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	185
Mutation landscape in patients with myelofibrosis receiving ruxolitinib or hydroxyurea	125
Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs)	124
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency	123
Mutated ASXL1 and number of somatic mutations as possible indicators of progression to chronic myelomonocytic leukemia of myelodysplastic syndromes with single or multilineage dysplasia	118
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing	110
THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS	107
Fundus phenotype in retinitis pigmentosa associated with EYS mutations	105
Germline Mutation in KIF1Bβ Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma	87
Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.	84
Characteristics and clinical correlates of NFE2 mutations in chronic Myeloproliferative neoplasms	67
Totale	1.235

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	145	0	0	0	0	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	365	25	64	37	116	123	0	0	0	0	0	0	0
Totale													1.235