CRIS Current Research Information System

NICOLETTI, ANNALISA
 Distribuzione geografica
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Continente #
NA - Nord America 1.990
AS - Asia 1.945
EU - Europa 1.392
AF - Africa 111
SA - Sud America 95
Continente sconosciuto - Info sul continente non disponibili 79
OC - Oceania 15
Totale 5.627
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Nazione #
US - Stati Uniti d'America 1.941
VN - Vietnam 705
SG - Singapore 433
CN - Cina 409
GB - Regno Unito 324
DE - Germania 246
SE - Svezia 169
IT - Italia 160
HK - Hong Kong 147
FR - Francia 90
UA - Ucraina 88
IN - India 79
BR - Brasile 67
RU - Federazione Russa 59
IE - Irlanda 58
NL - Olanda 57
JP - Giappone 38
CA - Canada 34
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
AU - Australia 15
IL - Israele 14
BG - Bulgaria 13
AR - Argentina 12
TR - Turchia 12
PH - Filippine 11
CZ - Repubblica Ceca 10
JO - Giordania 10
BD - Bangladesh 9
SC - Seychelles 9
AT - Austria 8
EC - Ecuador 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
JM - Giamaica 3
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
KM - Comore 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
LC - Santa Lucia 1
LU - Lussemburgo 1
MD - Moldavia 1
MK - Macedonia 1
MM - Myanmar 1
MQ - Martinica 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 5.549
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Città #
Singapore 309
Southend 282
Ashburn 192
Chandler 174
Ho Chi Minh City 161
San Jose 152
Hanoi 142
Hong Kong 134
Fairfield 97
Houston 90
Dong Ket 82
Santa Clara 74
Princeton 70
Wilmington 60
Jacksonville 59
Ann Arbor 57
Dublin 56
Beijing 54
Hefei 53
Council Bluffs 48
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
Helsinki 22
Munich 22
Nanjing 22
Bologna 21
Shenyang 21
Turin 21
Berlin 20
Haiphong 20
Lomé 20
Redwood City 20
Abeokuta 19
Falls Church 18
Medford 18
São Paulo 18
Dallas 17
Jinan 17
New York 17
Brussels 16
Seoul 15
Buffalo 14
Da Nang 14
Guangzhou 13
Sofia 13
Milan 12
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
Phoenix 6
Thái Nguyên 6
Vienna 6
Zhengzhou 6
Bengaluru 5
Burlington 5
Bắc Ninh 5
Chengdu 5
Hangzhou 5
Melle 5
Orem 5
Philadelphia 5
Totale 3.438
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Nome #
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. 529
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 405
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 264
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. 233
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material. 210
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA. 209
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 203
A molecular analysis of candidate genes for hypospadias in Italian subjects 195
Determination of BMP15 gene dosage in a woman with TS and spontaneous menarche. 192
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 186
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 184
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 184
Copy number determination of hypothyroidism genes by MLPA analysis in patients with hypothyroidism and thyroid hypoplasia 177
First Description of Partial Atrioventricular Septal Defect in a Rabbit 171
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 167
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 167
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 160
NKX2.1-Related Disorders: a novel mutation with mild clinical presentation. 158
Three new mutations in androgen receptor gene identified in patients with 46,XY SDS: Complications for genetic counselling 151
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS. 141
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 139
Low WT1 Expression Identifies a Subset of Acute Myeloid Leukemia with a Distinct Genotype 138
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. 136
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 132
SHOX dosage and final height (FH) in Turner syndrome (TS) treated with GH-therapy 131
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. 129
TSHR gene analysis in paediatric subjects with NASH (non autoimmune subclinical hypothyroidism) not selected by neonatal screening 128
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency 125
Non classical CAH: molecular evaluation of 287 subjects from northern and southern Italy with comparison between genetical and hormonal results. 114
Current Loss-Of-Function Mutations in The Thyrotropin Receptor Gene: When to Investigate, Clinical Effects, and Treatment. 92
null 77
Totale 5.627
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Categoria #
all - tutte 13.592
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 13.592
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022558 0 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
2025/20261.907 348 150 127 118 177 105 153 112 370 144 47 56
2026/202780 32 48 0 0 0 0 0 0 0 0 0 0
Totale 5.627