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Number of items: 6.


Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D, Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth
et al (show 137 more authors) (2022) Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11). pp. 1621-1629.


Becker, Jessica, Czamara, Darina, Scerri, Tom S, Ramus, Franck, Csepe, Valeria, Talcott, Joel B, Stein, John, Morris, Andrew, Ludwig, Kerstin U, Hoffmann, Per
et al (show 31 more authors) (2014) Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. EUROPEAN JOURNAL OF HUMAN GENETICS, 22 (5). pp. 675-680.


Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L, Wang, Carol A, Truong, Dongnhu T, Allegrini, Andrea G, Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G, Gerritse, Margot L
et al (show 85 more authors) (2022) Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America, 119 (35). e2202764119-e2202764119.


Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Brandler, William
et al (show 35 more authors) (2019) Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY, 9 (1). 77-.


Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Honbolygo, Ferenc
et al (show 39 more authors) (2021) Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY, 26 (7). pp. 3004-3017.


Price, Kaitlyn M, Wigg, Karen G, Eising, Else, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N, Guger, Sharon L, Abbondanza, Filippo, Allegrini, Andrea G
et al (show 80 more authors) (2022) Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. TRANSLATIONAL PSYCHIATRY, 12 (1). 495-.

This list was generated on Sat Mar 16 05:48:12 2024 GMT.