Detalhe da pesquisa
1.
Polymorphisms within Autophagy-Related Genes as Susceptibility Biomarkers for Multiple Myeloma: A Meta-Analysis of Three Large Cohorts and Functional Characterization.
Int J Mol Sci
; 24(10)2023 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37239846
2.
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes.
Hum Genomics
; 13(1): 37, 2019 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31429796
3.
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
Mol Med
; 24(1): 30, 2018 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30134812
4.
Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients.
BMC Cancer
; 18(1): 820, 2018 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30111286
5.
Bortezomib-induced peripheral neuropathy: A genome-wide association study on multiple myeloma patients.
Hematol Oncol
; 36(1): 232-237, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28317148
6.
Functional germline variants in driver genes of breast cancer.
Cancer Causes Control
; 28(4): 259-271, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28238063
7.
Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy: Replication of the Reported Candidate Susceptibility Loci.
Neurochem Res
; 42(3): 925-931, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27422265
8.
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS).
Eur J Haematol
; 99(1): 70-79, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28375557
9.
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype.
Blood
; 122(19): 3298-307, 2013 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23996088
10.
Polymorphisms within Autophagy-Related Genes Influence the Risk of Developing Colorectal Cancer: A Meta-Analysis of Four Large Cohorts.
Cancers (Basel)
; 13(6)2021 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33809172
11.
Loci associated with genomic damage levels in chronic kidney disease patients and controls.
Mutat Res Genet Toxicol Environ Mutagen
; 852: 503167, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32265040
12.
Epistatic effect of TLR3 and cGAS-STING-IKKε-TBK1-IFN signaling variants on colorectal cancer risk.
Cancer Med
; 9(4): 1473-1484, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31869529
13.
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma.
Commun Biol
; 2: 89, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30854481
14.
Association of NLRP1 Coding Polymorphism with Lung Function and Serum IL-1ß Concentration in Patients Diagnosed with Chronic Obstructive Pulmonary Disease (COPD).
Genes (Basel)
; 10(10)2019 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31601004
15.
Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma.
Nat Commun
; 10(1): 213, 2019 01 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30631080
16.
Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
Nat Commun
; 10(1): 157, 2019 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30622283
17.
Levels of DNA damage (Micronuclei) in patients suffering from chronic kidney disease. Role of GST polymorphisms.
Mutat Res Genet Toxicol Environ Mutagen
; 836(Pt A): 41-46, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30389161
18.
Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer.
PLoS One
; 13(2): e0192385, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29408916
19.
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma.
Nat Commun
; 9(1): 3707, 2018 09 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30213928
20.
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology.
Blood Cancer J
; 9(1): 1, 2018 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30602759