Volgen
Sonja Vernes
Sonja Vernes
Geverifieerd e-mailadres voor st-andrews.ac.uk - Homepage
Titel
Geciteerd door
Geciteerd door
Jaar
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
22212021
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
8822008
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
5792005
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
4002007
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
3412011
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
3212007
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
3192014
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
3032020
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 review of animal biosciences 6 (1), 23-46, 2018
2422018
The era of reference genomes in conservation genomics
G Formenti, K Theissinger, C Fernandes, I Bista, A Bombarely, C Bleidorn, ...
Trends in ecology & evolution 37 (3), 197-202, 2022
2362022
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
2162006
Universal DNA methylation age across mammalian tissues
AT Lu, Z Fei, A Haghani, TR Robeck, JA Zoller, CZ Li, R Lowe, Q Yan, ...
Nature aging 3 (9), 1144-1166, 2023
1952023
How genomics can help biodiversity conservation
K Theissinger, C Fernandes, G Formenti, I Bista, PR Berg, C Bleidorn, ...
Trends in genetics 39 (7), 545-559, 2023
1912023
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
1862018
DNA methylation predicts age and provides insight into exceptional longevity of bats
GS Wilkinson, DM Adams, A Haghani, AT Lu, J Zoller, CE Breeze, ...
Nature communications 12 (1), 1615, 2021
1442021
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
1272010
Universal DNA methylation age across mammalian tissues
AT Lu, Z Fei, A Haghani, TR Robeck, JA Zoller, CZ Li, R Lowe, Q Yan, ...
BioRxiv, 2021.01. 18.426733, 2021
1092021
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
1032013
DNA methylation networks underlying mammalian traits
A Haghani, CZ Li, TR Robeck, J Zhang, AT Lu, J Ablaeva, ...
Science 381 (6658), eabq5693, 2023
98*2023
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, 1-7, 2016
972016
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–20