statistiche ricercatore

Nome	#
Functional characterization of novel germline mutations affecting CDC42 highlighted their differential impact on multiple signaling pathways.	47
Phenotypic Assessment of Pathogenic Variants in GNAO1 and Response to Caffeine in C. elegans Models of the Disease	34
Novel de novo CDC42 variants cause variable functional alterations and heterogeneous spectrum of neurodevelopmental and immune-hematologic rare diseases	32
Caenorhabditis elegans provides an efficient drug screening platform for GNAO1-related disorders and highlights the potential role of caffeine in controlling dyskinesia	28
The recurrent pathogenic Pro890Leu substitution in CLTC causes a generalized defect in synaptic transmission in Caenorhabditis elegans	27
null	27
Mutations at the C-terminus of CDC42 cause distinct hematopoietic and autoinflammatory disorders	22
C. elegans-based chemosensation strategy for the early detection of cancer metabolites in urine samples	21
De novo mutations involving the C-terminal tail of CDC42 cause distinct dyshematopoietic and autoinflammatory disorders	20
Functional variability of novel CDC42 pathogenic variants is associated with phenotypic heterogeneity of neurodevelopmental and immune-hematologic related disorders	18
GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatments	17
Motor, epileptic, and developmental phenotypes in genetic disorders affecting G protein coupled receptors-cAMP signaling	16
Totale	309

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	8	0	0	0	0	0	0	7	1	0	0	0	0
2020/2021	8	0	0	0	0	1	2	0	0	0	0	0	5
2021/2022	51	2	0	1	0	2	3	1	2	16	2	8	14
2022/2023	44	7	3	0	1	6	5	4	4	10	1	1	2
2023/2024	151	3	8	11	29	27	8	8	7	8	13	12	17
2024/2025	47	6	10	18	13	0	0	0	0	0	0	0	0
Totale													309

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