statistiche ricercatore

Nome	#
A Comprehensive Bioinformatics Analysis of UBE2C in Cancers	157
A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment	44
Investigating the association between common DRD2/ANKK1 genetic polymorphisms and schizophrenia: a meta-analysis	43
Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: A case series	40
Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy	40
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia	39
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: A case report	38
A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: A case report	38
Expression signature of lncRNA APTR in clinicopathology of breast cancer: Its potential oncogenic function in dysregulation of ErbB signaling pathway	37
Expanding the molecular and clinical phenotypes of FUT8-CDG	37
A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: A Case report	34
Totale	547

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	40	2	1	3	2	2	4	4	4	7	4	3	4
2020/2021	34	2	4	4	4	3	2	0	3	1	2	3	6
2021/2022	250	16	3	46	53	13	7	2	15	1	10	44	40
2022/2023	153	13	8	12	3	5	31	12	10	22	6	21	10
2023/2024	70	13	24	4	3	5	2	5	1	0	8	5	0
Totale													547

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