Detalhe da pesquisa
1.
Single-cell functional genomics reveals determinants of sensitivity and resistance to natural killer cells in blood cancers.
Immunity
; 56(12): 2816-2835.e13, 2023 Dec 12.
Artigo
Inglês
| MEDLINE | ID: mdl-38091953
2.
Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci.
Hum Mol Genet
; 31(10): 1720-1732, 2022 05 19.
Artigo
Inglês
| MEDLINE | ID: mdl-35077545
3.
Molecular features encoded in the ctDNA reveal heterogeneity and predict outcome in high-risk aggressive B-cell lymphoma.
Blood
; 139(12): 1863-1877, 2022 03 24.
Artigo
Inglês
| MEDLINE | ID: mdl-34932792
4.
Integrated drug profiling and CRISPR screening identify essential pathways for CAR T-cell cytotoxicity.
Blood
; 135(9): 597-609, 2020 02 27.
Artigo
Inglês
| MEDLINE | ID: mdl-31830245
5.
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Cephalalgia
; 42(7): 631-644, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35166138
6.
Incidence Trends for SARS-CoV-2 Alpha and Beta Variants, Finland, Spring 2021.
Emerg Infect Dis
; 27(12): 3137-3141, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34708686
7.
Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: a population-based mtDNA sequencing study.
Hum Mol Genet
; 28(8): 1381-1391, 2019 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30629177
8.
Identifying haplotypes in recessive inherited retinal dystrophies using whole-genome linked-read sequencing.
Clin Genet
; 99(1): 193-198, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32901921
9.
The CRCbiome study: a large prospective cohort study examining the role of lifestyle and the gut microbiome in colorectal cancer screening participants.
BMC Cancer
; 21(1): 930, 2021 Aug 18.
Artigo
Inglês
| MEDLINE | ID: mdl-34407780
10.
Somatic mutations and T-cell clonality in patients with immunodeficiency.
Haematologica
; 105(12): 2757-2768, 2020 12 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33256375
11.
SLC18A3 variants lead to fetal akinesia deformation sequence early in pregnancy.
Am J Med Genet A
; 179(7): 1362-1365, 2019 07.
Artigo
Inglês
| MEDLINE | ID: mdl-31059209
12.
A novel class of somatic mutations in blood detected preferentially in CD8+ cells.
Clin Immunol
; 175: 75-81, 2017 02.
Artigo
Inglês
| MEDLINE | ID: mdl-27932211
13.
Copy number alterations define outcome in Philadelphia chromosome-positive acute lymphoblastic leukemia.
Haematologica
; 107(8): 1971-1976, 2022 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35484650
14.
Driver Gene and Novel Mutations in Asbestos-Exposed Lung Adenocarcinoma and Malignant Mesothelioma Detected by Exome Sequencing.
Lung
; 194(1): 125-35, 2016 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-26463840
15.
Somatic STAT3 mutations in large granular lymphocytic leukemia.
N Engl J Med
; 366(20): 1905-13, 2012 May 17.
Artigo
Inglês
| MEDLINE | ID: mdl-22591296
16.
Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency.
Gastroenterology
; 147(3): 595-598.e5, 2014 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-24941021
17.
Discovery of somatic STAT5b mutations in large granular lymphocytic leukemia.
Blood
; 121(22): 4541-50, 2013 May 30.
Artigo
Inglês
| MEDLINE | ID: mdl-23596048
18.
STAT3 mutations indicate the presence of subclinical T-cell clones in a subset of aplastic anemia and myelodysplastic syndrome patients.
Blood
; 122(14): 2453-9, 2013 Oct 03.
Artigo
Inglês
| MEDLINE | ID: mdl-23926297
19.
The analysis of clonal diversity and therapy responses using STAT3 mutations as a molecular marker in large granular lymphocytic leukemia.
Haematologica
; 100(1): 91-9, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25281507
20.
Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias.
Genes Chromosomes Cancer
; 53(7): 579-88, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24664538