nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A case of gastric adenocarcinoma with conspicuous binuclear cytologic features
|
Ito, Hideaki |
|
2013 |
233-234 |
7-8 |
p. 304-307 4 p. |
artikel |
2 |
A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity
|
Jeandidier, Eric |
|
2012 |
233-234 |
7-8 |
p. 365-372 8 p. |
artikel |
3 |
Analysis of Esophageal Adenocarcinoma Using Combined aCGH – SNP (CCMC v2+EA) Microarray Platform
|
Ahmad, Ausaf |
|
2012 |
233-234 |
7-8 |
p. 421-422 2 p. |
artikel |
4 |
A novel fumarate hydratase-deficient HLRCC kidney cancer cell line, UOK268: a model of the Warburg effect in cancer
|
Yang, Youfeng |
|
2012 |
233-234 |
7-8 |
p. 377-390 14 p. |
artikel |
5 |
A polymorphism at the miR-502 binding site in the 3′ untranslated region of the SET8 gene is associated with the risk of epithelial ovarian cancer
|
Wang, Cuiju |
|
2012 |
233-234 |
7-8 |
p. 373-376 4 p. |
artikel |
6 |
Array-Based Karyotyping Post Plasma Cell Enrichment for the Detection of Genomic Abnormalities in Multiple Myeloma
|
Zehentner, Barbara K. |
|
2012 |
233-234 |
7-8 |
p. 419- 1 p. |
artikel |
7 |
Ascertainment of Recurrent Translocations by Chromosomal Microarray Analysis
|
Gu, Guangyu |
|
2012 |
233-234 |
7-8 |
p. 420-421 2 p. |
artikel |
8 |
Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database
|
Xiang, Bixia |
|
2012 |
233-234 |
7-8 |
p. 420- 1 p. |
artikel |
9 |
BCR-PDGFRA fusion in a T lymphoblastic leukemia/lymphoma
|
Yigit, Nuri |
|
2015 |
233-234 |
7-8 |
p. 404-407 4 p. |
artikel |
10 |
Change in ploidy status from hyperdiploid to near-tetraploid in multiple myeloma associated with bortezomib/lenalidomide resistance
|
Pavlistova, Lenka |
|
2014 |
233-234 |
7-8 |
p. 326-331 6 p. |
artikel |
11 |
Chromosomal aberrations in childhood acute lymphoblastic leukemia: 15-year single center experience
|
Jarosova, Marie |
|
2016 |
233-234 |
7-8 |
p. 340-347 8 p. |
artikel |
12 |
Chronic lymphocytic leukemia with a FGFR3 translocation: case report and literature review of an uncommon cytogenetic event
|
Geller, Matthew D. |
|
2014 |
233-234 |
7-8 |
p. 340-343 4 p. |
artikel |
13 |
Clinical Laboratory Implementation of the Detection of Genomic Aberrations in Formalin-Fixed Paraffin-Embedded Small Lymphocytic Lymphoma Specimens by Array-CGH
|
Ma, Charles |
|
2012 |
233-234 |
7-8 |
p. 419- 1 p. |
artikel |
14 |
Clinical Utility of Single Nucleotide Polymorphism (SNP) Microarrays in Pediatric Cancer and Non-Malignant Hematologic Disorders
|
Lu, Xin-Yan |
|
2012 |
233-234 |
7-8 |
p. 420- 1 p. |
artikel |
15 |
Clinicopathology of diffuse intrinsic pontine glioma and its redefined genomic and epigenomic landscape
|
Panditharatna, Eshini |
|
2015 |
233-234 |
7-8 |
p. 367-373 7 p. |
artikel |
16 |
Complementation of non-tumorigenicity of HPV18-positive cervical carcinoma cells involves differential mRNA expression of cellular genes including potential tumor suppressor genes on chromosome 11q13
|
Kehrmann, Angela |
|
2013 |
233-234 |
7-8 |
p. 279-292 14 p. |
artikel |
17 |
Concordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: a report from the Children's Oncology Group
|
Vujkovic, Marijana |
|
2015 |
233-234 |
7-8 |
p. 408-413 6 p. |
artikel |
18 |
Copy number and expression analysis of FOSL1, GSTP1, NTSR1, FADD and CCND1 genes in primary breast tumors with axillary lymph node metastasis
|
Callegari, Cíntia C.F. |
|
2016 |
233-234 |
7-8 |
p. 331-339 9 p. |
artikel |
19 |
Cover 1
|
|
|
2014 |
233-234 |
7-8 |
p. OFC- 1 p. |
artikel |
20 |
Cover 1
|
|
|
2015 |
233-234 |
7-8 |
p. OFC- 1 p. |
artikel |
21 |
Cover 1
|
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|
2013 |
233-234 |
7-8 |
p. OFC- 1 p. |
artikel |
22 |
Cover 1
|
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|
2012 |
233-234 |
7-8 |
p. OFC- 1 p. |
artikel |
23 |
Cover_spine
|
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|
2016 |
233-234 |
7-8 |
p. CO1- 1 p. |
artikel |
24 |
Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
|
Walther, Charles |
|
2013 |
233-234 |
7-8 |
p. 299-303 5 p. |
artikel |
25 |
Cytogenetic, fluorescence in situ hybridization, and genomic array characterization of chronic myeloid leukemia with cryptic BCR-ABL1 fusions
|
Shao, Lina |
|
2015 |
233-234 |
7-8 |
p. 396-403 8 p. |
artikel |
26 |
Delineating Metastatic Breast Cancer Genome Using Chromosomal Microarray Analysis and Next Generation Sequencing
|
Li, Marilyn M. |
|
2012 |
233-234 |
7-8 |
p. 422- 1 p. |
artikel |
27 |
Diagnostic Utility of Array-CGH to Classify Renal Cell Carcinoma in Image-Guided Needle Biopsies
|
Gowrishankar, Banumathy |
|
2012 |
233-234 |
7-8 |
p. 422- 1 p. |
artikel |
28 |
Divergent gastrointestinal stromal tumors in syndromic settings
|
Ricci, Riccardo |
|
2016 |
233-234 |
7-8 |
p. 354-358 5 p. |
artikel |
29 |
Double minute chromosomes in acute myeloid leukemia, myelodysplastic syndromes, and chronic myelomonocytic leukemia are associated with micronuclei, MYC or MLL amplification, and complex karyotype
|
Huh, Yang O. |
|
2016 |
233-234 |
7-8 |
p. 313-320 8 p. |
artikel |
30 |
Editorial Board
|
|
|
2014 |
233-234 |
7-8 |
p. IFC- 1 p. |
artikel |
31 |
Editorial Board
|
|
|
2015 |
233-234 |
7-8 |
p. A1- 1 p. |
artikel |
32 |
Editorial Board
|
|
|
2016 |
233-234 |
7-8 |
p. CO2- 1 p. |
artikel |
33 |
Editorial Board
|
|
|
2013 |
233-234 |
7-8 |
p. IFC- 1 p. |
artikel |
34 |
Editorial Board
|
|
|
2012 |
233-234 |
7-8 |
p. IFC- 1 p. |
artikel |
35 |
Evaluation of rs62527607 [GT] single nucleotide polymorphism located in BAALC gene in children with acute leukemia using mismatch PCR-RFLP
|
Nadimi, Motahareh |
|
2016 |
233-234 |
7-8 |
p. 348-353 6 p. |
artikel |
36 |
Evaluation of SureFISHtm DNA-FISH Probes for Validation of Array-CGH Aberrations
|
Barenboim, Linda I. |
|
2012 |
233-234 |
7-8 |
p. 421- 1 p. |
artikel |
37 |
Ewing sarcoma mimicking atypical carcinoid tumor: detection of unexpected genomic alterations demonstrates the use of next generation sequencing as a diagnostic tool
|
Doyle, Leona A. |
|
2014 |
233-234 |
7-8 |
p. 335-339 5 p. |
artikel |
38 |
Exome-level comparison of primary well-differentiated neuroendocrine tumors and their cell lines
|
Boora, Ganesh K. |
|
2015 |
233-234 |
7-8 |
p. 374-381 8 p. |
artikel |
39 |
Expression of apoptosis-regulating miRNAs and target mRNAs in oral squamous cell carcinoma
|
Coutinho-Camillo, Cláudia Malheiros |
|
2015 |
233-234 |
7-8 |
p. 382-389 8 p. |
artikel |
40 |
Genomic characterization of recurrent high-grade astroblastoma
|
Bale, Tejus A. |
|
2016 |
233-234 |
7-8 |
p. 321-330 10 p. |
artikel |
41 |
Genomic Loss of Heterozygosity (LOH) in Pediatric Ovarian Germ Cell Tumors (OGCT)
|
Sutcliffe, Maxine J. |
|
2012 |
233-234 |
7-8 |
p. 423-424 2 p. |
artikel |
42 |
Genomic microarray analysis on formalin-fixed paraffin-embedded material for uveal melanoma prognostication
|
Minca, Eugen C. |
|
2014 |
233-234 |
7-8 |
p. 306-315 10 p. |
artikel |
43 |
HELIOS-BCL11B fusion gene involvement in a t(2;14)(q34;q32) in an adult T-cell leukemia patient
|
Fujimoto, Rika |
|
2012 |
233-234 |
7-8 |
p. 356-364 9 p. |
artikel |
44 |
Hyperhaploid plasma cell myeloma
|
Hoctor, Veronica T. |
|
2012 |
233-234 |
7-8 |
p. 414-418 5 p. |
artikel |
45 |
IGF2BP1: a novel IGH translocation partner in B acute lymphoblastic leukemia
|
Gu, Guangyu |
|
2014 |
233-234 |
7-8 |
p. 332-334 3 p. |
artikel |
46 |
Low incidence of IL6ST (gp130) mutations in exon 6 in lung cancer of a Chinese cohort
|
Sun, Luguo |
|
2014 |
233-234 |
7-8 |
p. 291-298 8 p. |
artikel |
47 |
Methylenetetrahydrofolate reductase gene polymorphisms and skin cancer risk: a meta-analysis
|
Deng, Feng |
|
2014 |
233-234 |
7-8 |
p. 299-305 7 p. |
artikel |
48 |
Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma
|
Racher, Hilary |
|
2016 |
233-234 |
7-8 |
p. 359-363 5 p. |
artikel |
49 |
Molecular classification, pathway addiction, and therapeutic targeting in diffuse large B cell lymphoma
|
Puvvada, Soham |
|
2013 |
233-234 |
7-8 |
p. 257-265 9 p. |
artikel |
50 |
Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone
|
Trombetta, Domenico |
|
2012 |
233-234 |
7-8 |
p. 410-413 4 p. |
artikel |
51 |
Molecular inversion probe analysis detects novel copy number alterations in Ewing sarcoma
|
Jahromi, Mona S. |
|
2012 |
233-234 |
7-8 |
p. 391-404 14 p. |
artikel |
52 |
Molecular inversion probes: a novel microarray technology and its application in cancer research
|
Wang, Yuker |
|
2012 |
233-234 |
7-8 |
p. 341-355 15 p. |
artikel |
53 |
Narrowing down the common deleted region of 5q to 6.0 Mb in blastic plasmacytoid dendritic cell neoplasms
|
Fu, Yumei |
|
2013 |
233-234 |
7-8 |
p. 293-298 6 p. |
artikel |
54 |
Polymorphisms in genes related to inflammation, NSAID use, and the risk of prostate cancer among Danish men
|
Kopp, Tine Iskov |
|
2013 |
233-234 |
7-8 |
p. 266-278 13 p. |
artikel |
55 |
Population-based characterization of the genetic landscape of chronic lymphocytic leukemia patients referred for cytogenetic testing in British Columbia, Canada: the role of provincial laboratory standardization
|
Gerrie, Alina S. |
|
2014 |
233-234 |
7-8 |
p. 316-325 10 p. |
artikel |
56 |
Recurrent Genetic Alterations in Hepatitis C-associated Hepatocellular Carcinoma Detected by CGH+SNP Array
|
Liu, Yajuan |
|
2012 |
233-234 |
7-8 |
p. 423- 1 p. |
artikel |
57 |
SNP Array Analysis Detects Genomic Alterations Associated with High-Risk Disease in Neuroblastoma
|
Ouyang, Karen J. |
|
2012 |
233-234 |
7-8 |
p. 423- 1 p. |
artikel |
58 |
Somatic c.34G>T KRAS mutation: a new prescreening test for MUTYH-associated polyposis?
|
Aimé, Adeline |
|
2015 |
233-234 |
7-8 |
p. 390-395 6 p. |
artikel |
59 |
Table of Contents
|
|
|
2014 |
233-234 |
7-8 |
p. A1- 1 p. |
artikel |
60 |
Table of Contents
|
|
|
2015 |
233-234 |
7-8 |
p. A3- 1 p. |
artikel |
61 |
Table of Contents
|
|
|
2016 |
233-234 |
7-8 |
p. A1- 1 p. |
artikel |
62 |
Table of Contents
|
|
|
2013 |
233-234 |
7-8 |
p. A1- 1 p. |
artikel |
63 |
Table of Contents
|
|
|
2012 |
233-234 |
7-8 |
p. A1-A2 nvt p. |
artikel |
64 |
The HEL Erythroleukemia Cell Line as a Test Case for Detailed Description of a Complex Karyotype by Combining SNP Array with Multiple FISH Approaches
|
MacKinnon, Ruth N. |
|
2012 |
233-234 |
7-8 |
p. 421- 1 p. |
artikel |
65 |
The NAB2–STAT6 gene fusion in solitary fibrous tumor can be reliably detected by anchored multiplexed PCR for targeted next-generation sequencing
|
Guseva, Natalya V. |
|
2016 |
233-234 |
7-8 |
p. 303-312 10 p. |
artikel |
66 |
Validation of Karyotypic Abnormalities in Human Pluripotent Stem Cells: Cytogenetic Progression in WA09 Mirrors Cancer
|
Nisler, Benjamin S. |
|
2012 |
233-234 |
7-8 |
p. 423- 1 p. |
artikel |
67 |
When are apparently non-clonal abnormalities in bone marrow chromosome studies actually clonal?
|
Hutchens, Chandra |
|
2012 |
233-234 |
7-8 |
p. 405-409 5 p. |
artikel |