Publications

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Author Title Type [ Year(Desc)]
Filters: Author is Quantitative Trait Working Group of the GenLang Consortium  [Clear All Filters]
2022
C. Doust, Fontanillas, P., Eising, E., Gordon, S. D., Wang, Z., Alagöz, G., Molz, B., Team, 23andM. Research, Consortium, Q. Trait Work, St Pourcain, B., Francks, C., Marioni, R. E., Zhao, J., Paracchini, S., Talcott, J. B., Monaco, A. P., Stein, J. F., Gruen, J. R., Olson, R. K., Willcutt, E. G., DeFries, J. C., Pennington, B. F., Smith, S. D., Wright, M. J., Martin, N. G., Auton, A., Bates, T. C., Fisher, S. E., and Luciano, M., “Discovery of 42 genome-wide significant loci associated with dyslexia”, Nature Genetics, vol. 54, pp. 1621–1629, 2022.
K. M. Price, Wigg, K. G., Eising, E., Feng, Y., Blokland, K., Wilkinson, M., Kerr, E. N., Guger, S. L., Consortium, Q. Trait Work, Fisher, S. E., Lovett, M. W., Strug, L. J., and Barr, C. L., “Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities”, Translational Psychiatry, vol. 12, p. 495, 2022.