Author

Antonio Benítez-Burraco

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Evolutionary Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Research Focus:host-pathogen & immune response· 1 Organism:non-human primate· 1

Frequent Co-Authors

Carles Lalueza-Fox· 1 shared Isabel Espejo-Portero· 1 shared Ma Salud Jiménez-Romero· 1 shared Montserrat Barcos-Martínez· 1 shared Paloma García-Bellido· 1 shared Pere Gelabert Xirinachs· 1 shared Raúl Torres-Ruiz· 1 shared Sandra Rodríguez-Perales· 1 shared

Activity by Year

2016-2017 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 13 mutual co-author links

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1 shared paperEvolutionary Biology

Carles Lalueza-Fox

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2 papers

Recent·Most cited

Evolutionary BiologybioRxivPreprintJun 28, 2017

Human-specific changes in two functional enhancers of FOXP2

Antonio Benítez-Burraco, Raúl Torres-Ruiz, Pere Gelabert Xirinachs…·Paloma García-Bellido

The paper identifies human-specific changes in two FOXP2 enhancers that may alter FOXP2 expression patterns compared to extinct hominins.

DOI 10.1101/157016

humannon-human primate

𝕏 PostBluesky

NeurosciencebioRxivPreprintApr 6, 2016

Language impairment resulting from a de novo deletion of 7q32.1-q33: a case report

Ma Salud Jiménez-Romero, Montserrat Barcos-Martínez, Isabel Espejo-Portero, Antonio Benítez-Burraco

This paper reports a case of language impairment caused by a de novo deletion in chromosome 7q32.1-q33, affecting genes related to brain development and language disorders.

DOI 10.1101/047241

𝕏 PostBluesky