Detalhe da pesquisa
1.
COMMUTE: Communication-efficient transfer learning for multi-site risk prediction.
J Biomed Inform
; 137: 104243, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36403757
2.
Common genetic variants influence human subcortical brain structures.
Nature
; 520(7546): 224-9, 2015 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25607358
3.
Pleiotropy in complex traits: challenges and strategies.
Nat Rev Genet
; 14(7): 483-95, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23752797
4.
Principles and methods of in-silico prioritization of non-coding regulatory variants.
Hum Genet
; 137(1): 15-30, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29288389
5.
Massively expedited genome-wide heritability analysis (MEGHA).
Proc Natl Acad Sci U S A
; 112(8): 2479-84, 2015 Feb 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25675487
6.
ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide.
Neuroimage
; 145(Pt B): 389-408, 2017 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26658930
7.
Levodopa dose maintenance or reduction in patients with Parkinson's disease transitioning to levodopa/carbidopa/entacapone.
Neurol India
; 65(4): 746-751, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28681744
8.
Is Dominant-Side Onset Associated With a Better Motor Compensation in Parkinson's Disease?
Mov Disord
; 30(14): 1921-5, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26408124
9.
Use of Tobacco Products and Suicide Attempts Among Elementary School-Aged Children.
JAMA Netw Open
; 7(2): e240376, 2024 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38407905
10.
Associations between behavioral and self-reported impulsivity, brain structure, and genetic influences in middle childhood.
Dev Cogn Neurosci
; 67: 101389, 2024 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38749217
11.
Individual differences in amygdala-medial prefrontal anatomy link negative affect, impaired social functioning, and polygenic depression risk.
J Neurosci
; 32(50): 18087-100, 2012 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-23238724
12.
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
Hum Mol Genet
; 20(18): 3699-709, 2011 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21665990
13.
INRICH: interval-based enrichment analysis for genome-wide association studies.
Bioinformatics
; 28(13): 1797-9, 2012 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22513993
14.
Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 162B(8): 779-88, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24039173
15.
Youth Team Sports Participation Associates With Reduced Dimensional Psychopathology Through Interaction With Biological Risk Factors.
Biol Psychiatry Glob Open Sci
; 3(4): 875-883, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37881582
16.
Genetic patterning for child psychopathology is distinct from that for adults and implicates fetal cerebellar development.
Nat Neurosci
; 26(6): 959-969, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37202553
17.
Modifiers and subtype-specific analyses in whole-genome association studies: a likelihood framework.
Hum Hered
; 72(1): 10-20, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21849790
18.
Identification of genetic variants influencing methylation in brain with pleiotropic effects on psychiatric disorders.
Prog Neuropsychopharmacol Biol Psychiatry
; 113: 110454, 2022 03 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34637873
19.
Associations Between Genetic Risk for Adult Suicide Attempt and Suicidal Behaviors in Young Children in the US.
JAMA Psychiatry
; 79(10): 971-980, 2022 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36044238
20.
Genetic Association of Attention-Deficit/Hyperactivity Disorder and Major Depression With Suicidal Ideation and Attempts in Children: The Adolescent Brain Cognitive Development Study.
Biol Psychiatry
; 92(3): 236-245, 2022 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216811