statistiche ricercatore

Nome	#
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome	116
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations	83
The copy number variation landscape of congenital anomalies of the kidney and urinary tract	75
Podocytes: the role of lysosomes in the development of nephrotic syndrome	52
MUSIC THERAPY REDUCES ANXIETY AND PAIN AND IMPROVES SATISFACTION IN PATIENTS UNDERGOING PERCUTANEOUS RENAL BIOPSY	42
null	32
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux	23
Erratum: Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789â802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))	17
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome	8
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis	4
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy	3
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease	3
Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis?	2
Totale	460

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	100	0	3	3	8	14	12	12	13	15	9	5	6
2020/2021	88	1	14	2	5	17	2	5	8	4	17	7	6
2021/2022	50	4	5	0	0	2	6	1	1	3	6	4	18
2022/2023	75	7	13	6	5	14	9	2	6	9	0	4	0
2023/2024	78	1	10	2	7	1	10	4	2	9	15	7	10
2024/2025	18	15	3	0	0	0	0	0	0	0	0	0	0
Totale													460