statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	1.440
GB - Regno Unito	409
RU - Federazione Russa	265
IT - Italia	210
DE - Germania	198
CN - Cina	164
SG - Singapore	145
IE - Irlanda	134
VN - Vietnam	80
SE - Svezia	78
FR - Francia	62
BR - Brasile	57
FI - Finlandia	57
UA - Ucraina	54
HK - Hong Kong	42
NL - Olanda	32
IN - India	22
ZA - Sudafrica	19
BE - Belgio	17
JP - Giappone	12
CA - Canada	11
TR - Turchia	11
ES - Italia	10
BD - Bangladesh	6
PL - Polonia	6
ID - Indonesia	5
IL - Israele	5
IQ - Iraq	5
KR - Corea	5
MX - Messico	5
PK - Pakistan	5
AT - Austria	3
CI - Costa d'Avorio	3
CZ - Repubblica Ceca	3
LT - Lituania	3
SA - Arabia Saudita	3
VE - Venezuela	3
AR - Argentina	2
AU - Australia	2
CO - Colombia	2
EC - Ecuador	2
IR - Iran	2
LB - Libano	2
PY - Paraguay	2
TM - Turkmenistan	2
TW - Taiwan	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
AM - Armenia	1
BO - Bolivia	1
BY - Bielorussia	1
EG - Egitto	1
ET - Etiopia	1
JM - Giamaica	1
KE - Kenya	1
KG - Kirghizistan	1
MD - Moldavia	1
MY - Malesia	1
NO - Norvegia	1
NZ - Nuova Zelanda	1
PE - Perù	1
PH - Filippine	1
PR - Porto Rico	1
PS - Palestinian Territory	1
SK - Slovacchia (Repubblica Slovacca)	1
SN - Senegal	1
TZ - Tanzania	1
UZ - Uzbekistan	1
Totale	3.629

Nome	#
Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation	406
iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome	394
Evidence of predisposing epimutation in retinoblastoma	378
Usefulness and limitations of comprehensive characterization of mRNA splicing profiles in the definition of the clinical relevance of BRCA1/2 variants of uncertain significance	341
Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism	327
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetuses	322
Parent inheritance of RB1 hypomorphic mutations and somatic mosaicism can explain low penetrance in retinoblastoma	300
Potentially treatable disorder diagnosed post Mortem by exome analysis in a boy with respiratory distress	288
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene	282
Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma	248
null	182
Urine-derived podocytes-lineage cells: A promising tool for precision medicine in Alport Syndrome	114
Compound heterozygous missense and deep intronic variants in NDUFAF6 unraveled by exome sequencing and mRNA analysis	82
Totale	3.664

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	162	0	0	0	0	0	0	0	0	0	101	32	29
2021/2022	232	20	28	12	22	7	6	10	3	12	31	34	47
2022/2023	287	14	30	39	39	32	47	9	26	27	7	10	7
2023/2024	243	15	5	21	17	10	64	79	5	1	7	8	11
2024/2025	518	15	16	47	28	54	62	55	54	65	12	43	67
2025/2026	932	76	97	92	177	244	41	116	25	29	35	0	0
Totale													3.664