MATTINA, Teresa
 Distribuzione geografica
Continente #
EU - Europa 183
NA - Nord America 60
AS - Asia 29
AF - Africa 9
OC - Oceania 3
SA - Sud America 2
Totale 286
Nazione #
IT - Italia 82
US - Stati Uniti d'America 54
FR - Francia 42
IE - Irlanda 20
CI - Costa d'Avorio 9
IN - India 9
DE - Germania 8
ES - Italia 7
VN - Vietnam 7
CZ - Repubblica Ceca 6
AU - Australia 3
KR - Corea 3
PT - Portogallo 3
TW - Taiwan 3
AT - Austria 2
CA - Canada 2
CO - Colombia 2
GB - Regno Unito 2
GT - Guatemala 2
NL - Olanda 2
PA - Panama 2
RS - Serbia 2
RU - Federazione Russa 2
TR - Turchia 2
CN - Cina 1
FI - Finlandia 1
GR - Grecia 1
IL - Israele 1
IR - Iran 1
LV - Lettonia 1
MY - Malesia 1
PL - Polonia 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
Totale 286
Città #
Dublin 20
Catania 19
Abidjan 9
Milan 6
Boardman 5
Bremen 5
Brescia 5
Dong Ket 5
Paris 5
Aci Catena 4
Bari 4
Rome 4
Ashburn 3
Delhi 3
Duluth 3
Florence 3
Linkou District 3
Lisbon 3
Palermo 3
Seoul 3
Vittoria 3
Zaragoza 3
Amsterdam 2
Biloxi 2
Chicago 2
Guatemala City 2
Houston 2
Juan Díaz 2
Melbourne 2
Miami 2
Milpitas 2
Oklahoma City 2
Padova 2
Pittsburgh 2
Seattle 2
Syracuse 2
Udine 2
Vienna 2
Vilanova i la Geltrú 2
Andhra Pradesh 1
Bangkok 1
Barcelona 1
Benton 1
Binetto 1
Bogotá 1
Bologna 1
Calgary 1
Carson 1
Cascina 1
Cheras 1
Châtellerault 1
Coimbatore 1
Corciano 1
Council Bluffs 1
Foggia 1
Hamilton 1
Hanoi 1
Hatfield 1
Helsinki 1
Hillsboro 1
Ho Chi Minh City 1
Iowa Falls 1
Istanbul 1
Kochi 1
Lake Forest 1
Leporano 1
Los Angeles 1
Lyon 1
Maglie 1
Manerbio 1
Messina 1
Monterey Park 1
Monza 1
Moratalla 1
Moscow 1
Mount Juliet 1
Mountain View 1
New Hyde Park 1
Odunpazari 1
Orlando 1
Pavia 1
Ranipet 1
Reggio Nell'emilia 1
Rehovot 1
Riga 1
Rohtak 1
Romano di Lombardia 1
Romeoville 1
San Jose 1
Santa Clara 1
Shenzhen 1
St Louis 1
Tampa 1
Trieste 1
Trnava 1
Užice 1
Vista 1
Wachtberg 1
Williamsburg 1
Totale 215
Nome #
Partial trisomy 21 map: Ten cases further supporting the highly restricted Down syndrome critical region (HR-DSCR) on human chromosome 21, file dfe4d22b-a676-bb0a-e053-d805fe0a78d9 143
Biallelic intragenic duplication in ADGRB3 (BAI3) gene associated with intellectual disability, cerebellar atrophy, and behavioral disorder, file dfe4d22b-669c-bb0a-e053-d805fe0a78d9 29
Phenotypic Expansion in Nasu-Hakola Disease: Immunological Findings in Three Patients and Proposal of a Unifying Pathogenic Hypothesis, file dfe4d22b-a677-bb0a-e053-d805fe0a78d9 22
Chromosome 15 structural abnormalities: effect on the IGF1R gene expression and function, file dfe4d228-b7c6-bb0a-e053-d805fe0a78d9 15
Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series, file dfe4d229-e320-bb0a-e053-d805fe0a78d9 9
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant, file dfe4d22b-b2dc-bb0a-e053-d805fe0a78d9 9
Decreased expression of GRAF1/OPHN-1-L in the X-linked alpha thalassemia mental retardation syndrome, file dfe4d227-a3d9-bb0a-e053-d805fe0a78d9 8
Early Motor Delay: An Outstanding, Initial Sign of Osteogenesis Imperfecta Type 1, file dfe4d228-9317-bb0a-e053-d805fe0a78d9 8
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants, file dfe4d229-93e6-bb0a-e053-d805fe0a78d9 8
A Customized Next-Generation Sequencing-Based Panel to Identify Novel Genetic Variants in Dementing Disorders: A Pilot Study, file dfe4d22d-cea6-bb0a-e053-d805fe0a78d9 6
Cryptic deletions are a common finding in "balanced'' reciprocal and complex chromosome rearrangements: A study of 59 patients, file 34f0d2fb-a9e3-4945-b70b-1b512bf3c935 4
Multiple malformations in a patient with unbalanced translocation 46,XY T(7;16) and ambiguous genitalia, file aadde8a9-19fd-47fc-8c16-fcf5e889779c 4
Familial 18q12.2 deletion supports the role of RNA-bindingprotein CELF4 in autism spectrum disorders, file 7d3b35d9-6402-44e4-a455-12d9fe9fa611 3
Balanced complex rearrangements: how many are really balanced?, file dfe4d227-39ba-bb0a-e053-d805fe0a78d9 3
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani, file dfe4d229-dd62-bb0a-e053-d805fe0a78d9 3
Duplication 9p due to unequal sister chromatid exchange, file dfe4d227-157a-bb0a-e053-d805fe0a78d9 2
Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform, file dfe4d227-2f96-bb0a-e053-d805fe0a78d9 2
Principi di genetica generale ed ereditarietà, file dfe4d227-4d20-bb0a-e053-d805fe0a78d9 2
IGF-1R: it is involved in etiopathogenesis of human gonadal abnormalities?, file dfe4d227-605f-bb0a-e053-d805fe0a78d9 2
Dysmegakaryopoietic thrombocytopenia in patients with distal chromosome 11q deletion, file dfe4d227-1ab3-bb0a-e053-d805fe0a78d9 1
B-cell acute lymphoblastic leukemia and isochromosome 7q, file dfe4d227-23ef-bb0a-e053-d805fe0a78d9 1
Mild cystic fibrosis in patients with the rare P5L CFTR mutation, file dfe4d227-2cb6-bb0a-e053-d805fe0a78d9 1
The 11q terminal deletion disorder: A prospective study of 110 cases (p NA), file dfe4d227-3ea0-bb0a-e053-d805fe0a78d9 1
Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders., file dfe4d22a-dff3-bb0a-e053-d805fe0a78d9 1
Small supernumerary marker chromosomes: A legacy of trisomy rescue?, file dfe4d22b-a675-bb0a-e053-d805fe0a78d9 1
Clinical correlates in children with autism spectrum disorder and CNVs: Systematic investigation in a clinical setting, file dfe4d22b-de19-bb0a-e053-d805fe0a78d9 1
Familiar osteopoikilosis: Case report with differential diagnosis and review of the literature, file dfe4d22e-3200-bb0a-e053-d805fe0a78d9 1
Totale 290
Categoria #
all - tutte 803
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 803


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203 0 0 0 0 0 0 0 0 0 0 2 1
2020/202118 1 1 0 0 2 0 2 2 3 0 1 6
2021/202228 2 1 1 2 3 6 0 4 3 2 2 2
2022/2023115 4 0 3 8 20 20 11 9 16 5 15 4
2023/2024125 0 6 7 17 14 32 20 17 7 5 0 0
Totale 290