statistiche ricercatore

Continente	#
NA - Nord America	354
AS - Asia	282
EU - Europa	253
SA - Sud America	46
AF - Africa	4
Continente sconosciuto - Info sul continente non disponibili	2
OC - Oceania	1
Totale	942

Nazione	#
US - Stati Uniti d'America	342
SG - Singapore	129
CN - Cina	80
IT - Italia	67
SE - Svezia	56
BR - Brasile	41
DE - Germania	31
FR - Francia	29
VN - Vietnam	21
GB - Regno Unito	11
IE - Irlanda	11
IN - India	10
NL - Olanda	10
ID - Indonesia	8
AT - Austria	6
CA - Canada	6
RU - Federazione Russa	6
BE - Belgio	5
FI - Finlandia	5
PL - Polonia	5
BD - Bangladesh	4
MX - Messico	4
PK - Pakistan	4
PT - Portogallo	4
TR - Turchia	4
AZ - Azerbaigian	2
CL - Cile	2
ES - Italia	2
HK - Hong Kong	2
JP - Giappone	2
KR - Corea	2
NP - Nepal	2
UZ - Uzbekistan	2
ZA - Sudafrica	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
CZ - Repubblica Ceca	1
EG - Egitto	1
EU - Europa	1
HN - Honduras	1
IL - Israele	1
IQ - Iraq	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
RO - Romania	1
SA - Arabia Saudita	1
TH - Thailandia	1
Totale	942

Nome	#
Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers	170
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome	162
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	145
Clinical genetics can solve the pitfalls of genome-wide investigations: Lesson from mismapping a loss-of-function variant in KANSL1	141
CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories	122
Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4	122
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	96
Totale	958

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	30	0	0	0	0	0	1	9	0	5	5	9	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	304	64	10	20	75	105	30	0	0	0	0	0	0
Totale													958

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