ZFIN ID: ZDB-LAB-190826-1
Gurnett Lab
PI/Director: Gurnett, Christina
Co-PI / Senior
Researcher:
Haller, Gabriel
Contact Person: Gurnett, Christina
Email: gurnettc@wustl.edu
URL:
Address:
Country: United States
Phone: 314-286-2723
Fax: 314-286-2894
Line Designation: stl


GENOMIC FEATURES ORIGINATING FROM THIS LAB
Show all 3 genomic features


STATEMENT OF RESEARCH INTERESTS
4938 Parkview Place
MPRB 5th floor Lab Entry 4
Washington University in St Louis
St Louis, MO 63110


LAB MEMBERS
Antunes, Lilian Graduate Student Whittle, Julia Graduate Student Sadler, Brooke Research Staff
McCall, Kevin Technical Staff Nikolov, Momchil Technical Staff


ZEBRAFISH PUBLICATIONS OF LAB MEMBERS
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