Detalhe da pesquisa
1.
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Nat Methods;
19(12): 1599-1611, 2022 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36303018
2.
Minimal Relationship between Local Gyrification and General Cognitive Ability in Humans.
Cereb Cortex;
30(6): 3439-3450, 2020 05 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32037459
3.
Neurocognitive impairment in type 2 diabetes: evidence for shared genetic aetiology.
Diabetologia;
63(5): 977-986, 2020 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32016567
4.
Family-based analyses reveal novel genetic overlap between cytokine interleukin-8 and risk for suicide attempt.
Brain Behav Immun;
80: 292-299, 2019 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30953777
5.
Contribution of Inbred Singletons to Variance Component Estimation of Heritability and Linkage.
Hum Hered;
83(2): 92-99, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30391948
6.
Epigenetic Age Acceleration Assessed with Human White-Matter Images.
J Neurosci;
37(18): 4735-4743, 2017 05 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28385874
7.
Shared Genetic Factors Influence Head Motion During MRI and Body Mass Index.
Cereb Cortex;
27(12): 5539-5546, 2017 12 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27744290
8.
A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers.
PLoS Genet;
11(10): e1005593, 2015 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26474483
9.
TRAK2, a novel regulator of ABCA1 expression, cholesterol efflux and HDL biogenesis.
Eur Heart J;
38(48): 3579-3587, 2017 12 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28655204
10.
Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants.
Hum Mol Genet;
24(16): 4674-85, 2015 Aug 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26022996
11.
Novel epigenetic determinants of type 2 diabetes in Mexican-American families.
Hum Mol Genet;
24(18): 5330-44, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26101197
12.
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes.
Hum Mol Genet;
24(5): 1504-12, 2015 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25378555
13.
ADAM19: A Novel Target for Metabolic Syndrome in Humans and Mice.
Mediators Inflamm;
2017: 7281986, 2017.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28265178
14.
HyCCAPP as a tool to characterize promoter DNA-protein interactions in Saccharomyces cerevisiae.
Genomics;
107(6): 267-73, 2016 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27184763
15.
Exome sequences of multiplex, multigenerational families reveal schizophrenia risk loci with potential implications for neurocognitive performance.
Am J Med Genet B Neuropsychiatr Genet;
174(8): 817-827, 2017 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28902459
16.
GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans.
BMC Genomics;
17: 276, 2016 Apr 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27039371
17.
Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits.
Am J Hum Genet;
93(6): 1087-99, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24314549
18.
Recurrent major depression and right hippocampal volume: A bivariate linkage and association study.
Hum Brain Mapp;
37(1): 191-202, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26485182
19.
A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).
PLoS Genet;
9(1): e1003147, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23326239
20.
Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging.
Proc Natl Acad Sci U S A;
110(47): 19006-11, 2013 Nov 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24191011