Katz, David M.

A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome

Buchovecky, C. M., Turley, S. D., Brown, H. M., Kyle, S. M., McDonald, J. G., Liu, B., Pieper, A. A., Huang, W., Katz, D. M., Russell, D. W., et al. (2013) · Nature Genetics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 234

Preclinical research in Rett syndrome: setting the foundation for translational success

Katz, D. M., Berger-Sweeney, J. E., Eubanks, J. H., Justice, M. J., Neul, J. L., Pozzo-Miller, L., Blue, M. E., Christian, D., Crawley, J. N., Giustetto, M., et al. (2012) · Disease Models & Mechanisms

Genetics and Neurodevelopmental DisordersAnimal testing and alternatives

Cited by 206

Dysregulation of Brain-Derived Neurotrophic Factor Expression and Neurosecretory Function in Mecp2 Null Mice

Wang, H., Chan, S.-A., Ogier, M., Hellard, D., Wang, Q., Smith, C., & Katz, D. M. (2006) · The Journal of Neuroscience

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 156

Brain Activity Mapping in Mecp2 Mutant Mice Reveals Functional Deficits in Forebrain Circuits, Including Key Nodes in the Default Mode Network, that are Reversed with Ketamine Treatment

Kron, M., Howell, C. J., Adams, I. T., Ransbottom, M., Christian, D., Ogier, M., & Katz, D. M. (2012) · The Journal of Neuroscience

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 154

A TrkB Small Molecule Partial Agonist Rescues TrkB Phosphorylation Deficits and Improves Respiratory Function in a Mouse Model of Rett Syndrome

Schmid, D. A., Yang, T., Ogier, M., Adams, I., Mirakhur, Y., Wang, Q., Massa, S. M., Longo, F. M., & Katz, D. M. (2012) · The Journal of Neuroscience

Genetics and Neurodevelopmental DisordersNeuroscience of respiration and sleep

Cited by 152

Rett Syndrome: Crossing the Threshold to Clinical Translation

Katz, D. M., Bird, A., Coenraads, M., Gray, S. J., Menon, D. U., Philpot, B. D., & Tarquinio, D. C. (2016) · Trends in Neurosciences

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 150

Secretion of brain‐derived neurotrophic factor from brain microvascular endothelial cells

Wang, H., Ward, N., Boswell, M., & Katz, D. M. (2006) · European Journal of Neuroscience

Nerve injury and regenerationBarrier Structure and Function Studies

Cited by 81

Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met

Shepherd, G. M., & Katz, D. M. (2011) · Current Opinion in Neurobiology

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 75

A BDNF loop-domain mimetic acutely reverses spontaneous apneas and respiratory abnormalities during behavioral arousal in a mouse model of Rett syndrome

Kron, M., Lang, M., Adams, I. T., Sceniak, M., Longo, F., & Katz, D. M. (2014) · Disease Models & Mechanisms

Genetics and Neurodevelopmental DisordersNeuroscience of respiration and sleep

Cited by 59

Activation of the Medial Prefrontal Cortex Reverses Cognitive and Respiratory Symptoms in a Mouse Model of Rett Syndrome

Howell, C. J., Sceniak, M. P., Lang, M., Krakowiecki, W., Abouelsoud, F. E., Lad, S. U., Yu, H., & Katz, D. M. (2017) · eneuro

Genetics and Neurodevelopmental DisordersNeuroscience of respiration and sleep

Cited by 23