Francesca Antonacci
Francesca Antonacci
Verified email at uniba.it
Title
Cited by
Cited by
Year
Mapping and sequencing of structural variation from eight human genomes
JM Kidd, GM Cooper, WF Donahue, HS Hayden, N Sampas, T Graves, ...
Nature 453 (7191), 56-64, 2008
12872008
Personalized copy number and segmental duplication maps using next-generation sequencing
C Alkan, JM Kidd, T Marques-Bonet, G Aksay, F Antonacci, F Hormozdiari, ...
Nature genetics 41 (10), 1061-1067, 2009
8162009
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
6482010
Resolving the complexity of the human genome using single-molecule sequencing
MJP Chaisson, J Huddleston, MY Dennis, PH Sudmant, M Malig, ...
Nature, 2014
6112014
A recurrent 16p12. 1 microdeletion supports a two-hit model for severe developmental delay
S Girirajan, JA Rosenfeld, GM Cooper, F Antonacci, P Siswara, A Itsara, ...
Nature genetics 42 (3), 203-209, 2010
5642010
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication
MY Dennis, X Nuttle, PH Sudmant, F Antonacci, TA Graves, M Nefedov, ...
Cell 149 (4), 912-922, 2012
3532012
Reconstructing complex regions of genomes using long-read sequencing technology
J Huddleston, S Ranade, M Malig, F Antonacci, M Chaisson, L Hon, ...
Genome research 24 (4), 688-696, 2014
2342014
Evolutionary toggling of the MAPT 17q21. 31 inversion region
MC Zody, Z Jiang, HC Fung, F Antonacci, LDW Hillier, MF Cardone, ...
Nature genetics 40 (9), 1076-1083, 2008
1672008
Characterization of missing human genome sequences and copy-number polymorphic insertions
JM Kidd, N Sampas, F Antonacci, T Graves, R Fulton, HS Hayden, ...
Nature methods 7 (5), 365-371, 2010
1532010
Programmed loss of millions of base pairs from a vertebrate genome
JJ Smith, F Antonacci, EE Eichler, CT Amemiya
Proceedings of the National Academy of Sciences 106 (27), 11212-11217, 2009
1392009
Evolutionary formation of new centromeres in macaque
M Ventura, F Antonacci, MF Cardone, R Stanyon, P D'Addabbo, ...
Science 316 (5822), 243-246, 2007
1352007
Characterization of six human disease-associated inversion polymorphisms
F Antonacci, JM Kidd, T Marques-Bonet, M Ventura, P Siswara, Z Jiang, ...
Human molecular genetics 18 (14), 2555-2566, 2009
1312009
Evolution and diversity of copy number variation in the great ape lineage
PH Sudmant, J Huddleston, CR Catacchio, M Malig, LDW Hillier, C Baker, ...
Genome research 23 (9), 1373-1382, 2013
1252013
Death and resurrection of the human IRGM gene
C Bekpen, T Marques-Bonet, C Alkan, F Antonacci, MB Leogrande, ...
PLoS genetics 5 (3), e1000403, 2009
1192009
Structural diversity and African origin of the 17q21. 31 inversion polymorphism
KM Steinberg, F Antonacci, PH Sudmant, JM Kidd, CD Campbell, L Vives, ...
Nature genetics 44 (8), 872-880, 2012
1092012
A large and complex structural polymorphism at 16p12. 1 underlies microdeletion disease risk
F Antonacci, JM Kidd, T Marques-Bonet, B Teague, M Ventura, S Girirajan, ...
Nature genetics 42 (9), 745-750, 2010
1002010
Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5
YZ Chen, MM Matsushita, P Robertson, M Rieder, S Girirajan, F Antonacci, ...
Archives of neurology 69 (5), 630-635, 2012
962012
Genome-wide characterization of centromeric satellites from multiple mammalian genomes
C Alkan, MF Cardone, CR Catacchio, F Antonacci, SJ O'Brien, OA Ryder, ...
Genome research 21 (1), 137-145, 2011
932011
Palindromic GOLGA8 core duplicons promote chromosome 15q13. 3 microdeletion and evolutionary instability
F Antonacci, MY Dennis, J Huddleston, PH Sudmant, KM Steinberg, ...
Nature genetics 46 (12), 1293-1302, 2014
832014
Copy number variation analysis in single‐suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis
HC Mefford, N Shafer, F Antonacci, JM Tsai, SS Park, AV Hing, MJ Rieder, ...
American Journal of Medical Genetics Part A 152 (9), 2203-2210, 2010
822010
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