| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acknowledgments to Our Reviewers for 2012
|
|
|
2013
|
214-215 |
1-2 |
p. 47-48
2 p.
|
artikel
|
| 2 |
Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participants
|
Laurie, Cathy C.
|
|
2014
|
214-215 |
1-2 |
p. 19-30
12 p.
|
artikel
|
| 3 |
A functional variant in miR-605 modifies the age of onset in Li-Fraumeni syndrome
|
Id Said, Badr
|
|
2015
|
214-215 |
1-2 |
p. 47-51
5 p.
|
artikel
|
| 4 |
A novel four-color fluorescence in situ hybridization assay for the detection of TMPRSS2 and ERG rearrangements in prostate cancer
|
Qu, Xiaoyu
|
|
2013
|
214-215 |
1-2 |
p. 1-11
11 p.
|
artikel
|
| 5 |
Association of interleukin-1β –511 C/T polymorphism with tobacco-associated cancer in northeast India: a study on oral and gastric cancer
|
Lakhanpal, Meena
|
|
2014
|
214-215 |
1-2 |
p. 1-11
11 p.
|
artikel
|
| 6 |
A t(17;22)(q21;q12) with partial ETV4 deletion in a soft tissue Ewing sarcoma
|
Rougemont, Anne-Laure
|
|
2012
|
214-215 |
1-2 |
p. 55-60
6 p.
|
artikel
|
| 7 |
Biallelic FANCD1/BRCA2 mutations predisposing to glioblastoma multiforme with multiple oncogenic amplifications
|
Dodgshun, Andrew J.
|
|
2016
|
214-215 |
1-2 |
p. 53-56
4 p.
|
artikel
|
| 8 |
Centrosome amplification in bladder washing cytology specimens is a useful prognostic biomarker for non-muscle invasive bladder cancer
|
Miyachika, Yoshihiro
|
|
2013
|
214-215 |
1-2 |
p. 12-18
7 p.
|
artikel
|
| 9 |
Change in HER2 (ERBB2) gene status after taxane-based chemotherapy for breast cancer: polyploidization can lead to diagnostic pitfalls with potential impact for clinical management
|
Valent, Alexander
|
|
2013
|
214-215 |
1-2 |
p. 37-41
5 p.
|
artikel
|
| 10 |
Characterization of the colorectal cancer–associated enhancer MYC-335 at 8q24: the role of rs67491583
|
Tuupanen, Sari
|
|
2012
|
214-215 |
1-2 |
p. 25-33
9 p.
|
artikel
|
| 11 |
Clinical characteristics and outcomes of BRCA-associated ovarian cancer: genotype and survival
|
Liu, Joyce
|
|
2012
|
214-215 |
1-2 |
p. 34-41
8 p.
|
artikel
|
| 12 |
Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors
|
Dougherty, Margaret J.
|
|
2012
|
214-215 |
1-2 |
p. 42-54
13 p.
|
artikel
|
| 13 |
Clonal evolution and clinical significance of copy number neutral loss of heterozygosity of chromosome arm 6p in acquired aplastic anemia
|
Betensky, Marisol
|
|
2016
|
214-215 |
1-2 |
p. 1-10
10 p.
|
artikel
|
| 14 |
Contribution of MLPA to routine diagnostic testing of recurrent genomic aberrations in chronic lymphocytic leukemia
|
Véronèse, Lauren
|
|
2013
|
214-215 |
1-2 |
p. 19-25
7 p.
|
artikel
|
| 15 |
Cover 1
|
|
|
2015
|
214-215 |
1-2 |
p. OFC-
1 p.
|
artikel
|
| 16 |
Cover 1
|
|
|
2014
|
214-215 |
1-2 |
p. OFC-
1 p.
|
artikel
|
| 17 |
Cover 1
|
|
|
2012
|
214-215 |
1-2 |
p. OFC-
1 p.
|
artikel
|
| 18 |
Cover 1
|
|
|
2013
|
214-215 |
1-2 |
p. OFC-
1 p.
|
artikel
|
| 19 |
Cover_spine
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|
2016
|
214-215 |
1-2 |
p. CO1-
1 p.
|
artikel
|
| 20 |
Cytogenetically cryptic and FISH-negative PML/RARA rearrangement in acute promyelocytic leukemia detected only by PCR: an exceedingly rare phenomenon
|
Blanco, Elvia Martinez
|
|
2014
|
214-215 |
1-2 |
p. 48-49
2 p.
|
artikel
|
| 21 |
Digitally guided microdissection aids somatic mutation detection in difficult to dissect tumors
|
Geiersbach, Katherine
|
|
2016
|
214-215 |
1-2 |
p. 42-49
8 p.
|
artikel
|
| 22 |
Editorial Board
|
|
|
2015
|
214-215 |
1-2 |
p. IFC-
1 p.
|
artikel
|
| 23 |
Editorial Board
|
|
|
2014
|
214-215 |
1-2 |
p. IFC-
1 p.
|
artikel
|
| 24 |
Editorial Board
|
|
|
2016
|
214-215 |
1-2 |
p. CO2-
1 p.
|
artikel
|
| 25 |
Editorial Board
|
|
|
2012
|
214-215 |
1-2 |
p. IFC-
1 p.
|
artikel
|
| 26 |
Editorial Board
|
|
|
2013
|
214-215 |
1-2 |
p. IFC-
1 p.
|
artikel
|
| 27 |
Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations
|
Sherman, Scott K.
|
|
2015
|
214-215 |
1-2 |
p. 41-46
6 p.
|
artikel
|
| 28 |
Evaluation of melanoma antigen (MAGE) gene expression in human cancers using The Cancer Genome Atlas
|
Li, Xiao
|
|
2015
|
214-215 |
1-2 |
p. 25-34
10 p.
|
artikel
|
| 29 |
Hotspot mutations in polyomavirus positive and negative Merkel cell carcinomas
|
Veija, Tuukka
|
|
2016
|
214-215 |
1-2 |
p. 30-35
6 p.
|
artikel
|
| 30 |
Integration of cytogenomic data for furthering the characterization of pediatric B-cell acute lymphoblastic leukemia: a multi-institution, multi-platform microarray study
|
Baughn, Linda B.
|
|
2015
|
214-215 |
1-2 |
p. 1-18
18 p.
|
artikel
|
| 31 |
Janet D. Rowley, MD (April 5, 1925–December 17, 2013)
|
Zeleznik-Le, Nancy J.
|
|
2014
|
214-215 |
1-2 |
p. 46-47
2 p.
|
artikel
|
| 32 |
Lymph node hyperplasia: clonal chromosomal and genomic rearrangements. Report of two new cases and literature review
|
Villa, Nicoletta
|
|
2014
|
214-215 |
1-2 |
p. 12-18
7 p.
|
artikel
|
| 33 |
Microarray CGH analyses of chromosomal 20q deletions in patients with hematopoietic malignancies
|
Okada, Michiko
|
|
2012
|
214-215 |
1-2 |
p. 18-24
7 p.
|
artikel
|
| 34 |
Modified cIg-FISH protocol for multiple myeloma in routine cytogenetic laboratory practice
|
Gole, Leena
|
|
2014
|
214-215 |
1-2 |
p. 31-34
4 p.
|
artikel
|
| 35 |
Monoclonality of multifocal epithelioid hemangioendothelioma of the liver by analysis of WWTR1-CAMTA1 breakpoints
|
Errani, Costantino
|
|
2012
|
214-215 |
1-2 |
p. 12-17
6 p.
|
artikel
|
| 36 |
Monosomal karyotype in acute myeloid leukemia defines a distinct subgroup within the adverse cytogenetic risk category
|
Voutiadou, Georgia
|
|
2013
|
214-215 |
1-2 |
p. 32-36
5 p.
|
artikel
|
| 37 |
Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine years
|
Concolino, Paola
|
|
2016
|
214-215 |
1-2 |
p. 36-41
6 p.
|
artikel
|
| 38 |
Papillary renal cell carcinoma with a somatic mutation in MET in a patient with autosomal dominant polycystic kidney disease
|
Zhang, Wanying
|
|
2016
|
214-215 |
1-2 |
p. 11-20
10 p.
|
artikel
|
| 39 |
Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background
|
Fishbein, Lauren
|
|
2012
|
214-215 |
1-2 |
p. 1-11
11 p.
|
artikel
|
| 40 |
Putative functional variants of XRCC1 identified by RegulomeDB were not associated with lung cancer risk in a Korean population
|
Yoo, Seung Soo
|
|
2015
|
214-215 |
1-2 |
p. 19-24
6 p.
|
artikel
|
| 41 |
RANBP2-ALK fusion combined with monosomy 7 in acute myelomonocytic leukemia
|
Lim, Ji-Hun
|
|
2014
|
214-215 |
1-2 |
p. 40-45
6 p.
|
artikel
|
| 42 |
Rare occurrence of a STAT5B N642H mutation in adult T-cell acute lymphoblastic leukemia
|
Ma, Xiaolin
|
|
2015
|
214-215 |
1-2 |
p. 52-53
2 p.
|
artikel
|
| 43 |
Replication of results of a genome-wide association study on lung cancer survival in a Korean population
|
Yoo, Seung Soo
|
|
2014
|
214-215 |
1-2 |
p. 35-39.e2
3866 p.
|
artikel
|
| 44 |
Systematic search for rare variants in Finnish early-onset colorectal cancer patients
|
Tanskanen, Tomas
|
|
2015
|
214-215 |
1-2 |
p. 35-40
6 p.
|
artikel
|
| 45 |
Table of Contents
|
|
|
2014
|
214-215 |
1-2 |
p. A1-
1 p.
|
artikel
|
| 46 |
Table of Contents
|
|
|
2016
|
214-215 |
1-2 |
p. A1-
1 p.
|
artikel
|
| 47 |
Table of Contents
|
|
|
2012
|
214-215 |
1-2 |
p. A1-
1 p.
|
artikel
|
| 48 |
Table of Contents
|
|
|
2013
|
214-215 |
1-2 |
p. A1-
1 p.
|
artikel
|
| 49 |
Table of Contents
|
|
|
2015
|
214-215 |
1-2 |
p. A1-
1 p.
|
artikel
|
| 50 |
The dominant role of G12C over other KRAS mutation types in the negative prediction of efficacy of epidermal growth factor receptor tyrosine kinase inhibitors in non–small cell lung cancer
|
Fiala, Ondrej
|
|
2013
|
214-215 |
1-2 |
p. 26-31
6 p.
|
artikel
|
| 51 |
Therapy-related myeloid neoplasms with isolated del(20q): comparison with cases of de novo myelodysplastic syndrome with del(20q)
|
Kanagal-Shamanna, Rashmi
|
|
2013
|
214-215 |
1-2 |
p. 42-46
5 p.
|
artikel
|
| 52 |
The rate of recurrent BRCA1, BRCA2, and TP53 mutations in the general population, and unselected ovarian cancer cases, in Belo Horizonte, Brazil
|
Schayek, Hagit
|
|
2016
|
214-215 |
1-2 |
p. 50-52
3 p.
|
artikel
|
| 53 |
Undifferentiated myxoid lipoblastoma with PLAG1–HAS2 fusion in an infant; morphologically mimicking primitive myxoid mesenchymal tumor of infancy (PMMTI)—diagnostic importance of cytogenetic and molecular testing and literature review
|
Warren, Mikako
|
|
2016
|
214-215 |
1-2 |
p. 21-29
9 p.
|
artikel
|
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