| A functional genetic link between distinct developmental language disorders SC Vernes, DF Newbury, BS Abrahams, L Winchester, J Nicod, M Groszer, ... New England Journal of Medicine 359 (22), 2337-2345, 2008 | 746 | 2008 |
| Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits KD MacDermot, E Bonora, N Sykes, AM Coupe, CSL Lai, SC Vernes, ... The American Journal of Human Genetics 76 (6), 1074-1080, 2005 | 503 | 2005 |
| Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain E Spiteri, G Konopka, G Coppola, J Bomar, M Oldham, J Ou, SC Vernes, ... The American Journal of Human Genetics 81 (6), 1144-1157, 2007 | 325 | 2007 |
| High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders SC Vernes, E Spiteri, J Nicod, M Groszer, JM Taylor, KE Davies, ... The American Journal of Human Genetics 81 (6), 1232-1250, 2007 | 265 | 2007 |
| Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain SC Vernes, PL Oliver, E Spiteri, HE Lockstone, R Puliyadi, JM Taylor, ... PLoS Genet 7 (7), e1002145, 2011 | 262 | 2011 |
| Shining a light on CNTNAP2: complex functions to complex disorders P Rodenas-Cuadrado, J Ho, SC Vernes European journal of human genetics 22 (2), 171-178, 2014 | 197 | 2014 |
| Functional genetic analysis of mutations implicated in a human speech and language disorder SC Vernes, J Nicod, FM Elahi, JA Coventry, N Kenny, AM Coupe, LE Bird, ... Human molecular genetics 15 (21), 3154-3167, 2006 | 188 | 2006 |
| Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex P Roll, SC Vernes, N Bruneau, J Cillario, M Ponsole-Lenfant, ... Human molecular genetics 19 (24), 4848-4860, 2010 | 108 | 2010 |
| FOXP2 targets show evidence of positive selection in European populations Q Ayub, B Yngvadottir, Y Chen, Y Xue, M Hu, SC Vernes, SE Fisher, ... The American Journal of Human Genetics 92 (5), 696-706, 2013 | 89 | 2013 |
| The efficacy of epidermal growth factor receptor–specific antibodies against glioma xenografts is influenced by receptor levels, activation status, and heterodimerization TG Johns, RM Perera, SC Vernes, AA Vitali, DX Cao, WK Cavenee, ... Clinical Cancer Research 13 (6), 1911-1925, 2007 | 80 | 2007 |
| Bat biology, genomes, and the Bat1K project: to generate chromosome-level genomes for all living bat species EC Teeling, SC Vernes, LM Dávalos, DA Ray, MTP Gilbert, E Myers, ... Annual Reviews, 2018 | 77 | 2018 |
| Characterisation of CASPR2 deficiency disorder-a syndrome involving autism, epilepsy and language impairment P Rodenas-Cuadrado, N Pietrafusa, T Francavilla, A La Neve, P Striano, ... BMC medical genetics 17 (1), 1-7, 2016 | 51 | 2016 |
| Taking turns: bridging the gap between human and animal communication S Pika, R Wilkinson, KH Kendrick, SC Vernes Proceedings of the Royal Society B 285 (1880), 20180598, 2018 | 49 | 2018 |
| A direct molecular link between the autism candidate gene RORa and the schizophrenia candidate MIR137 P Devanna, SC Vernes Scientific reports 4 (1), 1-7, 2014 | 48 | 2014 |
| Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia SC Vernes, KD MacDermot, AP Monaco, SE Fisher European Journal of Human Genetics 17 (10), 1354-1358, 2009 | 48 | 2009 |
| What bats have to say about speech and language SC Vernes Psychonomic Bulletin & Review 24 (1), 111-117, 2017 | 46 | 2017 |
| Genetics and the language sciences SE Fisher, SC Vernes Annu. Rev. Linguist. 1 (1), 289-310, 2015 | 46 | 2015 |
| The DISC1 promoter: characterization and regulation by FOXP2 RM Walker, AE Hill, AC Newman, G Hamilton, HS Torrance, SM Anderson, ... Human molecular genetics 21 (13), 2862-2872, 2012 | 44 | 2012 |
| FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways P Devanna, J Middelbeek, SC Vernes Frontiers in cellular neuroscience 8, 305, 2014 | 42 | 2014 |
| Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders P Devanna, XS Chen, J Ho, D Gajewski, SD Smith, A Gialluisi, C Francks, ... Molecular psychiatry 23 (5), 1375-1384, 2018 | 38 | 2018 |
Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsVerified email at mpi.nl
