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Sonja Vernes
Sonja Vernes
Max Planck Research Group Leader, Max Planck Institute for Psycholinguistics
Verified email at mpi.nl - Homepage
Title
Cited by
Cited by
Year
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
7962008
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
5282005
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
3522007
Towards complete and error-free genome assemblies of all vertebrate species
A Rhie, SA McCarthy, O Fedrigo, J Damas, G Formenti, S Koren, ...
Nature 592 (7856), 737-746, 2021
3102021
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 genetics 7 (7), e1002145, 2011
2922011
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
2812007
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
2392014
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
1972006
Bat biology, genomes, and the Bat1K project: to generate chromosome-level genomes for all living bat species
E Teeling, SC Vernes, LM Dávalos, DA Ray, MTP Gilbert, E Myers, ...
Annual review of animal biosciences 6, 23-46, 2018
1272018
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
1152010
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
1002013
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
952018
Six reference-quality genomes reveal evolution of bat adaptations
D Jebb, Z Huang, M Pippel, GM Hughes, K Lavrichenko, P Devanna, ...
Nature 583 (7817), 578-584, 2020
912020
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
802007
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
632016
Genetics and the language sciences
SE Fisher, SC Vernes
Annual Review of Linguistics 1, 289-310, 2015
572015
What bats have to say about speech and language
SC Vernes
Psychonomic bulletin & review 24 (1), 111-117, 2017
552017
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
542014
FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways
P Devanna, J Middelbeek, SC Vernes
Frontiers in cellular neuroscience 8, 305, 2014
522014
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
492009
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