- Plant evolutionary ecology
- Ph.D. ETH Zurich
- Bachelor, China Agricultural University, Beijing, China
- . . ‘Evolution of Alternative Splicing in Eudicots.’ Frontiers in Plant Science 10: 707-. doi: https://doi.org/10.3389/fpls.2019.00707.
- . . ‘Efficient genetic transformation and CRISPR/Cas9-mediated genome editing in Lemna aequinoctialis.’ Plant Biotechnology Journal 0, No. ja. doi: 10.1111/pbi.13128.
- . . ‘Low genetic variation is associated with low mutation rate in the giant duckweed.’ Nature Communications 10, No. 1: 1243-. doi: https://doi.org/10.1038/s41467-019-09235-5.
- . . ‘Species-specific regulation of herbivory-induced defoliation tolerance is associated with jasmonate inducibility.’ Ecology and Evolution 7, No. 11: 3703-3712. doi: 10.1002/ece3.2953.
- . . ‘Tissue-specific emission of (E)-alpha-bergamotene helps resolve the dilemma when pollinators are also herbivores.’ Current Biology 27, No. 9: 1336-1341. doi: 10.1016/j.cub.2017.03.017.
- . . ‘Evidence of an evolutionary hourglass pattern in herbivory-induced transcriptomic responses.’ New Phytologist 215, No. 3: 1264-1273. doi: 10.1111/nph.14644.
- . . ‘Introduction: integrative molecular ecology is rapidly advancing the study of adaptation and speciation.’ Molecular Ecology 26, No. 1: 1-6. doi: 10.1111/mec.13947.
- . . ‘NaMYB8 regulates distinct, optimally distributed herbivore defense traits.’ Journal of Integrative Plant Biology 59, No. 12: 844-850. doi: 10.1111/jipb.12593.
- . . ‘O-Acyl sugars protect a wild tobacco from both native fungal pathogens and a specialist herbivore.’ Plant Physiology 174, No. 1: 370-386. doi: 10.1104/pp.16.01904.
- . . ‘Wild tobacco genomes reveal the evolution of nicotine biosynthesis.’ Proceedings of the National Academy of Sciences of the United States of America 114, No. 23: 6133-6138. doi: 10.1073/pnas.1700073114.
- . . ‘Nicotiana attenuata Data Hub (NaDH): an integrative platform for exploring genomic, transcriptomic and metabolomic data in wild tobacco.’ BMC genomics 18, No. 1: 79. doi: 10.1186/s12864-016-3465-9.
- . . ‘Catechol, a major component of smoke, influences primary root growth and root hair elongation through reactive oxygen species-mediated redox signaling.’ New Phytologist 213, No. 4: 1755-1770. doi: 10.1111/nph.14317.
- . . ‘Molecular mechanisms of adaptation and speciation: why do we need an integrative approach?’ Molecular Ecology 26, No. 1: 277-290. doi: 10.1111/mec.13678.
- . . ‘Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana.’ eLife 5. doi: 10.7554/eLife.19531.
- . . ‘Auxin is rapidly induced by herbivore attack and regulates a subset of systemic, jasmonate-dependent defenses.’ Plant Physiology 172, No. 1: 521-32. doi: 10.1104/pp.16.00940.
- . . ‘Modeling the two-locus architecture of divergent pollinator adaptation: how variation in SAD paralogs affects fitness and evolutionary divergence in sexually deceptive orchids.’ Ecology and Evolution 5, No. 2: 493-502. doi: 10.1002/ece3.1378.
- . . ‘Insect herbivory elicits genome-wide alternative splicing responses in Nicotiana attenuata.’ Plant Journal 84, No. 1: 228-43. doi: 10.1111/tpj.12997.
- . . ‘Herbivore associated elicitor-induced defences are highly specific among closely related Nicotiana species.’ BMC Plant Biology 15: 2. doi: 10.1186/s12870-014-0406-0.
- . . ‘The rapidly evolving associations among herbivore associated elicitor-induced phytohormones in Nicotiana.’ Plant Signal and Behaviour 10, No. 7: e1035850. doi: 10.1080/15592324.2015.1035850.
- . . ‘Virus-induced gene silencing using tobacco rattle virus as a tool to study the interaction between Nicotiana attenuata and Rhizophagus irregularis.’ PLoS One 10, No. 8: e0136234. doi: 10.1371/journal.pone.0136234.
- . . ‘Transcriptome and proteome data reveal candidate genes for pollinator attraction in sexually deceptive orchids.’ PLoS One 8, No. 5: e64621. doi: 10.1371/journal.pone.0064621.
- . . ‘Pollinator shifts between Ophrys sphegodes populations: might adaptation to different pollinators drive population divergence?’ Journal of Evolutionary Biology 26, No. 10: 2197-208. doi: 10.1111/jeb.12216.
- . . ‘The genetic basis of pollinator adaptation in a sexually deceptive orchid.’ PLoS Genetics 8, No. 8: e1002889. doi: 10.1371/journal.pgen.1002889.
- . . ‘Stearoyl-acyl carrier protein desaturases are associated with floral isolation in sexually deceptive orchids.’ Proceedings of the National Academy of Sciences of the United States of America 108, No. 14: 5696-701. doi: 10.1073/pnas.1013313108.
- . . ‘Pollinator-driven speciation in sexually deceptive orchids.’ International Journal of Ecology 2012. doi: https://doi.org/10.1155/2012/285081.
- . . ‘Floral isolation is the main reproductive barrier among closely related sexually deceptive orchids.’ Evolution 65, No. 9: 2606-20. doi: 10.1111/j.1558-5646.2011.01323.x.
- . . ‘Gene conversion in the rice genome.’ BMC genomics 9: 93. doi: 10.1186/1471-2164-9-93.
- . . ‘High altitude adaptation and phylogenetic analysis of Tibetan horse based on the mitochondrial genome.’ Journal of Genetics and Genomics 34, No. 8: 720-9. doi: 10.1016/S1673-8527(07)60081-2.
- . . ‘Detection of HPV-2 and identification of novel mutations by whole genome sequencing from biopsies of two patients with multiple cutaneous horns.’ Journal of Clinic Virology 39, No. 1: 34-42. doi: 10.1016/j.jcv.2007.01.002.
- . . ‘Complete sequence and gene organization of the Tibetan chicken mitochondrial genome.’ Yi Chuan 28, No. 7: 769-77.
- . . ‘A mitochondrial genome sequence of the Tibetan antelope (Pantholops hodgsonii).’ Genomics Proteomics and Bioinformatics 3, No. 1: 5-17.