Liping Wei, Ph.D. - Publications

Affiliations: 
Stanford University, Palo Alto, CA 

114 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
2019 Cai L, He Q, Lu Y, Hu Y, Chen W, Wei L, Hu Y. Comorbidity of Pain and Depression in a Lumbar Disc Herniation Model: Biochemical Alterations and the Effects of Fluoxetine. Frontiers in Neurology. 10: 1022. PMID 31616368 DOI: 10.3389/fneur.2019.01022  1
2019 Wei L, Zhang Y, Qi X, Sun X, Li Y, Xu Y. Ubiquitin‑proteasomes are the dominant mediators of the regulatory effect of microRNA‑1 on cardiac remodeling after myocardial infarction. International Journal of Molecular Medicine. PMID 31485642 DOI: 10.3892/ijmm.2019.4330  1
2019 Li J, Wei L, Zhao C, Li J, Liu Z, Zhang M, Wang Y. Resveratrol Maintains Lipid Metabolism Homeostasis via One of the Mechanisms Associated with the Key Circadian Regulator Bmal1. Molecules (Basel, Switzerland). 24. PMID 31408938 DOI: 10.3390/molecules24162916  1
2019 Clark WT, Kasak L, Bakolitsa C, Hu Z, Andreoletti G, Babbi G, Bromberg Y, Casadio R, Dunbrack R, Folkman L, Ford CT, Jones D, Katsonis P, Kundu K, Lichtarge O, ... ... Wei L, et al. Assessment of predicted enzymatic activity of alpha-N-acetylglucosaminidase (NAGLU) variants of unknown significance for CAGI 2016. Human Mutation. PMID 31342580 DOI: 10.1002/humu.23875  1
2019 Wei M, Han A, Wei L, Ma L. A Neonatal Case With Perinatal Lethal Gaucher Disease Associated With Missense G234E and H413P Heterozygous Mutations. Frontiers in Pediatrics. 7: 201. PMID 31192173 DOI: 10.3389/fped.2019.00201  0.4
2019 Huang A, Qi X, Wei L, Zhang M, Zhou S. Non-HDL-c/TC: A Novel Lipid-Related Marker in the Assessment of Severity of Coronary Artery Lesions and Cardiovascular Outcomes. Cardiology Research and Practice. 2019: 5931975. PMID 31179126 DOI: 10.1155/2019/5931975  1
2019 Zhao B, Wu Q, Ye AY, Guo J, Zheng X, Yang X, Yan L, Liu QR, Hyde TM, Wei L, Huang AY. Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals. Plos Genetics. 15: e1008043. PMID 30973874 DOI: 10.1371/journal.pgen.1008043  1
2019 Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. ATP1A3 mosaicism in families with alternating hemiplegia of childhood. Clinical Genetics. PMID 30891744 DOI: 10.1111/cge.13539  1
2019 Sun X, Allison C, Wei L, Matthews FE, Auyeung B, Wu YY, Griffiths S, Zhang J, Baron-Cohen S, Brayne C. Autism prevalence in China is comparable to Western prevalence. Molecular Autism. 10: 7. PMID 30858963 DOI: 10.1186/s13229-018-0246-0  1
2019 Zhang Q, Yang X, Wang J, Li J, Wu Q, Wen Y, Zhao Y, Zhang X, Yao H, Wu X, Yu S, Wei L, Bao X. Correction: Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30783265 DOI: 10.1038/s41436-019-0461-x  1
2019 Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human Mutation. PMID 30763456 DOI: 10.1002/humu.23724  1
2018 Zhang Q, Yang X, Wang J, Li J, Wu Q, Wen Y, Zhao Y, Zhang X, Yao H, Wu X, Yu S, Wei L, Bao X. Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30405208 DOI: 10.1038/s41436-018-0348-2  1
2018 Yang C, Li J, Wu Q, Yang X, Huang AY, Zhang J, Ye AY, Dou Y, Yan L, Zhou WZ, Kong L, Wang M, Ai C, Yang D, Wei L. AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. Database : the Journal of Biological Databases and Curation. 2018. PMID 30339214 DOI: 10.1093/database/bay106  1
2018 Liu A, Yang X, Yang X, Wu Q, Zhang J, Sun D, Yang Z, Jiang Y, Wu X, Wei L, Zhang Y. Mosaicism and incomplete penetrance of mutations. Journal of Medical Genetics. PMID 30287595 DOI: 10.1136/jmedgenet-2017-105235  1
2018 Zhang H, Dou S, He F, Luo J, Wei L, Lu J. Genome-wide maps of ribosomal occupancy provide insights into adaptive evolution and regulatory roles of uORFs during Drosophila development. Plos Biology. 16: e2003903. PMID 30028832 DOI: 10.1371/journal.pbio.2003903  1
2018 Ye AY, Dou Y, Yang X, Wang S, Huang AY, Wei L. A model for postzygotic mosaicisms quantifies the allele fraction drift, mutation rate, and contribution to de novo mutations. Genome Research. PMID 29875290 DOI: 10.1101/gr.230003.117  1
2018 Huang AY, Yang X, Wang S, Zheng X, Wu Q, Ye AY, Wei L. Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs. Plos Genetics. 14: e1007395. PMID 29763432 DOI: 10.1371/journal.pgen.1007395  1
2018 Wang M, Tai C, E W, Wei L. DeFine: deep convolutional neural networks accurately quantify intensities of transcription factor-DNA binding and facilitate evaluation of functional non-coding variants. Nucleic Acids Research. PMID 29617928 DOI: 10.1093/nar/gky215  1
2017 Zeng Q, Yang X, Zhang J, Liu A, Yang Z, Liu X, Wu Y, Wu X, Wei L, Zhang Y. Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort. Journal of Human Genetics. PMID 29215089 DOI: 10.1038/s10038-017-0359-x  1
2017 Yang X, Liu A, Xu X, Yang X, Zeng Q, Ye AY, Yu Z, Wang S, Huang AY, Wu X, Wu Q, Wei L, Zhang Y. Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort. Scientific Reports. 7: 15677. PMID 29142202 DOI: 10.1038/s41598-017-15814-7  1
2017 An S, Feng X, Dai Y, Bo H, Wang X, Li M, Woo JZ, Liang X, Guo C, Liu CX, Wei L. Development and evaluation of a speech-generating AAC mobile app for minimally verbal children with autism spectrum disorder in Mainland China. Molecular Autism. 8: 52. PMID 29026509 DOI: 10.1186/s13229-017-0165-5  1
2017 Wang J, Gao H, Bao X, Zhang Q, Li J, Wei L, Wu X, Chen Y, Yu S. SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures. Bmc Medical Genetics. 18: 104. PMID 28923014 DOI: 10.1186/s12881-017-0460-1  1
2017 Zhang Q, Wang J, Li J, Bao X, Zhao Y, Zhang X, Wei L, Wu X. Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation. Bmc Medical Genetics. 18: 96. PMID 28851325 DOI: 10.1186/s12881-017-0455-y  1
2017 Kang YJ, Yang DC, Kong L, Hou M, Meng YQ, Wei L, Gao G. CPC2: a fast and accurate coding potential calculator based on sequence intrinsic features. Nucleic Acids Research. PMID 28521017 DOI: 10.1093/nar/gkx428  1
2017 Dou Y, Yang X, Li Z, Wang S, Zhang Z, Ye AY, Yan L, Yang C, Wu Q, Li J, Zhao B, Huang AY, Wei L. Post-zygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. Human Mutation. PMID 28503910 DOI: 10.1002/humu.23255  1
2017 Zhang Q, Zhao Y, Bao X, Luo J, Zhang X, Li J, Wei L, Wu X. Familial cases and male cases with MECP2 mutations. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28394482 DOI: 10.1002/ajmg.b.32534  1
2017 Luo J, Feng Q, Wei L, Luo M. Optogenetic activation of dorsal raphe neurons rescues the autistic-like social deficits in Shank3 knockout mice. Cell Research. PMID 28374752 DOI: 10.1038/cr.2017.52  1
2017 Zhou C, Wu F, Lu L, Wei L, Pai E, Yao Y, Song Y. Structure activity relationship and modeling studies of inhibitors of lysine specific demethylase 1. Plos One. 12: e0170301. PMID 28158205 DOI: 10.1371/journal.pone.0170301  1
2017 Huang AY, Zhang Z, Ye AY, Dou Y, Yan L, Yang X, Zhang Y, Wei L. MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples. Nucleic Acids Research. PMID 28132024 DOI: 10.1093/nar/gkx024  1
2016 Miao Z, Huo X, Gao F, Liao X, Wang C, Peng Y, Cao Y, Chen S, Zhang M, Jiang C, Peng X, Song C, Wei L, Zhu Q, Guo Z, et al. Endovascular therapy for Acute ischemic Stroke Trial (EAST): study protocol for a prospective, multicentre control trial in China. Stroke and Vascular Neurology. 1: 44-51. PMID 28959463 DOI: 10.1136/svn-2016-000022  1
2016 Liu D, Qi X, Li Q, Jia W, Wei L, Huang A, Liu K, Li Z. Increased complements and high-sensitivity C-reactive protein predict heart failure in acute myocardial infarction. Biomedical Reports. 5: 761-765. PMID 28105343 DOI: 10.3892/br.2016.793  1
2016 Hu G, Wu Y, Zhou Y, Wu Z, Wei L, Li Y, Peng G, Liang W, Ran P. Prognostic role of D-dimer for in-hospital and 1-year mortality in exacerbations of COPD. International Journal of Chronic Obstructive Pulmonary Disease. 11: 2729-2736. PMID 27843309 DOI: 10.2147/COPD.S112882  1
2016 Zhang Q, Li J, Zhao Y, Bao X, Wei L, Wang J. Gene mutation analysis of 175 Chinese patients with early-onset epileptic encephalopathy. Clinical Genetics. PMID 27779742 DOI: 10.1111/cge.12901  1
2016 Liu A, Xu X, Yang X, Jiang Y, Yang Z, Liu X, Wu Y, Wu X, Wei L, Zhang Y. The Clinical Spectrum of Female Epilepsy Patients with PCDH19 Mutations in a Chinese Population. Clinical Genetics. PMID 27527380 DOI: 10.1111/cge.12846  1
2016 Wang M, Wei L. iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers. Scientific Reports. 6: 31321. PMID 27527004 DOI: 10.1038/srep31321  1
2016 Li Z, He S, Wei L, Lin L, Xiong H, Li J, Chen P, Lai W. [Dexamethasone increases the expression of reversion-inducing cysteine-rich protein with Kazal motifs (RECK) in lung tissues of bronchial asthmatic mice]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi = Chinese Journal of Cellular and Molecular Immunology. 32: 604-8. PMID 27126937  1
2016 Hou T, Jian C, Xu J, Huang AY, Xi J, Hu K, Wei L, Cheng H, Wang X. Identification of EFHD1 as a novel Ca(2+) sensor for mitoflash activation. Cell Calcium. PMID 26975899 DOI: 10.1016/j.ceca.2016.03.002  1
2016 Feng Z, Yao Y, Zhou C, Chen F, Wu F, Wei L, Liu W, Dong S, Redell M, Mo Q, Song Y. Pharmacological inhibition of LSD1 for the treatment of MLL-rearranged leukemia. Journal of Hematology & Oncology. 9: 24. PMID 26970896 DOI: 10.1186/s13045-016-0252-7  0.32
2015 Yang X, Zhang Y, Yuan D, Xu X, Li S, Wei L, Wu Y, Xiong H, Liu X, Bao X, Jiang Y, Wu X. [ATP1A3 gene mutations in patients with alternating hemiplegia of childhood]. Zhonghua Er Ke Za Zhi. Chinese Journal of Pediatrics. 53: 835-9. PMID 26758322  1
2015 Wu F, Zhou C, Yao Y, Wei L, Feng Z, Deng L, Song Y. 3-(Piperidin-4-ylmethoxy)pyridine Containing Compounds Are Potent Inhibitors of Lysine Specific Demethylase 1. Journal of Medicinal Chemistry. PMID 26652247 DOI: 10.1021/acs.jmedchem.5b01361  0.32
2015 Thakkar M, Randhawa V, Mitra S, Wei L. Synthesis of diatom-FeOx composite for removing trace arsenic to meet drinking water standards. Journal of Colloid and Interface Science. 457: 169-73. PMID 26164249 DOI: 10.1016/j.jcis.2015.07.003  1
2015 Zhang X, Zhu D, Wei L, Zhao Z, Qi X, Li Z, Sun D. OSM Enhances Angiogenesis and Improves Cardiac Function after Myocardial Infarction. Biomed Research International. 2015: 317905. PMID 26146616 DOI: 10.1155/2015/317905  1
2015 Xu X, Yang X, Wu Q, Liu A, Yang X, Ye AY, Huang AY, Li J, Wang M, Yu Z, Wang S, Zhang Z, Wu X, Wei L, Zhang Y. Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Human Mutation. PMID 26096185 DOI: 10.1002/humu.22819  1
2015 Thakkar M, Wu Z, Wei L, Mitra S. Water defluoridation using a nanostructured diatom-ZrO₂ composite synthesized from algal biomass. Journal of Colloid and Interface Science. 450: 239-45. PMID 25823727 DOI: 10.1016/j.jcis.2015.03.017  0.52
2015 Sun D, Li S, Wu H, Zhang M, Zhang X, Wei L, Qin X, Gao E. Oncostatin M (OSM) protects against cardiac ischaemia/reperfusion injury in diabetic mice by regulating apoptosis, mitochondrial biogenesis and insulin sensitivity. Journal of Cellular and Molecular Medicine. 19: 1296-307. PMID 25752217 DOI: 10.1111/jcmm.12501  1
2015 Zhao HQ, Zhang P, Gao H, He X, Dou Y, Huang AY, Liu XM, Ye AY, Dong MQ, Wei L. Profiling the RNA editomes of wild-type C. elegans and ADAR mutants. Genome Research. 25: 66-75. PMID 25373143 DOI: 10.1101/gr.176107.114  1
2014 Zhou WZ, Ye AY, Sun ZK, Tian HH, Pu TZ, Wu YY, Wang DD, Zhao MZ, Lu SJ, Yang CH, Wei L. Statistical analysis of twenty years (1993 to 2012) of data from mainland China's first intervention center for children with autism spectrum disorder. Molecular Autism. 5: 52. PMID 25694804 DOI: 10.1186/2040-2392-5-52  1
2014 Ding Y, Wang M, He Y, Ye AY, Yang X, Liu F, Meng Y, Gao G, Wei L. "Bioinformatics: introduction and methods," a bilingual Massive Open Online Course (MOOC) as a new example for global bioinformatics education. Plos Computational Biology. 10: e1003955. PMID 25503717 DOI: 10.1371/journal.pcbi.1003955  1
2014 He B, Lanz RB, Fiskus W, Geng C, Yi P, Hartig SM, Rajapakshe K, Shou J, Wei L, Shah SS, Foley C, Chew SA, Eedunuri VK, Bedoya DJ, Feng Q, et al. GATA2 facilitates steroid receptor coactivator recruitment to the androgen receptor complex. Proceedings of the National Academy of Sciences of the United States of America. 111: 18261-6. PMID 25489091 DOI: 10.1073/pnas.1421415111  1
2014 Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, ... ... Wei L, et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature. 515: 216-21. PMID 25363768 DOI: 10.1038/nature13908  1
2014 Zhang L, Deng L, Chen F, Yao Y, Wu B, Wei L, Mo Q, Song Y. Inhibition of histone H3K79 methylation selectively inhibits proliferation, self-renewal and metastatic potential of breast cancer. Oncotarget. 5: 10665-77. PMID 25359765  1
2014 Huang AY, Xu X, Ye AY, Wu Q, Yan L, Zhao B, Yang X, He Y, Wang S, Zhang Z, Gu B, Zhao HQ, Wang M, Gao H, Gao G, ... ... Wei L, et al. Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals. Cell Research. 24: 1311-27. PMID 25312340 DOI: 10.1038/cr.2014.131  1
2014 Dong S, Walker MF, Carriero NJ, DiCola M, Willsey AJ, Ye AY, Waqar Z, Gonzalez LE, Overton JD, Frahm S, Keaney JF, Teran NA, Dea J, Mandell JD, Hus Bal V, ... ... Wei L, et al. De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. Cell Reports. 9: 16-23. PMID 25284784 DOI: 10.1016/j.celrep.2014.08.068  1
2014 Yang X, Gao H, Zhang J, Xu X, Liu X, Wu X, Wei L, Zhang Y. ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients. Plos One. 9: e97274. PMID 24842602 DOI: 10.1371/journal.pone.0097274  1
2014 Zhao Y, Zhang X, Bao X, Zhang Q, Zhang J, Cao G, Zhang J, Li J, Wei L, Pan H, Wu X. Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients. Bmc Medical Genetics. 15: 24. PMID 24564546 DOI: 10.1186/1471-2350-15-24  1
2014 Gao G, Vibranovski MD, Zhang L, Li Z, Liu M, Zhang YE, Li X, Zhang W, Fan Q, VanKuren NW, Long M, Wei L. A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster. Genome Research. 24: 629-38. PMID 24407956 DOI: 10.1101/gr.165837.113  1
2014 Tang H, Jin X, Li Y, Jiang H, Tang X, Yang X, Cheng H, Qiu Y, Chen G, Mei J, Zhou F, Wu R, Zuo X, Zhang Y, Zheng X, ... ... Wei L, et al. A large-scale screen for coding variants predisposing to psoriasis. Nature Genetics. 46: 45-50. PMID 24212883 DOI: 10.1038/ng.2827  1
2013 Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, ... ... Wei L, et al. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell. 155: 997-1007. PMID 24267886 DOI: 10.1016/j.cell.2013.10.020  1
2013 Wang W, Xue J, Tian T, Zhang J, Wei L, Shao J, Xie Z, Li Y. Total synthesis of (±)-δ-rubromycin. Organic Letters. 15: 2402-5. PMID 23635026 DOI: 10.1021/ol400864f  1
2013 Huang Y, Xie C, Ye AY, Li CY, Gao G, Wei L. Recent adaptive events in human brain revealed by meta-analysis of positively selected genes. Plos One. 8: e61280. PMID 23593450 DOI: 10.1371/journal.pone.0061280  1
2012 Qin Y, Chen X, Huang D, Wei L. [Distribution and drug resistance profiles of pathogenic bacteria isolated from patients with nosocomial infection in intensive care unit]. Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University. 32: 1513-5. PMID 23076198  1
2012 Wei L, Xue J, Liu H, Wang W, Li Y. Synthesis of (±)-γ-rubromycin via a new hypoiodite-catalytic oxidative cycloetherification. Organic Letters. 14: 5302-5. PMID 23050595 DOI: 10.1021/ol3024874  1
2012 Xie C, Zhang YE, Chen JY, Liu CJ, Zhou WZ, Li Y, Zhang M, Zhang R, Wei L, Li CY. Hominoid-specific de novo protein-coding genes originating from long non-coding RNAs. Plos Genetics. 8: e1002942. PMID 23028352 DOI: 10.1371/journal.pgen.1002942  1
2012 Zhang X, Bao X, Zhang J, Zhao Y, Cao G, Pan H, Zhang J, Wei L, Wu X. Molecular characteristics of Chinese patients with Rett syndrome. European Journal of Medical Genetics. 55: 677-81. PMID 22982301 DOI: 10.1016/j.ejmg.2012.08.009  1
2012 Yin Z, Fan L, Wei L, Gao H, Zhang R, Tao L, Cao F, Wang H. FTY720 protects cardiac microvessels of diabetes: a critical role of S1P1/3 in diabetic heart disease. Plos One. 7: e42900. PMID 22916176 DOI: 10.1371/journal.pone.0042900  1
2012 Lu F, Wei L, Azarpira A, Ralph J. Rapid syntheses of dehydrodiferulates via biomimetic radical coupling reactions of ethyl ferulate. Journal of Agricultural and Food Chemistry. 60: 8272-7. PMID 22846085 DOI: 10.1021/jf302140k  1
2012 Kang Y, Deng R, Wang C, Deng T, Peng P, Cheng X, Wang G, Qian M, Gao H, Han B, Chen Y, Hu Y, Geng R, Hu C, Zhang W, ... ... Wei L, et al. Etiologic diagnosis of lower respiratory tract bacterial infections using sputum samples and quantitative loop-mediated isothermal amplification. Plos One. 7: e38743. PMID 22719933 DOI: 10.1371/journal.pone.0038743  1
2012 Yue R, Li H, Liu H, Li Y, Wei B, Gao G, Jin Y, Liu T, Wei L, Du J, Pei G. Thrombin receptor regulates hematopoiesis and endothelial-to-hematopoietic transition. Developmental Cell. 22: 1092-100. PMID 22521721 DOI: 10.1016/j.devcel.2012.01.025  1
2012 Xu LM, Li JR, Huang Y, Zhao M, Tang X, Wei L. AutismKB: an evidence-based knowledgebase of autism genetics. Nucleic Acids Research. 40: D1016-22. PMID 22139918 DOI: 10.1093/nar/gkr1145  1
2011 Li CY, Zhou WZ, Zhang PW, Johnson C, Wei L, Uhl GR. Meta-analysis and genome-wide interpretation of genetic susceptibility to drug addiction. Bmc Genomics. 12: 508. PMID 21999673 DOI: 10.1186/1471-2164-12-508  1
2011 Du P, Wu J, Zhang J, Zhao S, Zheng H, Gao G, Wei L, Li Y. Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors. Plos Pathogens. 7: e1002176. PMID 21901091 DOI: 10.1371/journal.ppat.1002176  1
2011 Xie C, Mao X, Huang J, Ding Y, Wu J, Dong S, Kong L, Gao G, Li CY, Wei L. KOBAS 2.0: a web server for annotation and identification of enriched pathways and diseases. Nucleic Acids Research. 39: W316-22. PMID 21715386 DOI: 10.1093/nar/gkr483  1
2011 Liang C, Zhang X, Wei L, He H, Higbee AJ, Balser TC. Investigation of the molecular ion structure for aldononitrile acetate derivatized muramic acid. Journal of Microbiological Methods. 86: 224-30. PMID 21621564 DOI: 10.1016/j.mimet.2011.05.007  0.36
2010 Guo W, Li JT, Pan X, Wei L, Wu JY. Candidate Mycobacterium tuberculosis genes targeted by human microRNAs. Protein & Cell. 1: 419-21. PMID 21203954 DOI: 10.1007/s13238-010-0056-4  1
2010 Yuan Y, Wei L, Li F, Guo W, Li W, Luan R, Lv A, Wang H. Pulsed magnetic field induces angiogenesis and improves cardiac function of surgically induced infarcted myocardium in Sprague-Dawley rats. Cardiology. 117: 57-63. PMID 20924179 DOI: 10.1159/000321459  1
2010 Wei L, Thakkar M, Chen Y, Ntim SA, Mitra S, Zhang X. Cytotoxicity effects of water dispersible oxidized multiwalled carbon nanotubes on marine alga, Dunaliella tertiolecta. Aquatic Toxicology (Amsterdam, Netherlands). 100: 194-201. PMID 20673592 DOI: 10.1016/j.aquatox.2010.07.001  1
2010 Li CY, Zhang Y, Wang Z, Zhang Y, Cao C, Zhang PW, Lu SJ, Li XM, Yu Q, Zheng X, Du Q, Uhl GR, Liu QR, Wei L. A human-specific de novo protein-coding gene associated with human brain functions. Plos Computational Biology. 6: e1000734. PMID 20376170 DOI: 10.1371/journal.pcbi.1000734  1
2010 Wei L, Yin Z, Yuan Y, Hwang A, Lee A, Sun D, Li F, Di C, Zhang R, Cao F, Wang H. A PKC-beta inhibitor treatment reverses cardiac microvascular barrier dysfunction in diabetic rats. Microvascular Research. 80: 158-65. PMID 20079359 DOI: 10.1016/j.mvr.2010.01.003  1
2010 Wei L, Sun D, Yin Z, Yuan Y, Hwang A, Zhang Y, Si R, Zhang R, Guo W, Cao F, Wang H. A PKC-beta inhibitor protects against cardiac microvascular ischemia reperfusion injury in diabetic rats. Apoptosis : An International Journal On Programmed Cell Death. 15: 488-98. PMID 20044781 DOI: 10.1007/s10495-009-0439-2  1
2009 Zhao SQ, Wang J, Zhang L, Li JT, Gu X, Gao G, Wei L. BOAT: Basic Oligonucleotide Alignment Tool. Bmc Genomics. 10: S2. PMID 19958483 DOI: 10.1186/1471-2164-10-S3-S2  1
2009 Zhang Y, Lu S, Zhao S, Zheng X, Long M, Wei L. Positive selection for the male functionality of a co-retroposed gene in the hominoids. Bmc Evolutionary Biology. 9: 252. PMID 19832993 DOI: 10.1186/1471-2148-9-252  1
2009 Zhao M, Chen X, Gao G, Tao L, Wei L. RLEdb: a database of rate-limiting enzymes and their regulation in human, rat, mouse, yeast and E. coli. Cell Research. 19: 793-5. PMID 19468287 DOI: 10.1038/cr.2009.61  1
2009 Li Z, Liu M, Zhang L, Zhang W, Gao G, Zhu Z, Wei L, Fan Q, Long M. Detection of intergenic non-coding RNAs expressed in the main developmental stages in Drosophila melanogaster. Nucleic Acids Research. 37: 4308-14. PMID 19451167 DOI: 10.1093/nar/gkp334  1
2009 Gao G, Li JT, Kong L, Tao L, Wei L. Human herpesvirus miRNAs statistically preferentially target host genes involved in cell signaling and adhesion/junction pathways. Cell Research. 19: 665-7. PMID 19381166 DOI: 10.1038/cr.2009.45  1
2009 Li CY, Liu QR, Zhang PW, Li XM, Wei L, Uhl GR. OKCAM: an ontology-based, human-centered knowledgebase for cell adhesion molecules. Nucleic Acids Research. 37: D251-60. PMID 18790807 DOI: 10.1093/nar/gkn568  1
2008 Yu H, Gao Z, Feng Z, Shu Y, Xiang N, Zhou L, Huai Y, Feng L, Peng Z, Li Z, Xu C, Li J, Hu C, Li Q, Xu X, ... ... Wei L, et al. Clinical characteristics of 26 human cases of highly pathogenic avian influenza A (H5N1) virus infection in China. Plos One. 3: e2985. PMID 18716658 DOI: 10.1371/journal.pone.0002985  1
2008 Li JT, Zhang Y, Kong L, Liu QR, Wei L. Trans-natural antisense transcripts including noncoding RNAs in 10 species: implications for expression regulation. Nucleic Acids Research. 36: 4833-44. PMID 18653530 DOI: 10.1093/nar/gkn470  1
2008 Li CY, Mao X, Wei L. Genes and (common) pathways underlying drug addiction. Plos Computational Biology. 4: e2. PMID 18179280 DOI: 10.1371/journal.pcbi.0040002  1
2007 Kong L, Zhang Y, Ye ZQ, Liu XQ, Zhao SQ, Wei L, Gao G. CPC: assess the protein-coding potential of transcripts using sequence features and support vector machine. Nucleic Acids Research. 35: W345-9. PMID 17631615 DOI: 10.1093/nar/gkm391  1
2007 Xu Z, Liu H, Wei L. [Preservation of laryngeal function in treatment of pyriform sinus carcinoma]. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology, Head, and Neck Surgery. 21: 124-6. PMID 17441428  0.6
2007 Li CY, Yu Q, Ye ZQ, Sun Y, He Q, Li XM, Zhang W, Luo J, Gu X, Zheng X, Wei L. A nonsynonymous SNP in human cytosolic sialidase in a small Asian population results in reduced enzyme activity: potential link with severe adverse reactions to oseltamivir. Cell Research. 17: 357-62. PMID 17426694 DOI: 10.1038/cr.2007.27  1
2007 Ye ZQ, Zhao SQ, Gao G, Liu XQ, Langlois RE, Lu H, Wei L. Finding new structural and sequence attributes to predict possible disease association of single amino acid polymorphism (SAP). Bioinformatics (Oxford, England). 23: 1444-50. PMID 17384424 DOI: 10.1093/bioinformatics/btm119  1
2007 Zhang W, Zhang Y, Zheng H, Zhang C, Xiong W, Olyarchuk JG, Walker M, Xu W, Zhao M, Zhao S, Zhou Z, Wei L. SynDB: a Synapse protein DataBase based on synapse ontology. Nucleic Acids Research. 35: D737-41. PMID 17098931 DOI: 10.1093/nar/gkl876  1
2007 Zhang Y, Li J, Kong L, Gao G, Liu QR, Wei L. NATsDB: Natural Antisense Transcripts DataBase. Nucleic Acids Research. 35: D156-61. PMID 17082204 DOI: 10.1093/nar/gkl782  1
2006 Lu XC, Gong HQ, Huang ML, Bai SL, He YB, Mao X, Geng Z, Li SG, Wei L, Yuwen JS, Xu ZH, Bai SN. Molecular analysis of early rice stamen development using organ-specific gene expression profiling. Plant Molecular Biology. 61: 845-61. PMID 16927200 DOI: 10.1007/s11103-006-0054-3  1
2006 Cai Z, Mao X, Li S, Wei L. Genome comparison using Gene Ontology (GO) with statistical testing. Bmc Bioinformatics. 7: 374. PMID 16901353 DOI: 10.1186/1471-2105-7-374  1
2006 Zhang Y, Liu XS, Liu QR, Wei L. Genome-wide in silico identification and analysis of cis natural antisense transcripts (cis-NATs) in ten species. Nucleic Acids Research. 34: 3465-75. PMID 16849434 DOI: 10.1093/nar/gkl473  1
2006 Wu J, Mao X, Cai T, Luo J, Wei L. KOBAS server: a web-based platform for automated annotation and pathway identification. Nucleic Acids Research. 34: W720-4. PMID 16845106 DOI: 10.1093/nar/gkl167  1
2006 Ji X, Li W, Song J, Wei L, Liu XS. CEAS: cis-regulatory element annotation system. Nucleic Acids Research. 34: W551-4. PMID 16845068 DOI: 10.1093/nar/gkl322  1
2006 Gao G, Zhong Y, Guo A, Zhu Q, Tang W, Zheng W, Gu X, Wei L, Luo J. DRTF: a database of rice transcription factors. Bioinformatics (Oxford, England). 22: 1286-7. PMID 16551659 DOI: 10.1093/bioinformatics/btl107  1
2006 Li J, Li X, Guo L, Lu F, Feng X, He K, Wei L, Chen Z, Qu LJ, Gu H. A subgroup of MYB transcription factor genes undergoes highly conserved alternative splicing in Arabidopsis and rice. Journal of Experimental Botany. 57: 1263-73. PMID 16531467 DOI: 10.1093/jxb/erj094  1
2006 Zhou M, Xu H, Wei X, Ye Z, Wei L, Gong W, Wang Y, Zhu Z. Identification of a glyphosate-resistant mutant of rice 5-enolpyruvylshikimate 3-phosphate synthase using a directed evolution strategy. Plant Physiology. 140: 184-95. PMID 16361526 DOI: 10.1104/pp.105.068577  1
2005 Wu X, Walker MG, Luo J, Wei L. GBA server: EST-based digital gene expression profiling. Nucleic Acids Research. 33: W673-6. PMID 15980560 DOI: 10.1093/nar/gki480  1
2005 Mao X, Cai T, Olyarchuk JG, Wei L. Automated genome annotation and pathway identification using the KEGG Orthology (KO) as a controlled vocabulary. Bioinformatics (Oxford, England). 21: 3787-93. PMID 15817693 DOI: 10.1093/bioinformatics/bti430  1
2005 Guo A, He K, Liu D, Bai S, Gu X, Wei L, Luo J. DATF: a database of Arabidopsis transcription factors. Bioinformatics (Oxford, England). 21: 2568-9. PMID 15731212 DOI: 10.1093/bioinformatics/bti334  1
2004 Liu Y, Wei L, Batzoglou S, Brutlag DL, Liu JS, Liu XS. A suite of web-based programs to search for transcriptional regulatory motifs. Nucleic Acids Research. 32: W204-7. PMID 15215381 DOI: 10.1093/nar/gkh461  1
2004 Liu Y, Liu XS, Wei L, Altman RB, Batzoglou S. Eukaryotic regulatory element conservation analysis and identification using comparative genomics. Genome Research. 14: 451-8. PMID 14993210 DOI: 10.1101/gr.1327604  1
2003 Zhou Y, Tang J, Walker MG, Zhang X, Wang J, Hu S, Xu H, Deng Y, Dong J, Ye L, Lin L, Li J, Wang X, Xu H, Pan Y, ... ... Wei L, et al. Gene identification and expression analysis of 86,136 Expressed Sequence Tags (EST) from the rice genome. Genomics, Proteomics & Bioinformatics. 1: 26-42. PMID 15626331  1
2003 Wei L, Altman RB. Recognizing complex, asymmetric functional sites in protein structures using a Bayesian scoring function. Journal of Bioinformatics and Computational Biology. 1: 119-38. PMID 15290784  1
2003 Zhou Y, Zhou C, Ye L, Dong J, Xu H, Cai L, Zhang L, Wei L. Database and analyses of known alternatively spliced genes in plants. Genomics. 82: 584-95. PMID 14611800 DOI: 10.1016/S0888-7543(03)00204-0  1
2003 Long W, Barrett EJ, Wei L, Liu Z. Adrenalectomy enhances the insulin sensitivity of muscle protein synthesis. American Journal of Physiology. Endocrinology and Metabolism. 284: E102-9. PMID 12388148 DOI: 10.1152/ajpendo.00028.2002  0.52
2002 Wei L, Liu Y, Dubchak I, Shon J, Park J. Comparative genomics approaches to study organism similarities and differences. Journal of Biomedical Informatics. 35: 142-50. PMID 12474427  1
2002 Liu Z, Jahn LA, Wei L, Long W, Barrett EJ. Amino acids stimulate translation initiation and protein synthesis through an Akt-independent pathway in human skeletal muscle. The Journal of Clinical Endocrinology and Metabolism. 87: 5553-8. PMID 12466352 DOI: 10.1210/jc.2002-020424  0.52
2002 Zhou Y, Huang GM, Wei L. UniBLAST: a system to filter, cluster, and display BLAST results and assign unique gene annotation. Bioinformatics (Oxford, England). 18: 1268-9. PMID 12217921  1
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