Papers authored by Francesca Antonacci
Refreshing results…
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Megan Y. Dennis,
Dennis My,
John Huddleston,
Sudmant Ph,
Peter H. Sudmant ,
Steinberg Km,
Karyn Meltz Steinberg,
Jill A. Rosenfeld ,
Rosenfeld Ja,
Mattia Miroballo,
Tina A. Graves,
Graves Ta,
Laura Vives,
Maika Malig
and 13 other authors
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Mark Chaisson,
Sudmant Ph,
Lawrence Hon,
Peter H. Sudmant ,
Tina A. Graves,
Graves Ta,
Can Alkan,
Richard K. Wilson,
Megan Y. Dennis,
Stephen W. Turner,
Dennis My
and 4 other authors
Reconstructing complex regions of genomes using long-read sequencing technology
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Maika Malig,
Laura Vives,
Eichler Ee,
Evan E. Eichler,
Mario Ventura
Hominoid fission of chromosome 14/15 and the role of segmental duplications
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and 6 other authors
Evolution and diversity of copy number variation in the great ape lineage
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Marco Fichera,
Corrado Romano ,
Jay Shendure ,
Evan E. Eichler
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Peter H. Sudmant ,
Jeffrey M. Kidd,
Catarina D. Campbell,
Laura Vives,
Maika Malig,
Laura Scheinfeldt,
William Beggs,
Muntaser Ibrahim,
Godfrey Lema,
Thomas B. Nyambo,
Sabah A. Omar,
Jean-Marie Bodo,
Alain Froment
and 4 other authors
Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism
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Sudmant Ph,
Francesca Antonacci ,
Tina A. Graves,
Graves Ta,
Mikhail Nefedov,
Jill A. Rosenfeld,
Rosenfeld Ja,
Saba Sajjadian,
Maika Malig,
Holland Kotkiewicz,
Pieter J. de Jong
and 10 other authors
Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication.
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Peter Sudmant ,
Schulte Jh,
Johannes H. Schulte,
Roy Nv,
Nadine Van Roy,
Sarah Vergult,
Patrick G. Buckley,
Buckley Pg,
Paepe Ad
and 9 other authors
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Joseph F. Ryan,
Inna Hughes,
R. Blakesley,
G. Bouffard,
Ryan Jf,
J. McDowell,
B. Maskeri,
Nisc Comparative Sequencing Program,
N. Hansen,
Eichler Ee
and 7 other authors
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Stephen J. O'Brien,
Oliver A. Ryder,
Stefania Purgato,
Monica Zoli,
Giuliano Della Valle,
Evan E. Eichler,
Mario Ventura
Genome-wide characterization of centromeric satellites from multiple mammalian genomes
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Jesse M. Tsai,
Tsai Jm,
Park Ss,
Sarah S. Park,
Hing Av,
Anne V. Hing,
Rieder Mj,
Mark J. Rieder,
Smyth Md,
Matthew D. Smyth,
Speltz Ml
and 5 other authors
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Tina Graves,
Robert Fulton,
Hillary S. Hayden,
Hayden Hs,
Can Alkan,
Maika Malig,
Mario Ventura,
Giuliana Giannuzzi,
Joelle Kallicki,
Paige Anderson,
Yamada Na
and 10 other authors
Characterization of Missing Human Genome Sequences and Copy-number Polymorphic Insertions
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Kidd Jm,
Jeffrey M. Kidd,
Tomas Marques Bonet,
Brian Teague,
Mario Ventura,
Campbell Cd,
Santhosh Girirajan,
Can Alkan,
Rosenfeld Ja,
Catarina D. Campbell,
Laura Vives,
Ballif Bc,
Maika Malig,
Jill A. Rosenfeld
and 11 other authors
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
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Diversity of human copy number variation and multicopy genes
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Priscillia Siswara,
Andy Itsara,
Laura Vives,
Tom Walsh,
Shane E. McCarthy,
Carl Baker,
Heather C. Mefford,
Jeffrey M. Kidd,
Sharon R. Browning,
Brian L. Browning,
Diane E. Dickel
and 45 other authors
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
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Fereydoun Hormozdiari,
Kitzman Jo,
Jacob O. Kitzman,
Carl Baker,
Maika Malig,
Onur Mutlu,
S. Cenk Sahinalp,
S. Cenk Sahinalp
and 4 other authors
Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing
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Eichler Ee,
Evan E. Eichler,
Chris T. Amemiya,
Amemiya Ct
Programmed loss of millions of base pairs from a vertebrate genome
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M. F. Cardone,
G. Della Valle,
M. Malig,
M. Rocchi,
E. E. Eichler,
M. Ventura
New Insights into Centromere Organization and Evolution from the White-Cheeked Gibbon and Marmoset
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Kidd Jm,
Jeffrey M. Kidd,
Tomas Marques-Bonet,
Mario Ventura,
Priscillia Siswara,
Zhaoshi Jiang,
Eichler Ee,
Evan E. Eichler
Characterization of six human disease-associated inversion polymorphisms
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Maria Bruna Leogrande,
Mario Ventura,
Jeffrey M. Kidd,
Priscillia Siswara,
Jonathan C. Howard,
Evan E. Eichler
Death and Resurrection of the Human IRGM Gene
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