| 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 | 2107 | 2021 |
| 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 | 895 | 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 | 591 | 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 | 401 | 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 genetics 7 (7), e1002145, 2011 | 344 | 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 | 320 | 2014 |
| 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 | 319 | 2007 |
| 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 | 302 | 2020 |
| 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 | 244 | 2018 |
| 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 | 233 | 2022 |
| 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 | 220 | 2006 |
| 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 | 191 | 2018 |
| 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 | 189 | 2023 |
| 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 | 185 | 2023 |
| 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 | 145 | 2021 |
| 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 | 129 | 2010 |
| 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 | 106 | 2021 |
| 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 | 105 | 2013 |
| DNA methylation networks underlying mammalian traits A Haghani, CZ Li, TR Robeck, J Zhang, AT Lu, J Ablaeva, ... Science 381 (6658), eabq5693, 2023 | 97* | 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 | 94 | 2016 |
Simon E. FisherDirector, Max Planck Institute for Psycholinguisticsmpi.nl의 이메일 확인됨