BIGONI, Stefania
 Distribuzione geografica
Continente #
NA - Nord America 243
EU - Europa 123
AS - Asia 103
SA - Sud America 10
OC - Oceania 5
Totale 484
Nazione #
US - Stati Uniti d'America 175
CA - Canada 66
CN - Cina 54
IT - Italia 45
FR - Francia 22
TW - Taiwan 14
DE - Germania 12
GB - Regno Unito 12
SA - Arabia Saudita 8
AR - Argentina 7
JP - Giappone 7
CH - Svizzera 6
SE - Svezia 6
AU - Australia 5
IE - Irlanda 5
IN - India 5
KR - Corea 4
PT - Portogallo 4
MO - Macao, regione amministrativa speciale della Cina 3
NL - Olanda 3
AE - Emirati Arabi Uniti 2
DK - Danimarca 2
IR - Iran 2
MX - Messico 2
TH - Thailandia 2
BR - Brasile 1
CL - Cile 1
CO - Colombia 1
CZ - Repubblica Ceca 1
FI - Finlandia 1
GR - Grecia 1
HU - Ungheria 1
ID - Indonesia 1
IS - Islanda 1
RU - Federazione Russa 1
TR - Turchia 1
Totale 484
Città #
Santa Cruz 24
Ferrara 15
Ashburn 14
Cambridge 13
Beijing 10
Fairfield 9
Shanghai 8
Columbus 7
Federal 7
Florence 7
Wilmington 7
Chicago 5
Guangzhou 5
San Diego 5
Boston 4
Chang-hua 4
Changchun 4
Des Moines 4
Stockholm 4
Sursee 4
Yuanlin 4
Dublin 3
Houston 3
Saint-jérôme 3
Seoul 3
Taichung 3
Ann Arbor 2
Bengaluru 2
Bologna 2
Buffalo 2
Cedar Knolls 2
Dallas 2
Dearborn 2
Hefei 2
Jinan 2
Lake Forest 2
Marseille 2
Mohali 2
Nanjing 2
New York 2
Orange 2
Parma 2
Porto 2
Rotterdam 2
Saint Louis 2
Seattle 2
Tokyo 2
Toronto 2
Trebaseleghe 2
Woodbridge 2
Wuhan 2
Xian 2
Aarhus 1
Arlington Heights 1
Atlanta 1
Auerbach 1
Bartlesville 1
Boardman 1
Boulder 1
Bremen 1
Brooklyn 1
Budapest 1
Cork 1
Cuauhtémoc 1
Denver 1
Ellicott City 1
Eskilstuna 1
Este 1
Exeter 1
Falls Church 1
Farmington 1
Ferrara di Monte Baldo 1
Frankfurt Am Main 1
Gammertingen 1
Goole 1
Hangzhou 1
Heidelberg 1
Henderson 1
Jakarta 1
Kunming 1
Lappeenranta 1
Las Vegas 1
Limerick 1
Los Angeles 1
Lübeck 1
Memphis 1
Milpitas 1
Montpellier 1
Montréal 1
Nashville 1
Nigde 1
Odense 1
Ottawa 1
Padova 1
Paris 1
Pavia 1
Perth 1
Pijnacker 1
Poitiers 1
Reykjavík 1
Totale 279
Nome #
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria, file e309ade4-60b4-3969-e053-3a05fe0a2c94 372
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family, file e309ade2-1ad6-3969-e053-3a05fe0a2c94 45
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders, file e309ade0-29ca-3969-e053-3a05fe0a2c94 35
Identification of a new mutation in RSK2, the gene for coffin–lowry syndrome (CLS), in two related patients with mild and atypical phenotypes, file e309ade4-e7f0-3969-e053-3a05fe0a2c94 10
Non-Syndromic Sensorineural Prelingual and Postlingual Hearing Loss due to COL11A1 Gene Mutation, file d9b74b7c-2366-4bf7-b5bb-8b4f3759f921 7
THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder, file 9a940887-3ee1-4936-9897-3b6b3d962ca6 6
PURA-Related Developmental and Epileptic Encephalopathy Phenotypic and Genotypic Spectrum, file e309ade5-2fdd-3969-e053-3a05fe0a2c94 6
A Family with γ-Thalassemia and High Hb A2 Levels, file e309ade1-37e0-3969-e053-3a05fe0a2c94 5
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria, file e309ade4-377a-3969-e053-3a05fe0a2c94 3
Cochlear malformation and sensorineural hearing loss in the Silver-Russell Syndrome, file ed0be48d-c46b-4430-9d8e-ee7706501582 3
Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype, file e309ade2-b8b8-3969-e053-3a05fe0a2c94 2
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype, file db1d604f-07d8-4e67-99f5-3a222263d3a1 1
Universal neonatal screening for sickle cell disease and other haemoglobinopathies in Ferrara, Italy, file e309ade0-446b-3969-e053-3a05fe0a2c94 1
Thyroid function in Rett syndrome, file e309ade0-8dd8-3969-e053-3a05fe0a2c94 1
Unusual father-to-daughter transmission of incontinentia pigmenti due to mosaicism in IP males, file e309ade3-ad15-3969-e053-3a05fe0a2c94 1
Pura syndrome: an emerging neurodevelopmental disorder, file e309ade4-8ee6-3969-e053-3a05fe0a2c94 1
Auditory Neuropathy Spectrum Disorder in the White Sutton Syndrome, file f60f9424-0f8a-4d5d-bda9-b2408c44036e 1
Totale 500
Categoria #
all - tutte 1.532
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 1.532


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201 0 1 0 0 0 0 0 0 0 0 0 0
2020/20217 0 0 0 1 0 0 0 0 2 3 1 0
2021/2022354 0 8 34 29 25 40 48 49 52 29 27 13
2022/202370 1 3 16 12 6 6 5 2 2 2 11 4
2023/202468 2 3 22 1 5 8 0 5 2 6 14 0
Totale 500