IRIS
ANTONACCI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 2.383
EU - Europa 468
AS - Asia 165
AF - Africa 3
SA - Sud America 3
Totale 3.022
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Nazione #
US - Stati Uniti d'America 2.379
SE - Svezia 141
CN - Cina 132
IT - Italia 92
UA - Ucraina 58
DE - Germania 52
GB - Regno Unito 38
FI - Finlandia 36
FR - Francia 26
BE - Belgio 10
IN - India 7
VN - Vietnam 7
RO - Romania 6
CA - Canada 4
HK - Hong Kong 3
CH - Svizzera 2
DZ - Algeria 2
ES - Italia 2
ID - Indonesia 2
JP - Giappone 2
RU - Federazione Russa 2
TH - Thailandia 2
TR - Turchia 2
AR - Argentina 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
CO - Colombia 1
GE - Georgia 1
GH - Ghana 1
LB - Libano 1
LK - Sri Lanka 1
MY - Malesia 1
NL - Olanda 1
PE - Perù 1
PS - Palestinian Territory 1
PT - Portogallo 1
SG - Singapore 1
TW - Taiwan 1
Totale 3.022
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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 58
Beijing 47
Lawrence 44
Roxbury 43
Inglewood 32
Nanjing 32
Des Moines 24
Boardman 19
Strasbourg 19
Falls Church 14
San Diego 14
New York 13
Princeton 12
Grafing 10
London 10
Tianjin 10
Brussels 9
Changsha 9
Hebei 8
Jiaxing 7
Shenyang 7
Dearborn 6
Dong Ket 6
Los Angeles 6
Brooklyn 5
Helsinki 4
Norwalk 4
Paris 4
Redwood City 4
Nanchang 3
Barcelona 2
Haikou 2
Hong Kong 2
Indiana 2
Perugia 2
Pune 2
Quinto Vicentino 2
Rome 2
Santeramo in Colle 2
Tappahannock 2
Toronto 2
Ampang 1
Amsterdam 1
Auburn Hills 1
Bologna 1
Bucharest 1
Bursa 1
Chicago 1
Chiswick 1
Council Bluffs 1
Edinburgh 1
Enfield 1
Fuzhou 1
Ghaziabad 1
Ghent 1
Hanoi 1
Hefei 1
Hialeah 1
Hounslow 1
Hyderabad 1
Islington 1
Jinan 1
Kilburn 1
Kunming 1
Lausanne 1
Laval 1
Le Creusot 1
Montreal 1
Muenster 1
Nashua 1
New Bedfont 1
Novosibirsk 1
Odesa 1
Ouargla 1
Palwal 1
Prescot 1
Ramallah 1
San Francisco 1
Sarajevo 1
Seelze 1
Southwark 1
Taipei 1
Taranto 1
Tokyo 1
Triggiano 1
Washington 1
Zhengzhou 1
Totale 2.494
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Nome #
Characterization of six human disease-associated inversion polymorphisms 127
Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes 122
Inversion variants in human and primate genomes 121
Evolution and diversity of copy number variation in the great ape lineage 115
The birth of a human-specific neural gene by incomplete duplication and gene fusion 104
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility 101
Characterization of missing human genome sequences and copy-number polymorphic insertions 97
Genome-wide characterization of centromeric satellites from multiple mammalian genomes. 97
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk 93
Death and Resurrection of the Human IRGM Gene 90
Hominoid fission of chromosome 14/15 and the role of segmental duplications 85
The evolution and population diversity of human-specific segmental duplications 83
Evolutionary toggling of the MAPT 17q21.31 inversion region. 83
New Insights into Centromere Organization and Evolution from the White-cheeked Gibbon and Marmoset 82
Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication. 80
Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability 79
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. 78
Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses 77
Programmed loss of millions of base pairs from a vertebrate genome 76
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas 76
Diversity of Human Copy Number Variation and Multicopy Genes. 75
null 71
Reconstructing complex regions of genomes using long-read sequencing technology. 68
Discovery of large genomic inversions using long range information. 68
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus 67
Mapping and sequencing of structural variation from eight human genomes 66
Copy Number Variation Analysis in Single-Suture Craniosynostosis: Multiple Rare Variants Including RUNX2 Duplication in Two Cousins With Metopic Craniosynostosis 66
Evolutionary dynamics of the POTE gene family in human and nonhuman primates 64
Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions 63
Personalized copy number and segmental duplication maps using next-generation sequencing 62
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics 60
Evolutionary structural dynamics of macaque chromosome 6 neocentromere 59
Mapping of 5q35 chromosomal rearrangements within a genomically unstable region 49
Evolutionary formation of new centromeres in macaque 48
Discovery and characterization of Human/Great-Ape inversion polymorphisms 45
Unusual 8p inverted duplication deletion with telomere capture from 8q.(*First two authors contributed equally to this work) 41
A high-quality bonobo genome refines the analysis of hominid evolution 36
Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution 34
Recurrent inversion toggling and great ape genome evolution 33
Cytogenetic and array-cgh characterization of a simple case of reciprocal t(3;10) translocation reveals a hidden deletion at 5q12 32
Autosomal Dominant Familial Dyskinesia and Facial Myokymia Single Exome Sequencing Identifies a Mutation in Adenylyl Cyclase 5 31
Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility 30
Structural diversity and African origin of the 17q21.31 inversion polymorphism.(*First two authors contributed equally to this work) 27
Resolving the complexity of the human genome using single-molecule sequencing 23
A high-resolution map of small-scale inversions in the gibbon genome 10
Special issue: A tale of genes and genomes 10
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders 7
Structural Variation Evolution at the 15q11-q13 Disease-Associated Locus 2
A Rare Case of Concurrent 2q34q36 Duplication and 2q37 Deletion in a Neonate with Syndromic Features 2
Totale 3.115
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Categoria #
all - tutte 13.161
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 13.161
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019198 0 0 0 0 0 0 0 0 0 0 105 93
2019/2020851 112 46 22 63 90 58 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
2023/2024206 22 34 14 50 15 37 5 11 13 5 0 0
Totale 3.115