| Year |
Citation |
Score |
| 2024 |
Bukhari H, Nithianadam V, Battaglia RA, Cicalo A, Sarkar S, Comjean A, Hu Y, Leventhal MJ, Dong X, Feany MB. Transcriptional programs mediating neuronal toxicity and altered glial-neuronal signaling in a knock-in tauopathy model. Genome Research. PMID 38599684 DOI: 10.1101/gr.278576.123 |
0.325 |
|
| 2024 |
Leventhal MJ, Zanella CA, Kang B, Peng J, Gritsch D, Liao Z, Bukhari H, Wang T, Pao PC, Danquah S, Benetatos J, Nehme R, Farhi S, Tsai LH, Dong X, et al. A systems-biology approach connects aging mechanisms with Alzheimer's disease pathogenesis. Biorxiv : the Preprint Server For Biology. PMID 38559190 DOI: 10.1101/2024.03.17.585262 |
0.566 |
|
| 2024 |
Bukhari H, Nithianandam V, Battaglia RA, Cicalo A, Sarkar S, Comjean A, Hu Y, Leventhal MJ, Dong X, Feany MB. Transcriptional programs mediating neuronal toxicity and altered glial-neuronal signaling in a knock-in tauopathy model. Biorxiv : the Preprint Server For Biology. PMID 38352559 DOI: 10.1101/2024.02.02.578624 |
0.312 |
|
| 2023 |
Dong X, Bai Y, Liao Z, Gritsch D, Liu X, Wang T, Borges-Monroy R, Ehrlich A, Serrano GE, Feany MB, Beach TG, Scherzer CR. Circular RNAs in the human brain are tailored to neuron identity and neuropsychiatric disease. Nature Communications. 14: 5327. PMID 37723137 DOI: 10.1038/s41467-023-40348-0 |
0.605 |
|
| 2023 |
Dong X, Bai Y, Liao Z, Gritsch D, Liu X, Wang T, Borges-Monroy R, Ehrlich A, Serano GE, Feany MB, Beach TG, Scherzer CR. Circular RNAs in the human brain are tailored to neuron identity and neuropsychiatric disease. Biorxiv : the Preprint Server For Biology. PMID 37066229 DOI: 10.1101/2023.04.01.535194 |
0.604 |
|
| 2021 |
Domínguez-Baleón C, Ong JS, Scherzer CR, Rentería ME, Dong X. Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study. Scientific Reports. 11: 13980. PMID 34234189 DOI: 10.1038/s41598-021-93105-y |
0.518 |
|
| 2021 |
Dong X, Li X, Chang TW, Scherzer CR, Weiss ST, Qiu W. powerEQTL: An R package and shiny application for sample size and power calculation of bulk tissue and single-cell eQTL analysis. Bioinformatics (Oxford, England). PMID 34009297 DOI: 10.1093/bioinformatics/btab385 |
0.549 |
|
| 2021 |
Iwaki H, Leonard HL, Makarious MB, Bookman M, Landin B, Vismer D, Casey B, Gibbs JR, Hernandez DG, Blauwendraat C, Vitale D, Song Y, Kumar D, Dalgard CL, Sadeghi M, ... Dong X, et al. Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33960523 DOI: 10.1002/mds.28549 |
0.571 |
|
| 2021 |
Liu G, Peng J, Liao Z, Locascio JJ, Corvol JC, Zhu F, Dong X, Maple-Grødem J, Campbell MC, Elbaz A, Lesage S, Brice A, Mangone G, Growdon JH, Hung AY, et al. Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease. Nature Genetics. PMID 33958783 DOI: 10.1038/s41588-021-00847-6 |
0.556 |
|
| 2020 |
Tsuji J, Thomson T, Chan E, Brown CK, Oppenheimer J, Bigelow C, Dong X, Theurkauf WE, Weng Z, Schwartz LM. HIGH RESOLUTION ANALYSIS OF DIFFERENTIAL GENE EXPRESSION DURING SKELETAL MUSCLE ATROPHY AND PROGRAMMED CELL DEATH. Physiological Genomics. PMID 32926651 DOI: 10.1152/Physiolgenomics.00047.2020 |
0.525 |
|
| 2018 |
Dong X, Liao Z, Gritsch D, Hadzhiev Y, Bai Y, Locascio JJ, Guennewig B, Liu G, Blauwendraat C, Wang T, Adler CH, Hedreen JC, Faull RLM, Frosch MP, Nelson PT, et al. Publisher Correction: Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease. Nature Neuroscience. PMID 30482917 DOI: 10.1038/S41593-018-0277-Z |
0.566 |
|
| 2018 |
Dong X, Liao Z, Gritsch D, Hadzhiev Y, Bai Y, Locascio JJ, Guennewig B, Liu G, Blauwendraat C, Wang T, Adler CH, Hedreen JC, Faull RLM, Frosch MP, Nelson PT, et al. Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease. Nature Neuroscience. PMID 30224808 DOI: 10.1038/S41593-018-0223-0 |
0.63 |
|
| 2017 |
Mittal S, Bjørnevik K, Im DS, Flierl A, Dong X, Locascio JJ, Abo KM, Long E, Jin M, Xu B, Xiang YK, Rochet JC, Engeland A, Rizzu P, Heutink P, et al. β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's disease. Science (New York, N.Y.). 357: 891-898. PMID 28860381 DOI: 10.1126/Science.Aaf3934 |
0.613 |
|
| 2015 |
Dong X, Tsuji J, Labadorf A, Roussos P, Chen JF, Myers RH, Akbarian S, Weng Z. The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease. Plos One. 10: e0144398. PMID 26636336 DOI: 10.1371/Journal.Pone.0144398 |
0.639 |
|
| 2015 |
Locascio JJ, Eberly S, Liao Z, Liu G, Hoesing AN, Duong K, Trisini-Lipsanopoulos A, Dhima K, Hung AY, Flaherty AW, Schwarzschild MA, Hayes MT, Wills AM, Shivraj Sohur U, Mejia NI, ... ... Dong X, et al. Association between α-synuclein blood transcripts and early, neuroimaging-supported Parkinson's disease. Brain : a Journal of Neurology. 138: 2659-71. PMID 26220939 DOI: 10.1093/Brain/Awv202 |
0.633 |
|
| 2015 |
Bai G, Cheung I, Shulha HP, Coelho JE, Li P, Dong X, Jakovcevski M, Wang Y, Grigorenko A, Jiang Y, Hoss A, Patel K, Zheng M, Rogaev E, Myers RH, et al. Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains. Human Molecular Genetics. 24: 1441-56. PMID 25480889 DOI: 10.1093/Hmg/Ddu561 |
0.744 |
|
| 2014 |
Hoss AG, Kartha VK, Dong X, Latourelle JC, Dumitriu A, Hadzi TC, Macdonald ME, Gusella JF, Akbarian S, Chen JF, Weng Z, Myers RH. MicroRNAs located in the Hox gene clusters are implicated in huntington's disease pathogenesis. Plos Genetics. 10: e1004188. PMID 24586208 DOI: 10.1371/Journal.Pgen.1004188 |
0.5 |
|
| 2014 |
Haberle V, Li N, Hadzhiev Y, Plessy C, Previti C, Nepal C, Gehrig J, Dong X, Akalin A, Suzuki AM, van IJcken WF, Armant O, Ferg M, Strähle U, Carninci P, et al. Two independent transcription initiation codes overlap on vertebrate core promoters. Nature. 507: 381-5. PMID 24531765 DOI: 10.1038/Nature12974 |
0.643 |
|
| 2013 |
Dong X, Weng Z. The correlation between histone modifications and gene expression. Epigenomics. 5: 113-6. PMID 23566087 DOI: 10.2217/Epi.13.13 |
0.574 |
|
| 2013 |
Li XZ, Roy CK, Dong X, Bolcun-Filas E, Wang J, Han BW, Xu J, Moore MJ, Schimenti JC, Weng Z, Zamore PD. An ancient transcription factor initiates the burst of piRNA production during early meiosis in mouse testes. Molecular Cell. 50: 67-81. PMID 23523368 DOI: 10.1016/J.Molcel.2013.02.016 |
0.541 |
|
| 2013 |
Wang J, Zhuang J, Iyer S, Lin XY, Greven MC, Kim BH, Moore J, Pierce BG, Dong X, Virgil D, Birney E, Hung JH, Weng Z. Factorbook.org: a Wiki-based database for transcription factor-binding data generated by the ENCODE consortium. Nucleic Acids Research. 41: D171-6. PMID 23203885 DOI: 10.1093/Nar/Gks1221 |
0.698 |
|
| 2012 |
Wang J, Zhuang J, Iyer S, Lin X, Whitfield TW, Greven MC, Pierce BG, Dong X, Kundaje A, Cheng Y, Rando OJ, Birney E, Myers RM, Noble WS, Snyder M, et al. Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors. Genome Research. 22: 1798-812. PMID 22955990 DOI: 10.1101/Gr.139105.112 |
0.694 |
|
| 2012 |
Cheng C, Alexander R, Min R, Leng J, Yip KY, Rozowsky J, Yan KK, Dong X, Djebali S, Ruan Y, Davis CA, Carninci P, Lassman T, Gingeras TR, Guigó R, et al. Understanding transcriptional regulation by integrative analysis of transcription factor binding data. Genome Research. 22: 1658-67. PMID 22955978 DOI: 10.1101/Gr.136838.111 |
0.581 |
|
| 2012 |
Dong X, Greven MC, Kundaje A, Djebali S, Brown JB, Cheng C, Gingeras TR, Gerstein M, Guigó R, Birney E, Weng Z. Modeling gene expression using chromatin features in various cellular contexts. Genome Biology. 13: R53. PMID 22950368 DOI: 10.1186/Gb-2012-13-9-R53 |
0.549 |
|
| 2011 |
Fredman D, Dong X, Lenhard B. Making enhancers from spare parts of the genome. Genome Biology. 12: 138. PMID 22206586 DOI: 10.1186/Gb-2011-12-12-138 |
0.603 |
|
| 2011 |
Yildirim O, Li R, Hung JH, Chen PB, Dong X, Ee LS, Weng Z, Rando OJ, Fazzio TG. Mbd3/NURD complex regulates expression of 5-hydroxymethylcytosine marked genes in embryonic stem cells. Cell. 147: 1498-510. PMID 22196727 DOI: 10.1016/J.Cell.2011.11.054 |
0.585 |
|
| 2010 |
Dong X, Akalin A, Sharma Y, Lenhard B. Translog, a web browser for studying the expression divergence of homologous genes. Bmc Bioinformatics. 11: S59. PMID 20122234 DOI: 10.1186/1471-2105-11-S1-S59 |
0.631 |
|
| 2009 |
Dong X, Navratilova P, Fredman D, Drivenes Ø, Becker TS, Lenhard B. Exonic remnants of whole-genome duplication reveal cis-regulatory function of coding exons Nucleic Acids Research. 38: 1071-1085. PMID 19969543 DOI: 10.1093/Nar/Gkp1124 |
0.6 |
|
| 2009 |
Dong X, Fredman D, Lenhard B. Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomes. Genome Biology. 10: R86. PMID 19698106 DOI: 10.1186/Gb-2009-10-8-R86 |
0.601 |
|
| 2009 |
Akalin A, Fredman D, Arner E, Dong X, Bryne JC, Suzuki H, Daub CO, Hayashizaki Y, Lenhard B. Transcriptional features of genomic regulatory blocks. Genome Biology. 10: R38. PMID 19374772 DOI: 10.1186/Gb-2009-10-4-R38 |
0.652 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2008 |
Mungpakdee S, Seo HC, Angotzi AR, Dong X, Akalin A, Chourrout D. Differential evolution of the 13 Atlantic salmon Hox clusters. Molecular Biology and Evolution. 25: 1333-43. PMID 18424774 DOI: 10.1093/Molbev/Msn097 |
0.289 |
|
| 2021 |
Zhu Q, Cheng L, Deng C, Huang L, Li J, Wang Y, Li M, Yang Q, Dong X, Su J, Lee LP, Liu F. The genetic source tracking of human urinary exosomes. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34663731 DOI: 10.1073/pnas.2108876118 |
0.24 |
|
| 2022 |
Dai Y, Hu R, Liu A, Cho KS, Manuel AM, Li X, Dong X, Jia P, Zhao Z. WebCSEA: web-based cell-type-specific enrichment analysis of genes. Nucleic Acids Research. PMID 35610053 DOI: 10.1093/nar/gkac392 |
0.23 |
|
| 2023 |
Li F, Ming W, Lu W, Wang Y, Li X, Dong X, Bai Y. FLED: a full-length eccDNA detector for long-reads sequencing data. Briefings in Bioinformatics. 24. PMID 37930031 DOI: 10.1093/bib/bbad388 |
0.22 |
|
| 2023 |
Han X, Gharahkhani P, Hamel AR, Ong JS, Rentería ME, Mehta P, Dong X, Pasutto F, Hammond C, Young TL, Hysi P, Lotery AJ, Jorgenson E, Choquet H, Hauser M, et al. Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. Nature Genetics. PMID 37386247 DOI: 10.1038/s41588-023-01428-5 |
0.218 |
|
| 2021 |
Li C, Ou R, Chen Y, Gu X, Wei Q, Cao B, Zhang L, Hou Y, Liu K, Chen X, Song W, Zhao B, Wu Y, Li T, Dong X, et al. Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33884653 DOI: 10.1002/mds.28621 |
0.217 |
|
| 2023 |
Nithianandam V, Bukhari H, Leventhal MJ, Battaglia RA, Dong X, Fraenkel E, Feany MB. Integrative analysis reveals a conserved role for the amyloid precursor protein in proteostasis during aging. Nature Communications. 14: 7034. PMID 37923712 DOI: 10.1038/s41467-023-42822-1 |
0.212 |
|
| 2022 |
Hallacli E, Kayatekin C, Nazeen S, Wang XH, Sheinkopf Z, Sathyakumar S, Sarkar S, Jiang X, Dong X, Di Maio R, Wang W, Keeney MT, Felsky D, Sandoe J, Vahdatshoar A, et al. The Parkinson's disease protein alpha-synuclein is a modulator of processing bodies and mRNA stability. Cell. 185: 2035-2056.e33. PMID 35688132 DOI: 10.1016/j.cell.2022.05.008 |
0.203 |
|
| 2022 |
Mitchell BL, Saklatvala JR, Dand N, Hagenbeek FA, Li X, Min JL, Thomas L, Bartels M, Jan Hottenga J, Lupton MK, Boomsma DI, Dong X, Hveem K, Løset M, Martin NG, et al. Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. Nature Communications. 13: 702. PMID 35132056 DOI: 10.1038/s41467-022-28252-5 |
0.194 |
|
| 2009 |
Dong X. The brainstorm [Essay] Ieee Potentials. 28: 8-9. DOI: 10.1109/Mpot.2008.931159 |
0.179 |
|
| 2021 |
Wang T, Liu Y, Ruan J, Dong X, Wang Y, Peng J. A pipeline for RNA-seq based eQTL analysis with automated quality control procedures. Bmc Bioinformatics. 22: 403. PMID 34433407 DOI: 10.1186/s12859-021-04307-0 |
0.178 |
|
| 2021 |
Dong X, Liu C, Dozmorov M. Review of multi-omics data resources and integrative analysis for human brain disorders. Briefings in Functional Genomics. PMID 33969380 DOI: 10.1093/bfgp/elab024 |
0.162 |
|
| 2022 |
Campos AI, Ingold N, Huang Y, Mitchell BL, Kho PF, Han X, García-Marín LM, Ong JS, Law MH, Yokoyama JS, Martin NG, Dong X, Cuellar-Partida G, MacGregor S, Aslibekyan S, et al. Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep. PMID 36525587 DOI: 10.1093/sleep/zsac308 |
0.088 |
|
| 2021 |
Chen Y, Zhu Q, Cheng L, Wang Y, Li M, Yang Q, Hu L, Lou D, Li J, Dong X, Lee LP, Liu F. Exosome detection via the ultrafast-isolation system: EXODUS. Nature Methods. PMID 33432243 DOI: 10.1038/s41592-020-01034-x |
0.065 |
|
| 2012 |
Wang Q, Dong X, Pang Z, Du Y, Xia X, Wei Q, Huang F. Ammonia sensing behaviors of TiO2-PANI/PA6 composite nanofibers. Sensors (Basel, Switzerland). 12: 17046-57. PMID 23235446 DOI: 10.3390/s121217046 |
0.015 |
|
| Hide low-probability matches. |