Detalhe da pesquisa
1.
Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.
Nature;
555(7696): 371-376, 2018 03 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29489755
2.
Cancer germline predisposing variants and late mortality from subsequent malignant neoplasms among long-term childhood cancer survivors: a report from the St Jude Lifetime Cohort and the Childhood Cancer Survivor Study.
Lancet Oncol;
24(10): 1147-1156, 2023 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37797633
3.
indelPost: harmonizing ambiguities in simple and complex indel alignments.
Bioinformatics;
38(2): 549-551, 2022 01 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34431982
4.
Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants.
Genome Res;
29(9): 1555-1565, 2019 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31439692
5.
Therapy-induced mutations drive the genomic landscape of relapsed acute lymphoblastic leukemia.
Blood;
135(1): 41-55, 2020 01 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31697823
6.
RNAIndel: discovering somatic coding indels from tumor RNA-Seq data.
Bioinformatics;
36(5): 1382-1390, 2020 03 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31593214
7.
The landscape of coding RNA editing events in pediatric cancer.
BMC Cancer;
21(1): 1233, 2021 Nov 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34789196
8.
Inhibition of SF3B1 by molecules targeting the spliceosome results in massive aberrant exon skipping.
RNA;
24(8): 1056-1066, 2018 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29844105
9.
Estimated number of adult survivors of childhood cancer in United States with cancer-predisposing germline variants.
Pediatr Blood Cancer;
67(2): e28047, 2020 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31736278
10.
Germline Mutations in Predisposition Genes in Pediatric Cancer.
N Engl J Med;
373(24): 2336-2346, 2015 Dec 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26580448
11.
Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia.
PLoS Genet;
11(6): e1005262, 2015 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26102509
12.
RNAIndel: discovering somatic coding indels from tumor RNA-Seq data.
Bioinformatics;
36(14): 4231, 2020 08 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32572447
13.
Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study.
Lancet Oncol;
16(16): 1659-66, 2015 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26522332
14.
Corrigendum: Inhibition of SF3B1 by molecules targeting the spliceosome results in massive aberrant exon skipping.
RNA;
24(12): 1886, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30446591
15.
The most informative spacing test effectively discovers biologically relevant outliers or multiple modes in expression.
Bioinformatics;
30(10): 1400-8, 2014 May 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24458951
16.
Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project.
Blood;
121(3): 485-8, 2013 Jan 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23212523
17.
Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group.
Blood;
118(11): 3080-7, 2011 Sep 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21680795
18.
Defining the condensate landscape of fusion oncoproteins.
Nat Commun;
14(1): 6008, 2023 09 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37770423
19.
Bambino: a variant detector and alignment viewer for next-generation sequencing data in the SAM/BAM format.
Bioinformatics;
27(6): 865-6, 2011 Mar 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21278191
20.
Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint.
Cancer Cell;
39(1): 83-95.e4, 2021 01 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33434514