Li Wang - Publications

Affiliations: 
2012-2018 Molecular and Human Genetics Baylor College of Medicine, Houston, TX 
 2019- Neurology University of California, San Francisco, San Francisco, CA 

21 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
2023 Velmeshev D, Perez Y, Yan Z, Valencia JE, Castaneda-Castellanos DR, Wang L, Schirmer L, Mayer S, Wick B, Wang S, Nowakowski TJ, Paredes M, Huang EJ, Kriegstein AR. Single-cell analysis of prenatal and postnatal human cortical development. Science (New York, N.Y.). 382: eadf0834. PMID 37824647 DOI: 10.1126/science.adf0834  0.715
2023 Perez Y, Velmeshev D, Wang L, White M, Siebert C, Baltazar J, Dutton NG, Wang S, Haeussler M, Chamberlain S, Kriegstein A. Single cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism. Biorxiv : the Preprint Server For Biology. PMID 37790331 DOI: 10.1101/2023.09.22.559056  0.573
2023 Wang L, Pang K, Zhou L, Cebrián-Silla A, González-Granero S, Wang S, Bi Q, White ML, Ho B, Li J, Li T, Perez Y, Huang EJ, Winkler EA, Paredes MF, et al. A cross-species proteomic map reveals neoteny of human synapse development. Nature. PMID 37704727 DOI: 10.1038/s41586-023-06542-2  0.568
2023 Andrews MG, Siebert C, Wang L, White ML, Ross J, Morales R, Donnay M, Bamfonga G, Mukhtar T, McKinney AA, Gemenes K, Wang S, Bi Q, Crouch EE, Parikshak N, et al. LIF signaling regulates outer radial glial to interneuron fate during human cortical development. Cell Stem Cell. PMID 37673072 DOI: 10.1016/j.stem.2023.08.009  0.709
2023 Wang L, Kriegstein AR. Non-muscle myosins control the integrity of cortical radial glial endfeet. Plos Biology. 21: e3002032. PMID 36854254 DOI: 10.1371/journal.pbio.3002032  0.502
2022 Andrews MG, Mukhtar T, Eze UC, Simoneau CR, Ross J, Parikshak N, Wang S, Zhou L, Koontz M, Velmeshev D, Siebert CV, Gemenes KM, Tabata T, Perez Y, Wang L, et al. Tropism of SARS-CoV-2 for human cortical astrocytes. Proceedings of the National Academy of Sciences of the United States of America. 119: e2122236119. PMID 35858406 DOI: 10.1073/pnas.2122236119  0.678
2022 Long H, Jia Q, Wang L, Fang W, Wang Z, Jiang T, Zhou F, Jin Z, Huang J, Zhou L, Hu C, Wang X, Zhang J, Ba Y, Gong Y, ... ... Wang L, ... ... Wang L, et al. Tumor-induced erythroid precursor-differentiated myeloid cells mediate immunosuppression and curtail anti-PD-1/PD-L1 treatment efficacy. Cancer Cell. PMID 35594863 DOI: 10.1016/j.ccell.2022.04.018  0.301
2022 Jia M, Li Q, Guo J, Shi W, Zhu L, Huang Y, Li Y, Wang L, Ma S, Zhuang T, Wang X, Pan Q, Wei X, Qin Y, Li X, et al. Deletion of BACH1 Attenuates Atherosclerosis by Reducing Endothelial Inflammation. Circulation Research. CIRCRESAHA121319540. PMID 35196865 DOI: 10.1161/CIRCRESAHA.121.319540  0.403
2021 Li T, Yu D, Oak HC, Zhu B, Wang L, Jiang X, Molday RS, Kriegstein A, Piao X. Phospholipid-flippase chaperone CDC50A is required for synapse maintenance by regulating phosphatidylserine exposure. The Embo Journal. e107915. PMID 34585770 DOI: 10.15252/embj.2021107915  0.478
2020 Wang L, Kriegstein A. Mitochondria Control Cortical Cell Fate after Mitosis. Developmental Cell. 55: 120-122. PMID 33108754 DOI: 10.1016/j.devcel.2020.09.028  0.51
2020 Huang W, Bhaduri A, Velmeshev D, Wang S, Wang L, Rottkamp CA, Alvarez-Buylla A, Rowitch DH, Kriegstein AR. Origins and Proliferative States of Human Oligodendrocyte Precursor Cells. Cell. PMID 32679030 DOI: 10.1016/j.cell.2020.06.027  0.556
2020 Pang K, Wang L, Wang W, Zhou J, Cheng C, Han K, Zoghbi HY, Liu Z. Coexpression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders. Genome Research. PMID 32554779 DOI: 10.1101/Gr.254987.119  0.503
2019 Chen CA, Wang W, Pedersen SE, Raman A, Seymour ML, Ruiz FR, Xia A, van der Heijden ME, Wang L, Yin J, Lopez J, Rech ME, Lewis RA, Wu SM, Liu Z, et al. Nr2f1 heterozygous knockout mice recapitulate neurological phenotypes of Bosch-Boonstra-Schaaf optic atrophy syndrome and show impaired hippocampal synaptic plasticity. Human Molecular Genetics. PMID 31600777 DOI: 10.1093/Hmg/Ddz233  0.615
2019 Meng X, McGraw CM, Wang W, Jing J, Yeh SY, Wang L, Lopez J, Brown AM, Lin T, Chen W, Xue M, Sillitoe RV, Jiang X, Zoghbi HY. Neurexophilin4 is a selectively expressed α-neurexin ligand that modulates specific cerebellar synapses and motor functions. Elife. 8. PMID 31524598 DOI: 10.7554/Elife.46773  0.724
2019 Wang L, Adamski CJ, Bondar VV, Craigen E, Collette JR, Pang K, Han K, Jain A, Y Jung S, Liu Z, Sifers RN, Holder JL, Zoghbi HY. A kinome-wide RNAi screen identifies ERK2 as a druggable regulator of Shank3 stability. Molecular Psychiatry. PMID 30696942 DOI: 10.1038/S41380-018-0325-9  0.468
2019 Wang L, Pang K, Han K, Adamski CJ, Wang W, He L, Lai JK, Bondar VV, Duman JG, Richman R, Tolias KF, Barth P, Palzkill T, Liu Z, Holder JL, et al. An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function. Molecular Psychiatry. PMID 30610205 DOI: 10.1038/S41380-018-0324-X  0.726
2018 Bondar VV, Adamski CJ, Onur TS, Tan Q, Wang L, Diaz-Garcia J, Park J, Orr HT, Botas J, Zoghbi HY. PAK1 regulates ATXN1 levels providing an opportunity to modify its toxicity in Spinocerebellar ataxia type 1. Human Molecular Genetics. PMID 29860311 DOI: 10.1093/Hmg/Ddy200  0.686
2018 Gennarino VA, Palmer EE, McDonell LM, Wang L, Adamski CJ, Koire A, See L, Chen CA, Schaaf CP, Rosenfeld JA, Panzer JA, Moog U, Hao S, Bye A, Kirk EP, et al. A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures. Cell. 172: 924-936.e11. PMID 29474920 DOI: 10.1016/j.cell.2018.02.006  0.595
2018 Yin J, Chen W, Chao ES, Soriano S, Wang L, Wang W, Cummock SE, Tao H, Pang K, Liu Z, Pereira FA, Samaco RC, Zoghbi HY, Xue M, Schaaf CP. Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. American Journal of Human Genetics. 102: 296-308. PMID 29395075 DOI: 10.1016/J.Ajhg.2018.01.005  0.733
2018 Gulinello M, Mitchell HA, Chang Q, Timothy O'Brien W, Zhou Z, Abel T, Wang L, Corbin JG, Veeraragavan S, Samaco RC, Andrews NA, Fagiolini M, Cole TB, Burbacher TM, Crawley JN. Rigor and Reproducibility in Rodent Behavioral Research. Neurobiology of Learning and Memory. PMID 29307548 DOI: 10.1016/J.Nlm.2018.01.001  0.637
2013 Han JJ, Xie de R, Wang LL, Liu YQ, Wu GF, Sun Q, Chen YX, Wei Y, Huang ZQ, Li HG. Significance of glutathione peroxidase 1 and caudal-related homeodomain transcription factor in human gastric adenocarcinoma. Gastroenterology Research and Practice. 2013: 380193. PMID 24228025 DOI: 10.1155/2013/380193  0.327
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