about
In vivo and in vitro genetic evidence of involvement of neuregulin 1 in immune system dysregulationArguments for the sake of endophenotypes: examining common misconceptions about the use of endophenotypes in psychiatric geneticsThe epsin 4 gene is associated with psychotic disorders in families of Latin American originMitochondrial polymorphisms are associated both with increased and decreased longevityAssociation of apolipoprotein E-e4 and dementia declines with age.Assessment of genetic ancestry and population substructure in Costa Rica by analysis of individuals with a familial history of mental disorder.High mitochondrial mutation rates estimated from deep-rooting Costa Rican pedigrees.Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational familiesIs subclinical anxiety an endophenotype for bipolar I patients? A study from a Costa Rican sample.Suggestive evidence for association between L-type voltage-gated calcium channel (CACNA1C) gene haplotypes and bipolar disorder in Latinos: a family-based association study.Meta-analysis of 32 genome-wide linkage studies of schizophrenia.The serotonin transporter 5-HTTPR polymorphism is associated with current and lifetime depression in persons with chronic psychotic disorders.Global signaling effects of a schizophrenia-associated missense mutation in neuregulin 1: an exploratory study using whole genome and novel kinome approaches.Clozapine treatment causes oxidation of proteins involved in energy metabolism in lymphoblastoid cells: a possible mechanism for antipsychotic-induced metabolic alterations.Family-based association of an ANK3 haplotype with bipolar disorder in Latino populations.Identification of circadian gene variants in bipolar disorder in Latino populations.Genetic studies of neuropsychiatric disorders in Costa Rica: a model for the use of isolated populations.Social and clinical comparison between schizophrenia and bipolar disorder type I with psychosis in Costa Rica.Malic enzyme 2 and susceptibility to psychosis and mania.A genome-wide linkage scan of bipolar disorder in Latino families identifies susceptibility loci at 8q24 and 14q32.A genome-wide scan for schizophrenia and psychosis susceptibility loci in families of Mexican and Central American ancestry.Association analyses of the neuregulin 1 gene with schizophrenia and manic psychosis in a Hispanic population.Mitochondrial polymorphisms associated with differential longevity do not impact lifetime-reproductive success.Evidence of genetic overlap of schizophrenia and bipolar disorder: linkage disequilibrium analysis of chromosome 18 in the Costa Rican population.Rediscovering the value of families for psychiatric genetics researchDNase activity in Costa Rican crotaline snake venoms: Quantification of activity and identification of electrophoretic variantsGenetic structure of personality factors and bipolar disorder in families segregating bipolar disorderHeritability of age of onset of psychosis in schizophreniaA Schizophrenia Gene Locus on Chromosome 17q21 in a New Set of Families of Mexican and Central American Ancestry: Evidence From the NIMH Genetics of Schizophrenia in Latino Populations StudyCannabinoid receptor 1 gene (CNR1) and susceptibility to a quantitative phenotype for hebephrenic schizophreniaAdjudicating neurocognitive endophenotypes for schizophreniaTGFB-induced factor (TGIF): a candidate gene for psychosis on chromosome 18pA Novel Missense Mutation in the Transmembrane Domain of Neuregulin 1 is Associated with SchizophreniaLinkage disequilibrium analyses in the Costa Rican population suggests discrete gene loci for schizophrenia at 8p23.1 and 8q13.3
P50
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P50
description
hulumtuese
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onderzoeker
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researcher
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հետազոտող
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name
Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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Henriette Raventós
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P106
P1153
9041500800
P2038
Henriette_Raventos
P21
P31
P496
0000-0001-9423-8308