statistiche ricercatore

Continente	#
NA - Nord America	257
AS - Asia	239
EU - Europa	165
SA - Sud America	26
Continente sconosciuto - Info sul continente non disponibili	11
AF - Africa	5
OC - Oceania	2
Totale	705

Nome	#
LOW-FREQUENCY ALLELE VARIANTS IN NGS MULTI-GENE PANELS FOR HEREDITARY CANCER TESTING: ARTIFACTS, CHIP OR MOSAICS? MANAGING THE RESULTS IN THE LABORATORY ROUTINE	161
Clinically relevant low-frequency Next Generation Sequencing variants in hereditary cancer patients: an operational multi-step algorithm for laboratory managing	158
Homologous recombination deficiency in pancreatic neuroendocrine tumors	137
Characterization of copy number variants in hereditary cancer patients through NGS shows a distinctive PALB2 contribution to the diagnostic yield	108
GENOMIC SCREENING OF PRIMARY REFRACTORY ACUTE MYELOID LEUKEMIA WITHOUT TP53 ALTERATIONS BY OPTICAL GENOME MAPPING (OGM)	36
Optical genome mapping reveals multiple apoptotic and cell-cycle pathway aberrations in B-cell prolymphocytic leukemia: a report of three cases	36
ASSOCIATION BETWEEN TYPE AND LOCATION OF GERMLINE BRCA1/2 PATHOGENIC OR LIKELY PATHOGENIC VARIANTS WITH PHENOTYPE AND PROGNOSIS IN YOUNG PATIENTS WITH BREAST CANCER: RESULTS FROM AN INTERNATIONAL COHORT STUDY.	26
Citogenomica nelle leucemie a cellule B: potenziamento della caratterizzazione genetica e individuazione di biomarcatori prognostici e target terapeutici tramite NGS e mappatura ottica del genoma	22
OPTICAL GENOME MAPPING IDENTIFIES MULTIPLE STRUCTURAL VARIATION AND CATASTROPHIC REARRANGEMENTS IN B-CELL PROLYMPHOCYTIC LEUKEMIA	21
Totale	705

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2023/2024	38	0	0	0	0	0	0	18	6	1	4	6	3
2024/2025	170	2	0	8	4	19	22	14	8	19	17	26	31
2025/2026	410	32	20	24	24	47	21	43	22	32	48	59	38
2026/2027	87	38	49	0	0	0	0	0	0	0	0	0	0
Totale													705