Xing, Jinchuan

Evolutionary and biomedical insights from the rhesus macaque genome.

Gibbs, R. A., Rogers, J., Katze, M. G., Bumgarner, R., Weinstock, G. M., Mardis, E. R., Remington, K. A., Strausberg, R. L., Venter, J. C., Wilson, R. K., et al. (2007) · Science

Genomics and Phylogenetic StudiesChromosomal and Genetic Variations

Cited by 1,403

Genetic Evidence for High-Altitude Adaptation in Tibet

Simonson, T. S., Yang, Y., Huff, C. D., Yun, H., Qin, G., Witherspoon, D. J., Bai, Z., Lorenzo, F. R., Xing, J., Jorde, L. B., et al. (2010) · Science

High Altitude and HypoxiaForensic and Genetic Research

Cited by 1,227

A comprehensive map of mobile element insertion polymorphisms in humans

Stewart, C., Kural, D., Strömberg, M. P., Walker, J. A., Konkel, M. K., Stütz, A. M., Urban, A. E., Grubert, F., Lam, H. Y. K., Lee, W.-P., et al. (2011) · PLoS Genetics

Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities

Cited by 307

Worldwide patterns of genomic variation and admixture in gray wolves

Fan, Z., Silva, P., Gronau, I., Wang, S., Armero, A. S., Schweizer, R. M., Ramirez, O., Pollinger, J., Galaverni, M., Ortega Del-Vecchyo, D., et al. (2016) · Genome Research

Genetic diversity and population structureHuman-Animal Interaction Studies

Cited by 209

SIRT7 mediates L1 elements transcriptional repression and their association with the nuclear lamina

Vazquez, B. N., Thackray, J. K., Simonet, N. G., Chahar, S., Kane-Goldsmith, N., Newkirk, S. J., Lee, S., Xing, J., Verzi, M. P., An, W., et al. (2019) · Nucleic Acids Research

Nuclear Structure and FunctionSirtuins and Resveratrol in Medicine

Cited by 79

Targeted re-sequencing approach of candidate genes implicates rare potentially functional variants in Tourette Syndrome etiology

Alexander, J., Potamianou, H., Xing, J., Deng, L., Karagiannidis, I., Tsetsos, F., Drineas, P., Tarnok, Z., Rizzo, R., Wolanczyk, T., et al. (2016) · Frontiers in Neuroscience

Obsessive-Compulsive Spectrum DisordersGenomics and Rare Diseases

Cited by 27

De Novo Coding Variants Are Strongly Associated with Tourette Syndrome

Willsey, J., Fernandez, T., Yu, D., King, R., Dietrich, A., Xing, J., Sanders, S., Mandell, J., Neale, B., Coppola, G., et al. (2019) · European Neuropsychopharmacology

Obsessive-Compulsive Spectrum DisordersGenomics and Rare Diseases

Cited by 2