Detalhe da pesquisa
1.
Novel genes and sex differences in COVID-19 severity.
Hum Mol Genet
; 31(22): 3789-3806, 2022 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35708486
2.
Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.
Int J Mol Sci
; 24(2)2023 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36674414
3.
Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population.
J Clin Periodontol
; 48(7): 896-906, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33745150
4.
Genetic Susceptibility to Periodontal Disease in Down Syndrome: A Case-Control Study.
Int J Mol Sci
; 22(12)2021 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34200970
5.
In utero and childhood exposure to tobacco smoke and multi-layer molecular signatures in children.
BMC Med
; 18(1): 243, 2020 08 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32811491
6.
Differential admixture in Latin American populations and its impact on the study of colorectal cancer.
Genet Mol Biol
; 43(4): e20200143, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33306774
7.
The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability.
J Hum Genet
; 64(3): 221-231, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30518945
8.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Alzheimers Dement
; 15(10): 1333-1347, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31473137
9.
Enhanced localization of genetic samples through linkage-disequilibrium correction.
Am J Hum Genet
; 92(6): 882-94, 2013 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23726367
10.
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.
PLoS Genet
; 9(3): e1003349, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23555275
11.
Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations.
Int J Cancer
; 137(8): 1870-8, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25855579
12.
Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome.
Am J Med Genet A
; 167(6): 1369-73, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25898976
13.
A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features.
Am J Med Genet A
; 167(6): 1315-22, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25847113
14.
Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion.
Am J Med Genet A
; 167A(12): 3121-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26332054
15.
Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder.
Am J Med Genet A
; 167A(12): 3113-20, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26284580
16.
Clonal chromosomal mosaicism and loss of chromosome Y in elderly men increase vulnerability for SARS-CoV-2.
Commun Biol
; 7(1): 202, 2024 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374351
17.
An Insertion Within SIRPß1 Shows a Dual Effect Over Alzheimer's Disease Cognitive Decline Altering the Microglial Response.
J Alzheimers Dis
; 98(2): 601-618, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38427484
18.
A Genome-Wide Association Study of Small Cell Lung Cancer.
Arch Bronconeumol
; 59(10): 645-650, 2023 Oct.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-37500326
19.
Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood.
Elife
; 112022 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35302492
20.
Multi-omics signatures of the human early life exposome.
Nat Commun
; 13(1): 7024, 2022 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36411288