Michael Coulter, MD, PhD
Postdoctoral Scholar
Physiology
School of Medicine

Grants and Projects

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• Linking Hippocampal Replay Content to Learning and Decision-Making, NIH, 2020-2023
• A Novel Essential Gene for Human Cognitive Function, NIH, 2013-2018

Publications (17)

Top publication keywords:
Developmental DisabilitiesEndosomal Sorting Complexes Required for TransportAbnormalities, MultipleMutation RateHippocampusExtracellular VesiclesMicroarray AnalysisMicrocephalyHedgehog ProteinsVolitionBrain DiseasesSpatial NavigationWhole Genome SequencingBrain-Computer InterfacesDNA Adducts

• Spyglass: a framework for reproducible and shareable neuroscience research.
  bioRxiv : the preprint server for biology 2024 Lee KH, Denovellis EL, Ly R, Magland J, Soules J, Comrie AE, Gramling DP, Guidera JA, Nevers R, Adenekan P, Brozdowski C, Bray SR, Monroe E, Bak JH, Coulter ME, Sun X, Broyles E, Shin D, Chiang S, …
• The neural basis of mental navigation in rats.
  Science (New York, N.Y.) 2023 Coulter ME, Kemere C
• Hippocampal replay of experience at real-world speeds.
  eLife 2021 Denovellis EL, Gillespie AK, Coulter ME, Sosa M, Chung JE, Eden UT, Frank LM
• Hippocampal replay reflects specific past experiences rather than a plan for subsequent choice.
  Neuron 2021 Gillespie AK, Astudillo Maya DA, Denovellis EL, Liu DF, Kastner DB, Coulter ME, Roumis DK, Eden UT, Frank LM
• DNA Adductomics by mass tag prelabeling.
  Rapid communications in mass spectrometry : RCM 2021 Wang P, Roider E, Coulter ME, Walsh CA, Kramer CS, Beuning PJ, Giese RW

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• Jettison-MS of Nucleic Acid Species.
  Journal of the American Society for Mass Spectrometry 2020 Wang P, Shah GL, Landau H, Coulter ME, Walsh CA, Roider E, Kramer CS, Beuning PJ, Giese RW
• 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 2020 Coulter ME, Musaev D, DeGennaro EM, Zhang X, Henke K, James KN, Smith RS, Hill RS, Partlow JN, Kamumbu AS, Hatem N, Barkovich AJ, Aziza J, Chassaing N, Zaki MS, Sultan T, Burglen L, Rajab A, Al-Gazali…
• Linked-read analysis identifies mutations in single-cell DNA-sequencing data.
  Nature genetics 2019 Bohrson CL, Barton AR, Lodato MA, Rodin RE, Luquette LJ, Viswanadham VV, Gulhan DC, Cortés-Ciriano I, Sherman MA, Kwon M, Coulter ME, Galor A, Walsh CA, Park PJ
• The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles.
  Cell reports 2018 Coulter ME, Dorobantu CM, Lodewijk GA, Delalande F, Cianferani S, Ganesh VS, Smith RS, Lim ET, Xu CS, Pang S, Wong ET, Lidov HGW, Calicchio ML, Yang E, Gonzalez DM, Schlaeger TM, Mochida GH, Hess H, …
• PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation.
  Nucleic acids research 2018 Sherman MA, Barton AR, Lodato MA, Vitzthum C, Coulter ME, Walsh CA, Park PJ
• Aging and neurodegeneration are associated with increased mutations in single human neurons.
  Science (New York, N.Y.) 2017 Lodato MA, Rodin RE, Bohrson CL, Coulter ME, Barton AR, Kwon M, Sherman MA, Vitzthum CM, Luquette LJ, Yandava CN, Yang P, Chittenden TW, Hatem NE, Ryu SC, Woodworth MB, Park PJ, Walsh CA
• Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.
  Genome research 2017 Evrony GD, Cordero DR, Shen J, Partlow JN, Yu TW, Rodin RE, Hill RS, Coulter ME, Lam AN, Jayaraman D, Gerrelli D, Diaz DG, Santos C, Morrison V, Galli A, Tschulena U, Wiemann S, Martel MJ, Spooner B, …
• Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.
  American journal of human genetics 2015 Nakayama T, Al-Maawali A, El-Quessny M, Rajab A, Khalil S, Stoler JM, Tan WH, Nasir R, Schmitz-Abe K, Hill RS, Partlow JN, Al-Saffar M, Servattalab S, LaCoursiere CM, Tambunan DE, Coulter ME, Elhosary…
• METTL23, a transcriptional partner of GABPA, is essential for human cognition.
  Human molecular genetics 2014 Reiff RE, Ali BR, Baron B, Yu TW, Ben-Salem S, Coulter ME, Schubert CR, Hill RS, Akawi NA, Al-Younes B, Kaya N, Evrony GD, Al-Saffar M, Felie JM, Partlow JN, Sunu CM, Schembri-Wismayer P, Alkuraya FS,…
• Using whole-exome sequencing to identify inherited causes of autism.
  Neuron 2013 Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, …
• Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.
  PLoS genetics 2012 Chahrour MH, Yu TW, Lim ET, Ataman B, Coulter ME, Hill RS, Stevens CR, Schubert CR, ARRA Autism Sequencing Collaboration, Greenberg ME, Gabriel SB, Walsh CA
• Chromosomal microarray testing influences medical management.
  Genetics in medicine : official journal of the American College of Medical Genetics 2011 Coulter ME, Miller DT, Harris DJ, Hawley P, Picker J, Roberts AE, Sobeih MM, Irons M