statistiche ricercatore

Continente	#
EU - Europa	857
Totale	857

Nazione	#
IT - Italia	857
Totale	857

Nome	#
Prognostic value of specific chromosome imbalances, mutation profile, and BAP1 expression in uveal melanoma	172
Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma	171
Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma	117
How many mutations does it take to make a uveal melanoma?	83
Genetic Workup for Charcot–Marie–Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years	67
ROLE OF MME IN LATE ONSET AXONAL CMT: ANALYSIS OF AN ITALIAN CMT2 COHORT	53
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia	46
null	35
A CASE OF BIALLELIC SORD MUTATIONS ASSOCIATED WITH DISTAL WEAKNESS AND HISTOLOGICAL SIGNS OF MYOPATHY	30
A misleading presentation of Mohr–Tranebjaerg syndrome: what is hidden behind an axonal neuropathy?	29
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation	25
Skeletal muscle involvement in biallelic SORD mutations: case report and review of the literature	24
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement	21
Case report: Episodic ataxia without ataxia?	16
A PROPOSAL FOR IMPROVEMENT OF ACMG GUIDELINES FOR VARIANTS EVALUATION IN CHARCOT-MARIE-TOOTH DISEASE MOLECULAR DIAGNOSIS	13
Totale	902

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	91	0	0	0	0	0	0	18	10	18	21	18	6
2020/2021	50	1	6	1	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	189	16	28	11	40	61	33	0	0	0	0	0	0
Totale													902