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Francesca Antonacci

Francesca Antonacci,University of Washington,Genetics & Genealogy,Molecular Biology,Evolutionary Studies

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Francesca Antonacci

University of Washington

Publications: 19 | Citations: 558

Fields: Genetics & Genealogy, Molecular Biology, Evolutionary Studies

Collaborated with 186 co-authors from 2005 to 2011 | Cited by 3347 authors

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Publications (19)

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Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses

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Journal: BMC Evolutionary Biology - BMC EVOL BIOL , vol. 11, no. 1, pp. 23-18, 2011

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay (Citations: 49)

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Journal: Nature Genetics - NAT GENET , vol. 42, no. 3, pp. 203-209, 2010

Characterization of missing human genome sequences and copy-number polymorphic insertions (Citations: 19)

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Journal: Nature Methods - NAT METHODS , vol. 7, no. 5, pp. 365-371, 2010

Diversity of Human Copy Number Variation and Multicopy Genes (Citations: 6)

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Journal: Science , vol. 330, 2010

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk (Citations: 5)

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Journal: Nature Genetics - NAT GENET , vol. 42, no. 9, pp. 745-750, 2010

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Citations (558 times by 494 publications)

Insights into hominid evolution from the gorilla genome sequence

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Journal: Nature , vol. 483, no. 7388, pp. 169-175, 2012

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

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Journal: PLOS Genetics - PLOS GENET , vol. 8, no. 2, 2012

Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans

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Journal: PLOS Biology - PLOS BIOL , vol. 10, no. 3, 2012

Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3

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Journal: PLOS Genetics - PLOS GENET , vol. 8, no. 5, 2012

Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics

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Journal: European Journal of Human Genetics - EUR J HUMAN GENET , vol. 20, no. 2, pp. 161-165, 2012

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