statistiche ricercatore

Nome	#
Transcriptional hallmarks of noonan syndrome and noonan-like syndrome with loose anagen hair	220
Analisi del profilo di trascrizione genetica nella sindrome di Noonan.	215
The KCNQ1OT1 Imprinting Control Region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.	175
Convergent mutations and kinase fusions lead to oncogenic STAT3 activation in anaplastic large cell lymphoma	131
Molecular dissection of Noonan syndrome by transcriptiome analysis	127
Prevalence of beckwith-wiedemann syndrome in North West of Italy	82
Genotypic and phenotypic spectrum of 44 patients with Noonan syndrome	81
ARRAY-CGH analysis in 92 children with complex syndromic phenotype	72
Molecular and clinical characterization of 37 patients with Noonan syndrome	71
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome.	67
The overlap between Sotos and Beckwith-Wiedemann syndromes	63
Eyebrow anomalies as a diagnostic sign of genomic disorders	62
Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome.	61
Incidence of Beckwith-Wiedemann syndrome	60
SLC25A19 deficiency and bilateral striatal necrosis with polyneuropathy: a new case and review of the literature	40
Clinical, biochemical, and molecular spectrum of short/branched-chain acyl-CoA dehydrogenase deficiency: two new cases and review of literature	2
Totale	1.529

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	165	12	5	8	24	9	30	27	11	7	21	9	2
2020/2021	109	17	5	8	6	5	5	11	6	6	11	5	24
2021/2022	298	25	13	19	36	19	18	26	20	16	12	54	40
2022/2023	373	31	42	11	47	21	79	24	30	52	15	13	8
2023/2024	124	22	24	7	9	5	6	5	9	3	6	13	15
Totale													1.529

CINECA IRIS Institutional Research Information System