Detalhe da pesquisa
1.
Medication effects on the gut microbiome in allo-HCT.
Cell
; 186(12): 2520-2523, 2023 06 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37295398
2.
The tumour microenvironment shapes innate lymphoid cells in patients with hepatocellular carcinoma.
Gut
; 71(6): 1161-1175, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34340996
3.
Tumor heterogeneity assessed by sequencing and fluorescence in situ hybridization (FISH) data.
Bioinformatics
; 37(24): 4704-4711, 2021 12 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34289030
4.
Integration of adeno-associated virus (AAV) into the genomes of most Thai and Mongolian liver cancer patients does not induce oncogenesis.
BMC Genomics
; 22(1): 814, 2021 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34763675
5.
PhISCS-BnB: a fast branch and bound algorithm for the perfect tumor phylogeny reconstruction problem.
Bioinformatics
; 36(Suppl_1): i169-i176, 2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32657358
6.
High Levels of Chromosomal Copy Number Alterations and TP53 Mutations Correlate with Poor Outcome in Younger Breast Cancer Patients.
Am J Pathol
; 190(8): 1643-1656, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32416097
7.
Aneuploidy, TP53 mutation, and amplification of MYC correlate with increased intratumor heterogeneity and poor prognosis of breast cancer patients.
Genes Chromosomes Cancer
; 57(4): 165-175, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29181861
8.
A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct.
J Med Genet
; 54(10): 665-673, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28780564
9.
Phylogenetic analysis of multiple FISH markers in oral tongue squamous cell carcinoma suggests that a diverse distribution of copy number changes is associated with poor prognosis.
Int J Cancer
; 138(1): 98-109, 2016 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26175310
10.
Inferring models of multiscale copy number evolution for single-tumor phylogenetics.
Bioinformatics
; 31(12): i258-67, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26072490
11.
Inherited biallelic CSF3R mutations in severe congenital neutropenia.
Blood
; 123(24): 3811-7, 2014 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24753537
12.
Potential non-B DNA regions in the human genome are associated with higher rates of nucleotide mutation and expression variation.
Nucleic Acids Res
; 42(20): 12367-79, 2014 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25336616
13.
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.
Am J Hum Genet
; 90(6): 986-1001, 2012 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-22608502
14.
The phenotype of human STK4 deficiency.
Blood
; 119(15): 3450-7, 2012 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-22294732
15.
Chromosome 7 to the rescue: overcoming chromosome 10 loss in gliomas.
bioRxiv
; 2024 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38313282
16.
Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance.
Hum Genet
; 132(4): 385-96, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23239121
17.
Accuracy and coverage assessment of Oryctolagus cuniculus (rabbit) genes encoding immunoglobulins in the whole genome sequence assembly (OryCun2.0) and localization of the IGH locus to chromosome 20.
Immunogenetics
; 65(10): 749-62, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23925440
18.
Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.
N Engl J Med
; 361(21): 2033-45, 2009 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19890111
19.
Predicting cancer prognosis and drug response from the tumor microbiome.
Nat Commun
; 13(1): 2896, 2022 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35610202
20.
Deconvolving Clinically Relevant Cellular Immune Cross-talk from Bulk Gene Expression Using CODEFACS and LIRICS Stratifies Patients with Melanoma to Anti-PD-1 Therapy.
Cancer Discov
; 12(4): 1088-1105, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34983745