FOXP2 and the neuroanatomy of speech and language

Parallel Organization of Functionally Segregated Circuits Linking Basal Ganglia and Cortex

1986 • 8,208 citations

A forkhead-domain gene is mutated in a severe speech and language disorder

2001 • 1,949 citations

Basal ganglia and cerebellar loops: motor and cognitive circuits

2000 • 1,869 citations

Molecular evolution of FOXP2, a gene involved in speech and language

2002 • 1,520 citations

Cerebellar Loops with Motor Cortex and Prefrontal Cortex of a Nonhuman Primate

2003 • 1,517 citations

Evaluation of the role of phonological STM in the development of vocabulary in children: A longitudinal study

1989 • 1,011 citations

Forkhead Transcription Factors: Key Players in Development and Metabolism

2002 • 824 citations

Parallel neural networks for learning sequential procedures

1999 • 777 citations

Role for supplementary motor area cells in planning several movements ahead

1994 • 669 citations

Localisation of a gene implicated in a severe speech and language disorder

1998 • 476 citations

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain

2003 • 476 citations

Re-examining the brain regions crucial for orchestrating speech articulation

2004 • 470 citations

Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder.

1995 • 431 citations

Sequential Organization of Multiple Movements: Involvement of Cortical Motor Areas

2001 • 413 citations

FoxP2Expression in Avian Vocal Learners and Non-Learners

2004 • 395 citations

Neural basis of an inherited speech and language disorder

1998 • 385 citations

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder

2003 • 370 citations

An extended Family with a Dominantly Inherited Speech Disorder

1990 • 345 citations

Characterization of a New Subfamily of Winged-helix/Forkhead (Fox) Genes That Are Expressed in the Lung and Act as Transcriptional Repressors

2001 • 345 citations

Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia

2002 • 342 citations

MRI analysis of an inherited speech and language disorder: structural brain abnormalities

2002 • 335 citations

Language fMRI abnormalities associated with FOXP2 gene mutation

2003 • 316 citations

Transcriptional and DNA Binding Activity of the Foxp1/2/4 Family Is Modulated by Heterotypic and Homotypic Protein Interactions

2003 • 311 citations

ParallelFoxP1andFoxP2Expression in Songbird and Human Brain Predicts Functional Interaction

2004 • 310 citations

Accelerated Protein Evolution and Origins of Human-Specific Features: FOXP2 as an Example

2002 • 250 citations

Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

2003 • 217 citations

The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder

2000 • 206 citations

Language Function, Foot of the Third Frontal Gyrus, and Rolandic Operculum

1981 • 165 citations

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia

2003 • 162 citations

Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum

2003 • 157 citations

The “Pure form” of the phonetic disintegration syndrome (pure anarthria); anatomo-clinical report of a historical case

1976 • 143 citations

Foxp4: a novel member of the Foxp subfamily of winged-helix genes co-expressed with Foxp1 and Foxp2 in pulmonary and gut tissues

2002 • 118 citations

The role of the left mesial frontal cortex in fluent speech: Evidence from a case of left supplementary motor area hemorrhage

1997 • 115 citations

Oral Dyspraxia in Inherited Speech and Language Impairment and Acquired Dysphasia

2000 • 107 citations

Periventricular Leukomalacia: Ultrasonic and Neuropathological Correlations

1990 • 107 citations

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

2003 • 83 citations

Speech and language defects

1990 • 82 citations

Detecting bilateral abnormalities with voxel-based morphometry

2000 • 53 citations

Pure Anarthria with Predominantly Sequencing Errors in Phoneme Articulation: A Case Report

2001 • 24 citations

Deleted Work

1955 • 0 citations