David Housman

Massachusetts Institute of Technology, Cambridge, MA, United States 
Human Genetics, Huntington's disease, Myotonic dystrophy, Fragile-X syndrome
"David Housman"
Mean distance: 14.54 (cluster 11)


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Harvey F. Lodish post-doc (Cell Biology Tree)


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J. Michael Andresen research assistant UMN
James (Jim) F. Gusella grad student
Robert Levenson grad student MIT
David Nelson grad student MIT (GenetiTree)
Heather L. Hinds grad student 1991-1993 MIT
Eric T Wang grad student 2006-2012 MIT
Jill R. Crittenden post-doc MIT
Daniel A. Haber post-doc MIT (Cell Biology Tree)
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Crittenden JR, Zhai S, Sauvage M, et al. (2021) CalDAG-GEFI mediates striatal cholinergic modulation of dendritic excitability, synaptic plasticity and psychomotor behaviors. Neurobiology of Disease. 105473
Crittenden JR, Gipson TA, Smith AC, et al. (2021) Striatal transcriptome changes linked to drug-induced repetitive behaviors. The European Journal of Neuroscience
Wang ET, Treacy D, Eichinger K, et al. (2018) Transcriptome alterations in myotonic dystrophy skeletal muscle and heart. Human Molecular Genetics
Fratta P, Sivakumar P, Humphrey J, et al. (2018) Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. The Embo Journal
Sivakumar P, Humphrey J, Lo K, et al. (2018) Dissecting TDP-43 gain- and loss-of-function in neurodegeneration Neuromuscular Disorders. 28
McGinty RJ, Puleo F, Aksenova AY, et al. (2017) A Defective mRNA Cleavage and Polyadenylation Complex Facilitates Expansions of Transcribed (GAA)n Repeats Associated with Friedreich's Ataxia. Cell Reports. 20: 2490-2500
Sivakumar P, Humphrey J, Ule A, et al. (2017) Investigating dysfunctional RNA processing in TDP-43 mouse mutants Neuromuscular Disorders. 27: S32
Crittenden JR, Tillberg PW, Riad MH, et al. (2016) Striosome-dendron bouquets highlight a unique striatonigral circuit targeting dopamine-containing neurons. Proceedings of the National Academy of Sciences of the United States of America
Bugiardini E, Meola G, Alvarez C, et al. (2014) Consensus on cerebral involvement in myotonic dystrophy. Workshop report: May 24-27, 2013, Ferrere (AT), Italy Neuromuscular Disorders. 24: 445-452
Gipson TA, Neueder A, Wexler NS, et al. (2013) Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis. Rna Biology. 10: 1647-52
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