ZFIN Person: Gurnett, Christina

ZFIN ID: ZDB-PERS-190826-1

Gurnett, Christina

Email:	gurnettc@wustl.edu
URL:
Affiliation:	Gurnett Lab
Address:	Christina A. Gurnett, MD PhD A. Ernest and Jane G. Stein Professor of Developmental Neurology Professor of Neurology, Pediatrics, and Orthopaedic Surgery Head, Division of Pediatric and Developmental Neurology Washington University School of Medicine Neurologist-in-Chief, St Louis Children’s Hospital 4938 Parkview Place MPRB 5th floor Lab Entry 4 Washington University in St Louis St Louis, MO 63110
Country:	United States
Phone:	314-286-2723
Fax:	314-286-2894
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Rebello, D., Wohler, E., Erfani, V., Li, G., Aguilera, A.N., Santiago-Cornier, A., Zhao, S., Hwang, S.W., Steiner, R.D., Zhang, T.J., Gurnett, C.A., Raggio, C., Wu, N., Sobreira, N., Giampietro, P.F., Ciruna, B. (2023) COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis. Human molecular genetics. 32(19):2913-2928

McAdow, J., Yang, S., Ou, T., Huang, G., Dobbs, M.B., Gurnett, C.A., Greenberg, M.J., Johnson, A.N. (2022) A pathogenic mechanism associated with myopathies and structural birth defects involves TPM2 directed myogenesis. JCI insight. 7(12)

Terhune, E.A., Cuevas, M.T., Monley, A.M., Wethey, C.I., Chen, X., Cattel, M.V., Bayrak, M.N., Bland, M.R., Sutphin, B., Devon Trahan, G., Taylor, M.R.G., Niswander, L.A., Jones, K.L., Baschal, E.E., Antunes, L., Dobbs, M., Gurnett, C., Appel, B., Gray, R., Miller, N.H. (2020) Mutations in KIF7 Implicated in Idiopathic Scoliosis in Humans and Axial Curvatures in Zebrafish. Human Mutation. 42(4):392-407

Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A.T., Gannon, S.R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Burnetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A., Garrett, M.E., Soldano, K., Macaya, A., Conrad, D., Strahle, J., Dobbs, M.B., Turner, T.N., Shannon, C.N., Brockmeyer, D., Limbrick, D.D., Gurnett, C.A., Haller, G. (2020) Rare and de novo coding variants in chromodomain genes in Chiari I malformation. American journal of human genetics. 108(1):100-114

Whittle, J., Antunes, L., Harris, M., Upshaw, Z., Sepich, D.S., Johnson, A.N., Mokalled, M., Solnica-Krezel, L., Dobbs, M.B., Gurnett, C.A. (2020) MYH3-associated distal arthrogryposis zebrafish model is normalized with para-aminoblebbistatin. EMBO Molecular Medicine. 12(11):e12356

Haller, G., McCall, K., Jenkitkasemwong, S., Sadler, B., Antunes, L., Nikolov, M., Whittle, J., Upshaw, Z., Shin, J., Baschal, E., Cruchaga, C., Harms, M., Raggio, C., Morcuende, J.A., Giampietro, P., Miller, N.H., Wise, C., Gray, R.S., Solnica-Krezel, L., Knutson, M., Dobbs, M.B., Gurnett, C.A. (2018) A missense variant in SLC39A8 is associated with severe idiopathic scoliosis. Nature communications. 9:4171

NON-ZEBRAFISH PUBLICATIONS