Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency by A. Ayanna Wade, A. Ayanna Wade, Kenneth Lim, Kenneth Lim, Rinaldo Catta-Preta, Rinaldo Catta-Preta, Alex S. Nord, Alex S. Nord

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Genomic analysis of transcriptional networks directing progression of cell states during MGE development by Magnus Sandberg, Leila Taher, Jianxin Hu, Brian L. Black, Alex S. Nord, John L. R. Rubenstein

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Transcriptional Pathology Evolves over Time in Rat Hippocampus after Lateral Fluid Percussion Traumatic Brain Injury by Rinaldo Catta-Preta, Iva Zdilar, Bradley Jenner, Emily T. Doisy, Kayleen Tercovich, Alex S. Nord, Gene G. Gurkoff

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In vivo targeted DamID identifies CHD8 genomic targets in fetal mouse brain by A. Ayanna Wade, Jelle van den Ameele, Seth W. Cheetham, Rebecca Yakob, Andrea H. Brand, Alex S. Nord

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Tissue-specific RNA expression marks distant-acting developmental enhancers. by Han Wu, Alex S Nord, Jennifer A Akiyama, Malak Shoukry, Veena Afzal, Edward M Rubin, Len A Pennacchio, Axel Visel

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Genomic Resolution of DLX-Orchestrated Transcriptional Circuits Driving Development of Forebrain GABAergic Neurons by Susan Lindtner, Rinaldo Catta-Preta, Hua Tian, Linda Su-Feher, James D. Price, Diane E. Dickel, Vanille Greiner, Shanni N. Silberberg, Gabriel L. McKinsey, Michael T. McManus, Len A. Pennacchio, Axel Visel, Alex S. Nord, John L.R. Rubenstein

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A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risks⃞ by Dana C. Crawford, Alex S. Nord, Michael D. Badzioch, Jane Ranchalis, Laura A. McKinstry, Magdalena Ahearn, Caterina Bertucci, Cynthia Shephard, Michelle Wong, Mark J. Rieder, Gerard D. Schellenberg, Deborah A. Nickerson, Patrick J. Heagerty, Ellen M. Wijsman, Gail P. Jarvik

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Parallel functional testing identifies enhancers active in early postnatal mouse brain by Jason T Lambert, Linda Su-Feher, Karol Cichewicz, Tracy L Warren, Iva Zdilar, Yurong Wang, Kenneth J Lim, Jessica L Haigh, Sarah J Morse, Cesar P Canales, Tyler W Stradleigh, Erika Castillo Palacios, Viktoria Haghani, Spencer D Moss, Hannah Parolini, Diana Quintero, Diwash Shrestha, Daniel Vogt, Leah C Byrne, Alex S Nord

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Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice by Jessica L. Haigh, Anna Adhikari, Nycole A. Copping, Tyler Stradleigh, A. Ayanna Wade, Rinaldo Catta-Preta, Linda Su-Feher, Iva Zdilar, Sarah Morse, Timothy A. Fenton, Anh Nguyen, Diana Quintero, Samrawit Agezew, Michael Sramek, Ellie J. Kreun, Jasmine Carter, Andrea Gompers, Jason T. Lambert, Cesar P. Canales, Len A. Pennacchio, Axel Visel, Diane E. Dickel, Jill L. Silverman, Alex S. Nord

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Sequential perturbations to mouse corticogenesis following in utero maternal immune activation by Cesar P Canales, Myka L Estes, Karol Cichewicz, Kartik Angara, John Paul Aboubechara, Scott Cameron, Kathryn Prendergast, Linda Su-Feher, Iva Zdilar, Ellie J Kreun, Emma C Connolly, Jin Myeong Seo, Jack B Goon, Kathleen Farrelly, Tyler W Stradleigh, Deborah van der List, Lori Haapanen, Judy Van de Water, Daniel Vogt, A Kimberley McAllister, Alex S Nord

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