Detalhe da pesquisa
1.
Transposable element sequence fragments incorporated into coding and noncoding transcripts modulate the transcriptome of human pluripotent stem cells.
Nucleic Acids Res
; 49(16): 9132-9153, 2021 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34390351
2.
Application of T-cell receptor repertoire as a novel monitor in dynamic tracking and assessment: A cohort-study based on RA patients.
J Cell Mol Med
; 26(24): 6042-6055, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36440548
3.
Key findings from the UKCCMP cohort of 877 patients with haematological malignancy and COVID-19: disease control as an important factor relative to recent chemotherapy or anti-CD20 therapy.
Br J Haematol
; 196(4): 892-901, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34761389
4.
Integrative analysis of spontaneous CLL regression highlights genetic and microenvironmental interdependency in CLL.
Blood
; 135(6): 411-428, 2020 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31794600
5.
TKTL1 Knockdown Impairs Hypoxia-Induced Glucose-6-phosphate Dehydrogenase and Glyceraldehyde-3-phosphate Dehydrogenase Overexpression.
Int J Mol Sci
; 23(7)2022 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35408935
6.
Severity of COVID-19 in children with cancer: Report from the United Kingdom Paediatric Coronavirus Cancer Monitoring Project.
Br J Cancer
; 124(4): 754-759, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33299130
7.
COVID-19 mortality in patients with cancer on chemotherapy or other anticancer treatments: a prospective cohort study.
Lancet
; 395(10241): 1919-1926, 2020 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32473682
8.
COVID-19 prevalence and mortality in patients with cancer and the effect of primary tumour subtype and patient demographics: a prospective cohort study.
Lancet Oncol
; 21(10): 1309-1316, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32853557
9.
Novel putative drugs and key initiating genes for neurodegenerative disease determined using network-based genetic integrative analysis.
J Cell Biochem
; 120(4): 5459-5471, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30302804
10.
Candidate gene variant effects on language disorders in Robinson Crusoe Island.
Ann Hum Biol
; 46(2): 109-119, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31132892
11.
Molecular genetics of the transcription factor GLIS3 identifies its dual function in beta cells and neurons.
Genomics
; 110(2): 98-111, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28911974
12.
Harnessing genomics to improve outcomes for women with cancer in India: key priorities for research.
Lancet Oncol
; 19(2): e102-e112, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29413464
13.
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
PLoS Genet
; 11(3): e1004925, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25781923
14.
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis.
Hum Mol Genet
; 23(12): 3200-11, 2014 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24463883
15.
Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development.
J Pathol
; 236(2): 155-64, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25712196
16.
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
Nat Genet
; 39(8): 984-8, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17618284
17.
Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.
Clin Immunol
; 160(2): 301-14, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26122175
18.
mQTL.NMR: an integrated suite for genetic mapping of quantitative variations of (1)H NMR-based metabolic profiles.
Anal Chem
; 87(8): 4377-84, 2015 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-25803548
19.
Circulating lipid levels and risk of coronary artery disease in a large group of patients undergoing coronary angiography.
J Thromb Thrombolysis
; 39(1): 15-22, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24788070
20.
Recessive mutations in SPTBN2 implicate ß-III spectrin in both cognitive and motor development.
PLoS Genet
; 8(12): e1003074, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23236289