statistiche ricercatore

Nome	#
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.	96
Spectrum and prevalence of mutations involving BrS1-12 susceptibility genes in a cohort of unrelated patients referred for Brugada Syndrome genetic testing: implications for genetic testing.	77
FGF12 is a candidate Brugada syndrome locus.	77
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.	77
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study	70
Condizioni cliniche associate ad anomalie dell'intervallo QT: Implicazioni cliniche [Clinical conditions associated with abnormal QT interval: clinical implications].	55
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene	49
From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2	48
Torsades de Pointes following Acute Myocardial Infarction: Evidence for a Deadly Link with a Common Genetic Variant.	47
Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.	46
The genetics underlying acquired long QT syndrome: impact for genetic screening.	42
Totale	684

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	7	0	0	0	0	0	0	0	0	0	0	5	2
2019/2020	164	43	54	2	7	1	9	1	7	3	23	12	2
2020/2021	82	9	7	3	7	5	9	3	15	3	10	10	1
2021/2022	70	2	3	2	2	4	6	2	7	4	2	11	25
2022/2023	219	28	18	3	15	20	20	0	12	93	0	8	2
2023/2024	62	5	21	1	3	6	15	3	5	0	3	0	0
Totale													684