CRIS Current Research Information System

NICOLETTI, ANNALISA
 Distribuzione geografica
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Continente #
AS - Asia 1.937
NA - Nord America 1.931
EU - Europa 1.384
AF - Africa 110
SA - Sud America 94
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 1
Totale 5.468
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Nazione #
US - Stati Uniti d'America 1.888
VN - Vietnam 705
SG - Singapore 429
CN - Cina 407
GB - Regno Unito 324
DE - Germania 245
SE - Svezia 169
IT - Italia 154
HK - Hong Kong 146
FR - Francia 90
UA - Ucraina 88
IN - India 79
BR - Brasile 66
RU - Federazione Russa 59
IE - Irlanda 57
NL - Olanda 57
JP - Giappone 38
CA - Canada 32
FI - Finlandia 32
ZA - Sudafrica 26
CI - Costa d'Avorio 24
EE - Estonia 23
NG - Nigeria 20
TG - Togo 20
KR - Corea 19
BE - Belgio 18
IL - Israele 14
BG - Bulgaria 13
AR - Argentina 12
TR - Turchia 12
AU - Australia 11
PH - Filippine 11
CZ - Repubblica Ceca 10
JO - Giordania 10
AT - Austria 8
BD - Bangladesh 8
EC - Ecuador 8
SC - Seychelles 8
PK - Pakistan 7
TH - Thailandia 7
CH - Svizzera 6
GR - Grecia 6
IQ - Iraq 6
MX - Messico 6
PL - Polonia 6
RO - Romania 6
AE - Emirati Arabi Uniti 5
CL - Cile 5
ES - Italia 5
ID - Indonesia 5
IR - Iran 5
TW - Taiwan 5
EG - Egitto 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
MA - Marocco 3
KE - Kenya 2
KH - Cambogia 2
LT - Lituania 2
NP - Nepal 2
PS - Palestinian Territory 2
BO - Bolivia 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
ET - Etiopia 1
HN - Honduras 1
JM - Giamaica 1
KM - Comore 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
LU - Lussemburgo 1
MD - Moldavia 1
MK - Macedonia 1
MM - Myanmar 1
MY - Malesia 1
NI - Nicaragua 1
NO - Norvegia 1
PE - Perù 1
PY - Paraguay 1
SK - Slovacchia (Repubblica Slovacca) 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 5.468
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Città #
Singapore 307
Southend 282
Ashburn 190
Chandler 174
Ho Chi Minh City 161
San Jose 152
Hanoi 142
Hong Kong 134
Fairfield 97
Houston 90
Dong Ket 82
Santa Clara 71
Princeton 70
Wilmington 60
Jacksonville 59
Ann Arbor 57
Dublin 55
Beijing 53
Hefei 53
Seattle 42
Woodbridge 38
Los Angeles 36
Boardman 34
Lauterbourg 29
Tokyo 29
Westminster 29
Cambridge 26
Abidjan 24
Padova 24
Frankfurt am Main 23
Council Bluffs 22
Helsinki 22
Munich 22
Nanjing 22
Bologna 21
Shenyang 21
Berlin 20
Haiphong 20
Lomé 20
Redwood City 20
Abeokuta 19
Turin 19
Falls Church 18
Medford 18
São Paulo 18
Jinan 17
Brussels 16
Dallas 16
New York 16
Seoul 15
Buffalo 14
Da Nang 14
Guangzhou 13
Sofia 13
Milan 11
Tacoma 11
Tianjin 11
Amman 10
Chennai 10
Hải Dương 10
Prague 10
Turku 10
Can Tho 9
Düsseldorf 9
Hebei 9
Mülheim 9
Saint Petersburg 9
Bremen 8
Brookhaven 8
Chicago 8
Dortmund 8
Rishon LeTsiyyon 8
Toronto 8
Biên Hòa 7
Dearborn 7
Ha Long 7
Hagen 7
Jiaxing 7
Mountain View 7
Norwalk 7
Redondo Beach 7
San Francisco 7
Changsha 6
Falkenstein 6
Leawood 6
London 6
Mahé 6
Nanchang 6
Thái Nguyên 6
Vienna 6
Zhengzhou 6
Bengaluru 5
Burlington 5
Bắc Ninh 5
Chengdu 5
Hangzhou 5
Melle 5
Orem 5
Phoenix 5
Quận Mười 5
Totale 3.397
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Nome #
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. 515
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 403
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 261
Study of the NR5A1 gene in a cohort of Italian patients with 46,XY Disorders of Sex Development (DSD) without adrenal insufficiency: identification of 7 novel mutations. 231
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA. 207
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material. 205
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 201
A molecular analysis of candidate genes for hypospadias in Italian subjects 193
Determination of BMP15 gene dosage in a woman with TS and spontaneous menarche. 191
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 183
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 183
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 181
Copy number determination of hypothyroidism genes by MLPA analysis in patients with hypothyroidism and thyroid hypoplasia 176
First Description of Partial Atrioventricular Septal Defect in a Rabbit 169
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 165
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 164
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 158
NKX2.1-Related Disorders: a novel mutation with mild clinical presentation. 157
Three new mutations in androgen receptor gene identified in patients with 46,XY SDS: Complications for genetic counselling 150
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS. 138
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 137
HESX1 gene analysis in a population of 45 patients with posterior pituitari ectopia (PPE) and GH deficiency (GHD): two novel mutations associated with a mild phenotype. 133
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 130
SHOX dosage and final height (FH) in Turner syndrome (TS) treated with GH-therapy 129
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. 128
Low WT1 Expression Identifies a Subset of Acute Myeloid Leukemia with a Distinct Genotype 127
TSHR gene analysis in paediatric subjects with NASH (non autoimmune subclinical hypothyroidism) not selected by neonatal screening 127
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency 124
Non classical CAH: molecular evaluation of 287 subjects from northern and southern Italy with comparison between genetical and hormonal results. 112
Current Loss-Of-Function Mutations in The Thyrotropin Receptor Gene: When to Investigate, Clinical Effects, and Treatment. 91
null 77
Totale 5.546
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Categoria #
all - tutte 13.080
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 13.080
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021115 0 0 0 0 0 0 0 0 0 0 0 115
2021/2022661 103 29 23 61 52 39 20 35 25 35 121 118
2022/2023736 77 95 45 87 61 62 24 37 140 22 60 26
2023/2024201 6 26 32 18 18 19 10 12 17 18 16 9
2024/2025754 28 128 52 66 89 53 24 27 1 89 27 170
2025/20261.906 348 150 127 118 177 105 153 112 370 144 47 55
Totale 5.546