Anthony P. Monaco, M.D., Ph.D.
Affiliations: | President | Tufts University, Boston |
Area:
neurodevelopmental disorders, autism, specific language impairment, dyslexia, chorea acanthocytosis and menkes diseaseWebsite:
http://www.ndm.ox.ac.uk/principal-investigators/researcher/anthony-monacoGoogle:
"Anthony Monaco"Mean distance: 53433
Cross-listing: Evolution Tree - CSD Tree
Children
Sign in to add trainee| Claudio Toma | grad student | WTCHG (Evolution Tree) | |
| Fanny Mojdeh Elahi | grad student | 2004-2007 | Oxford |
| Silvia Paracchini | post-doc | Oxford (Evolution Tree) | |
| Antonio Velayos-Baeza | post-doc | Oxford (Evolution Tree) | |
| Simon E. Fisher | post-doc | 1996-2002 | Oxford |
| Elena Maestrini | research scientist | Oxford (Evolution Tree) |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Doust C, Fontanillas P, Eising E, et al. (2023) Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics |
| Doust C, Fontanillas P, Eising E, et al. (2022) Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics |
| Eising E, Mirza-Schreiber N, de Zeeuw EL, et al. (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: e2202764119 |
| Perrino PA, Chasse RY, Monaco AP, et al. (2022) Rapid auditory processing and medial geniculate nucleus anomalies in Kiaa0319 knockout mice. Genes, Brain, and Behavior. e12808 |
| Gialluisi A, Andlauer TFM, Mirza-Schreiber N, et al. (2020) Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry |
| Monaco AP. (2020) An epigenetic, transgenerational model of increased mental health disorders in children, adolescents and young adults. European Journal of Human Genetics : Ejhg |
| Gialluisi A, Andlauer TFM, Mirza-Schreiber N, et al. (2019) Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry. 9: 77 |
| Yeshaw WM, van der Zwaag M, Pinto F, et al. (2019) Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility. Elife. 8 |
| Yeshaw WM, Zwaag Mvd, Pinto F, et al. (2019) Author response: Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility Elife |
| Guidi LG, Velayos-Baeza A, Martinez-Garay I, et al. (2018) The Neuronal Migration Hypothesis of Dyslexia: A Critical Evaluation Thirty Years On. The European Journal of Neuroscience |