Kellen D. Winden

Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits

Olga Peñagarikano, Brett S. Abrahams, Edward I. Herman et al. · Cell · 2011 · 1.1K citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Molecular Neuroscience +14

Human-specific transcriptional regulation of CNS development genes by FOXP2

Geneviève Konopka, Jamee M. Bomar, Kellen D. Winden et al. · Nature · 2009 · 394 citations · Full text

Transcriptional Regulation, Developmental Biology, Molecular Neuroscience +7

Human-Specific Transcriptional Networks in the Brain

Geneviève Konopka, Tara Friedrich, Jeremy Davis‐Turak et al. · Neuron · 2012 · 280 citations · Full text

Transcriptional Regulation, Human-specific Transcriptional Networks, Molecular Neuroscience +6

Functional Genomic Analyses Identify Pathways Dysregulated by Progranulin Deficiency, Implicating Wnt Signaling

Ezra Y. Rosen, Eric Wexler, Revital Versano et al. · Neuron · 2011 · 130 citations · Full text

Transcriptional Regulation, Implicating Wnt, Signal Transduction +10

Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin

Maria Sundberg, Ivan Tochitsky, David E. Buchholz et al. · Molecular Psychiatry · 2018 · 129 citations

Neurophysiology, Neuroanatomy, Reduced Fmrp Levels +10