statistiche ricercatore

Nome	#
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center	160
Mutation landscape in patients with myelofibrosis receiving ruxolitinib or hydroxyurea	94
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency	89
Mutated ASXL1 and number of somatic mutations as possible indicators of progression to chronic myelomonocytic leukemia of myelodysplastic syndromes with single or multilineage dysplasia	88
Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs)	82
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing	81
Fundus phenotype in retinitis pigmentosa associated with EYS mutations	76
THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS	74
Germline Mutation in KIF1Bβ Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma	63
Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.	57
Characteristics and clinical correlates of NFE2 mutations in chronic Myeloproliferative neoplasms	39
Totale	903

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	163	0	4	1	13	16	26	25	23	23	15	13	4
2020/2021	160	4	5	23	28	3	10	5	11	13	33	17	8
2021/2022	87	13	4	3	1	1	9	4	1	6	6	15	24
2022/2023	265	20	52	22	25	15	38	27	16	34	0	5	11
2023/2024	127	8	12	14	5	16	18	4	21	3	11	10	5
2024/2025	33	25	8	0	0	0	0	0	0	0	0	0	0
Totale													903