Michael Coulter • UCSF Profiles

Michael Coulter, MD, PhD

Title(s)	Postdoctoral Scholar, Physiology
School	School of Medicine
Address	675 Nelson Rising Lane San Francisco CA 94158
Phone	--
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Research

Research Activities and Funding

Linking Hippocampal Replay Content to Learning and Decision-Making
NIH F32MH123003Jun 1, 2020 - May 31, 2023
Role: Principal Investigator

A Novel Essential Gene for Human Cognitive Function
NIH F30MH102909Sep 30, 2013 - Sep 29, 2018
Role: Principal Investigator

Bibliographic

Publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

Altmetrics Details

PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.

Hippocampal replay of experience at real-world speeds. Elife. 2021 09 27; 10. Denovellis EL, Gillespie AK, Coulter ME, Sosa M, Chung JE, Eden UT, Frank LM. PMID: 34570699; PMCID: PMC8476125.

View in: PubMed Mentions: 2 Fields:
Bio Biology
Hippocampal replay reflects specific past experiences rather than a plan for subsequent choice. Neuron. 2021 10 06; 109(19):3149-3163.e6. Gillespie AK, Astudillo Maya DA, Denovellis EL, Liu DF, Kastner DB, Coulter ME, Roumis DK, Eden UT, Frank LM. PMID: 34450026; PMCID: PMC8497431.

View in: PubMed Mentions: Fields:
Neu Neurology
DNA Adductomics by mass tag prelabeling. Rapid Commun Mass Spectrom. 2021 Jul 15; 35(13):e9095. Wang P, Roider E, Coulter ME, Walsh CA, Kramer CS, Beuning PJ, Giese RW. PMID: 33821547.

View in: PubMed Mentions: Fields:
Che Chemistry Techniques
Jettison-MS of Nucleic Acid Species. J Am Soc Mass Spectrom. 2020 Jul 09. Wang P, Shah GL, Landau H, Coulter ME, Walsh CA, Roider E, Kramer CS, Beuning PJ, Giese RW. PMID: 32551641.

View in: PubMed Mentions: Fields:
Che Chemistry Techniques
Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genet Med. 2020 06; 22(6):1040-1050. 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 L, Mochida GH, Harris MP, Gleeson JG, Walsh CA. PMID: 32103185; PMCID: PMC7272323.

View in: PubMed Mentions: 2 Fields:
Gen Genetics
Translation:Humans Animals
Linked-read analysis identifies mutations in single-cell DNA-sequencing data. Nat Genet. 2019 04; 51(4):749-754. 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. PMID: 30886424; PMCID: PMC6900933.

View in: PubMed Mentions: 16 Fields:
Gen Genetics
Translation:Humans
The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Rep. 2018 07 24; 24(4):973-986.e8. 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, Lee WA, Lehtinen MK, Kirchhausen T, Haussler D, Jacobs FMJ, Gaudin R, Walsh CA. PMID: 30044992; PMCID: PMC6178983.

View in: PubMed Mentions: 23 Fields:
Cel Cell Biology Mol Molecular Biology
Translation:Humans Animals Cells
PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation. Nucleic Acids Res. 2018 02 28; 46(4):e20. Sherman MA, Barton AR, Lodato MA, Vitzthum C, Coulter ME, Walsh CA, Park PJ. PMID: 29186545; PMCID: PMC5829578.

View in: PubMed Mentions: 8 Fields:
Bio Biochemistry
Translation:Humans
Aging and neurodegeneration are associated with increased mutations in single human neurons. Science. 2018 02 02; 359(6375):555-559. 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. PMID: 29217584; PMCID: PMC5831169.

View in: PubMed Mentions: 117 Fields:
Sci Science
Translation:Humans Cells
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Genome Res. 2017 08; 27(8):1323-1335. 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, Ryu SC, Elhosary PC, Richardson JM, Tierney D, Robinson CA, Chibbar R, Diudea D, Folkerth R, Wiebe S, Barkovich AJ, Mochida GH, Irvine J, Lemire EG, Blakley P, Walsh CA. PMID: 28630177; PMCID: PMC5538549.

View in: PubMed Mentions: 17 Fields:
Gen Genetics
Translation:Humans Animals Cells
Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. Am J Hum Genet. 2015 May 07; 96(5):709-19. 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 PC, Gorski G, Barkovich AJ, Markianos K, Poduri A, Mochida GH. PMID: 25865492; PMCID: PMC4570282.

View in: PubMed Mentions: 23 Fields:
Gen Genetics
Translation:Humans
METTL23, a transcriptional partner of GABPA, is essential for human cognition. Hum Mol Genet. 2014 Jul 01; 23(13):3456-66. 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, Meyer BF, Walsh CA, Al-Gazali L, Mochida GH. PMID: 24501276; PMCID: PMC4049305.

View in: PubMed Mentions: 19 Fields:
Gen Genetics Mol Molecular Biology
Translation:Humans Cells
Using whole-exome sequencing to identify inherited causes of autism. Neuron. 2013 Jan 23; 77(2):259-73. 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, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, LeClair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA. PMID: 23352163; PMCID: PMC3694430.

View in: PubMed Mentions: 167 Fields:
Neu Neurology
Translation:Humans Animals Cells
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. PLoS Genet. 2012; 8(4):e1002635. 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. PMID: 22511880; PMCID: PMC3325173.

View in: PubMed Mentions: 85 Fields:
Gen Genetics
Translation:Humans Cells
Chromosomal microarray testing influences medical management. Genet Med. 2011 Sep; 13(9):770-6. Coulter ME, Miller DT, Harris DJ, Hawley P, Picker J, Roberts AE, Sobeih MM, Irons M. PMID: 21716121.

View in: PubMed Mentions: 43 Fields:
Gen Genetics
Translation:Humans Cells