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Martina Proietti Onori, PhD - Publications

Affiliations: 
2014-2020 Neuroscience Erasmus Medical Center Rotterdam, Rotterdam, Netherlands 
 2020- Zuckerman Institute Columbia University, New York, NY 
Area:
human specific duplicated gene, development, genetic
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5 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Rigter PMF, de Konink C, Dunn MJ, Proietti Onori M, Humberson JB, Thomas M, Barnes C, Prada CE, Weaver KN, Ryan TD, Caluseriu O, Conway J, Calamaro E, Fong CT, Wuyts W, et al. Role of CAMK2D in neurodevelopment and associated conditions. American Journal of Human Genetics. PMID 38272033 DOI: 10.1016/j.ajhg.2023.12.016  0.596
2021 Proietti Onori M, Koene LMC, Schäfer CB, Nellist M, de Brito van Velze M, Gao Z, Elgersma Y, van Woerden GM. RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity. Plos Biology. 19: e3001279. PMID 34038402 DOI: 10.1371/journal.pbio.3001279  0.555
2021 Proietti Onori M, van Woerden GM. Role of calcium/calmodulin-dependent kinase 2 in neurodevelopmental disorders. Brain Research Bulletin. 171: 209-220. PMID 33774142 DOI: 10.1016/j.brainresbull.2021.03.014  0.603
2019 Koene LMC, van Grondelle SE, Proietti Onori M, Wallaard I, Kooijman NHRM, van Oort A, Schreiber J, Elgersma Y. Effects of antiepileptic drugs in a new TSC/mTOR-dependent epilepsy mouse model. Annals of Clinical and Translational Neurology. 6: 1273-1291. PMID 31353861 DOI: 10.1002/acn3.50829  0.495
2017 Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HAF, Pujol A, Distel B, Robak LA, Bernstein JA, et al. De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. American Journal of Human Genetics. 101: 768-788. PMID 29100089 DOI: 10.1016/J.Ajhg.2017.10.003  0.58
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