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Qian Peng, Ph.D.

Assistant Professor of Mcn
Department of Neuroscience
California Campus
Scripps VIVO Scientific Profile
qpeng@scripps.edu
(858) 784-7215

Professional Experience

2016-2017 Assistant Professor of MCN, Molecular and Cellular Neuroscience (MCN), The Scripps Research Institute
2015-2016 Research Associate, Molecular and Cellular Neuroscience (MCN), The Scripps Research Institute
-2015 Research Associate, Salk Institute for Biological Studies

Selected References

All Publications

Peng, Q., Schork, N. J., Wilhelmsen, K. C. & Ehlers, C. L. Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population. (2017). American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 174(4), 435-450. PMCID: PMC5435561.

Peng, Q., Schork, A., Bartsch, H., Lo, M. T., Panizzon, M. S., Pediatric Imaging, Neurocognition and Genetics Study, Alzheimer’s Disease Neuroimaging Initiative, Westlye, L. T., Kremen, W. S., Jernigan, T. L., Le Hellard, S., Steen, V. M., et al. Conservation of distinct enetically-mediated human cortical pattern. (2016). PLoS Genetics, 12. PMCID: PMC4961377.

Ehlers, C. L., Gizer, I. R., Bizon, C., Slutske, W., Peng, Q., Schork, N. J. & Wilhelmsen, K. C. Single nucleotide polymorphisms in the REG-CTNNA2 region of chromosome 2 and NEIL3 associated with impulsivity in a Native American sample. (2016). Genes Brain and Behavior, 15(6), 568-577. PMCID: PMC4935619.

Chen, C. H., Schork, A. J., Lo, M. T., Fan, C. C., Wang, Y., Desikan, R. S., Bettella, F., Hagler, D. J., Pediatric Imaging, Neurocognition, Alzheimer's Disease Neuroimaging Initiative, Westlye, L. T., Kremen, W. S. Large-scale genomics unveil polygenic architecture of human cortical surface area. (2015). Nature Communications, 6, 7549. PMCID: PMC4518289.

Gizer, I. R., Libiger, O., Bizon, C., Wilhelmsen, K. C., Schork, N. J. & Ehlers, C. L. Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample. (2014). American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 165(8), 673-683. PMCID: PMC4364382.

Peng, Q. & Ecker, J. R. Detection of allele-specific methylation through a generalized heterogeneous epigenome model. (2012). Bioinformatics, 28(12), I163-I171. PMCID: PMC3371863.

Chekanova, J. A., Gregory, B. D., Reverdatto, S. V., Chen, H., Kumar, R., Hooker, T., Yazaki, J., Li, P., Skiba, N., Peng, Q., Alonso, J., Brukhin, V., et al. Genome-wide high-resolution mapping of exosome substrates reveals hidden features in the Arabidopsis transcriptome. (2007). Cell, 131(7), 1340-1353.