Michael E. Coulter

Affiliations: 
2008-2018 Harvard University, Cambridge, MA, United States 
 2018- University of California, San Francisco, San Francisco, CA 
Area:
neurobiology
Google:
"Michael Coulter"
Mean distance: (not calculated yet)
 

Parents

Sign in to add mentor
Chris A. Walsh grad student 2012-2018
Loren Frank post-doc 2018-
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.

Wang P, Shah GL, Landau HJ, et al. (2020) Jettison-MS of Nucleic Acid Species. Journal of the American Society For Mass Spectrometry
Coulter ME, Musaev D, DeGennaro EM, et al. (2020) Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Bohrson CL, Barton AR, Lodato MA, et al. (2019) Linked-read analysis identifies mutations in single-cell DNA-sequencing data. Nature Genetics
Coulter ME, Dorobantu CM, Lodewijk GA, et al. (2018) The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Reports. 24: 973-986.e8
Lodato MA, Rodin RE, Bohrson CL, et al. (2017) Aging and neurodegeneration are associated with increased mutations in single human neurons. Science (New York, N.Y.)
Sherman MA, Barton AR, Lodato MA, et al. (2017) PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation. Nucleic Acids Research
Evrony GD, Cordero DR, Shen J, et al. (2017) Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Genome Research
Nakayama T, Al-Maawali A, El-Quessny M, et al. (2015) Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. American Journal of Human Genetics. 96: 709-19
Reiff RE, Ali BR, Baron B, et al. (2014) METTL23, a transcriptional partner of GABPA, is essential for human cognition. Human Molecular Genetics. 23: 3456-66
Yu TW, Chahrour MH, Coulter ME, et al. (2013) Using whole-exome sequencing to identify inherited causes of autism. Neuron. 77: 259-73
See more...