Publications

Herrera-Masurel, A., Altay, S. & Mercier, H. (2023). Does nuclear energy produce neodymium? Negative perception of nuclear energy drives the assumption that it is polluting. Journal of experimental psychology. Applied, 29(3), 572-583. doi:10.1037/xap0000477

Latimier, A. , Riegert, A. , Ly, S. , Peyre, H., Casati, R. & Ramus, F. (2019). Does pre-testing promote better retention than post-testing? npj Science of Learning, 4(15). doi:10.1038/s41539-019-0053-1

De Araujo, E. , Yesilaltay , S., Bor, A. & Mercier, H. (2021). Dominant Jerks: People Infer Dominance From the Utterance of Challenging and Offensive Statements. Social Psychological Bulletin, 16(4), e6999. doi:10.32872/spb.6999

Ramus, F. (2001). Dyslexia: Talk of two theories. Nature, 412(6845), 393-395. doi:10.1038/35086683

Mari, A. (2014). Each Other, Asymmetry and Reasonable Futures. Journal of Semantics, 31 (2), 209-261

Dezecache, G. & Mercier, H. (2022). Emotional Vigilance. The Oxford Handbook of Evolution and the Emotions

Peyre, H., Ramus, F., Melchior, M., Forhan, A., Heude, B. & Gauvrit, N. (2016). Emotional, behavioral and social difficulties among high-IQ children during the preschool period: Results of the EDEN mother-child cohort. Personality and Individual Differences, 94, 366-371. doi:10.1016/j.paid.2016.02.014

Järvinen-Pasley, A., Wallace, G., Ramus, F., Happé, F. & Heaton, P. (2008). Enhanced perceptual processing of speech in autism. Developmental science, 11(1), 109-21. doi:10.1111/j.1467-7687.2007.00644.x

Ramus, F., Di Folco , C. , Guez, A. & Peyre, H. (2021). Epidémiologie des troubles de la lecture en France : une comparaison du DSM-5 et de la CIM-11. Approche neuropsychologique des apprentissages chez l'enfant, 175, 639-649

Di Folco , C. , Guez, A., Peyre, H. & Ramus, F. (2021). Epidemiology of reading disability: A comparison of DSM-5 and ICD-11 criteria. Scientific Studies of Reading, NA. doi:10.1080/10888438.2021.1998067

O'Madagain, C. (2019). Epistemic Injustice at the Conceptual Level: Are We Entitled to Our Own Concepts? Studia Philosophica Estonica, 12, 64-80

Cova, F., Strickland, B., Abatista, A., Allard, A. , Andow, J., Attie, M., Beebe, J., Berniūnas, R., Boudesseul, J., Colombo, M., Cushman, F., Diaz, R., N’djaye Nikolai Van Dongen, N., Dranseika, V., Earp, B., Torres, A. , Hannikainen, I., Hernández-Conde, J., Hu, W., Jaquet, F., Khalifa, K., Kim, H., Kneer, M., Knobe, J., Kurthy, M., Lantian, A., Liao, S., Machery, E., Moerenhout, T., Mott, C., Phelan, M., Phillips, J., Rambharose, N., Reuter, K., Romero, F., Sousa, P., Sprenger, J. , Thalabard, E., Tobia, K., Viciana, H. , Wilkenfeld, D. & Zhou, X. (2021). Estimating the Reproducibility of Experimental Philosophy. Review of Philosophy and Psychology, 12(1), 9-44. doi:10.1007/s13164-018-0400-9

Strickland, B., Geraci, C., Chemla, E., Schlenker, P., Kelepir, M. & Pfau, R. (2015). Event representations constrain the structure of language: Sign language as a window into universally accessible linguistic biases. Proceedings of the National Academy of Sciences of the United States of America, 112(19), 5968-73. doi:10.1073/pnas.1423080112

Ramus, F. (2002). Evidence for a domain-specific deficit in developmental dyslexia. Behavioral and Brain Sciences, 25(6), 767-768. doi:10.1017/S0140525X02390137

Szenkovits, G. & Ramus, F. (2005). Exploring dyslexics' phonological deficit I: lexical vs sub-lexical and input vs output processes. Dyslexia (Chichester, England), 11(4), 253-68.

Szenkovits, G., Darma, Q., Darcy, I. & Ramus, F. (2016). Exploring dyslexics' phonological deficit II: Phonological grammar. First Language, 36(3), 316-337. doi:10.1177/0142723716648841

Soroli, E., Szenkovits, G. & Ramus, F. (2010). Exploring dyslexics' phonological deficit III: foreign speech perception and production. Dyslexia (Chichester, England), 16(4), 318-40. doi:10.1002/dys.415

Martinot, P. , Bernard, J., Peyre, H., De Agostini, M., Charles, M., Plancoulaine, S. & Barbara, H. (2021). Exposure to screens and children’s language development in the EDEN mother–child cohort. Scientific Reports, 11, 11863. doi:10.1038/s41598-021-90867-3

Roux, P., Brunet-Gouet, E., Passerieux, C. & Ramus, F. (2016). Eye-tracking reveals a slowdown of social context processing during intention attribution in patients with schizophrenia. Journal of psychiatry & neuroscience : JPN, 41(2), E13-21.

Yesilaltay , S. & Mercier, H. (2020). Framing messages for vaccination supporters. Journal of Experimental Psychology Applied, 26(4). doi:10.1037/xap0000271

Galaburda, A., Loturco, J., Ramus, F., Fitch, R. & Rosen, G. (2006). From genes to behavior in developmental dyslexia. Nature neuroscience, 9(10), 1213-7. doi:10.1038/nn1772

Forgeot D'Arc, B., Delorme, R., Zalla, T., Lefebvre, A., Amsellem, F., Moukawane, S., Letellier, L., Leboyer, M., Mouren, M. & Ramus, F. (2017). Gaze direction detection in autism spectrum disorder. Autism : the international journal of research and practice, 21(1), 100-107. doi:10.1177/1362361316630880

Falck, A. & Strickland, B. (2021). Gaze following and mental state attribution: the agent’s line of sight moderates the gaze cueing effect. Journal of Vision, 21(9), 2569-2569. doi:10.1167/jov.21.9.2569

Ramus, F. (2017). General intelligence is an emerging property, not an evolutionary puzzle. The Behavioral and brain sciences, 40, e217. doi:10.1017/S0140525X1600176X

Ramus, F. (2006). Genes, brain, and cognition: a roadmap for the cognitive scientist. Cognition, 101(2), 247-69. doi:10.1016/j.cognition.2006.04.003

Becker, J., Czamara, D., Scerri, T., Ramus, F., Csépe, V., Talcott, J., Stein, J., Morris, A., Ludwig, K., Hoffmann, P., Honbolygó, F., Tóth, D., Fauchereau, F., Bogliotti, C., Iannuzzi, S., Chaix, Y., Valdois, S., Billard, C., George, F., Soares-Boucaud, I., Gérard, C., Van Der Mark, S., Schulz, E., Vaessen, A., Maurer, U., Lohvansuu, K., Lyytinen, H., Zucchelli, M., Brandeis, D., Blomert, L., Leppänen, P., Bruder, J., Monaco, A., Müller-Myhsok, B., Kere, J., Landerl, K., Nöthen, M., Schulte-Körne, G., Paracchini, S., Peyrard-Janvid, M. & Schumacher, J. (2014). Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. European journal of human genetics : EJHG, 22(5), 675-80. doi:10.1038/ejhg.2013.199

Ramus, F. (2008). Génétique de la dyslexie développementale. ANAE - Approche Neuropsychologique des Apprentissages chez l'Enfant, 20, 9-14

Eising, E. , Mirza-Schreiber, N. , de Zeeuw, E. , ..., .., Ramus, F. & (Et Al), . (2022). Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. PNAS, 19(35), e2202764119. doi:10.1073/pnas.2202764119

Gialluisi, A., Andlauer, T., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., Ludwig, K., Czamara, D., St Pourcain, B., Brandler, W., Honbolygó, F., Tóth, D., Csépe, V., Huguet, G., Morris, A., Hulslander, J., Willcutt, E., Defries, J., Olson, R., Smith, S., Pennington, B., Vaessen, A., Maurer, U., Lyytinen, H., Peyrard-Janvid, M., Leppänen, P., Brandeis, D., Bonte, M., Stein, J., Talcott, J., Fauchereau, F., Wilcke, A., Francks, C., Bourgeron, T., Monaco, A., Ramus, F., Landerl, K., Kere, J., Scerri, T., Paracchini, S., Fisher, S., Schumacher, J., Nöthen, M., Müller-Myhsok, B. & Schulte-Körne, G. (2019). Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational psychiatry, 9(1), 77. doi:10.1038/s41398-019-0402-0

Gialluisi, A., Andlauer, T., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., Ludwig, K., Czamara, D., Pourcain, B. , Honbolygó, F., Tóth, D., Csépe, V., Huguet, G., Chaix, Y., Iannuzzi, S., Démonet, J., Morris, A., Hulslander, J., Willcutt, E., Defries, J., Olson, R., Smith, S., Pennington, B., Vaessen, A., Maurer, U., Lyytinen, H., Peyrard-Janvid, M., Leppänen, P., Brandeis, D., Bonte, M., Stein, J., Talcott, J., Fauchereau, F., Wilcke, A., Kirsten, H., Müller, B., Francks, C., Bourgeron, T., Monaco, A., Ramus, F., Landerl, K., Kere, J., Scerri, T., Paracchini, S., Fisher, S., Schumacher, J., Nöthen, M., Müller-Myhsok, B. & Schulte-Körne, G. (2021). Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry, 26 (7), 3004-3017. doi:10.1038/s41380-020-00898-x