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Number of items: 8.


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.


Nichols, Emma, Steinmetz, Jaimie D, Vollset, Stein Emil, Fukutaki, Kai, Chalek, Julian, Abd-Allah, Foad, Abdoli, Amir, Abualhasan, Ahmed, Abu-Gharbieh, Eman, Akram, Tayyaba Tayyaba
et al (show 254 more authors) (2022) Estimation of the global prevalence of dementia in 2019 and forecasted prevalence in 2050: an analysis for the Global Burden of Disease 2019. LANCET PUBLIC HEALTH, 7 (2). E105-E125.


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-.


Gialluisi, Alessandro ORCID: 0000-0002-7388-4463, Reccia, Mafalda Giovanna, Modugno, Nicola, Nutile, Teresa, Lombardi, Alessia, Di Giovannantonio, Luca Giovanni, Pietracupa, Sara, Ruggiero, Daniela ORCID: 0000-0003-3898-7827, Scala, Simona, Gambardella, Stefano
et al (show 8 more authors) (2021) Identification of sixteen novel candidate genes for late onset Parkinson's disease. Molecular neurodegeneration, 16 (1). 35-.


Castelpietra, Giulio, Knudsen, Ann Kristin Skrindo, Agardh, Emilie E, Armocida, Benedetta, Beghi, Massimiliano, Iburg, Kim Moesgaard, Logroscino, Giancarlo, Ma, Rui, Starace, Fabrizio, Steel, Nicholas
et al (show 104 more authors) (2022) The burden of mental disorders, substance use disorders and self-harm among young people in Europe, 1990-2019: Findings from the Global Burden of Disease Study 2019. The Lancet regional health. Europe, 16. p. 100341.

This list was generated on Sun Apr 14 12:21:50 2024 BST.