0000000000733099

AUTHOR

Amparo Tolosa

showing 5 related works from this author

Rapid evolving RNA gene HAR1A and schizophrenia

2008

GeneticsPsychiatry and Mental healthExonLinkage disequilibriumPolymorphism (computer science)Schizophrenia (object-oriented programming)HaplotypeGenotypeRNABiologyGeneBiological PsychiatrySchizophrenia Research
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Potential involvement of serotonin receptor genes with age of onset and gender in schizophrenia: a preliminary study in a Spanish sample.

2009

Malemedicine.medical_specialtySample (statistics)BioinformaticsPolymorphism Single NucleotidePolymorphism (computer science)MedicineHumansAge of OnsetPsychiatryReceptorGeneBiological Psychiatry5-HT receptorSex Characteristicsbusiness.industrymedicine.diseasePsychiatry and Mental healthSchizophreniaSpainReceptors SerotoninSchizophreniaFemaleAge of onsetbusinessSex characteristicsPsychiatry research
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FOXP2 polymorphisms in patients with schizophrenia.

2005

Abstract Background FOXP2 was described as the first gene involved in our ability to acquire spoken language. The main objective of this study was to compare the distribution of FOXP2 gene polymorphisms between patients with schizophrenia and healthy controls. Methods Two FOXP2 polymorphisms, Intron3a and SNP 923875, and the G→A transition in exon 14 were analysed in 149 patients with schizophrenia and schizoaffective disorders according to DSM-IV, as well as in 137 controls. All the patients showed a history of auditory hallucinations. Results The transition G→A at exon 14, detected in all the affected members in KE family, was not found in any of the analyzed samples from patients or cont…

OncologyAdultMalemedicine.medical_specialtyPsychosisGenotypeHallucinationsSeverity of Illness IndexExonPolymorphism (computer science)Internal medicinemedicineSNPHumansGenetic Predisposition to DiseaseAlleleBiological PsychiatryAllelesAgedDNA PrimersRetrospective StudiesGeneticsLanguage DisordersFOXP2 GenePolymorphism GeneticTransition (genetics)business.industryForkhead Transcription FactorsExonsMiddle Agedmedicine.diseaseIntronsDiagnostic and Statistical Manual of Mental DisordersPsychiatry and Mental healthSchizophreniaSchizophreniaFemalebusinessTranscription FactorsSchizophrenia research
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FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies

2010

Abstract Background Schizophrenia is considered a language related human specific disease. Previous studies have reported evidence of positive selection for schizophrenia-associated genes specific to the human lineage. FOXP2 shows two important features as a convincing candidate gene for schizophrenia vulnerability: FOXP2 is the first gene related to a language disorder, and it has been subject to positive selection in the human lineage. Methods Twenty-seven SNPs of FOXP2 were genotyped in a cohort of 293 patients with schizophrenia and 340 controls. We analyzed in particular the association with the poverty of speech and the intensity of auditory hallucinations. Potential expansion of thre…

Candidate genelcsh:Internal medicineGenotypeHallucinationslcsh:QH426-470Epigenetics of schizophreniaSingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideEpigenesis GeneticCohort StudiesmedicineGeneticsHumansLanguage disorderGenetics(clinical)lcsh:RC31-1245Genetics (clinical)GeneticsPsychiatric Status Rating ScalesLanguage DisordersFOXP2 GeneFOXP2Forkhead Transcription FactorsExonsDNA Methylationmedicine.diseaselcsh:GeneticsSchizophreniaDNA methylationSchizophreniaParahippocampal GyrusCpG IslandsResearch Article
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178 – Promoter region of foxp2 gene: epigenetic and evolutionary analysis

2008

GeneticsPsychiatry and Mental healthFOXP2 GeneEpigenetics of physical exercisePromoterEpigeneticsBiologyBiological PsychiatrySchizophrenia Research
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