Detalhe da pesquisa
1.
Rare coding variants in ten genes confer substantial risk for schizophrenia.
Nature
; 604(7906): 509-516, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396579
2.
Genetic substrates of bipolar disorder risk in Latino families.
Mol Psychiatry
; 28(1): 154-167, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35948660
3.
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
Mol Psychiatry
; 25(10): 2455-2467, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31591465
4.
EXPLORATORY ANALYSIS OF POLYGENIC RISK SCORES FOR PSYCHIATRIC DISORDERS: APPLIED TO DUAL DIAGNOSIS.
Rev Invest Clin
; 71(5): 321-329, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31599879
5.
Fine-mapping scan of bipolar disorder susceptibility loci in Latino pedigrees.
Am J Med Genet B Neuropsychiatr Genet
; 180(3): 213-222, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30779416
6.
A genome-wide quantitative trait locus (QTL) linkage scan of NEO personality factors in Latino families segregating bipolar disorder.
Am J Med Genet B Neuropsychiatr Genet
; 174(7): 683-690, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28556497
7.
Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort.
Bipolar Disord
; 18(6): 520-527, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27759212
8.
Global signaling effects of a schizophrenia-associated missense mutation in neuregulin 1: an exploratory study using whole genome and novel kinome approaches.
J Neural Transm (Vienna)
; 121(5): 479-90, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24380930
9.
NRG3 gene is associated with the risk and age at onset of Alzheimer disease.
J Neural Transm (Vienna)
; 121(2): 183-92, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24061483
10.
A genome-wide linkage scan of bipolar disorder in Latino families identifies susceptibility loci at 8q24 and 14q32.
Am J Med Genet B Neuropsychiatr Genet
; 165B(6): 479-91, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25044503
11.
Suggestive evidence for association between L-type voltage-gated calcium channel (CACNA1C) gene haplotypes and bipolar disorder in Latinos: a family-based association study.
Bipolar Disord
; 15(2): 206-14, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23437964
12.
The genomic psychiatry cohort: partners in discovery.
Am J Med Genet B Neuropsychiatr Genet
; 162B(4): 306-12, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23650244
13.
Substance use disorder and schizophrenia: prevalence and sociodemographic characteristics in the Latin American population.
Actas Esp Psiquiatr
; 39(2): 123-30, 2011.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-21404151
14.
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.
Schizophr Bull
; 47(2): 517-529, 2021 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33169155
15.
Assessment of genetic ancestry and population substructure in Costa Rica by analysis of individuals with a familial history of mental disorder.
Ann Hum Genet
; 74(6): 516-24, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20946256
16.
Association of serotonin transporter promoter gene polymorphism (5-HTTLPR) with depression in Costa Rican schizophrenic patients.
J Neurogenet
; 24(2): 83-9, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20397838
17.
The role of complex emotions in inconsistent diagnoses of schizophrenia.
J Nerv Ment Dis
; 198(9): 609-13, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20823720
18.
Social and clinical comparison between schizophrenia and bipolar disorder type I with psychosis in Costa Rica.
Soc Psychiatry Psychiatr Epidemiol
; 45(6): 675-80, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19727533
19.
Psychiatric syndromes in individuals with chromosome 18 abnormalities.
Am J Med Genet B Neuropsychiatr Genet
; 153B(3): 837-45, 2010 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19927307
20.
Heritability of age of onset of psychosis in schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 153B(1): 298-302, 2010 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19350535