Foxp2 regulates anatomical features that may be relevant for vocal behaviors and bipedal locomotion

Phonological working memory and FOXP2

(2018) Katrin Schulze et al.   NEUROPSYCHOLOGIA

Hip extensor mechanics and the evolution of walking and climbing capabilities in humans, apes, and fossil hominins

(2018) Elaine E. Kozma et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The evolution of modern human brain shape

(2018) Simon Neubauer et al.   Science Advances

Foxp1 regulation of neonatal vocalizations via cortical development

(2017) Noriyoshi Usui et al.   GENES & DEVELOPMENT

Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization

(2017) Henning Fröhlich et al.   HUMAN MOLECULAR GENETICS

Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders

(2017) Elliot Sollis et al.   HUMAN MUTATION

FOXP1 controls mesenchymal stem cell commitment and senescence during skeletal aging

(2017) Hanjun Li et al.   JOURNAL OF CLINICAL INVESTIGATION

Speech and Language: Translating the Genome

(2017) Pelagia Deriziotis et al.   TRENDS IN GENETICS

Insights into the Neural and Genetic Basis of Vocal Communication

(2016) Genevieve Konopka et al.   CELL

Mice produce ultrasonic vocalizations by intra-laryngeal planar impinging jets

(2016) Elena Mahrt et al.   CURRENT BIOLOGY

Ultrasonic vocalizations of adult maleFoxp2-mutant mice: behavioral contexts of arousal and emotion

(2016) S. Gaub et al.   GENES BRAIN AND BEHAVIOR

FOXP2variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

(2016) Miriam S Reuter et al.   JOURNAL OF MEDICAL GENETICS

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

(2016) Sara B. Estruch et al.   Journal of Neurodevelopmental Disorders

Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c

(2016) Yi-Chuan Chen et al.   NATURE NEUROSCIENCE

A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice

(2016) Jonathan Chabout et al.   Frontiers in Behavioral Neuroscience

Foxp1/2/4 regulate endochondral ossification as a suppresser complex

(2015) Haixia Zhao et al.   DEVELOPMENTAL BIOLOGY

Identification and functional characterization ofde novo FOXP1variants provides novel insights into the etiology of neurodevelopmental disorder

(2015) Elliot Sollis et al.   HUMAN MOLECULAR GENETICS

Osteogenesis and neurogenesis: a robust link also for language evolution

(2015) Cedric Boeckx et al.   Frontiers in Cellular Neuroscience

Universal mechanisms of sound production and control in birds and mammals

(2015) C.P.H Elemans et al.   Nature Communications

What can mice tell us about Foxp2 function?

(2014) Catherine A French et al.   CURRENT OPINION IN NEUROBIOLOGY

Specific expression of FOXP2 in cerebellum improves ultrasonic vocalization in heterozygous but not in homozygous Foxp2 (R552H) knock-in pups

(2014) Eriko Fujita-Jimbo et al.   NEUROSCIENCE LETTERS

Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance

(2014) Christiane Schreiweis et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

(2013) Samantha J Turner et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Diminished FoxP2 Levels Affect Dopaminergic Modulation of Corticostriatal Signaling Important to Song Variability

(2013) Malavika Murugan et al.   NEURON

Foxp2 Mutations Impair Auditory-Motor Association Learning

(2012) Simone Kurt et al.   PLoS One

Phenotype of FOXP2 haploinsufficiency in a mother and son

(2011) Gregory M. Rice et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Subglottal pressure, tracheal airflow, and intrinsic laryngeal muscle activity during rat ultrasound vocalization

(2011) Tobias Riede   JOURNAL OF NEUROPHYSIOLOGY

An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning

(2011) C A French et al.   MOLECULAR PSYCHIATRY

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

(2011) Sonja C. Vernes et al.   PLoS Genetics

Chiari I malformation, delayed gross motor skills, severe speech delay and epileptiform discharges in a child with FOXP1 haploinsufficiency

(2010) Christopher W Carr et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Knockdown of FoxP2 alters spine density in Area X of the zebra finch

(2010) S. B. Schulz et al.   GENES BRAIN AND BEHAVIOR

A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice

(2009) Wolfgang Enard et al.   CELL

A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis

(2009) Mitchel J. Pariani et al.   European Journal of Medical Genetics

Human-specific transcriptional regulation of CNS development genes by FOXP2

(2009) Genevieve Konopka et al.   NATURE

FOXP2 as a molecular window into speech and language

(2009) Simon E. Fisher et al.   TRENDS IN GENETICS

Evolution of human vocal production

(2008) Asif A. Ghazanfar et al.   CURRENT BIOLOGY

Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits

(2008) Matthias Groszer et al.   CURRENT BIOLOGY

Birdsong Decreases Protein Levels of FoxP2, a Molecule Required for Human Speech

(2008) Julie E. Miller et al.   JOURNAL OF NEUROPHYSIOLOGY

The Timing of Selection at the Human FOXP2 Gene

(2008) Graham Coop et al.   MOLECULAR BIOLOGY AND EVOLUTION

Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

(2008) E. Fujita et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA