statistiche ricercatore

Continente	#
EU - Europa	1.576
NA - Nord America	1.540
AS - Asia	531
SA - Sud America	72
Continente sconosciuto - Info sul continente non disponibili	35
AF - Africa	27
OC - Oceania	3
Totale	3.784

Nazione	#
US - Stati Uniti d'America	1.518
GB - Regno Unito	410
RU - Federazione Russa	265
IT - Italia	238
DE - Germania	198
CN - Cina	167
SG - Singapore	145
IE - Irlanda	134
VN - Vietnam	81
SE - Svezia	78
FR - Francia	62
BR - Brasile	57
FI - Finlandia	57
UA - Ucraina	54
HK - Hong Kong	43
NL - Olanda	32
IN - India	22
ZA - Sudafrica	19
BE - Belgio	17
CA - Canada	13
JP - Giappone	12
ES - Italia	11
TR - Turchia	11
BD - Bangladesh	6
PL - Polonia	6
ID - Indonesia	5
IL - Israele	5
IQ - Iraq	5
KR - Corea	5
MX - Messico	5
PK - Pakistan	5
AR - Argentina	3
AT - Austria	3
CI - Costa d'Avorio	3
CO - Colombia	3
CZ - Repubblica Ceca	3
LT - Lituania	3
SA - Arabia Saudita	3
VE - Venezuela	3
AE - Emirati Arabi Uniti	2
AU - Australia	2
EC - Ecuador	2
IR - Iran	2
LB - Libano	2
PY - Paraguay	2
TM - Turkmenistan	2
TW - Taiwan	2
AL - Albania	1
AM - Armenia	1
BO - Bolivia	1
BY - Bielorussia	1
CR - Costa Rica	1
EG - Egitto	1
ET - Etiopia	1
JM - Giamaica	1
KE - Kenya	1
KG - Kirghizistan	1
MD - Moldavia	1
MY - Malesia	1
NI - Nicaragua	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	3.749

Nome	#
Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation	412
iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome	397
Evidence of predisposing epimutation in retinoblastoma	390
Usefulness and limitations of comprehensive characterization of mRNA splicing profiles in the definition of the clinical relevance of BRCA1/2 variants of uncertain significance	358
Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism	342
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetuses	330
Parent inheritance of RB1 hypomorphic mutations and somatic mosaicism can explain low penetrance in retinoblastoma	315
Potentially treatable disorder diagnosed post Mortem by exome analysis in a boy with respiratory distress	299
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene	295
Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma	257
null	182
Urine-derived podocytes-lineage cells: A promising tool for precision medicine in Alport Syndrome	119
Compound heterozygous missense and deep intronic variants in NDUFAF6 unraveled by exome sequencing and mRNA analysis	88
Totale	3.784

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	184	0	0	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	992	76	97	92	177	244	41	116	25	29	42	18	35
2026/2027	60	23	19	18	0	0	0	0	0	0	0	0	0
Totale													3.784