Detalhe da pesquisa
1.
High karyotypic complexity is an independent prognostic factor in patients with CLL treated with venetoclax combinations.
Blood
; 142(5): 446-459, 2023 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37172204
2.
Fixed-duration venetoclax plus obinutuzumab improves quality of life and geriatric impairments in FCR-unfit patients with CLL.
Blood
; 142(13): 1131-1142, 2023 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37363833
3.
Activity of venetoclax in patients with relapsed or refractory chronic lymphocytic leukaemia: analysis of the VENICE-1 multicentre, open-label, single-arm, phase 3b trial.
Lancet Oncol
; 25(4): 463-473, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38467131
4.
Minimal residual disease-guided stop and start of venetoclax plus ibrutinib for patients with relapsed or refractory chronic lymphocytic leukaemia (HOVON141/VISION): primary analysis of an open-label, randomised, phase 2 trial.
Lancet Oncol
; 23(6): 818-828, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35654052
5.
Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch Caribbean.
Am J Med Genet A
; 188(6): 1777-1791, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35253369
6.
Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity: a multi-center study.
Haematologica
; 106(1): 87-97, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31974198
7.
Does non-invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population-based register study.
Prenat Diagn
; 41(10): 1351-1359, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34176145
8.
Oral-facial-digital syndrome type 1 in males: Congenital heart defects are included in its phenotypic spectrum.
Am J Med Genet A
; 173(5): 1383-1389, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28371265
9.
Trisomy 4 mosaicism: Delineation of the phenotype.
Am J Med Genet A
; 170A(4): 1040-5, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26789019
10.
The idiopathic preterm delivery methylation profile in umbilical cord blood DNA.
BMC Genomics
; 16: 736, 2015 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26419829
11.
Venetoclax consolidation after fixed-duration venetoclax plus obinutuzumab for previously untreated chronic lymphocytic leukaemia (HOVON 139/GiVe): primary endpoint analysis of a multicentre, open-label, randomised, parallel-group, phase 2 trial.
Lancet Haematol
; 9(3): e190-e199, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35240075
12.
Venetoclax Plus Rituximab in Relapsed Chronic Lymphocytic Leukemia: 4-Year Results and Evaluation of Impact of Genomic Complexity and Gene Mutations From the MURANO Phase III Study.
J Clin Oncol
; 38(34): 4042-4054, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32986498
13.
PRRT2-related phenotypes in patients with a 16p11.2 deletion.
Eur J Med Genet
; 62(4): 265-269, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30125676
14.
Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates.
PLoS One
; 13(3): e0194938, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29601581
15.
Generation and characterization of a human iPSC line SANi005-A containing the gray platelet associated heterozygous mutation p.Q287* in GFI1B.
Stem Cell Res
; 25: 34-37, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29055225
16.
Generation and characterization of human iPSC lines SANi001-A and SANi002-A from mobilized peripheral blood derived megakaryoblasts.
Stem Cell Res
; 25: 42-45, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29055227
17.
Generation and characterization of human iPSC line MML-6838-Cl2 from mobilized peripheral blood derived megakaryoblasts.
Stem Cell Res
; 18: 26-28, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28395797
18.
Clinicobiological characteristics and treatment efficacy of novel agents in chronic lymphocytic leukemia with IGLV3-21R110.
Leukemia
; 36(7): 1935-1938, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35585140
19.
Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies.
Eur J Hum Genet
; 20(2): 166-70, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21915152
20.
The importance of chromosome studies in Roberts syndrome/SC phocomelia and other cohesinopathies.
Eur J Med Genet
; 53(1): 40-4, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-19878742