Ponzi, Emanuela
 Distribuzione geografica
Continente #
NA - Nord America 283
EU - Europa 257
AS - Asia 91
SA - Sud America 11
AF - Africa 1
Totale 643
Nazione #
US - Stati Uniti d'America 281
DE - Germania 84
SG - Singapore 48
IT - Italia 32
SE - Svezia 29
UA - Ucraina 29
CN - Cina 23
FR - Francia 21
GB - Regno Unito 15
FI - Finlandia 13
BR - Brasile 11
IE - Irlanda 11
RU - Federazione Russa 10
PL - Polonia 7
ID - Indonesia 6
IN - India 6
HK - Hong Kong 3
BE - Belgio 2
CA - Canada 1
GR - Grecia 1
IL - Israele 1
IQ - Iraq 1
IS - Islanda 1
KZ - Kazakistan 1
LK - Sri Lanka 1
ML - Mali 1
MX - Messico 1
NL - Olanda 1
RO - Romania 1
TH - Thailandia 1
Totale 643
Città #
Chandler 67
Singapore 21
Ann Arbor 18
Ashburn 17
Jacksonville 14
New York 14
San Mateo 12
Dublin 11
Moscow 7
Detroit 6
Helsinki 6
Jakarta 6
Nanjing 6
Seattle 6
Wilmington 6
Woodbridge 6
Boston 5
Dearborn 5
Florence 5
Houston 5
Lawrence 5
Marseille 5
Boardman 4
Cattolica 4
Frankfurt am Main 4
Fremont 4
Lancaster 4
Nanchang 4
Norwalk 4
Nürnberg 4
Warsaw 4
Rome 3
Bari 2
Besana in Brianza 2
Boulder 2
Brussels 2
Campinas 2
Castel Maggiore 2
Fairfield 2
Formigine 2
Guidonia 2
Hong Kong 2
Los Angeles 2
Polska 2
Portsmouth 2
Redwood City 2
Roubaix 2
Shenyang 2
Turku 2
Almaty 1
Amsterdam 1
Athens 1
Bamako 1
Bay Shore 1
Beijing 1
Bexley 1
Boa Vista 1
Buffalo 1
Chennai 1
Colombo 1
Contagem 1
Currais Novos 1
Dalian 1
Duhok 1
Düsseldorf 1
Formosa 1
Goiana 1
Gravataí 1
Gunzenhausen 1
Ha Kwai Chung 1
Indiana 1
Kilburn 1
Kunming 1
Lauterbourg 1
Leawood 1
Leeds 1
Linhares 1
Magé 1
Milan 1
Monmouth Junction 1
Mountain View 1
Napoli 1
Nuremberg 1
Palermo 1
Paris 1
Phoenix 1
Princeton 1
Providence 1
Pune 1
Richmond 1
San Diego 1
San Fernando 1
Santa Clara 1
Simi Valley 1
Tappahannock 1
Tel Aviv 1
Termoli 1
Toronto 1
Velikiy Novgorod 1
Totale 376
Nome #
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 138
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype 124
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients 115
The ring 14 syndrome 113
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype. 93
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype. 74
Totale 657
Categoria #
all - tutte 2.513
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 2.513


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20208 0 0 0 0 0 0 0 0 0 0 0 8
2020/202155 4 8 1 6 9 0 4 0 7 4 12 0
2021/202253 3 4 0 6 2 1 0 12 3 4 5 13
2022/2023144 22 21 9 23 5 23 5 11 15 0 4 6
2023/202475 1 16 1 12 1 21 3 0 0 1 8 11
2024/2025112 6 4 7 1 15 8 2 3 24 13 20 9
Totale 657