statistiche ricercatore

Continente	#
NA - Nord America	1.173
AS - Asia	679
EU - Europa	366
SA - Sud America	80
Continente sconosciuto - Info sul continente non disponibili	15
AF - Africa	13
OC - Oceania	2
Totale	2.328

Nazione	#
US - Stati Uniti d'America	1.117
SG - Singapore	265
CN - Cina	148
IT - Italia	116
HK - Hong Kong	72
GB - Regno Unito	64
VN - Vietnam	62
BR - Brasile	57
BD - Bangladesh	43
SE - Svezia	37
CA - Canada	28
DE - Germania	27
RU - Federazione Russa	24
FI - Finlandia	22
FR - Francia	19
KR - Corea	19
ID - Indonesia	14
IN - India	11
NL - Olanda	10
JP - Giappone	9
MX - Messico	9
TR - Turchia	8
UA - Ucraina	8
AR - Argentina	6
BG - Bulgaria	6
CZ - Repubblica Ceca	6
ES - Italia	6
PH - Filippine	5
CL - Cile	4
CO - Colombia	4
CR - Costa Rica	4
PY - Paraguay	4
ZA - Sudafrica	4
AT - Austria	3
LT - Lituania	3
MA - Marocco	3
PL - Polonia	3
PR - Porto Rico	3
RS - Serbia	3
TT - Trinidad e Tobago	3
VE - Venezuela	3
HN - Honduras	2
IL - Israele	2
IQ - Iraq	2
MY - Malesia	2
OM - Oman	2
PK - Pakistan	2
PT - Portogallo	2
SV - El Salvador	2
UZ - Uzbekistan	2
AE - Emirati Arabi Uniti	1
AI - Anguilla	1
AL - Albania	1
AU - Australia	1
AZ - Azerbaigian	1
BE - Belgio	1
BH - Bahrain	1
BO - Bolivia	1
CW - ???statistics.table.value.countryCode.CW???	1
DZ - Algeria	1
EC - Ecuador	1
EG - Egitto	1
ET - Etiopia	1
GE - Georgia	1
GR - Grecia	1
GT - Guatemala	1
HT - Haiti	1
HU - Ungheria	1
IE - Irlanda	1
JO - Giordania	1
KE - Kenya	1
KH - Cambogia	1
LB - Libano	1
LK - Sri Lanka	1
LV - Lettonia	1
MM - Myanmar	1
MN - Mongolia	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
PA - Panama	1
RO - Romania	1
SN - Senegal	1
TN - Tunisia	1
TW - Taiwan	1
Totale	2.314

Nome	#
Diprosopus: A Rare Case of Craniofacial Duplication and a Systematic Review of the Literature	345
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care	300
Growth hormone deficiency in a child with benign hereditary chorea caused by a de novo mutation of the TITF1/NKX2-1 gene	235
Mowat-Wilson syndrome: growth charts	224
Focal dermal hypoplasia (goltz-gorlin syndrome): A new case with a novel variant in the PORCN gene (c.1250T>C:p.F417S) and unusual spinal anomaly	223
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature	212
Risk of congenital anomalies around a municipal solid waste incinerator	196
Developmental and epileptic encephalopathy in a young Italian woman with a de novo missense variant in the CLCN4 gene: A case report	182
Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation	152
Correspondence on “Disorder of sex development associated with a novel homozygous nonsense mutation in COG6 expands the phenotypic spectrum of COG6-CDG”	144
An uncommon case of neonatal asphyxia associated with infantile-onset Pompe disease	115
Totale	2.328

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	86	0	0	0	0	0	8	15	7	5	5	31	15
2022/2023	114	14	15	7	9	16	21	0	10	13	2	5	2
2023/2024	114	9	3	7	8	16	12	5	16	5	3	7	23
2024/2025	433	9	3	9	26	82	69	38	18	61	20	42	56
2025/2026	1.020	64	35	69	134	188	69	136	48	80	86	46	65
2026/2027	276	35	46	59	104	32	0	0	0	0	0	0	0
Totale													2.328