| Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits O Peñagarikano, BS Abrahams, EI Herman, KD Winden, A Gdalyahu, ... Cell 147 (1), 235-246, 2011 | 1054 | 2011 |
| Human-specific transcriptional regulation of CNS development genes by FOXP2 G Konopka, JM Bomar, K Winden, G Coppola, ZO Jonsson, F Gao, ... Nature 462 (7270), 213-217, 2009 | 525 | 2009 |
| Human-specific transcriptional networks in the brain G Konopka, T Friedrich, J Davis-Turak, K Winden, MC Oldham, F Gao, ... Neuron 75 (4), 601-617, 2012 | 276 | 2012 |
| Abnormal mTOR activation in autism KD Winden, D Ebrahimi-Fakhari, M Sahin Annual review of neuroscience 41, 1-23, 2018 | 174 | 2018 |
| Functional genomic analyses identify pathways dysregulated by progranulin deficiency, implicating Wnt signaling EY Rosen, EM Wexler, R Versano, G Coppola, F Gao, KD Winden, ... Neuron 71 (6), 1030-1042, 2011 | 151 | 2011 |
| The organization of the transcriptional network in specific neuronal classes KD Winden, MC Oldham, K Mirnics, PJ Ebert, CH Swan, P Levitt, ... Molecular systems biology 5 (1), 291, 2009 | 134 | 2009 |
| Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin M Sundberg, I Tochitsky, DE Buchholz, K Winden, V Kujala, K Kapur, ... Molecular psychiatry 23 (11), 2167-2183, 2018 | 97 | 2018 |
| Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex E Ercan, JM Han, A Di Nardo, K Winden, MJ Han, L Hoyo, A Saffari, ... Journal of Experimental Medicine 214 (3), 681-697, 2017 | 91 | 2017 |
| A systems level, functional genomics analysis of chronic epilepsy KD Winden, SL Karsten, A Bragin, LC Kudo, L Gehman, J Ruidera, ... PloS one 6 (6), e20763, 2011 | 83 | 2011 |
| Biallelic mutations in TSC2 lead to abnormalities associated with cortical tubers in human iPSC-derived neurons KD Winden, M Sundberg, C Yang, SMA Wafa, S Dwyer, PF Chen, ... Journal of Neuroscience 39 (47), 9294-9305, 2019 | 71 | 2019 |
| CCDC22: a novel candidate gene for syndromic X-linked intellectual disability I Voineagu, L Huang, K Winden, M Lazaro, E Haan, J Nelson, ... Molecular psychiatry 17 (1), 4-7, 2012 | 60 | 2012 |
| Arthritis flares mediated by tissue-resident memory T cells in the joint MH Chang, A Levescot, N Nelson-Maney, RB Blaustein, KD Winden, ... Cell reports 37 (4), 2021 | 56 | 2021 |
| Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophy MH Wertz, K Winden, P Neveu, SY Ng, E Ercan, M Sahin Human molecular genetics 25 (11), 2168-2181, 2016 | 49 | 2016 |
| Megalencephaly and macrocephaly KD Winden, CJ Yuskaitis, A Poduri Seminars in neurology 35 (03), 277-287, 2015 | 45 | 2015 |
| Substrate sequence influences γ-secretase modulator activity, role of the transmembrane domain of the amyloid precursor protein SA Sagi, CB Lessard, KD Winden, H Maruyama, JC Koo, S Weggen, ... Journal of Biological Chemistry 286 (46), 39794-39803, 2011 | 43 | 2011 |
| 16p11. 2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro M Sundberg, H Pinson, RS Smith, KD Winden, P Venugopal, DJC Tai, ... Nature communications 12 (1), 2897, 2021 | 37 | 2021 |
| Phenotypic screen with TSC-deficient neurons reveals heat-shock machinery as a druggable pathway for mTORC1 and reduced cilia A Di Nardo, I Lenoël, KD Winden, A Rühmkorf, ME Modi, L Barrett, ... Cell reports 31 (12), 2020 | 17 | 2020 |
| Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profile K Giannikou, Z Zhu, J Kim, KD Winden, ME Tyburczy, D Marron, JS Parker, ... Modern Pathology 34 (2), 264-279, 2021 | 16 | 2021 |
| Stroke in primary hyperoxaluria type I NM Rao, A Yallapragada, KD Winden, J Saver, DS Liebeskind Journal of Neuroimaging 24 (4), 411-413, 2014 | 15 | 2014 |
| Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy KD Winden, A Bragin, J Engel, DH Geschwind Neurobiology of disease 78, 35-44, 2015 | 14 | 2015 |
