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
7462008
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
5032005
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
3252007
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
2652007
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
2622011
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
1972014
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
1882006
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
1082010
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
892013
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
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
772018
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
512016
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
492018
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
482014
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
482009
What bats have to say about speech and language
SC Vernes
Psychonomic Bulletin & Review 24 (1), 111-117, 2017
462017
Genetics and the language sciences
SE Fisher, SC Vernes
Annu. Rev. Linguist. 1 (1), 289-310, 2015
462015
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
442012
FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways
P Devanna, J Middelbeek, SC Vernes
Frontiers in cellular neuroscience 8, 305, 2014
422014
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
382018
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