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Emanuela Iovino
Emanuela Iovino
在 unibo.it 的电子邮件经过验证
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引用次数
引用次数
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SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect
A McNeill, E Iovino, L Mansard, C Vache, D Baux, E Bedoukian, H Cox, ...
Brain 143 (8), 2380-2387, 2020
462020
The role of neurohypophyseal hormones vasopressin and oxytocin in neuropsychiatric disorders
M Iovino, T Messana, G De Pergola, E Iovino, F Dicuonzo, ...
Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug …, 2018
392018
Synaptic inputs of neural afferent pathways to vasopressin-and oxytocin-secreting neurons of supraoptic and paraventricular hypothalamic nuclei
M Iovino, V Angelo Giagulli, B Licchelli, E Iovino, E Guastamacchia, ...
Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug …, 2016
342016
Neuroendocrine mechanisms involved in male sexual and emotional behavior
M Iovino, T Messana, E Iovino, G De Pergola, E Guastamacchia, ...
Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug …, 2019
272019
Vasopressin in heart failure
M Iovino, M Iacoviello, G De Pergola, B Licchelli, E Iovino, ...
Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug …, 2018
212018
Role of central and peripheral chemoreceptors in vasopressin secretion control
M Iovino, E Guastamacchia, V Angelo Giagulli, G Fiore, B Licchelli, ...
Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug …, 2013
192013
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy
L Gozzelino, G Kochlamazashvili, S Baldassari, AI Mackintosh, ...
Brain 145 (7), 2313-2331, 2022
152022
Molecular mechanisms involved in the control of neurohypophyseal hormones secretion
M Iovino, E Guastamacchia, VA Giagulli, B Licchelli, E Iovino, V Triggiani
Current Pharmaceutical Design 20 (42), 6702-6713, 2014
142014
Brain angiotensinergic regulation of the immune system: implications for cardiovascular and neuroendocrine responses
M Iovino, T Messana, G De Pergola, E Iovino, E Guastamacchia, ...
Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug …, 2020
122020
Vigilance states: central neural pathways, neurotransmitters and neurohormones
M Iovino, T Messana, G De Pergola, E Iovino, E Guastamacchia, ...
Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug …, 2019
102019
Exploration of tools for the interpretation of human non-coding variants
N Tabarini, E Biagi, P Uva, E Iovino, T Pippucci, M Seri, A Cavalli, ...
International Journal of Molecular Sciences 23 (21), 12977, 2022
92022
Long read sequencing on its way to the routine diagnostics of genetic diseases
G Olivucci, E Iovino, G Innella, D Turchetti, T Pippucci, P Magini
Frontiers in Genetics 15, 1374860, 2024
52024
Ultra-Rare Variants Identify Biological Pathways and Candidate Genes in the Pathobiology of Non-Syndromic Cleft Palate Only
E Iovino, L Scapoli, A Palmieri, R Sgarzani, N Nouri, A Pellati, F Carinci, ...
Biomolecules 13 (2), 236, 2023
12023
Bradykinin Signal Pathways Modulate Neurohypophyseal Hormones Secretion
M Iovino, E Guastamacchia, VA Giagulli, E Iovino, B Licchelli
Autacoids 3 (104), 2161-0479.1000104, 2014
12014
SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X‐Linked Intellectual Disability
A Roychaudhury, YR Lee, TI Choi, MG Thomas, TN Khan, H Yousaf, ...
Annals of Neurology, 2024
2024
Integrating structural variant calling, annotation and prioritization into whole genome analysis workflows: a practical application in the molecular diagnosis of …
E Iovino
alma, 2023
2023
Correction to: SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect
A McNeill, E Iovino, L Mansard, C Vache, D Baux, E Bedoukian, H Cox, ...
Brain 146 (e26), e26, 2023
2023
WHOLE GENOME SEQUENCING
E Iovino
European Neuropsychopharmacology 63, e312, 2022
2022
unCOVERApp: an interactive graphical application for clinical assessment of sequence coverage at the base-pair level
E Iovino, M Seri, T Pippucci
Bioinformatics 37 (5), 723-725, 2021
2021
unCOVERApp: an interactive graphical web-application for clinical assessment of sequence coverage at the base-pair level
E Iovino, T Pippucci
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 662-662, 2020
2020
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