Quentin Thomas

Quentin Thomas

Postdoc

ORCID: 0000-0002-3522-5125

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  1. 2022

  2. ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model

    Vitobello, A., Mazel, B., Lelianova, V. G., Zangrandi, A., Petitto, E., Suckling, J., Salpietro, V., Meyer, R., Elbracht, M., Kurth, I., Eggermann, T., Benlaouer, O., Lall, G., Tonevitsky, A. G., Scott, D. A., Chan, K. M., Rosenfeld, J. A., Nambot, S., Safraou, H., Bruel, A. L. & 20 others, Denommé-Pichon, A. S., Tran Mau-Them, F., Philippe, C., Duffourd, Y., Guo, H., Petersen, A. K., Granger, L., Crunk, A., Bayat, Allan, Striano, P., Zara, F., Scala, M., Thomas, Quentin, Delahaye, A., de Sainte Agathe, J. M., Buratti, J., Kozlov, S. V., Faivre, L., Thauvin-Robinet, C. & Ushkaryov, Y., 2022, In: American Journal of Human Genetics. 109, 8, p. 1436-1457 22 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis

    Zhong, Z., Wang, Y., Wang, M., Yang, F., Thomas, Quentin, Xue, Y., Zhang, Y., Liu, W., Jami-Alahmadi, Y., Xu, L., Feng, S., Marquardt, Sebastian, Wohlschlegel, J. A., Ausin, I. & Jacobsen, S. E., 2022, In: Nature Communications. 13, 15 p., 6970.

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 183888639