statistiche ricercatore

Continente	#
NA - Nord America	441
AS - Asia	369
EU - Europa	286
SA - Sud America	48
AF - Africa	5
Continente sconosciuto - Info sul continente non disponibili	2
OC - Oceania	1
Totale	1.152

Nazione	#
US - Stati Uniti d'America	426
SG - Singapore	172
CN - Cina	87
IT - Italia	76
SE - Svezia	56
BR - Brasile	43
DE - Germania	38
FR - Francia	38
VN - Vietnam	37
GB - Regno Unito	12
IE - Irlanda	12
HK - Hong Kong	11
IN - India	11
NL - Olanda	10
BD - Bangladesh	8
ID - Indonesia	8
CA - Canada	7
RU - Federazione Russa	7
AT - Austria	6
FI - Finlandia	6
BE - Belgio	5
JP - Giappone	5
PL - Polonia	5
TR - Turchia	5
ES - Italia	4
MX - Messico	4
PK - Pakistan	4
PT - Portogallo	4
KR - Corea	3
ZA - Sudafrica	3
AZ - Azerbaigian	2
CL - Cile	2
IQ - Iraq	2
NP - Nepal	2
RO - Romania	2
SA - Arabia Saudita	2
UZ - Uzbekistan	2
A2 - ???statistics.table.value.countryCode.A2???	1
AR - Argentina	1
AU - Australia	1
BN - Brunei Darussalam	1
CH - Svizzera	1
CI - Costa d'Avorio	1
CR - Costa Rica	1
CZ - Repubblica Ceca	1
DK - Danimarca	1
EG - Egitto	1
EU - Europa	1
HN - Honduras	1
IL - Israele	1
IR - Iran	1
JO - Giordania	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LT - Lituania	1
NO - Norvegia	1
OM - Oman	1
PA - Panama	1
PE - Perù	1
PY - Paraguay	1
SV - El Salvador	1
TH - Thailandia	1
Totale	1.152

Nome	#
Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers	219
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome	201
A novel truncating variant within exon 7 of KAT6B associated with features of both SayâBarberâBiesekerâYoungâSimpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders	170
Clinical genetics can solve the pitfalls of genome-wide investigations: Lesson from mismapping a loss-of-function variant in KANSL1	162
CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories	159
Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4	149
Syndromic craniosynostosis can define new candidate genes for suture development or result from the non-specifc effects of pleiotropic genes: Rasopathies and chromatinopathies as examples	112
Totale	1.172

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	1	0	0	0	0	0	0	0	0	0	0	0	1
2021/2022	83	13	0	1	11	1	1	0	9	9	4	15	19
2022/2023	185	26	26	14	30	2	22	7	12	11	16	14	5
2023/2024	103	3	17	4	8	3	17	9	6	2	3	12	19
2024/2025	191	2	4	8	8	31	9	4	11	29	19	37	29
2025/2026	518	64	10	20	75	105	34	97	25	38	21	19	10
Totale													1.172

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