| Year |
Citation |
Score |
| 2024 |
Lee KH, Denovellis E, Ly R, Magland J, Soules J, Comrie AE, Gramling DP, Guidera JA, Nevers R, Adenekan P, Brozdowski C, Bray S, Monroe E, Bak JH, Coulter M, et al. Spyglass: a data analysis framework for reproducible and shareable neuroscience research. Biorxiv : the Preprint Server For Biology. PMID 38328074 DOI: 10.1101/2024.01.25.577295 |
0.709 |
|
| 2023 |
Coulter ME, Kemere C. The neural basis of mental navigation in rats. Science (New York, N.Y.). 382: 517-518. PMID 37917674 DOI: 10.1126/science.adl0806 |
0.62 |
|
| 2022 |
Bae T, Fasching L, Wang Y, Shin JH, Suvakov M, Jang Y, Norton S, Dias C, Mariani J, Jourdon A, Wu F, Panda A, Pattni R, Chahine Y, Yeh R, ... ... Coulter M, et al. Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability. Science (New York, N.Y.). 377: 511-517. PMID 35901164 DOI: 10.1126/science.abm6222 |
0.735 |
|
| 2021 |
Denovellis EL, Gillespie AK, Coulter ME, Sosa M, Chung JE, Eden UT, Frank LM. Hippocampal replay of experience at real-world speeds. Elife. 10. PMID 34570699 DOI: 10.7554/eLife.64505 |
0.69 |
|
| 2021 |
Gillespie AK, Astudillo Maya DA, Denovellis EL, Liu DF, Kastner DB, Coulter ME, Roumis DK, Eden UT, Frank LM. Hippocampal replay reflects specific past experiences rather than a plan for subsequent choice. Neuron. PMID 34450026 DOI: 10.1016/j.neuron.2021.07.029 |
0.684 |
|
| 2020 |
Wang P, Shah GL, Landau HJ, Coulter ME, Walsh CA, Roider E, Kramer CS, Beuning PJ, Giese RW. Jettison-MS of Nucleic Acid Species. Journal of the American Society For Mass Spectrometry. PMID 32551641 DOI: 10.1021/Jasms.0C00084 |
0.435 |
|
| 2020 |
Coulter ME, Musaev D, DeGennaro EM, Zhang X, Henke K, James KN, Smith RS, Hill RS, Partlow JN, Muna Al-Saffar, Kamumbu AS, Hatem N, Barkovich AJ, Aziza J, Chassaing N, et al. 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. PMID 32103185 DOI: 10.1038/S41436-020-0758-9 |
0.719 |
|
| 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. Linked-read analysis identifies mutations in single-cell DNA-sequencing data. Nature Genetics. PMID 30886424 DOI: 10.1038/S41588-019-0366-2 |
0.768 |
|
| 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, et al. The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Reports. 24: 973-986.e8. PMID 30044992 DOI: 10.1016/J.Celrep.2018.06.100 |
0.76 |
|
| 2017 |
Lodato MA, Rodin RE, Bohrson CL, Coulter ME, Barton AR, Kwon M, Sherman MA, Vitzthum CM, Luquette LJ, Yandava C, Yang P, Chittenden TW, Hatem NE, Ryu SC, Woodworth MB, et al. Aging and neurodegeneration are associated with increased mutations in single human neurons. Science (New York, N.Y.). PMID 29217584 DOI: 10.1126/Science.Aao4426 |
0.765 |
|
| 2017 |
Sherman MA, Barton AR, Lodato MA, Vitzthum C, Coulter ME, Walsh CA, Park PJ. PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation. Nucleic Acids Research. PMID 29186545 DOI: 10.1093/Nar/Gkx1195 |
0.736 |
|
| 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, et al. Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Genome Research. PMID 28630177 DOI: 10.1101/Gr.219899.116 |
0.775 |
|
| 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, et al. Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. American Journal of Human Genetics. 96: 709-19. PMID 25865492 DOI: 10.1016/J.Ajhg.2015.03.003 |
0.436 |
|
| 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, et al. METTL23, a transcriptional partner of GABPA, is essential for human cognition. Human Molecular Genetics. 23: 3456-66. PMID 24501276 DOI: 10.1093/Hmg/Ddu054 |
0.759 |
|
| 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, et al. Using whole-exome sequencing to identify inherited causes of autism. Neuron. 77: 259-73. PMID 23352163 DOI: 10.1016/J.Neuron.2012.11.002 |
0.743 |
|
| 2013 |
Yu TW, Coulter M, Chahrour M, Walsh CA. Autism Spectrum Disorders Genomic and Personalized Medicine. 2: 1067-1074. DOI: 10.1016/B978-0-12-382227-7.00090-2 |
0.731 |
|
| 2012 |
Chahrour MH, Yu TW, Lim ET, Ataman B, Coulter ME, Hill RS, Stevens CR, Schubert CR, Greenberg ME, Gabriel SB, Walsh CA. Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. Plos Genetics. 8: e1002635. PMID 22511880 DOI: 10.1371/Journal.Pgen.1002635 |
0.785 |
|
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