Detalhe da pesquisa
1.
Sex-heterogeneous SNPs disproportionately influence gene expression and health.
PLoS Genet
; 18(5): e1010147, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35511767
2.
Directional dominance on stature and cognition in diverse human populations.
Nature
; 523(7561): 459-462, 2015 Jul 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26131930
3.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
Am J Hum Genet
; 100(6): 865-884, 2017 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28552196
4.
Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.
PLoS Genet
; 13(1): e1006516, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28076348
5.
Correction: Pleiotropic Mechanisms Indicated for Sex Differences in Autism.
PLoS Genet
; 13(6): e1006831, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28591140
6.
Pleiotropic Mechanisms Indicated for Sex Differences in Autism.
PLoS Genet
; 12(11): e1006425, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27846226
7.
Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies.
PLoS Genet
; 12(2): e1005874, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26910538
8.
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes.
J Am Soc Nephrol
; 29(1): 335-348, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29093028
9.
Seventy-five genetic loci influencing the human red blood cell.
Nature
; 492(7429): 369-75, 2012 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23222517
10.
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine.
Pflugers Arch
; 469(1): 91-103, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27915449
11.
A general approach for haplotype phasing across the full spectrum of relatedness.
PLoS Genet
; 10(4): e1004234, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24743097
12.
A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings.
Rev Endocr Metab Disord
; 17(2): 209-19, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27129595
13.
A genome-wide association study of early menopause and the combined impact of identified variants.
Hum Mol Genet
; 22(7): 1465-72, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23307926
14.
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.
J Am Soc Nephrol
; 25(8): 1869-82, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24578125
15.
TMPRSS6 rs855791 modulates hepcidin transcription in vitro and serum hepcidin levels in normal individuals.
Blood
; 118(16): 4459-62, 2011 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21873547
16.
The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis.
BMC Nephrol
; 14: 48, 2013 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-23433094
17.
Neuronal APOE4 removal protects against tau-mediated gliosis, neurodegeneration and myelin deficits.
Nat Aging
; 3(3): 275-296, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37118426
18.
APOE4-promoted gliosis and degeneration in tauopathy are ameliorated by pharmacological inhibition of HMGB1 release.
Cell Rep
; 42(10): 113252, 2023 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37863057
19.
In vivo protein turnover rates in varying oxygen tensions nominate MYBBP1A as a mediator of the hyperoxia response.
Sci Adv
; 9(49): eadj4884, 2023 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38064566
20.
The APOE-R136S mutation protects against APOE4-driven Tau pathology, neurodegeneration and neuroinflammation.
Nat Neurosci
; 26(12): 2104-2121, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37957317