Simon E. Fisher, D.Phil.

Affiliations: 
Wellcome Trust Centre for Human Genetics University of Oxford, Oxford, United Kingdom 
Area:
speech, language
Website:
http://www.well.ox.ac.uk/simon-e-fisher-homepage
Google:
"Simon Fisher"
Mean distance: 53433
 
Cross-listing: LinguisTree - CSD Tree

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Publications

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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
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