DI STAZIO, MARIATERESA
 Distribuzione geografica
Continente #
NA - Nord America 486
EU - Europa 164
AS - Asia 101
AF - Africa 12
OC - Oceania 2
SA - Sud America 2
Totale 767
Nazione #
US - Stati Uniti d'America 481
IT - Italia 66
CN - Cina 65
FR - Francia 40
NL - Olanda 11
ID - Indonesia 10
VN - Vietnam 10
ZA - Sudafrica 10
PL - Polonia 8
RU - Federazione Russa 8
UA - Ucraina 8
DE - Germania 6
CA - Canada 5
CZ - Repubblica Ceca 5
GB - Regno Unito 4
JP - Giappone 4
FI - Finlandia 3
HK - Hong Kong 3
AT - Austria 2
CL - Cile 2
IR - Iran 2
KR - Corea 2
NZ - Nuova Zelanda 2
TW - Taiwan 2
BE - Belgio 1
CM - Camerun 1
DK - Danimarca 1
IN - India 1
NO - Norvegia 1
PK - Pakistan 1
SN - Senegal 1
TR - Turchia 1
Totale 767
Città #
Ashburn 61
Fairfield 53
Beijing 44
Houston 35
Santa Cruz 35
Buffalo 33
Cambridge 25
Trieste 25
Seattle 20
Wilmington 20
Woodbridge 17
Ann Arbor 10
Dong Ket 10
Bologna 9
Paris 9
Warsaw 8
Boardman 7
Las Vegas 7
Mountain View 7
Cape Town 6
Redmond 6
Harmelen 4
Muizenberg 4
Riva 4
San Diego 4
Tucson 4
University Park 4
Venezia 4
Wuhan 4
Chicago 3
Clearwater 3
Des Moines 3
Henderson 3
Los Angeles 3
Miami 3
Ottawa 3
Phoenix 3
Saint Petersburg 3
Barletta 2
Chions 2
Dallas 2
Fairfax Station 2
Helsinki 2
Lake Forest 2
Livingston 2
Milan 2
New York 2
Rho 2
Shanghai 2
Sunnyvale 2
Taipei 2
Tokyo 2
Victoria 2
Wellington 2
Austin 1
Bremen 1
Brussels 1
Casalbordino 1
Cedar Knolls 1
Chongqing 1
City of Westminster 1
Council Bluffs 1
Crugers 1
Dakar 1
Dresden 1
Easton 1
Florence 1
Forlì 1
Gilleleje 1
Grenoble 1
Groningen 1
Guwahati 1
Hangzhou 1
Herndon 1
Incheon 1
Islington 1
Istanbul 1
Karachi 1
Kawagoe 1
Kenmore 1
Langen 1
Lappeenranta 1
Lutzingen 1
Lviv 1
Milpitas 1
Montpellier 1
Moscow 1
Nashville 1
Park Ridge 1
Peoria 1
Portland 1
Redwood City 1
Roermond 1
Rome 1
San Francisco 1
San Jose 1
Scranton 1
Seongnam-si 1
Suita 1
Trondheim 1
Totale 584
Nome #
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss, file e2913fda-b346-f688-e053-3705fe0a67e0 139
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss, file e2913fdc-822b-f688-e053-3705fe0a67e0 138
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss, file e2913fdc-7405-f688-e053-3705fe0a67e0 131
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss, file e2913fda-70dd-f688-e053-3705fe0a67e0 127
New age-related hearing loss candidate genes in humans: an ongoing challenge, file e2913fdd-7e8b-f688-e053-3705fe0a67e0 51
New age-related hearing loss candidate genes in humans: an ongoing challenge, file e2913fdd-90a5-f688-e053-3705fe0a67e0 49
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders, file a0645099-df64-4da6-95bb-160f5aece7ac 37
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss, file e2913fda-7da3-f688-e053-3705fe0a67e0 36
Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique, file e2913fde-86f8-f688-e053-3705fe0a67e0 22
Identification of a New Mutation in RSK2, the Gene for Coffin–Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes, file e2913fde-e2b5-f688-e053-3705fe0a67e0 16
What Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian Study, file 303cb7b4-7501-4d14-9fa5-0bb2de6b6741 14
A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family, file e2913fd9-48de-f688-e053-3705fe0a67e0 11
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders, file 1387fba6-ea05-4eeb-808b-7853c0d1c109 10
New age-related hearing loss candidate genes in humans: an ongoing challenge, file e2913fdd-7e66-f688-e053-3705fe0a67e0 4
New age-related hearing loss candidate genes in humans: an ongoing challenge, file e2913fdd-9ec1-f688-e053-3705fe0a67e0 3
Clinical and genetic aspects Bernard-Soulier syndrome: searching for genotype/phenotype correlations., file e2913fd9-048a-f688-e053-3705fe0a67e0 2
Mutations in the 5′ UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2, file e2913fda-2f23-f688-e053-3705fe0a67e0 1
TBL1Y: a new gene involved in syndromic hearing loss, file e2913fdc-cd85-f688-e053-3705fe0a67e0 1
Totale 792
Categoria #
all - tutte 1.801
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 1.801


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201963 0 0 0 0 0 0 0 0 0 19 21 23
2019/2020147 15 10 11 20 14 14 13 9 17 8 10 6
2020/202191 8 7 6 7 13 9 10 8 4 7 6 6
2021/2022122 4 5 9 9 9 7 8 5 8 8 34 16
2022/2023147 8 4 26 15 7 13 16 9 9 18 20 2
2023/2024175 6 2 14 7 10 54 27 35 12 8 0 0
Totale 792