun, Peeters, Hilde, Nordenskjöld, Magnus, Schenck, Annette, Bernier, Raphael A., Eichler, Evan E.
Publicado no Nat Genet (2017)