Regulation of the Epigenome by Vitamin C von Young, Juan I, Züchner, Stephan, Wang, Gaofeng

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Ascorbate Induces Ten-Eleven Translocation (Tet) Methylcytosine Dioxygenase-mediated Generation of 5-Hydroxymethylcytosine von Minor, Emily A., Court, Brenda L., Young, Juan I., Wang, Gaofeng

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Epigenome-wide meta-analysis of DNA methylation differences in prefrontal cortex implicates the immune processes in Alzheimer’s disease von Zhang, Lanyu, Silva, Tiago C., Young, Juan I., Gomez, Lissette, Schmidt, Michael A., Hamilton-Nelson, Kara L., Kunkle, Brian W., Chen, Xi, Martin, Eden R., Wang, Lily

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Cross-tissue analysis of blood and brain epigenome-wide association studies in Alzheimer’s disease von C. Silva, Tiago, Young, Juan I., Zhang, Lanyu, Gomez, Lissette, Schmidt, Michael A., Varma, Achintya, Chen, X. Steven, Martin, Eden R., Wang, Lily

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Ascorbate-induced generation of 5-hydroxymethylcytosine is unaffected by varying levels of iron and 2-oxoglutarate von Dickson, Kevin M., Gustafson, Christopher B., Young, Juan I., Züchner, Stephan, Wang, Gaofeng

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Critical evaluation of the reliability of DNA methylation probes on the Illumina MethylationEPIC v1.0 BeadChip microarrays von Zhang, Wei, Young, Juan I, Gomez, Lissette, Schmidt, Michael A, Lukacsovich, David, Varma, Achintya, Chen, X Steven, Kunkle, Brian, Martin, Eden R, Wang, Lily

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Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease von Krall, Paola, Canales, Cesar P, Kairath, Pamela, Carmona-Mora, Paulina, Molina, Jessica, Carpio, J Daniel, Ruiz, Phillip, Mezzano, Sergio A, Li, Jing, Wei, Changli, Reiser, Jochen, Young, Juan I, Walz, Katherina

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Regulation of RNA Splicing by the Methylation-Dependent Transcriptional Repressor Methyl-CpG Binding Protein 2 von Juan I. Young, Eugene P. Hong, John C. Castle, Juan Crespo-Barreto, Bowman, Aaron B., Matthew F. Rose, Dongcheul Kang, Richman, Ron, Johnson, Jason M., Susan Berget, Zoghbi, Huda Y.

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Sex-specific DNA methylation differences in Alzheimer's disease pathology von Zhang, Lanyu, Young, Juan I., Gomez, Lissette, Silva, Tiago C., Schmidt, Michael A., Cai, Jesse, Chen, Xi, Martin, Eden R., Wang, Lily

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Distinct sex-specific DNA methylation differences in Alzheimer's disease von C Silva, Tiago, Zhang, Wei, Young, Juan I, Gomez, Lissette, Schmidt, Michael A, Varma, Achintya, Chen, X Steven, Martin, Eden R, Wang, Lily

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Distinct CSF biomarker-associated DNA methylation in Alzheimer's disease and cognitively normal subjects von Zhang, Wei, Young, Juan I, Gomez, Lissette, Schmidt, Michael A, Lukacsovich, David, Varma, Achintya, Chen, X Steven, Martin, Eden R, Wang, Lily

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Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models von Ricard, Guénola, Molina, Jessica, Chrast, Jacqueline, Gu, Wenli, Gheldof, Nele, Pradervand, Sylvain, Schütz, Frédéric, Young, Juan I, Lupski, James R, Reymond, Alexandre, Walz, Katherina

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Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning von Abad, Clemer, Robayo, Maria C., Muñiz-Moreno, Maria del Mar, Bernardi, Maria T., Otero, Maria G., Kosanovic, Christina, Griswold, Anthony J., Pierson, Tyler Mark, Walz, Katherina, Young, Juan I.

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DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and Palate von Young, Juan I., Slifer, Susan, Hecht, Jacqueline T., Blanton, Susan H.

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Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2–associated schwannomas reveals differences in efficacy and drug resistance development von Fuse, Marisa A, Dinh, Christine T, Vitte, Jeremie, Kirkpatrick, Joanna, Mindos, Thomas, Plati, Stephani Klingeman, Young, Juan I, Huang, Jie, Carlstedt, Annemarie, Franco, Maria Clara, Brnjos, Konstantin, Nagamoto, Jackson, Petrilli, Alejandra M, Copik, Alicja J, Soulakova, Julia N, Bracho, Olena, Yan, Denise, Mittal, Rahul, Shen, Rulong, Telischi, Fred F, Morrison, Helen, Giovannini, Marco, Liu, Xue-Zhong, Chang, Long-Sheng, Fernandez-Valle, Cristina

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Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome von Walz, Katherina, Cohen, Devon, Neilsen, Paul M., Foster, Joseph, Brancati, Francesco, Demir, Korcan, Fisher, Richard, Moffat, Michelle, Verbeek, Nienke E., Bjørgo, Kathrine, Lo Castro, Adriana, Curatolo, Paolo, Novelli, Giuseppe, Abad, Clemer, Lei, Cao, Zhang, Lily, Diaz-Horta, Oscar, Young, Juan I., Callen, David F., Tekin, Mustafa

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Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome von Kerr, Bredford, Silva, Pamela A, Walz, Katherina, Young, Juan I

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SLITRK6 mutations cause myopia and deafness in humans and mice von Tekin, Mustafa, Chioza, Barry A, Matsumoto, Yoshifumi, Diaz-Horta, Oscar, Cross, Harold E, Duman, Duygu, Kokotas, Haris, Moore-Barton, Heather L, Sakoori, Kazuto, Ota, Maya, Odaka, Yuri S, Foster, 2nd, Joseph, Cengiz, F Basak, Tokgoz-Yilmaz, Suna, Tekeli, Oya, Grigoriadou, Maria, Petersen, Michael B, Sreekantan-Nair, Ajith, Gurtz, Kay, Xia, Xia-Juan, Pandya, Arti, Patton, Michael A, Young, Juan I, Aruga, Jun, Crosby, Andrew H

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Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes von KERR, Bredford, SOTO C, Jessica, SAEZ, Mauricio, ABRAMS, Alexander, WALZ, Katherina, YOUNG, Juan I

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Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons von Seabra, Catarina M., Aneichyk, Tatsiana, Erdin, Serkan, Tai, Derek J. C., De Esch, Celine E. F., Razaz, Parisa, An, Yu, Manavalan, Poornima, Ragavendran, Ashok, Stortchevoi, Alexei, Abad, Clemer, Young, Juan, Maciel, Patricia, Talkowski, Michael E., Gusella, James F.

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