Detalhe da pesquisa
1.
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet
; 17(7): e1009679, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34324492
2.
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet
; 17(9): e1009809, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34547032
3.
CRISPR/Cas9-induced knockout reveals the role of ABCB1 in the response to temozolomide, carmustine and lomustine in glioblastoma multiforme.
Pharmacol Res
; 185: 106510, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36252775
4.
Genome sequencing in families with congenital limb malformations.
Hum Genet
; 140(8): 1229-1239, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34159400
5.
Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study.
Br J Cancer
; 123(4): 619-623, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32451468
6.
Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3).
Genes Chromosomes Cancer
; 55(9): 677-87, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27121553
7.
A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma.
Blood
; 123(8): 1187-98, 2014 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-24398325
8.
Genotype/phenotype correlation in a female patient with 21q22.3 and 12p13.33 duplications.
Am J Med Genet A
; 170A(4): 1050-8, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26749249
9.
A familial disorder of altered DNA-methylation.
J Med Genet
; 51(6): 407-12, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24721835
10.
Recurrent mutation of JAK3 in T-cell prolymphocytic leukemia.
Genes Chromosomes Cancer
; 53(4): 309-16, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24446122
11.
Janus--a comprehensive tool investigating the two faces of transcription.
Bioinformatics
; 29(13): 1600-6, 2013 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23620359
12.
Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.
Am J Hum Genet
; 86(2): 279-84, 2010 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20137775
13.
Clonal evolution in tyrosine kinase inhibitor-resistance: lessons from in vitro-models.
Front Oncol
; 13: 1200897, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37384296
14.
Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B-cell and Burkitt lymphomas.
Int J Cancer
; 131(5): E830-5, 2012 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22213068
15.
Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma.
Br J Haematol
; 157(6): 702-8, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22469134
16.
Immunoglobulin heavy chain locus chromosomal translocations in B-cell precursor acute lymphoblastic leukemia: rare clinical curios or potent genetic drivers?
Blood
; 115(8): 1490-9, 2010 Feb 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-20042721
17.
Presence of the P2RY8-CRLF2 rearrangement is associated with a poor prognosis in non-high-risk precursor B-cell acute lymphoblastic leukemia in children treated according to the ALL-BFM 2000 protocol.
Blood
; 115(26): 5393-7, 2010 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20378752
18.
Statistical inference of allelic imbalance from transcriptome data.
Hum Mutat
; 32(1): 98-106, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21120951
19.
Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemia.
Blood
; 114(13): 2688-98, 2009 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-19641190
20.
Rare occurrence of biallelic CYLD gene mutations in classical Hodgkin lymphoma.
Genes Chromosomes Cancer
; 49(9): 803-9, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20607853