RAHMAN, SARAH IFFAT
 Distribuzione geografica
Continente #
EU - Europa 257
NA - Nord America 121
AS - Asia 79
SA - Sud America 10
Continente sconosciuto - Info sul continente non disponibili 8
AF - Africa 1
Totale 476
Nazione #
RU - Federazione Russa 182
US - Stati Uniti d'America 119
IT - Italia 54
SG - Singapore 25
VN - Vietnam 20
CN - Cina 18
BR - Brasile 6
GB - Regno Unito 5
HK - Hong Kong 4
IN - India 4
SE - Svezia 4
KR - Corea 3
NL - Olanda 3
JP - Giappone 2
SA - Arabia Saudita 2
AR - Argentina 1
AT - Austria 1
BG - Bulgaria 1
CA - Canada 1
CL - Cile 1
CW - ???statistics.table.value.countryCode.CW??? 1
DE - Germania 1
DZ - Algeria 1
EC - Ecuador 1
FI - Finlandia 1
FR - Francia 1
GT - Guatemala 1
HU - Ungheria 1
IE - Irlanda 1
LU - Lussemburgo 1
OM - Oman 1
PT - Portogallo 1
VE - Venezuela 1
Totale 469
Città #
Moscow 59
Ashburn 22
San Jose 21
Singapore 14
Council Bluffs 12
Naples 9
Milan 8
Hanoi 7
Hefei 6
Rome 5
Hong Kong 4
Santa Clara 4
Viterbo 4
Ho Chi Minh City 3
Houston 3
Los Angeles 3
Padua 3
Remanzacco 3
Seoul 3
Amsterdam 2
Aversa 2
Beijing 2
Bengaluru 2
Castellammare di Stabia 2
Da Nang 2
Dallas 2
Kolkata 2
London 2
North Bergen 2
North Kansas City 2
Afragola 1
Ancona 1
Atlanta 1
Bay Saint Louis 1
Berrouaghia 1
Biên Hòa 1
Boardman 1
Bologna 1
Boynton Beach 1
Braga 1
Brasília 1
Bình Dương 1
Caarapó 1
Campo Grande 1
Caracas 1
Changchun 1
Charlotte 1
Covington 1
Cuenca 1
Dammam 1
Dublin 1
Forlì 1
Frankfurt am Main 1
Giugliano in Campania 1
Guatemala City 1
Helsinki 1
Innisfil 1
Jeddah 1
Ligonier 1
Limeira 1
Luxembourg 1
Manchester 1
Nashville 1
Pagani 1
Palestine 1
Philadelphia 1
Phoenix 1
Phú Thọ 1
Piscataway 1
Pleasant Prairie 1
Porto Alegre 1
Poughkeepsie 1
Quảng Ninh 1
Quận Hai 1
Rafael Castillo 1
Rialto 1
Rimini 1
Rio Grande City 1
Rotterdam 1
San Diego 1
San Giorgio delle Pertiche 1
Santiago 1
Seeb 1
St Louis 1
São Paulo 1
Tam Kỳ 1
Turin 1
Umatilla 1
Vigonza 1
Vũng Tàu 1
Washington 1
Willemstad 1
Totale 277
Nome #
Nanopore Sequencing Solves an Elusive Case of Sotos Syndrome 138
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18) 121
Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From RNU4-2 Variants to Clinical Phenotypes 96
Common Ancestry from Southern Italy: Two Families with Dilated Cardiomyopathy Share the Same Homozygous Loss-of-Function Variant in NRAP 55
Exploring the Genetic Landscape of Psychotic Disorders Using Trio-based Short and Long Reads Sequencing 36
Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases 30
Totale 476
Categoria #
all - tutte 1.338
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 1.338


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/202517 0 0 0 0 0 0 0 0 0 9 1 7
2025/2026332 12 19 16 13 32 165 24 13 12 9 9 8
2026/2027127 11 27 43 46 0 0 0 0 0 0 0 0
Totale 476