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|
|den Hoed J, Devaraju K, Fisher SE. (2021) Molecular networks of the FOXP2 transcription factor in the brain. Embo Reports. e52803|
|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|
|Carrion-Castillo A, Estruch SB, Maassen B, et al. (2021) Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family. Human Genetics|
|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|
|Jansen NA, Braden RO, Srivastava S, et al. (2021) Clinical delineation of SETBP1 haploinsufficiency disorder. European Journal of Human Genetics : Ejhg|
|Kong XZ, Postema M, Schijven D, et al. (2021) Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew. Cerebral Cortex (New York, N.Y. : 1991)|
|Sønderby IE, van der Meer D, Moreau C, et al. (2021) 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry. 11: 182|
|Postema MC, Hoogman M, Ambrosino S, et al. (2021) Analysis of structural brain asymmetries in attention-deficit/hyperactivity disorder in 39 datasets. Journal of Child Psychology and Psychiatry, and Allied Disciplines|
|Sha Z, Schijven D, Carrion-Castillo A, et al. (2021) The genetic architecture of structural left-right asymmetry of the human brain. Nature Human Behaviour|