Fingerprint
Dive into the research topics where Chao Xing is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
A recurrent ACAA2 variant causes a dominant syndrome of lipodystrophy, lipomatosis, infantile steatohepatitis, and hypoglycemia
Simha, V., LoPiccolo, M. K., Platt, A., Brown, R. J., Johnson, X., Carere, D. A., Donnelly, C., Snyder, M. T., Xing, C., Mathews, T. P., Gopal, P., Ward, S. C., Tomchick, D. R., Agarwal, A. K., DeBerardinis, R. J. & Garg, A., Jan 2 2026, In: The Journal of clinical investigation. 136, 1Research output: Contribution to journal › Article › peer-review
Open Access3 Link opens in a new tab Scopus citations -
Defects in nephrogenesis result in an expansion of the Foxd1+ stromal progenitor population
Michalopoulos, M. G., Liu, Y., Raju, D. R., Lafin, J. T., Ma, Y., Gaur, D., Khadka, S., Xing, C., Mcmahon, A. P., Carroll, T. J. & Drake, K. A., Jan 2026, In: Development (Cambridge). 153, 1Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Scopus citations -
EPOP restricts PRC2.1 targeting to chromatin by directly modulating enzyme complex dimerization
Gong, L., Liu, X., Yang, X., Yu, Z., Bhat, M. Y., Chen, S., Lemoff, A., Xing, C. & Liu, X., Dec 2026, In: Nature communications. 17, 1, 1565.Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Scopus citations -
Erratum. Gain of Function NOTCH3 Variants Cause Familial Partial Lipodystrophy Due to Activation of Senescence Pathways. Diabetes 2025;74:427–438
Garg, A., Xing, C., Agarwal, A. K., Westfall, A. K., Tomchick, D. R., Zhang, X., Xing, M. & Brown, R. J., Jan 2026, In: Diabetes. 75, 1, p. 223 1 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access -
Erythrokeratodermia-Cardiomyopathy Syndrome: Expanding the DSP Mutational Spectrum Beyond Proline Substitutions
Hamzehlou, S., Mortlock, R. D., Echeandia-Francis, C., Zhou, J., Xing, C., Agim, N. G., Choate, K. A. & Glass, D. A., Mar 1 2026, In: Pediatric dermatology. 43, 2, p. 444-447 4 p.Research output: Contribution to journal › Article › peer-review
Open Access