IRIS
ANTONACCI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 2.432
EU - Europa 544
AS - Asia 268
AF - Africa 4
SA - Sud America 3
Totale 3.251
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Nazione #
US - Stati Uniti d'America 2.427
CN - Cina 162
SE - Svezia 141
IT - Italia 111
SG - Singapore 74
DE - Germania 60
UA - Ucraina 59
GB - Regno Unito 39
FI - Finlandia 38
RU - Federazione Russa 37
FR - Francia 27
BE - Belgio 10
IN - India 7
VN - Vietnam 7
RO - Romania 6
CA - Canada 5
CZ - Repubblica Ceca 5
HK - Hong Kong 3
CH - Svizzera 2
DZ - Algeria 2
ES - Italia 2
ID - Indonesia 2
JP - Giappone 2
LT - Lituania 2
NL - Olanda 2
TH - Thailandia 2
TR - Turchia 2
AR - Argentina 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
CO - Colombia 1
DK - Danimarca 1
GE - Georgia 1
GH - Ghana 1
LB - Libano 1
LK - Sri Lanka 1
MY - Malesia 1
PE - Perù 1
PS - Palestinian Territory 1
PT - Portogallo 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 3.251
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Città #
Fairfield 356
Chandler 234
Woodbridge 229
Ashburn 172
Houston 168
Seattle 153
Cambridge 136
Jacksonville 134
Wilmington 127
Ann Arbor 120
Nyköping 114
Bari 60
Singapore 52
Beijing 48
Lawrence 44
Roxbury 43
Inglewood 32
Nanjing 32
Des Moines 24
Boardman 22
Strasbourg 19
Falls Church 14
San Diego 14
New York 13
Princeton 12
London 11
Tianjin 11
Changsha 10
Grafing 10
Grottaglie 10
Brussels 9
Hebei 8
Jiaxing 7
Los Angeles 7
Shenyang 7
Dearborn 6
Dong Ket 6
Helsinki 6
Brno 5
Brooklyn 5
Santa Clara 5
Norwalk 4
Paris 4
Redwood City 4
Hefei 3
Nanchang 3
Nuremberg 3
Toronto 3
Amsterdam 2
Barcelona 2
Frankfurt am Main 2
Guangzhou 2
Haikou 2
Hangzhou 2
Hong Kong 2
Indiana 2
Jinan 2
Munich 2
Perugia 2
Pune 2
Quinto Vicentino 2
Rome 2
Santeramo in Colle 2
Shijiazhuang 2
Tappahannock 2
Ampang 1
Auburn Hills 1
Bologna 1
Bucharest 1
Bursa 1
Chicago 1
Chiswick 1
Copenhagen 1
Council Bluffs 1
Edinburgh 1
Enfield 1
Fuzhou 1
Ghaziabad 1
Ghent 1
Hanoi 1
Hialeah 1
Hounslow 1
Hyderabad 1
Islington 1
Kilburn 1
Kunming 1
Lausanne 1
Lauterbourg 1
Laval 1
Le Creusot 1
Lishui 1
Montreal 1
Muenster 1
Nashua 1
New Bedfont 1
Newark 1
Novosibirsk 1
Odesa 1
Ouargla 1
Palwal 1
Totale 2.588
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Nome #
Characterization of six human disease-associated inversion polymorphisms 130
Inversion variants in human and primate genomes 130
Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes 130
Evolution and diversity of copy number variation in the great ape lineage 122
The birth of a human-specific neural gene by incomplete duplication and gene fusion 106
Characterization of missing human genome sequences and copy-number polymorphic insertions 105
Genome-wide characterization of centromeric satellites from multiple mammalian genomes. 105
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility 105
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk 100
Death and Resurrection of the Human IRGM Gene 94
Hominoid fission of chromosome 14/15 and the role of segmental duplications 90
Evolutionary toggling of the MAPT 17q21.31 inversion region. 88
The evolution and population diversity of human-specific segmental duplications 86
Evolutionary dynamics of the POTE gene family in human and nonhuman primates 86
New Insights into Centromere Organization and Evolution from the White-cheeked Gibbon and Marmoset 85
Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication. 85
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. 82
Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability 82
Programmed loss of millions of base pairs from a vertebrate genome 80
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas 80
Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses 79
Diversity of Human Copy Number Variation and Multicopy Genes. 79
null 72
Discovery of large genomic inversions using long range information. 72
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus 72
Copy Number Variation Analysis in Single-Suture Craniosynostosis: Multiple Rare Variants Including RUNX2 Duplication in Two Cousins With Metopic Craniosynostosis 71
Reconstructing complex regions of genomes using long-read sequencing technology. 69
Mapping and sequencing of structural variation from eight human genomes 68
Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions 67
Personalized copy number and segmental duplication maps using next-generation sequencing 63
Evolutionary structural dynamics of macaque chromosome 6 neocentromere 62
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics 62
Evolutionary formation of new centromeres in macaque 53
Mapping of 5q35 chromosomal rearrangements within a genomically unstable region 51
Discovery and characterization of Human/Great-Ape inversion polymorphisms 50
A high-quality bonobo genome refines the analysis of hominid evolution 49
Unusual 8p inverted duplication deletion with telomere capture from 8q.(*First two authors contributed equally to this work) 44
Recurrent inversion toggling and great ape genome evolution 44
Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution 44
Cytogenetic and array-cgh characterization of a simple case of reciprocal t(3;10) translocation reveals a hidden deletion at 5q12 39
Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility 38
Autosomal Dominant Familial Dyskinesia and Facial Myokymia Single Exome Sequencing Identifies a Mutation in Adenylyl Cyclase 5 35
Structural diversity and African origin of the 17q21.31 inversion polymorphism.(*First two authors contributed equally to this work) 29
Resolving the complexity of the human genome using single-molecule sequencing 27
A high-resolution map of small-scale inversions in the gibbon genome 23
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders 13
Special issue: A tale of genes and genomes 13
A Rare Case of Concurrent 2q34q36 Duplication and 2q37 Deletion in a Neonate with Syndromic Features 10
Structural Variation Evolution at the 15q11-q13 Disease-Associated Locus 5
Totale 3.374
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Categoria #
all - tutte 16.257
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 16.257
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020460 0 0 0 0 0 0 94 104 109 56 75 22
2020/2021502 48 23 58 18 30 34 48 34 65 67 47 30
2021/2022384 9 66 6 3 30 24 25 16 29 33 65 78
2022/2023610 64 82 29 49 82 92 7 73 97 5 13 17
2023/2024224 22 34 14 50 15 37 5 11 13 5 6 12
2024/2025241 24 30 64 24 24 68 7 0 0 0 0 0
Totale 3.374