Linda J. Richards

Affiliations: 
University of Queensland, Saint Lucia, Queensland, Australia 
Google:
"Linda Richards"
Mean distance: 16.69 (cluster 6)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Morcom L, Edwards TJ, Rider E, et al. (2021) DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation. Elife. 10
Morcom L, Gobius I, Marsh AP, et al. (2021) DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation. Elife. 10
Chen KS, Lynton Z, Lim JWC, et al. (2020) NFIA and NFIB function as tumour suppressors in high-grade glioma in mice. Carcinogenesis
Edwards TJ, Fenlon LR, Dean RJ, et al. (2020) Altered structural connectivity networks in a mouse model of complete and partial dysgenesis of the corpus callosum. Neuroimage. 116868
Szczupak D, Liu C, Yen CCC, et al. (2020) Long Long-distance aberrant heterotopic connectivity in a mouse strain with a high incidence of callosal anomalies. Neuroimage. 116875
Adams A, Albin S, Amunts K, et al. (2020) Erratum: International Brain Initiative: An Innovative Framework for Coordinated Global Brain Research Efforts (Neuron (2020) 105(2) (212–216), (S0896627320300027), (10.1016/j.neuron.2020.01.002)) Neuron. 105
Lennox AL, Hoye ML, Jiang R, et al. (2020) Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development. Neuron
Adams A, Albin S, Amunts K, et al. (2020) International Brain Initiative: An Innovative Framework for Coordinated Global Brain Research Efforts Neuron. 105: 212-216
Zenker M, Bunt J, Schanze I, et al. (2019) Variants in nuclear factor I genes influence growth and development. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
Schanze I, Bunt J, Lim JWC, et al. (2018) NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. American Journal of Human Genetics. 103: 752-768
See more...