nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Advances in the understanding of constitutional and somatic genomic alterations in neuroblastoma
|
Deyell, Rebecca J. |
|
2011 |
212-213 |
3 |
p. 113-121 9 p. |
artikel |
2 |
Amplification of EVI1 on cytogenetically cryptic double minutes as new mechanism for increased expression of EVI1
|
Volkert, Sarah |
|
2014 |
212-213 |
3 |
p. 103-108 6 p. |
artikel |
3 |
Analysis of miRNA-gene expression-genomic profiles reveals complex mechanisms of microRNA deregulation in osteosarcoma
|
Maire, Georges |
|
2011 |
212-213 |
3 |
p. 138-146 9 p. |
artikel |
4 |
A new rearrangement giving rise to a very rare MLL-MLLT10 fusion mRNA in an infant acute myeloid leukemia
|
Burillo-Sanz, Sergio |
|
2015 |
212-213 |
3 |
p. 101-102 2 p. |
artikel |
5 |
A novel BAP1 mutation is associated with melanocytic neoplasms and thyroid cancer
|
McDonnell, Kevin J. |
|
2016 |
212-213 |
3 |
p. 75-81 7 p. |
artikel |
6 |
A t(11;14)(p13;q11.2) in myelofibrosis following polycythemia vera
|
Jeong, Ji Hun |
|
2016 |
212-213 |
3 |
p. 112-116 5 p. |
artikel |
7 |
BCL2, BCL6, IGH, TP53, and MYC protein expression and gene rearrangements as prognostic markers in diffuse large B-cell lymphoma: a study of 44 Turkish patients
|
Akay, Olga Meltem |
|
2014 |
212-213 |
3 |
p. 87-93 7 p. |
artikel |
8 |
CD5-positive, cyclinD1-negative mantle cell lymphoma with a translocation involving the CCND2 gene and the IGL locus
|
Shiller, Shirley Michelle |
|
2011 |
212-213 |
3 |
p. 162-164 3 p. |
artikel |
9 |
Chronic lymphocytic leukemia: a clinical and molecular heterogenous disease
|
Rodríguez-Vicente, Ana E. |
|
2013 |
212-213 |
3 |
p. 49-62 14 p. |
artikel |
10 |
Clinical significance of papillary thyroid cancer risk loci identified by genome-wide association studies
|
Wei, Wen-Jun |
|
2015 |
212-213 |
3 |
p. 68-75 8 p. |
artikel |
11 |
Clonal chromosomal abnormalities in Ph-negative cells in chronic myeloid leukemia: an unusual case evolving to secondary acute myeloid leukemia
|
Van Obbergh, Florence |
|
2015 |
212-213 |
3 |
p. 102-104 3 p. |
artikel |
12 |
Combinations of genetic data in a study of neuroblastoma risk genotypes
|
Capasso, Mario |
|
2014 |
212-213 |
3 |
p. 94-97 4 p. |
artikel |
13 |
Comparison of chromosomal aberrations in primary colorectal carcinomas to their pulmonary metastases
|
Danner, Bernhard C. |
|
2011 |
212-213 |
3 |
p. 122-128 7 p. |
artikel |
14 |
Constance A. Griffin, MD (June 8, 1951–January 8, 2012)
|
Axilbund, Jennifer E. |
|
2012 |
212-213 |
3 |
p. 78-79 2 p. |
artikel |
15 |
Copy neutral loss of heterozygosity in 20q in chronic lymphocytic leukemia/small lymphocytic lymphoma
|
Pei, Jianming |
|
2014 |
212-213 |
3 |
p. 98-102 5 p. |
artikel |
16 |
Cover 1
|
|
|
2015 |
212-213 |
3 |
p. OFC- 1 p. |
artikel |
17 |
Cover 1
|
|
|
2012 |
212-213 |
3 |
p. OFC- 1 p. |
artikel |
18 |
Cover 1
|
|
|
2011 |
212-213 |
3 |
p. OFC- 1 p. |
artikel |
19 |
Cover 1
|
|
|
2013 |
212-213 |
3 |
p. OFC- 1 p. |
artikel |
20 |
Cover 1
|
|
|
2014 |
212-213 |
3 |
p. OFC- 1 p. |
artikel |
21 |
Cover_spine
|
|
|
2016 |
212-213 |
3 |
p. CO1- 1 p. |
artikel |
22 |
Crizotinib resistance in acute myeloid leukemia with inv(2)(p23q13)/RAN binding protein 2 (RANBP2) anaplastic lymphoma kinase (ALK) fusion and monosomy 7
|
Takeoka, Kayo |
|
2015 |
212-213 |
3 |
p. 85-90 6 p. |
artikel |
23 |
Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome
|
Manola, Kalliopi N. |
|
2013 |
212-213 |
3 |
p. 63-72 10 p. |
artikel |
24 |
Development of t(8;21) and RUNX1–RUNX1T1 in the Philadelphia-positive clone of a patient with chronic myelogenous leukemia: additional evidence for multiple steps involved in disease progression
|
Najfeld, Vesna |
|
2011 |
212-213 |
3 |
p. 165-170 6 p. |
artikel |
25 |
Disruption of the APC gene by t(5;7) translocation in a Turcot family
|
Sahnane, Nora |
|
2016 |
212-213 |
3 |
p. 107-111 5 p. |
artikel |
26 |
Distinct set of chromosomal aberrations in childhood hepatocellular carcinoma is correlated to hepatitis B virus infection
|
Tan, Lu |
|
2016 |
212-213 |
3 |
p. 87-96 10 p. |
artikel |
27 |
Down-regulation of FoxM1 leads to the inhibition of the epithelial-mesenchymal transition in gastric cancer cells
|
Miao, Lifeng |
|
2014 |
212-213 |
3 |
p. 75-82 8 p. |
artikel |
28 |
Editorial Board
|
|
|
2014 |
212-213 |
3 |
p. IFC- 1 p. |
artikel |
29 |
Editorial Board
|
|
|
2015 |
212-213 |
3 |
p. IFC- 1 p. |
artikel |
30 |
Editorial Board
|
|
|
2016 |
212-213 |
3 |
p. CO2- 1 p. |
artikel |
31 |
Editorial Board
|
|
|
2012 |
212-213 |
3 |
p. A1- 1 p. |
artikel |
32 |
Editorial Board
|
|
|
2011 |
212-213 |
3 |
p. IFC- 1 p. |
artikel |
33 |
Editorial Board
|
|
|
2013 |
212-213 |
3 |
p. IFC- 1 p. |
artikel |
34 |
Effectiveness of dasatinib in accelerated-phase chronic myeloid leukemia with p190 BCR-ABL1 and a second Philadelphia chromosome
|
Rabenau, Karen E. |
|
2014 |
212-213 |
3 |
p. 109-110 2 p. |
artikel |
35 |
Evolution in a transmissible cancer: a study of the chromosomal changes in devil facial tumor (DFT) as it spreads through the wild Tasmanian devil population
|
Pearse, Anne-Maree |
|
2012 |
212-213 |
3 |
p. 101-112 12 p. |
artikel |
36 |
Expression of Kit and Etv1 in restricted brain regions supports a brain-cell progenitor as an origin for cranial germinomas
|
Tan, Chris |
|
2015 |
212-213 |
3 |
p. 55-61 7 p. |
artikel |
37 |
High frequency of allelic loss at the BRCA1 locus in ovarian cancers: clinicopathologic and molecular associations
|
Rzepecka, Iwona K. |
|
2012 |
212-213 |
3 |
p. 94-100 7 p. |
artikel |
38 |
High resolution array comparative genomic hybridization identifies copy number alterations in diffuse large B-cell lymphoma that predict response to immuno-chemotherapy
|
Kreisel, F. |
|
2011 |
212-213 |
3 |
p. 129-137 9 p. |
artikel |
39 |
Identification of the TAF15–ZNF384 fusion gene in two new cases of acute lymphoblastic leukemia with a t(12;17)(p13;q12)
|
Nyquist, Kaja Beate |
|
2011 |
212-213 |
3 |
p. 147-152 6 p. |
artikel |
40 |
Investigation of a putative melanoma susceptibility locus at chromosome 3q29
|
Tuominen, Rainer |
|
2014 |
212-213 |
3 |
p. 70-74 5 p. |
artikel |
41 |
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia
|
Gorello, Paolo |
|
2013 |
212-213 |
3 |
p. 92-96 5 p. |
artikel |
42 |
Matrix metalloproteinase 13: a potential intermediate between low expression of microRNA-125b and increasing metastatic potential of non–small cell lung cancer
|
Yu, Xiaozhou |
|
2015 |
212-213 |
3 |
p. 76-84 9 p. |
artikel |
43 |
Melanoma risk associated with MC1R gene variants in Latvia and the functional analysis of rare variants
|
Ozola, Aija |
|
2013 |
212-213 |
3 |
p. 81-91 11 p. |
artikel |
44 |
MicroRNA-26a regulates tumorigenic properties of EZH2 in human lung carcinoma cells
|
Dang, Xiaomin |
|
2012 |
212-213 |
3 |
p. 113-123 11 p. |
artikel |
45 |
Monosomy and ring chromosome 13 in a thyroid nodular goiter—do we underestimate its relevance in benign thyroid lesions?
|
Sendt, Wolfgang |
|
2012 |
212-213 |
3 |
p. 128-130 3 p. |
artikel |
46 |
MYC amplification in multiple marker chromosomes and EZH2 microdeletion in a man with acute myeloid leukemia
|
Xiang, Zhifu |
|
2015 |
212-213 |
3 |
p. 96-100 5 p. |
artikel |
47 |
Oncogenic KIAA1549-BRAF fusion with activation of the MAPK/ERK pathway in pediatric oligodendrogliomas
|
Kumar, Anupam |
|
2015 |
212-213 |
3 |
p. 91-95 5 p. |
artikel |
48 |
Optimal strategy for obtaining routine chromosome analysis by using negative fractions of CD138 enriched plasma cells
|
Ortega, Veronica |
|
2016 |
212-213 |
3 |
p. 82-86 5 p. |
artikel |
49 |
Overview of recurrent chromosomal losses in retinoblastoma detected by low coverage next generation sequencing
|
García-Chequer, A.J. |
|
2016 |
212-213 |
3 |
p. 57-69 13 p. |
artikel |
50 |
22q11-q13 as a hot spot for prediction of disease-free survival in bile duct cancer: integrative analysis of copy number variations
|
Kang, Mee Joo |
|
2014 |
212-213 |
3 |
p. 57-69 13 p. |
artikel |
51 |
Rare germline variant (rs78378222) in the TP53 3' UTR: Evidence for a new mechanism of cancer predisposition in Li-Fraumeni syndrome
|
Macedo, Gabriel S. |
|
2016 |
212-213 |
3 |
p. 97-106 10 p. |
artikel |
52 |
Simultaneous occurrence of ETV6-RUNX1 and BCR-ABL1 (e1a2) transcripts in a child with B-cell acute lymphoblastic leukemia
|
Balatzenko, Gueorgui |
|
2013 |
212-213 |
3 |
p. 97-101 5 p. |
artikel |
53 |
SNP-based arrays complement classic cytogenetics in the detection of chromosomal aberrations in Wilms’ tumor
|
Zin, Reena |
|
2012 |
212-213 |
3 |
p. 80-93 14 p. |
artikel |
54 |
Somatic loss of an EXT2 gene mutation during malignant progression in a patient with hereditary multiple osteochondromas
|
Musso, Nicolò |
|
2015 |
212-213 |
3 |
p. 62-67 6 p. |
artikel |
55 |
Table of Contents
|
|
|
2014 |
212-213 |
3 |
p. A1- 1 p. |
artikel |
56 |
Table of Contents
|
|
|
2015 |
212-213 |
3 |
p. A1- 1 p. |
artikel |
57 |
Table of Contents
|
|
|
2016 |
212-213 |
3 |
p. A1- 1 p. |
artikel |
58 |
Table of Contents
|
|
|
2012 |
212-213 |
3 |
p. A3- 1 p. |
artikel |
59 |
Table of Contents
|
|
|
2011 |
212-213 |
3 |
p. A1-A2 nvt p. |
artikel |
60 |
Table of Contents
|
|
|
2013 |
212-213 |
3 |
p. A1- 1 p. |
artikel |
61 |
The characteristics and prognostic analysis in 213 myeloid malignancy patients with del(20q): a report of a single-center case series
|
Pan, Jinlan |
|
2014 |
212-213 |
3 |
p. 51-56 6 p. |
artikel |
62 |
The first case of Philadelphia chromosome-negative acute promyelocytic leukemia following imatinib for chronic myelogenous leukemia
|
Wakim, Jad J. |
|
2012 |
212-213 |
3 |
p. 124-127 4 p. |
artikel |
63 |
The genetics of gestational trophoblastic disease: a rare complication of pregnancy
|
Hoffner, Lori |
|
2012 |
212-213 |
3 |
p. 63-77 15 p. |
artikel |
64 |
The peculiar 11q-gain/loss aberration reported in a subset of MYC-negative high-grade B-cell lymphomas can also occur in a MYC-rearranged lymphoma
|
Havelange, Violaine |
|
2016 |
212-213 |
3 |
p. 117-118 2 p. |
artikel |
65 |
The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers
|
Laitman, Yael |
|
2016 |
212-213 |
3 |
p. 70-74 5 p. |
artikel |
66 |
Translocation t(2;7)(p11;q21) associated with the CDK6/IGK rearrangement is a rare but recurrent abnormality in B-cell lymphoproliferative malignancies
|
Douet-Guilbert, Nathalie |
|
2014 |
212-213 |
3 |
p. 83-86 4 p. |
artikel |
67 |
Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20q
|
MacKinnon, Ruth N. |
|
2011 |
212-213 |
3 |
p. 153-161 9 p. |
artikel |
68 |
Utility of serum DNA and pyrosequencing for the detection of EGFR mutations in non-small cell lung cancer
|
Akca, Hakan |
|
2013 |
212-213 |
3 |
p. 73-80 8 p. |
artikel |