Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaFEUK, Lars; KALERVO, Aino; RIVLIN, Joseph et al.American journal of human genetics. 2006, Vol 79, Num 5, pp 965-972, issn 0002-9297, 8 p.Article

The DISC1 promoter: characterization and regulation by FOXP2WALKER, Rosie M; HILL, Alison E; FISHER, Simon E et al.Human molecular genetics (Print). 2012, Vol 21, Num 13, pp 2862-2872, issn 0964-6906, 11 p.Article

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complexROLL, Patrice; VERNES, Sonja C; SZEPETOWSKI, Pierre et al.Human molecular genetics (Print). 2010, Vol 19, Num 24, pp 4848-4860, issn 0964-6906, 13 p.Article

Maternally and Paternally Inherited Deletion of 7q31 Involving the FOXP2 Gene in Two FamiliesZILINA, O; REIMAND, T; ZJABLOVSKAJA, P et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 254-256, issn 1552-4825, 3 p.Article

Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human BrainSPITERI, Elizabeth; KONOPKA, Genevieve; COPPOLA, Giovanni et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1144-1157, issn 0002-9297, 14 p.Article

High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language DisordersVERNES, Sonja C; SPITERI, Elizabeth; NICOD, Jérome et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1232-1250, issn 0002-9297, 19 p.Article

Human-specific transcriptional regulation of CANS development genes by FOXP2KONOPKA, Genevieve; BOMAR, Jamee M; WINDEN, Kellen et al.Nature (London). 2009, Vol 462, Num 7270, pp 213-217, issn 0028-0836, 5 p.Article

Association between the FOXP2 gene and autistic disorder in Chinese populationXIAOHONG GONG; MEIXIANG JIA; DAI ZHANG et al.American journal of medical genetics. 2004, Vol 127B, Num 1, pp 113-116, issn 0148-7299, 4 p.Article

¿Homo loquens neanderthalensis? En torno a las capacidades simbólicas y lingüísticas del Neandertal = Homo loquens neanderthalensis? On the symbolic and linguistic capacities of NeandertalsBALARI, Sergio; BENITEZ BURRACO, Antonio; CAMPS, Marta et al.Munibe. Antropologia-arkeologia. 2008, Num 59, pp 3-24, issn 1132-2217, 22 p.Article

FOXP2 polymorphisms in patients with schizophreniaSANJUAN, Julio; TOLOSA, Amparo; GONZALEZ, Jose Carlos et al.Schizophrenia research. 2005, Vol 73, Num 2-3, pp 253-256, issn 0920-9964, 4 p.Article

Language evolution : A brief guide for linguistsBICKERTON, Derek.Lingua (Haarlem. Print). 2007, Vol 117, Num 3, pp 510-526, issn 0024-3841, 17 p.Article

FOXP2 as a molecular window into speech and languageFISHER, Simon E; SCHARFF, Constance.Trends in genetics (Regular ed.). 2009, Vol 25, Num 4, pp 166-177, issn 0168-9525, 12 p.Article

Evaluation of FOXP2 as an autism susceptibility geneWASSINK, Thomas H; PIVEN, Joseph; VIELAND, Veronica J et al.American journal of medical genetics. 2002, Vol 114, Num 5, pp 566-569, issn 0148-7299Article

Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patientsSPANIEL, Filip; HORACEK, Jiří; TINTERA, Jaroslav et al.Neuroscience letters. 2011, Vol 493, Num 3, pp 131-135, issn 0304-3940, 5 p.Article

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2ZEESMAN, Susan; NOWACZYK, Malgorzata J. M; TESHIMA, Ikuko et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 5, pp 509-514, issn 1552-4825, 6 p.Article

From manual gesture to speech : A gradual transitionGENTILUCCI, Maurizio; CORBALLIS, Michael C.Neuroscience and biobehavioral reviews. 2006, Vol 30, Num 7, pp 949-960, issn 0149-7634, 12 p.Article

Deciphering the genetic basis of speech and language disordersFISHER, Simon E; LAI, Cecilia S. L; MONACO, Anthony P et al.Annual review of neuroscience. 2003, Vol 26, pp 57-80, issn 0147-006X, 24 p.Article

HISTAMINE IS REQUIRED DURING NEURAL STEM CELL PROLIFERATION TO INCREASE NEURON DIFFERENTIATIONRODRIGUEZ-MARTINEZ, G; VELASCO, I; GARCIA-LOPEZ, G et al.Neuroscience. 2012, Vol 216, pp 10-17, issn 0306-4522, 8 p.Article

Tangled webs : Tracing the connections between genes and cognitionFISHER, Simon E.Cognition. 2006, Vol 101, Num 2, pp 270-297, issn 0010-0277, 28 p.Article

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorderLAI, Cecilia S. L; GERRELLI, Dianne; MONACO, Anthony P et al.Brain. 2003, Vol 126, pp 2455-2462, issn 0006-8950, 8 p., 11Article

Breakpoint Localization Using Array-CGH in Three Siblings With an Unbalanced 4q;16q Translocation and Childhood Apraxia of Speech (CAS)SHRIBERG, Lawrence D; JAKIELSKI, Kathy J; EL-SHANTI, Hatem et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 17, pp 2227-2233, issn 1552-4825, 7 p.Article

Multidisciplinary approaches in evolutionary linguisticsTAO GONG; LAN SHUAI; YICHENG WU et al.Language sciences (Oxford). 2013, Vol 37, pp 1-13, issn 0388-0001, 13 p.Article

Language-impaired children: No sign of the FOXP2 mutationMEABURN, E; DALE, P. S; CRAIG, I. W et al.Neuroreport (Oxford). 2002, Vol 13, Num 8, pp 1075-1077, issn 0959-4965Article

Facteurs génétiques dans les troubles spécifiques du développement du langage : Dysphasie = Genetic factors in developmental speech and language disordersPHILIPPE, A.ANAE. Approche neuropsychologique des apprentissages chez l'enfant. 2004, Num 76-77, pp 34-37, issn 0999-792X, 4 p.Article

HUMANIZED Foxp2 SPECIFICALLY AFFECTS CORTICO-BASAL GANGLIA CIRCUITSREIMERS-KIPPING, S; HEVERS, W; PÄÄBO, S et al.Neuroscience. 2011, Vol 175, pp 75-84, issn 0306-4522, 10 p.Article