FOXP1mutations cause intellectual disability and a recognizable phenotype

The Role of the FOXP Family of Transcription Factors in ASD

(2013) J. Michael Bowers et al.   DISEASE MARKERS

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

(2012) Michael E. Talkowski et al.   CELL

The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders

(2012) Claire Bacon et al.   HUMAN GENETICS

3p Interstitial Deletion

(2012) Andreea Cristina Ţuţulan-Cuniţă et al.   JOURNAL OF CHILD NEUROLOGY

Meta-analysis of association between PITX3 gene polymorphism and Parkinson's disease

(2012) Lanhua Tang et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Exome sequencing and the genetics of intellectual disability

(2011) S Topper et al.   CLINICAL GENETICS

Endophenotypes of FOXP2: Dysfunction within the human articulatory network

(2011) F. Liégeois et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

(2011) Jillian P. Casey et al.   HUMAN GENETICS

Regulation of MET by FOXP2, Genes Implicated in Higher Cognitive Dysfunction and Autism Risk

(2011) Z. Mukamel et al.   JOURNAL OF NEUROSCIENCE

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

(2011) Brian J O'Roak et al.   NATURE GENETICS

Transcription factor Foxp1 exerts essential cell-intrinsic regulation of the quiescence of naive T cells

(2011) Xiaoming Feng et al.   NATURE IMMUNOLOGY

The involvement of epigenetic defects in mental retardation

(2011) Tamara B. Franklin et al.   NEUROBIOLOGY OF LEARNING AND MEMORY

Evidence Report: Genetic and metabolic testing on children with global developmental delay: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society

(2011) D. J. Michelson et al.   NEUROLOGY

Forkhead transcription factors: key players in health and disease

(2011) Bérénice A. Benayoun et al.   TRENDS IN GENETICS

De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

(2010) Fadi F. Hamdan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

FOXP1 expression and its clinicopathologic significance in nodal and extranodal diffuse large B-cell lymphoma

(2010) BaoHua Yu et al.   ANNALS OF HEMATOLOGY

The genetics of neurodevelopmental disease

(2010) Kevin J Mitchell   CURRENT OPINION IN NEUROBIOLOGY

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

Foxp1 coordinates cardiomyocyte proliferation through both cell-autonomous and nonautonomous mechanisms

(2010) Y. Zhang et al.   GENES & DEVELOPMENT

New genetic associations detected in a host response study to hepatitis B vaccine

(2010) S Davila et al.   GENES AND IMMUNITY

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

(2010) Denise Horn et al.   HUMAN MUTATION

FoxP1 promotes midbrain identity in embryonic stem cell-derived dopamine neurons by regulating Pitx3

(2010) Constantine James Konstantoulas et al.   JOURNAL OF NEUROCHEMISTRY

Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL)

(2010) Andre Franke et al.   NATURE GENETICS

Common variants in FOXP1 are associated with generalized vitiligo

(2010) Ying Jin et al.   NATURE GENETICS

Foxp1 and Lhx1 Coordinate Motor Neuron Migration with Axon Trajectory Choice by Gating Reelin Signalling

(2010) Elena Palmesino et al.   PLOS BIOLOGY

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

(2009) Sonja C Vernes et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

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

The evolution of Fox genes and their role in development and disease

(2009) Sridhar Hannenhalli et al.   NATURE REVIEWS GENETICS

The forkhead transcription factors, Foxp1 and Foxp2, identify different subpopulations of projection neurons in the mouse cerebral cortex

(2009) T. Hisaoka et al.   NEUROSCIENCE

FOXP2 as a molecular window into speech and language

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

Down-regulation of the forkhead transcription factor Foxp1 is required for monocyte differentiation and macrophage function

(2008) C. Shi et al.   BLOOD

Hox Repertoires for Motor Neuron Diversity and Connectivity Gated by a Single Accessory Factor, FoxP1

(2008) Jeremy S. Dasen et al.   CELL

Developmental neuroscience: Hox and Fox

(2008) Samuel L. Pfaff   NATURE

Coordinated Actions of the Forkhead Protein Foxp1 and Hox Proteins in the Columnar Organization of Spinal Motor Neurons

(2008) David L. Rousso et al.   NEURON