statistiche ricercatore

Nome	#
Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma	208
Prognostic value of specific chromosome imbalances, mutation profile, and BAP1 expression in uveal melanoma	185
Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma	148
Genetic Workup for Charcot–Marie–Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years	119
How many mutations does it take to make a uveal melanoma?	116
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia	89
ROLE OF MME IN LATE ONSET AXONAL CMT: ANALYSIS OF AN ITALIAN CMT2 COHORT	87
A CASE OF BIALLELIC SORD MUTATIONS ASSOCIATED WITH DISTAL WEAKNESS AND HISTOLOGICAL SIGNS OF MYOPATHY	78
A PROPOSAL FOR IMPROVEMENT OF ACMG GUIDELINES FOR VARIANTS EVALUATION IN CHARCOT-MARIE-TOOTH DISEASE MOLECULAR DIAGNOSIS	75
A misleading presentation of Mohr–Tranebjaerg syndrome: what is hidden behind an axonal neuropathy?	65
Skeletal muscle involvement in biallelic SORD mutations: case report and review of the literature	64
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement	64
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation	64
Case report: Episodic ataxia without ataxia?	51
null	35
Case report: A single novel calpain 3 gene variant associated with mild myopathy	11
Totale	1.459

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	42	0	0	0	4	4	6	1	9	0	6	7	5
2021/2022	120	7	8	10	4	3	4	10	17	10	11	20	16
2022/2023	154	6	10	1	12	14	24	8	18	20	5	30	6
2023/2024	233	17	6	11	43	11	37	13	15	16	14	14	36
2024/2025	495	16	28	11	40	61	33	48	101	31	28	48	50
2025/2026	251	109	29	56	57	0	0	0	0	0	0	0	0
Totale													1.459