The Story of Rett Syndrome: From Clinic to Neurobiology von Chahrour, Maria, Zoghbi, Huda Y.

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Parkinson's Disease Genetics and Pathophysiology von Vázquez-Vélez, Gabriel E, Zoghbi, Huda Y

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Loss of MeCP2 in Parvalbumin-and Somatostatin-Expressing Neurons in Mice Leads to Distinct Rett Syndrome-like Phenotypes von Ito-Ishida, Aya, Ure, Kerstin, Chen, Hongmei, Swann, John W., Zoghbi, Huda Y.

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Rett Syndrome and the Ongoing Legacy of Close Clinical Observation von Zoghbi, Huda Y.

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Presymptomatic training mitigates functional deficits in a mouse model of Rett syndrome von Achilly, Nathan P., Wang, Wei, Zoghbi, Huda Y.

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Trinucleotide repeat disorders von ORR, Harry T, ZOGHBI, Huda Y

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Solving the Autism Puzzle a Few Pieces at a Time von Schaaf, Christian P., Zoghbi, Huda Y.

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MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome von Chen, Lin, Chen, Kaifu, Lavery, Laura A., Baker, Steven Andrew, Shaw, Chad A., Li, Wei, Zoghbi, Huda Y.

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Reduction of Nuak1 Decreases Tau and Reverses Phenotypes in a Tauopathy Mouse Model von Lasagna-Reeves, Cristian A., de Haro, Maria, Hao, Shuang, Park, Jeehye, Rousseaux, Maxime W.C., Al-Ramahi, Ismael, Jafar-Nejad, Paymaan, Vilanova-Velez, Luis, See, Lauren, De Maio, Antonia, Nitschke, Larissa, Wu, Zhenyu, Troncoso, Juan C., Westbrook, Thomas F., Tang, Jianrong, Botas, Juan, Zoghbi, Huda Y.

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? von Zoghbi, Huda Y.

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The distinct methylation landscape of maturing neurons and its role in Rett syndrome pathogenesis von Lavery, Laura A, Zoghbi, Huda Y

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Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides von Sztainberg, Yehezkel, Chen, Hong-mei, Swann, John W., Hao, Shuang, Tang, Bin, Wu, Zhenyu, Tang, Jianrong, Wan, Ying-Wooi, Liu, Zhandong, Rigo, Frank, Zoghbi, Huda Y.

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Cerebellar Transcriptome Profiles of ATXN1 Transgenic Mice Reveal SCA1 Disease Progression and Protection Pathways von Ingram, Melissa, Wozniak, Emily A.L., Duvick, Lisa, Yang, Rendong, Bergmann, Paul, Carson, Robert, O’Callaghan, Brennon, Zoghbi, Huda Y., Henzler, Christine, Orr, Harry T.

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MeCP2 Controls Excitatory Synaptic Strength by Regulating Glutamatergic Synapse Number von Chao, Hsiao-Tuan, Zoghbi, Huda Y., Rosenmund, Christian

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Molecular profiling predicts meningioma recurrence and reveals loss of DREAM complex repression in aggressive tumors von Patel, Akash J., Wan, Ying-Wooi, Al-Ouran, Rami, Revelli, Jean-Pierre, Cardenas, Maria F., Oneissi, Mazen, Xi, Liu, Jalali, Ali, Magnotti, John F., Muzny, Donna M., Doddapaneni, HarshaVardhan, Sebastian, Sherly, Heck, Kent A., Goodman, J. Clay, Gopinath, Shankar P., Liu, Zhandong, Rao, Ganesh, Plon, Sharon E., Yoshor, Daniel, Wheeler, David A., Zoghbi, Huda Y., Klisch, Tiemo J.

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MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription von Chahrour, Maria, Jung, Sung Yun, Shaw, Chad, Zhou, Xiaobo, Wong, Stephen T.C, Qin, Jun, Zoghbi, Huda Y

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Pathogenic Mechanisms of a Polyglutamine-mediated Neurodegenerative Disease, Spinocerebellar Ataxia Type 1 von Zoghbi, Huda Y., Orr, Harry T.

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Pumilio1 Haploinsufficiency Leads to SCA1-like Neurodegeneration by Increasing Wild-Type Ataxin1 Levels von Gennarino, Vincenzo A., Singh, Ravi K., White, Joshua J., De Maio, Antonia, Han, Kihoon, Kim, Ji-Yoen, Jafar-Nejad, Paymaan, di Ronza, Alberto, Kang, Hyojin, Sayegh, Layal S., Cooper, Thomas A., Orr, Harry T., Sillitoe, Roy V., Zoghbi, Huda Y.

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MeCP2 dysfunction in Rett syndrome and related disorders von Moretti, Paolo, Zoghbi, Huda Y

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Math1 Expression Redefines the Rhombic Lip Derivatives and Reveals Novel Lineages within the Brainstem and Cerebellum von Wang, Vincent Y., Rose, Matthew F., Zoghbi, Huda Y.

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