RAHMAN, SARAH IFFAT
 Distribuzione geografica
Continente #
EU - Europa 227
AS - Asia 77
NA - Nord America 54
SA - Sud America 9
Continente sconosciuto - Info sul continente non disponibili 7
AF - Africa 1
Totale 375
Nazione #
RU - Federazione Russa 182
US - Stati Uniti d'America 53
IT - Italia 28
SG - Singapore 25
VN - Vietnam 20
CN - Cina 18
BR - Brasile 6
HK - Hong Kong 4
SE - Svezia 4
GB - Regno Unito 3
KR - Corea 3
NL - Olanda 3
IN - India 2
JP - Giappone 2
SA - Arabia Saudita 2
AR - Argentina 1
AT - Austria 1
BG - Bulgaria 1
CA - Canada 1
CL - Cile 1
DE - Germania 1
DZ - Algeria 1
EC - Ecuador 1
FI - Finlandia 1
FR - Francia 1
IE - Irlanda 1
OM - Oman 1
PT - Portogallo 1
Totale 368
Città #
Moscow 59
Singapore 14
San Jose 12
Ashburn 11
Naples 9
Hanoi 7
Hefei 6
Hong Kong 4
Viterbo 4
Ho Chi Minh City 3
Los Angeles 3
Seoul 3
Amsterdam 2
Aversa 2
Beijing 2
Bengaluru 2
Castellammare di Stabia 2
Council Bluffs 2
Da Nang 2
Houston 2
London 2
North Kansas City 2
Atlanta 1
Berrouaghia 1
Biên Hòa 1
Boardman 1
Braga 1
Brasília 1
Bình Dương 1
Caarapó 1
Campo Grande 1
Changchun 1
Cuenca 1
Dallas 1
Dammam 1
Dublin 1
Frankfurt am Main 1
Giugliano in Campania 1
Helsinki 1
Innisfil 1
Jeddah 1
Ligonier 1
Limeira 1
Manchester 1
Milan 1
Nashville 1
Padua 1
Pagani 1
Palestine 1
Philadelphia 1
Phoenix 1
Phú Thọ 1
Piscataway 1
Porto Alegre 1
Quảng Ninh 1
Quận Hai 1
Rafael Castillo 1
Rialto 1
Rotterdam 1
San Diego 1
Santa Clara 1
Santiago 1
Seeb 1
St Louis 1
São Paulo 1
Tam Kỳ 1
Vũng Tàu 1
Totale 200
Nome #
Nanopore Sequencing Solves an Elusive Case of Sotos Syndrome 126
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18) 109
Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From RNU4-2 Variants to Clinical Phenotypes 82
Common Ancestry from Southern Italy: Two Families with Dilated Cardiomyopathy Share the Same Homozygous Loss-of-Function Variant in NRAP 35
Exploring the Genetic Landscape of Psychotic Disorders Using Trio-based Short and Long Reads Sequencing 13
Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases 10
Totale 375
Categoria #
all - tutte 987
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 987


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
2026/202726 11 15 0 0 0 0 0 0 0 0 0 0
Totale 375