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Brie A. Wamsley - Publications

Affiliations: 
Columbia University, New York, NY 
Area:
Axon Guidance, Cell Migration, Development, Synaptogenesis
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Wamsley B, Bicks L, Cheng Y, Kawaguchi R, Quintero D, Margolis M, Grundman J, Liu J, Xiao S, Hawken N, Mazariegos S, Geschwind DH. Molecular cascades and cell type-specific signatures in ASD revealed by single-cell genomics. Science (New York, N.Y.). 384: eadh2602. PMID 38781372 DOI: 10.1126/science.adh2602  0.366
2024 Emani PS, Liu JJ, Clarke D, Jensen M, Warrell J, Gupta C, Meng R, Lee CY, Xu S, Dursun C, Lou S, Chen Y, Chu Z, Galeev T, Hwang A, ... ... Wamsley B, et al. Single-cell genomics and regulatory networks for 388 human brains. Science (New York, N.Y.). 384: eadi5199. PMID 38781369 DOI: 10.1126/science.adi5199  0.319
2024 Emani PS, Liu JJ, Clarke D, Jensen M, Warrell J, Gupta C, Meng R, Lee CY, Xu S, Dursun C, Lou S, Chen Y, Chu Z, Galeev T, Hwang A, ... ... Wamsley B, et al. Single-cell genomics and regulatory networks for 388 human brains. Biorxiv : the Preprint Server For Biology. PMID 38562822 DOI: 10.1101/2024.03.18.585576  0.313
2023 Wamsley B, Bicks L, Cheng Y, Kawaguchi R, Quintero D, Grundman J, Liu J, Xiao S, Hawken N, Margolis M, Mazariegos S, Geschwind DH. Molecular cascades and cell-type specific signatures in ASD revealed by single cell genomics. Biorxiv : the Preprint Server For Biology. PMID 36945369 DOI: 10.1101/2023.03.10.530869  0.387
2022 Gandal MJ, Haney JR, Wamsley B, Yap CX, Parhami S, Emani PS, Chang N, Chen GT, Hoftman GD, de Alba D, Ramaswami G, Hartl CL, Bhattacharya A, Luo C, Jin T, et al. Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD. Nature. PMID 36323788 DOI: 10.1038/s41586-022-05377-7  0.302
2022 Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics. PMID 35982160 DOI: 10.1038/s41588-022-01104-0  0.302
2018 Wamsley B, Jaglin XH, Favuzzi E, Quattrocolo G, Nigro MJ, Yusuf N, Khodadadi-Jamayran A, Rudy B, Fishell G. Rbfox1 Mediates Cell-type-Specific Splicing in Cortical Interneurons. Neuron. PMID 30318414 DOI: 10.1016/J.Neuron.2018.09.026  0.326
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