Richards, Linda J.

Agenesis of the corpus callosum: Genetic, developmental and functional aspects of connectivity

Paul, L. K., Brown, W. S., Adolphs, R., Tyszka, J. M., Richards, L. J., Mukherjee, P., & Sherr, E. H. (2007) · Nature Reviews Neuroscience

Fetal and Pediatric Neurological DisordersAdvanced Neuroimaging Techniques and Applications

Cited by 830

Anatomical characterization of human fetal brain development with diffusion tensor magnetic resonance imaging

Huang, H., Xue, R., Zhang, J., Ren, T., Richards, L. J., Yarowsky, P., Miller, M. I., & Mori, S. (2009) · The Journal of Neuroscience

Advanced Neuroimaging Techniques and ApplicationsFetal and Pediatric Neurological Disorders

Cited by 364

The transcription factor Nfixis essential for normal brain development

Campbell, C. E., Piper, M., Plachez, C., Yeh, Y.-T., Baizer, J. S., Osinski, J. M., Litwack, E. D., Richards, L. J., & Gronostajski, R. M. (2008) · BMC Developmental Biology

Neurogenesis and neuroplasticity mechanismsFetal and Pediatric Neurological Disorders

Cited by 179

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

Marsh, A. P. L., Heron, D., Edwards, T. J., Quartier, A., Galea, C., Nava, C., Rastetter, A., Moutard, M.-L., Anderson, V., Bitoun, P., et al. (2017) · Nature Genetics

Fetal and Pediatric Neurological DisordersGenetics and Neurodevelopmental Disorders

Cited by 101

Contralateral targeting of the corpus callosum in normal and pathological brain function

Fenlon, L. R., & Richards, L. J. (2015) · Trends in Neurosciences

Fetal and Pediatric Neurological DisordersAxon Guidance and Neuronal Signaling

Cited by 87

NFIB haploinsufficiency is associated with intellectual disability and macrocephaly

Schanze, I., Bunt, J., Lim, J. W. C., Schanze, D., Dean, R. J., Alders, M., Blanchet, P., Attié-Bitach, T., Berland, S., Boogert, S., et al. (2018) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 63

Mapk/Erk activation in an animal model of social deficits shows a possible link to autism

Faridar, A., Jones-Davis, D., Rider, E., Li, J., Gobius, I., Morcom, L., Richards, L. J., Sen, S., & Sherr, E. H. (2014) · Molecular Autism

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 63