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

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

(2012) Michael E. Talkowski et al.   CELL

CNTNAP2variants affect early language development in the general population

(2012) A. J. O. Whitehouse et al.   GENES BRAIN AND BEHAVIOR

Forkhead box protein p1 is a transcriptional repressor of immune signaling in the CNS: implications for transcriptional dysregulation in Huntington disease

(2012) Bin Tang et al.   HUMAN MOLECULAR GENETICS

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

(2011) Anne Gregor et al.   BMC Medical Genetics

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

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

MicroRNA miR-9 Modifies Motor Neuron Columns by a Tuning Regulation of FoxP1 Levels in Developing Spinal Cords

(2011) G. Otaegi et al.   JOURNAL OF NEUROSCIENCE

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

(2011) C A French et al.   MOLECULAR PSYCHIATRY

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

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

Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment

(2011) C. Palka et al.   PEDIATRICS

Genetics of autism spectrum disorders

(2011) Daniel H. Geschwind   TRENDS IN COGNITIVE SCIENCES

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

(2011) Sonja C. Vernes et al.   PLoS 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

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies

(2010) Amparo Tolosa et al.   BMC Medical Genetics

An Atlas of Combinatorial Transcriptional Regulation in Mouse and Man

(2010) Timothy Ravasi et al.   CELL

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

Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

(2010) H. J. Williams et al.   HUMAN MOLECULAR GENETICS

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

(2010) Denise Horn et al.   HUMAN MUTATION

Foxp1/2/4-NuRD Interactions Regulate Gene Expression and Epithelial Injury Response in the Lung via Regulation of Interleukin-6

(2010) Ann L. Chokas et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

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

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

The genetic basis of non-syndromic intellectual disability: a review

(2010) Liana Kaufman et al.   Journal of Neurodevelopmental Disorders

Common variants in FOXP1 are associated with generalized vitiligo

(2010) Ying Jin et al.   NATURE GENETICS

Genetic Advances in the Study of Speech and Language Disorders

(2010) D.F. Newbury et al.   NEURON

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

(2010) Elena Palmesino et al.   PLOS BIOLOGY

CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila

(2009) Christiane Zweier et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development

(2009) X. Feng et al.   BLOOD

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

(2009) Wolfgang Enard et al.   CELL

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

Human-specific transcriptional regulation of CNS development genes by FOXP2

(2009) Genevieve Konopka et al.   NATURE

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

(2009) Sridhar Hannenhalli et al.   NATURE REVIEWS GENETICS

FOXP2 as a molecular window into speech and language

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

Language Features in a Mother and Daughter of a Chromosome 7;13 Translocation Involving FOXP2

(2009) J. Bruce Tomblin et al.   JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH

Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

(2008) Maricela Alarcón et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Foxp2 Inhibits Nkx2.1-Mediated Transcription of SP-C via Interactions with the Nkx2.1 Homeodomain

(2008) Beiyun Zhou et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

FOXP1 is an androgen-responsive transcription factor that negatively regulates androgen receptor signaling in prostate cancer cells

(2008) Kenichi Takayama et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Methylation Mediated Silencing of MicroRNA-1 Gene and Its Role in Hepatocellular Carcinogenesis

(2008) J. Datta et al.   CANCER RESEARCH

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

(2008) Jeremy S. Dasen et al.   CELL

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

(2008) Matthias Groszer et al.   CURRENT BIOLOGY

Cooperative regulation in development by SMRT and FOXP1

(2008) K. Jepsen et al.   GENES & DEVELOPMENT

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

(2008) Manuel A R Ferreira et al.   NATURE GENETICS

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

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE