Detalhe da pesquisa
1.
Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.
Am J Hum Genet
; 109(10): 1727-1741, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36055244
2.
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 575(7783): E4, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31686056
3.
Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 572(7769): 323-328, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31367044
4.
Association of structural variation with cardiometabolic traits in Finns.
Am J Hum Genet
; 108(4): 583-596, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33798444
5.
Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder.
Mol Psychiatry
; 26(9): 5229-5238, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32606377
6.
Genetic analysis of activity, brain and behavioral associations in extended families with heavy genetic loading for bipolar disorder.
Psychol Med
; 51(3): 494-502, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31813409
7.
The Contribution of GWAS Loci in Familial Dyslipidemias.
PLoS Genet
; 12(5): e1006078, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27227539
8.
Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder.
PLoS Genet
; 12(5): e1006046, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27176483
9.
Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder.
Proc Natl Acad Sci U S A
; 113(6): E754-61, 2016 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26712028
10.
Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.
PLoS Genet
; 10(1): e1004147, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24497850
11.
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder.
Brain
; 138(Pt 7): 2087-102, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25943422
12.
Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits.
BMC Biol
; 13: 41, 2015 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-26092298
13.
Geospatial investigations in Colombia reveal variations in the distribution of mood and psychotic disorders.
Commun Med (Lond)
; 4(1): 26, 2024 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38383761
14.
Power of IRT in GWAS: successful QTL mapping of sum score phenotypes depends on interplay between risk allele frequency, variance explained by the risk allele, and test characteristics.
Genet Epidemiol
; 36(8): 882-9, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22965845
15.
Phenotype mining in CNV carriers from a population cohort.
Hum Mol Genet
; 20(13): 2686-95, 2011 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21505072
16.
Predicting diagnostic conversion from major depressive disorder to bipolar disorder: an EHR based study from Colombia.
medRxiv
; 2023 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37873340
17.
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.
Nat Commun
; 13(1): 1644, 2022 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35347128
18.
Identifying heritable brain phenotypes in an extended pedigree of vervet monkeys.
J Neurosci
; 29(9): 2867-75, 2009 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-19261882
19.
Distinct and shared contributions of diagnosis and symptom domains to cognitive performance in severe mental illness in the Paisa population: a case-control study.
Lancet Psychiatry
; 7(5): 411-419, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32353276
20.
Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.
Transl Psychiatry
; 10(1): 74, 2020 02 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32094344