statistiche ricercatore

Nome	#
Identification and functional characterization of LDLR mutations in familial hypercholesterolemia patients from Southern Italy	44
Identification of deletions in LDLR gene by Multiplex Ligation-Dependent Probe Amplification Analysis.	42
Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population.	42
Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis of the Polygenic Form of Clinical Familial Hypercholesterolemia and Replication in Samples from 6 Countries.	40
Investigation of Single Nucleotide Polymorphisms Associated to Familial Combined Hyperlipidemia with Random Forests.	39
An improved method on stimulated T-lymphocytes to functionally characterize novel and known LDLR mutations.	36
Identification and functional characterization of a new mutation leading to defective uptake of LDL-LDLR complex.	34
Functional characterization of mutant genes associated with autosomal dominant familial hypercholesterolemia: Integration and evolution of genetic diagnosis	34
Familial hypercholesterolemia: a flow chart for the molecular diagnosis.	33
Identification of Single Nucleotide Polymorphisms associated to Familial Combined Hyperlipidemia.	32
The novel variant p.Ser465Leu in the PCSK9 gene does not account for the decreased LDLR activity in members of a FH family	27
Totale	403

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	9	0	0	0	0	0	0	1	0	0	0	2	6
2020/2021	37	0	1	4	0	0	5	0	2	1	2	17	5
2021/2022	78	1	0	0	0	0	1	2	1	10	1	32	30
2022/2023	100	11	0	2	2	20	12	0	10	16	22	4	1
2023/2024	64	0	16	3	5	0	6	1	10	0	2	8	13
2024/2025	51	12	21	0	10	8	0	0	0	0	0	0	0
Totale													403