Detalhe da pesquisa
1.
High-dimensional immune profiling identifies a biomarker to monitor dimethyl fumarate response in multiple sclerosis.
Proc Natl Acad Sci U S A
; 119(31): e2205042119, 2022 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35881799
2.
Meta-analysis of ACE inhibitor-induced angioedema identifies novel risk locus.
J Allergy Clin Immunol
; 153(4): 1073-1082, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38300190
3.
Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus.
Neuroimage
; 273: 120095, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37030412
4.
Integrative genomic analysis of pediatric T-cell lymphoblastic lymphoma reveals candidates of clinical significance.
Blood
; 137(17): 2347-2359, 2021 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33152759
5.
Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach.
Br J Psychiatry
; : 1-10, 2022 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35225756
6.
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.
Mol Psychiatry
; 26(4): 1286-1298, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712721
7.
Association of polygenic score for major depression with response to lithium in patients with bipolar disorder.
Mol Psychiatry
; 26(6): 2457-2470, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32203155
8.
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.
Mol Psychiatry
; 26(8): 4179-4190, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712720
9.
Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.
Cereb Cortex
; 30(2): 801-811, 2020 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-31402375
10.
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.
PLoS Genet
; 12(10): e1006343, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27792727
11.
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.
Int J Cancer
; 143(11): 2800-2813, 2018 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29987844
12.
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities.
J Neural Transm (Vienna)
; 125(2): 259-271, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29147782
13.
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Brain
; 140(6): 1561-1578, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28459997
14.
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.
Lancet
; 387(10023): 1085-1093, 2016 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26806518
15.
Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach - CORRIGENDUM.
Br J Psychiatry
; 221(2): 494, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35505515
16.
Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array.
Genet Epidemiol
; 39(8): 601-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26497834
17.
SUCLG2 identified as both a determinator of CSF Aß1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.
Hum Mol Genet
; 23(24): 6644-58, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25027320
18.
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
Hum Mol Genet
; 23(22): 6069-80, 2014 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24939913
19.
Runs of homozygosity and inbreeding in thyroid cancer.
BMC Cancer
; 16: 227, 2016 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26984635
20.
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts.
Behav Genet
; 46(2): 151-69, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26392368