HAY MELE, Bruno
 Distribuzione geografica
Continente #
EU - Europa 187
AS - Asia 126
NA - Nord America 65
SA - Sud America 13
Totale 391
Nazione #
RU - Federazione Russa 116
US - Stati Uniti d'America 63
SG - Singapore 51
CN - Cina 31
IT - Italia 26
HK - Hong Kong 20
IE - Irlanda 19
BR - Brasile 12
FR - Francia 9
IN - India 7
KR - Corea 6
VN - Vietnam 6
DE - Germania 5
NL - Olanda 5
CA - Canada 2
GB - Regno Unito 2
PK - Pakistan 2
AT - Austria 1
BD - Bangladesh 1
BE - Belgio 1
JO - Giordania 1
JP - Giappone 1
LT - Lituania 1
NO - Norvegia 1
PE - Perù 1
PL - Polonia 1
Totale 391
Città #
Moscow 36
Singapore 23
Hong Kong 20
Dublin 19
Santa Clara 17
Hefei 12
Ashburn 11
Seoul 6
Amsterdam 5
Caserta 5
New York 5
Paris 5
Viterbo 5
Aversa 4
Bengaluru 4
Beijing 3
Bắc Ninh 3
Dallas 3
Delhi 3
Falkenstein 3
Los Angeles 3
Boydton 2
Capua 2
Massa Lubrense 2
Naples 2
Pomigliano d'Arco 2
São Paulo 2
Toronto 2
Amman 1
Angelina 1
Boardman 1
Bremen 1
Brooklyn 1
Brussels 1
Cabo Frio 1
Cajazeiras 1
Can Tho 1
Changsha 1
Clifton 1
Contagem 1
Curitiba 1
Dadu 1
Dhaka 1
Duque de Caxias 1
Espírito Santo do Pinhal 1
Frankfurt am Main 1
Guarulhos 1
Haiphong 1
Ipubi 1
Islamabad 1
Makhachkala 1
Manchester 1
Marseille 1
Oslo 1
Piscataway 1
Pouso Alegre 1
Pozzuoli 1
Quận Một 1
Roubaix 1
Sanmenxia 1
Santa Maria Capua Vetere 1
Succivo 1
Tokyo 1
Vienna 1
Warsaw 1
Totale 246
Nome #
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 92
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances 84
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex 84
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 75
Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances 34
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans 29
Totale 398
Categoria #
all - tutte 1.448
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 1.448


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202338 0 0 0 2 4 1 1 1 16 0 8 5
2023/202428 4 0 1 3 5 9 0 0 0 0 2 4
2024/202595 0 4 0 5 13 15 11 13 19 8 6 1
2025/2026237 18 28 20 9 76 86 0 0 0 0 0 0
Totale 398