Simon E. Fisher, D.Phil.
|Wellcome Trust Centre for Human Genetics||University of Oxford, Oxford, United Kingdom|
Mean distance: 53433
Cross-listing: LinguisTree - CSD Tree
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|Shapland CY, Verhoef E, Davey Smith G, et al. (2021) Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies. Npj Science of Learning. 6: 23|
|Blok LS, Goosen YM, van Haaften L, et al. (2021) Speech-language profiles in the context of cognitive and adaptive functioning in SATB2-associated syndrome. Genes, Brain, and Behavior. e12761|
|Braden RO, Amor DJ, Fisher SE, et al. (2021) Severe speech impairment is a distinguishing feature of FOXP1-related disorder. Developmental Medicine and Child Neurology|
|Morgan A, Braden R, Wong MMK, et al. (2021) Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics : Ejhg|
|Snijders Blok L, Vino A, den Hoed J, et al. (2020) Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities. Genetics in Medicine : Official Journal of the American College of Medical Genetics|
|Gialluisi A, Andlauer TFM, Mirza-Schreiber N, et al. (2020) Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry|
|Verhoef E, Shapland CY, Fisher SE, et al. (2020) The developmental origins of genetic factors influencing language and literacy: Associations with early-childhood vocabulary. Journal of Child Psychology and Psychiatry, and Allied Disciplines|
|Connaughton DM, Dai R, Owen DJ, et al. (2020) Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. American Journal of Human Genetics|
|Kong XZ, Postema MC, Guadalupe T, et al. (2020) Mapping brain asymmetry in health and disease through the ENIGMA consortium. Human Brain Mapping|
|Hildebrand MS, Jackson VE, Scerri TS, et al. (2020) Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation. Neurology|