statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	1.360
GB - Regno Unito	405
RU - Federazione Russa	265
IT - Italia	200
DE - Germania	198
CN - Cina	161
IE - Irlanda	134
SG - Singapore	131
SE - Svezia	77
FI - Finlandia	56
UA - Ucraina	54
FR - Francia	52
BR - Brasile	49
HK - Hong Kong	37
NL - Olanda	32
VN - Vietnam	19
BE - Belgio	17
IN - India	17
JP - Giappone	10
TR - Turchia	10
ES - Italia	9
CA - Canada	8
ZA - Sudafrica	6
BD - Bangladesh	5
IL - Israele	5
KR - Corea	5
PL - Polonia	5
ID - Indonesia	4
IQ - Iraq	4
MX - Messico	4
PK - Pakistan	4
AT - Austria	3
CI - Costa d'Avorio	3
CZ - Repubblica Ceca	3
LT - Lituania	3
VE - Venezuela	3
AR - Argentina	2
AU - Australia	2
CO - Colombia	2
IR - Iran	2
LB - Libano	2
TM - Turkmenistan	2
TW - Taiwan	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
AM - Armenia	1
BY - Bielorussia	1
JM - Giamaica	1
MY - Malesia	1
NO - Norvegia	1
NZ - Nuova Zelanda	1
PE - Perù	1
PR - Porto Rico	1
PS - Palestinian Territory	1
PY - Paraguay	1
SA - Arabia Saudita	1
SK - Slovacchia (Repubblica Slovacca)	1
SN - Senegal	1
TZ - Tanzania	1
UZ - Uzbekistan	1
Totale	3.389

Nome	#
Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation	395
iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome	358
Evidence of predisposing epimutation in retinoblastoma	352
Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism	313
Usefulness and limitations of comprehensive characterization of mRNA splicing profiles in the definition of the clinical relevance of BRCA1/2 variants of uncertain significance	311
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetuses	286
Parent inheritance of RB1 hypomorphic mutations and somatic mosaicism can explain low penetrance in retinoblastoma	277
Potentially treatable disorder diagnosed post Mortem by exome analysis in a boy with respiratory distress	275
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene	267
Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma	232
null	182
Urine-derived podocytes-lineage cells: A promising tool for precision medicine in Alport Syndrome	104
Compound heterozygous missense and deep intronic variants in NDUFAF6 unraveled by exome sequencing and mRNA analysis	72
Totale	3.424

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	279	0	0	0	0	0	25	16	45	31	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	692	76	97	92	177	244	6	0	0	0	0	0	0
Totale													3.424