Detalhe da pesquisa
1.
Recurrent tissue-specific mtDNA mutations are common in humans.
PLoS Genet
; 9(11): e1003929, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24244193
2.
Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography.
Hum Genet
; 133(1): 85-93, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24026422
3.
Genetic modification of the relationship between phosphorylated tau and neurodegeneration.
Alzheimers Dement
; 10(6): 637-645.e1, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24656848
4.
White matter integrity deficits in prefrontal-amygdala pathways in Williams syndrome.
Neuroimage
; 59(2): 887-94, 2012 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22008369
5.
Electrophysiological biomarkers and age characterize phenotypic heterogeneity among individuals with major depressive disorder.
Front Hum Neurosci
; 16: 1055685, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36699961
6.
Iron-regulatory genes are associated with Neuroimaging measures in HIV infection.
Brain Imaging Behav
; 14(5): 2037-2049, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31273671
7.
Genetics, statistics and human disease: analytical retooling for complexity.
Trends Genet
; 20(12): 640-7, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15522460
8.
Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic data.
BMC Bioinformatics
; 7: 204, 2006 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-16611359
9.
Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium.
Neurobiol Aging
; 38: 141-150, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26827652
10.
Resting-State Functional Connectivity in Individuals with Down Syndrome and Williams Syndrome Compared with Typically Developing Controls.
Brain Connect
; 5(8): 461-75, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25712025
11.
GSK3ß Interactions with Amyloid Genes: An Autopsy Verification and Extension.
Neurotox Res
; 28(3): 232-8, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26194614
12.
Interactions between GSK3ß and amyloid genes explain variance in amyloid burden.
Neurobiol Aging
; 35(3): 460-5, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24112793
13.
Genetic variation modifies risk for neurodegeneration based on biomarker status.
Front Aging Neurosci
; 6: 183, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25140149
14.
Neural correlates of amusia in williams syndrome.
Brain Sci
; 4(4): 594-612, 2014 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-25422929
15.
Genetic interactions within inositol-related pathways are associated with longitudinal changes in ventricle size.
J Alzheimers Dis
; 38(1): 145-54, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24077433
16.
Impact of family structure and common environment on heritability estimation for neuroimaging genetics studies using Sequential Oligogenic Linkage Analysis Routines.
J Med Imaging (Bellingham)
; 1(1): 014005, 2014 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-25558465
17.
Differences in age-related effects on brain volume in Down syndrome as compared to Williams syndrome and typical development.
J Neurodev Disord
; 6(1): 8, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24713364
18.
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
PLoS One
; 9(6): e94661, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24922517
19.
Genetic interactions associated with 12-month atrophy in hippocampus and entorhinal cortex in Alzheimer's Disease Neuroimaging Initiative.
Neurobiol Aging
; 34(5): 1518.e9-18, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23107432
20.
Associations between KCNJ6 (GIRK2) gene polymorphisms and pain-related phenotypes.
Pain
; 154(12): 2853-2859, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23994450