Detalhe da pesquisa
1.
Whole-Exome Sequencing Reveals Uncaptured Variation and Distinct Ancestry in the Southern African Population of Botswana.
Am J Hum Genet
; 102(5): 731-743, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29706352
2.
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Hum Mol Genet
; 25(11): 2331-2341, 2016 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26965164
3.
Protective variant for hippocampal atrophy identified by whole exome sequencing.
Ann Neurol
; 77(3): 547-52, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25559091
4.
Association of plasma and cortical amyloid beta is modulated by APOE ε4 status.
Alzheimers Dement
; 10(1): e9-e18, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23541187
5.
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.
Neuroimage
; 53(3): 1051-63, 2010 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20100581
6.
Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans.
Alzheimers Dement
; 6(3): 265-73, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20451875
7.
Edematous severe acute malnutrition is characterized by hypomethylation of DNA.
Nat Commun
; 10(1): 5791, 2019 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31857576
8.
Characteristics of Bipolar I patients grouped by externalizing disorders.
J Affect Disord
; 178: 206-14, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25827505
9.
A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome.
PLoS One
; 10(7): e0131797, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26176221
10.
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi Syndrome.
Invest Ophthalmol Vis Sci
; 56(6): 3896-904, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26091538
11.
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers.
Brain Imaging Behav
; 8(2): 183-207, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24092460
12.
Effect of complement CR1 on brain amyloid burden during aging and its modification by APOE genotype.
Biol Psychiatry
; 73(5): 422-8, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23022416
13.
PARP1 gene variation and microglial activity on [11C]PBR28 PET in older adults at risk for Alzheimer's disease.
Multimodal Brain Image Anal (2013)
; 8159: 150-158, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-25383391
14.
Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel.
PLoS One
; 8(7): e70269, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23894628
15.
Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study.
Curr Alzheimer Res
; 9(7): 801-14, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22486522
16.
Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.
PLoS One
; 7(12): e50640, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23227193
17.
Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort.
Brain Imaging Behav
; 6(1): 1-15, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21901424
18.
The effect of reference panels and software tools on genotype imputation.
AMIA Annu Symp Proc
; 2011: 1013-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22195161
19.
Hippocampal surface mapping of genetic risk factors in AD via sparse learning models.
Med Image Comput Comput Assist Interv
; 14(Pt 2): 376-83, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21995051
20.
Identifying Neuroimaging and Proteomic Biomarkers for MCI and AD via the Elastic Net.
Multimodal Brain Image Anal (2011)
; 7012: 27-34, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27054198