Fisher, Simon E.

Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

de Boer, E., Ockeloen, C. W., Kampen, R. A., Hampstead, J. E., Dingemans, A. J. M., Rots, D., Lütje, L., Ashraf, T., Baker, R., Barat-Houari, M., et al. (2022) · Genetics in Medicine

Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders

Cited by 28

Exome-wide analysis implicates rare protein-altering variants in human handedness

Schijven, D., Soheili-Nezhad, S., Fisher, S. E., & Francks, C. (2023) · Nature Communications

Hemispheric Asymmetry in NeuroscienceGenetic Associations and Epidemiology

Cited by 27

Exome-wide analysis implicates rare protein-altering variants in human handedness

Schijven, D., Soheili-Nezhad, S., Fisher, S. E., & Francks, C. (2024) · Nature Communications

Hemispheric Asymmetry in NeuroscienceGenetic Associations and Epidemiology

Cited by 27

Erratum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

O'Roak, B. J., Deriziotis, P., Lee, C., Vives, L., Schwartz, J. J., Girirajan, S., Karakoc, E., MacKenzie, A. P., Ng, S. B., Baker, C., et al. (2012) · Nature Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 15

A Pooled Genome-Wide Association Study of Asperger Syndrome

Warrier, V., Chakrabarti, B., Murphy, L., Chan, A., Craig, I., Mallya, U., Lakatošová, S., Rehnstrom, K., Peltonen, L., Wheelwright, S., et al. (2015) · PLOS ONE

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 11

Erratum: A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2

Fedorenko, E., Morgan, A., Murray, E., Cardinaux, A., Mei, C., Tager-Flusberg, H., Fisher, S. E., & Kanwisher, N. (2016) · European Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesLanguage Development and Disorders

Cited by 6