Detalhe da pesquisa
1.
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.
Am J Hum Genet
; 108(7): 1350-1355, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34115965
2.
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes.
Am J Hum Genet
; 102(5): 874-889, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29727688
3.
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 180(3): 223-231, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30801977
4.
Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders.
Trends Genet
; 25(12): 528-35, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19883952
5.
Casirivimab and Imdevimab Treatment Reduces Viral Load and Improves Clinical Outcomes in Seropositive Hospitalized COVID-19 Patients with Nonneutralizing or Borderline Neutralizing Antibodies.
mBio
; 13(6): e0169922, 2022 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36255239
6.
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease.
Nat Genet
; 54(4): 382-392, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35241825
7.
Altered DNA methylation associated with a translocation linked to major mental illness.
NPJ Schizophr
; 4(1): 5, 2018 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29555928
8.
Unlocking the treasure trove: from genes to schizophrenia biology.
Schizophr Bull
; 40(3): 492-6, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24674812
9.
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.
Eur J Hum Genet
; 19(6): 727-31, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21448237
10.
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Nat Genet
; 42(3): 203-9, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20154674
11.
Microduplications of 16p11.2 are associated with schizophrenia.
Nat Genet
; 41(11): 1223-7, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19855392
12.
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Science
; 320(5875): 539-43, 2008 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-18369103