Amaia Carrión-Castillo

Carrión-Castillo, A., & Boeckx, C. (2024). Insights into the genetic architecture of cerebellar lobules derived from the UK Biobank. Scientific Reports, 14(1). Doi:10.1038/s41598-024-59699-9

Knol, M.J., Poot, R.A., Evans, T.E., Satizabal, C.L., Mishra, A., Sargurupremraj, M., van der Auwera, S., Duperron, M.G., Jian, X., Hostettler, I.C., van Dam-Nolen, D.H.K., Lamballais, S., Pawlak, M.A., Lewis, C.E., Carrion-Castillo, A., van Erp, T.G.M., Reinbold, C.S., Shin, J., Scholz, M., Håberg, A.K., Kämpe, A., Li, G.H.Y., Avinun, R., Atkins, J.R., Hsu, F.C., Amod, A.R., Lam, M., Tsuchida, A., Teunissen, M.W.A., Aygün, N., Patel, Y., Liang, D., Beiser, A.S., Beyer, F., Bis, J.C., Bos, D., Bryan, R.N., Bülow, R., Caspers, S., Catheline, G., Cecil, C.A.M., Dalvie, S., Dartigues, J.F., DeCarli, C., Enlund-Cerullo, M., Ford, J.M., Franke, B., Freedman, B.I., Friedrich, N., Green, M.J., Haworth, S., Helmer, C., Hoffmann, P., Homuth, G., Ikram, M.K., Jack, C.R., Jahanshad, N., Jockwitz, C., Kamatani, Y., Knodt, A.R., Li, S., Lim, K., Longstreth, W.T., Macciardi, F., Amouyel, P., Arfanakis, K., Aribisala, B.S., Bastin, M.E., Chauhan, G., Chen, C., Cheng, C.Y., de Jager, P.L., Deary, I.J., Fleischman, D.A., Gottesman, R.F., Gudnason, V., Hilal, S., Hofer, E., Janowitz, D., Jukema, J.W., Liewald, D.C.M., Lopez, L.M., Lopez, O., Luciano, M., Martinez, O., Niessen, W.J., Nyquist, P., Rotter, J.I., Rundek, T., Sacco, R.L., Schmidt, H., Tiemeier, H., Trompet, S., van der Grond, J., Völzke, H., Wardlaw, J.M., Yanek, L., Yang, J., Agartz, I., & Alhusaini, S. (2024). Genetic variants for head size share genes and pathways with cancer. Cell Reports Medicine, 5(5). Doi:10.1016/j.xcrm.2024.101529

Amelink, J.S., Postema, M.C., Kong, X.Z., Schijven, D., Carrión-Castillo, A., Soheili-Nezhad, S., Sha, Z., Molz, B., Joliot, M., Fisher, S.E., & Francks, C. (2024). Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness. Communications Biology, 7(1). Doi:10.1038/s42003-024-06890-3

Carrión-Castillo, A., Paz-Alonso, P.M., & Carreiras, M. (2023). Brain structure, phenotypic and genetic correlates of reading performance. Nature Human Behaviour, 7(7), 1120-1134. Doi:10.1038/s41562-023-01583-z

Mekki, Y., Guillemot, V., Lemaître, H., Carrión-Castillo, A., Forkel, S., Frouin, V., & Philippe, C. (2022). The genetic architecture of language functional connectivity. NeuroImage, 249. Doi:10.1016/j.neuroimage.2021.118795

Sha, Z., Pepe, A., Schijven, D., Carrion-Castillo, A., Roe, J.M., Westerhausen, R., Joliot, M., Fisher, S.E., Crivello, F., & Francks, C. (2021). Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals. Proceedings of the National Academy of Sciences of the United States of America, 118(47). Doi:10.1073/pnas.2113095118

Kong, X.Z., Postema, M., Schijven, D., Castillo, A.C., Pepe, A., Crivello, F., Joliot, M., Mazoyer, B., Fisher, S.E., & Francks, C. (2021). Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew. Cerebral Cortex, 31(9), 4151-4168. Doi:10.1093/cercor/bhab075

Sha, Z., Schijven, D., Carrion-Castillo, A., Joliot, M., Mazoyer, B., Fisher, S.E., Crivello, F., & Francks, C. (2021). The genetic architecture of structural left–right asymmetry of the human brain. Nature Human Behaviour, 5(9), 1226-1239. Doi:10.1038/s41562-021-01069-w

Carrion-Castillo, A., Estruch, S.B., Maassen, B., Franke, B., Francks, C., & Fisher, S.E. (2021). Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family. Human Genetics, 140(8), 1183-1200. Doi:10.1007/s00439-021-02289-w

Postema, M.C., Carrion-Castillo, A., Fisher, S.E., Vingerhoets, G., & Francks, C. (2020). The genetics of situs inversus without primary ciliary dyskinesia. Scientific Reports, 10(1). Doi:10.1038/s41598-020-60589-z

Carrion-Castillo, A., Pepe, A., Kong, X.Z., Fisher, S.E., Mazoyer, B., Tzourio-Mazoyer, N., Crivello, F., & Francks, C. (2020). Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment. Cortex, 124, 137-153. Doi:10.1016/j.cortex.2019.11.006

Shin, J., Ma, S., Hofer, E., Patel, Y., Vosberg, D.E., Tilley, S., Roshchupkin, G.V., Sousa, A.M.M., Jian, X., Gottesman, R., Mosley, T.H., Fornage, M., Saba, Y., Pirpamer, L., Schmidt, R., Schmidt, H., Carrion-Castillo, A., Crivello, F., Mazoyer, B., Bis, J.C., Li, S., Yang, Q., Luciano, M., Karama, S., Lewis, L., Bastin, M.E., Harris, M.A., Wardlaw, J.M., Deary, I.E., Scholz, M., Loeffler, M., Witte, A.V., Beyer, F., Villringer, A., Armstrong, N.J., Mather, K.A., Ames, D., Jiang, J., Kwok, J.B., Schofield, P.R., Thalamuthu, A., Trollor, J.N., Wright, M.J., Brodaty, H., Wen, W., Sachdev, P.S., Terzikhan, N., Evans, T.E., Adams, H.H.H.H., Ikram, M.A., Frenzel, S., van der Auwera-Palitschka, S., Wittfeld, K., Bülow, R., Grabe, H.J., Tzourio, C., Mishra, A., Maingault, S., Debette, S., Gillespie, N.A., Franz, C.E., Kremen, W.S., Ding, L., Jahanshad, N., Sestan, N., Pausova, Z., Seshadri, S., & Paus, T. (2020). Global and regional development of the human cerebral cortex: Molecular architecture and occupational aptitudes. Cerebral Cortex, 30(7), 4121-4139. Doi:10.1093/CERCOR/BHAA035

Amaia Carrión Castillo (2019). Zer genek laguntzen digute irakurtzen?. Elhuyar aldizkaria, zientzia eta teknologia, 33, 64–68.

de Kovel, C.G.F., Carrión-Castillo, A., & Francks, C. (2019). A large-scale population study of early life factors influencing left-handedness. Scientific Reports, 9(1). Doi:10.1038/s41598-018-37423-8

Eising, E., Carrion-Castillo, A., Vino, A., Strand, E.A., Jakielski, K.J., Scerri, T.S., Hildebrand, M.S., Webster, R., Ma, A., Mazoyer, B., Francks, C., Bahlo, M., Scheffer, I.E., Morgan, A.T., Shriberg, L.D., & Fisher, S.E. (2019). A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. Molecular Psychiatry, 24(7), 1065-1078. Doi:10.1038/s41380-018-0020-x

Carrion-Castillo, A., Van der Haegen, L., Tzourio-Mazoyer, N., Kavaklioglu, T., Badillo, S., Chavent, M., Saracco, J., Brysbaert, M., Fisher, S.E., Mazoyer, B., & Francks, C. (2019). Genome sequencing for rightward hemispheric language dominance. Genes, Brain and Behavior, 18(5). Doi:10.1111/gbb.12572

Carrion-Castillo, A., Maassen, B., Franke, B., Heister, A., Naber, M., Van Der Leij, A., Francks, C., & Fisher, S.E. (2017). Association analysis of dyslexia candidate genes in a Dutch longitudinal sample. European Journal of Human Genetics, 25(4), 452-460. Doi:10.1038/ejhg.2016.194

Carrion-Castillo, A., van Bergen, E., Vino, A., van Zuijen, T., de Jong, P.F., Francks, C., & Fisher, S.E. (2016). Evaluation of results from genome-wide studies of language and reading in a novel independent dataset. Genes, Brain and Behavior, 15(6), 531-541. Doi:10.1111/gbb.12299

Agus, T.R., Carrión-Castillo, A., Pressnitzer, D., & Ramus, F. (2014). Perceptual learning of acoustic noise by individuals with dyslexia. Journal of Speech, Language, and Hearing Research, 57(3), 1069-1077. Doi:10.1044/1092-4388(2013/13-0020)

Carrion-Castillo, A., Franke, B., & Fisher, S.E. (2013). Molecular genetics of dyslexia: An overview. Dyslexia, 19(4), 214-240. Doi:10.1002/dys.1464