| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aberrant expression of the microRNA cluster in 14q32 is associated with del(5q) myelodysplastic syndrome and lenalidomide treatment
|
Krejčík, Zdeněk
|
|
2015
|
|
4 |
p. 156-161
6 p.
|
artikel
|
| 2 |
Acquired isochromosome 12p, somatic TP53 and PTEN mutations, and a germline ATM variant in an adolescent male with concurrent acute megakaryoblastic leukemia and mediastinal germ cell tumor
|
Oshrine, Benjamin R.
|
|
2014
|
|
4 |
p. 153-159
7 p.
|
artikel
|
| 3 |
A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromes
|
MacKinnon, Ruth N.
|
|
2011
|
|
4 |
p. 187-194
8 p.
|
artikel
|
| 4 |
A der(11)t(4;11)(q21;p15) in a T-ALL/LBL patient
|
Colli, Sandra
|
|
2016
|
|
4 |
p. 166-170
5 p.
|
artikel
|
| 5 |
Adult acute lymphoblastic leukemia with a rare b3a3 type BCR/ABL1 fusion transcript
|
Kurita, Daisuke
|
|
2016
|
|
4 |
p. 161-165
5 p.
|
artikel
|
| 6 |
Analysis of genomic abnormalities in tumors: a review of available methods for Illumina two-color SNP genotyping and evaluation of performance
|
Oros, Kathleen Klein
|
|
2013
|
|
4 |
p. 103-115
13 p.
|
artikel
|
| 7 |
Analysis of the predictive efficiency of S100P on adverse prognosis and the pathogenesis of S100P-mediated invasion and metastasis of colon adenocarcinoma
|
Shen, Zhi-Yong
|
|
2016
|
|
4 |
p. 143-153
11 p.
|
artikel
|
| 8 |
Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation
|
Kato, Takema
|
|
2014
|
|
4 |
p. 133-140
8 p.
|
artikel
|
| 9 |
A new variant of KMT2A(MLL)-FLNA fusion transcript in acute myeloid leukemia with ins(X;11)(q28;q23q23)
|
Matveeva, Elena
|
|
2015
|
|
4 |
p. 148-151
4 p.
|
artikel
|
| 10 |
A novel variant in the 3' untranslated region of the CDK4 gene: interference with microRNA target sites and role in increased risk of cutaneous melanoma
|
Pedace, Lucia
|
|
2014
|
|
4 |
p. 168-169
2 p.
|
artikel
|
| 11 |
A polymorphism at the microRNA binding site in the 3′ untranslated region of C14orf101 is associated with non-Hodgkin lymphoma overall survival
|
Yang, Bo
|
|
2014
|
|
4 |
p. 141-146
6 p.
|
artikel
|
| 12 |
Are ER+PR+ and ER+PR− breast tumors genetically different? A CGH array study
|
Carracedo, Alma
|
|
2012
|
|
4 |
p. 138-146
9 p.
|
artikel
|
| 13 |
A ZMYM2-FGFR1 8p11 myeloproliferative neoplasm with a novel nonsense RUNX1 mutation and tumor lysis upon imatinib treatment
|
Buijs, Arjan
|
|
2013
|
|
4 |
p. 140-144
5 p.
|
artikel
|
| 14 |
CHEK2 c.1100delC allele is rarely identified in Greek breast cancer cases
|
Apostolou, Paraskevi
|
|
2015
|
|
4 |
p. 129-134
6 p.
|
artikel
|
| 15 |
Chromosomal microarray provides enhanced targetable gene aberration detection when paired with next generation sequencing panel in profiling lung and colorectal tumors
|
Mukherjee, S.
|
|
2016
|
|
4 |
p. 119-129
11 p.
|
artikel
|
| 16 |
Chromosome banding analysis of cells from fine-needle aspiration biopsy samples from soft tissue and bone tumors: is it clinically meaningful?
|
Walther, Charles
|
|
2011
|
|
4 |
p. 203-206
4 p.
|
artikel
|
| 17 |
Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patients
|
Ghazwani, Yahya
|
|
2016
|
|
4 |
p. 171-176
6 p.
|
artikel
|
| 18 |
Clonal karyotypic abnormalities associated with reactive lymphoid hyperplasia
|
Montgomery, Nathan D.
|
|
2013
|
|
4 |
p. 135-139
5 p.
|
artikel
|
| 19 |
Correlation of WT1 expression with the burden of total and residual leukemic blasts in bone marrow samples of acute myeloid leukemia patients
|
Alonso-Dominguez, Juan Manuel
|
|
2012
|
|
4 |
p. 190-191
2 p.
|
artikel
|
| 20 |
Cover 1
|
|
|
2015
|
|
4 |
p. OFC-
1 p.
|
artikel
|
| 21 |
Cover 1
|
|
|
2012
|
|
4 |
p. OFC-
1 p.
|
artikel
|
| 22 |
Cover 1
|
|
|
2013
|
|
4 |
p. OFC-
1 p.
|
artikel
|
| 23 |
Cover 1
|
|
|
2011
|
|
4 |
p. OFC-
1 p.
|
artikel
|
| 24 |
Cover 1
|
|
|
2014
|
|
4 |
p. OFC-
1 p.
|
artikel
|
| 25 |
Cover_spine
|
|
|
2016
|
|
4 |
p. CO1-
1 p.
|
artikel
|
| 26 |
Cytogenetic characterization of the murine bladder cancer model MB49 and the derived invasive line MB49-I
|
Fabris, Victoria T.
|
|
2012
|
|
4 |
p. 168-176
9 p.
|
artikel
|
| 27 |
Cytogenetic findings in 14 benign cartilaginous neoplasms
|
Sakai Junior, Nilo
|
|
2011
|
|
4 |
p. 180-186
7 p.
|
artikel
|
| 28 |
Cytogenetic profile of locally advanced and metastatic schistosoma-related bladder cancer and response to chemotherapy
|
Aly, Magdy Sayed
|
|
2012
|
|
4 |
p. 156-162
7 p.
|
artikel
|
| 29 |
Deep intronic point mutations of the KIT gene in a female patient with cutaneous clear cell sarcoma and her family
|
Gambichler, Thilo
|
|
2012
|
|
4 |
p. 182-185
4 p.
|
artikel
|
| 30 |
Detection of an early adult T-cell leukemia-lymphoma clone in lymph nodes with anaplastic lymphoma kinase-negative anaplastic large cell lymphoma involvement
|
Tokunaga, Masahito
|
|
2016
|
|
4 |
p. 138-142
5 p.
|
artikel
|
| 31 |
Detection of the FCGR3a polymorphism using a real-time polymerase chain reaction assay
|
Burchard, Paul R.
|
|
2013
|
|
4 |
p. 130-134
5 p.
|
artikel
|
| 32 |
Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors
|
Roth, Jacquelyn J.
|
|
2014
|
|
4 |
p. 111-123
13 p.
|
artikel
|
| 33 |
Editorial Board
|
|
|
2014
|
|
4 |
p. IFC-
1 p.
|
artikel
|
| 34 |
Editorial Board
|
|
|
2015
|
|
4 |
p. A4-
1 p.
|
artikel
|
| 35 |
Editorial Board
|
|
|
2016
|
|
4 |
p. CO2-
1 p.
|
artikel
|
| 36 |
Editorial Board
|
|
|
2012
|
|
4 |
p. IFC-
1 p.
|
artikel
|
| 37 |
Editorial Board
|
|
|
2013
|
|
4 |
p. IFC-
1 p.
|
artikel
|
| 38 |
Editorial Board
|
|
|
2011
|
|
4 |
p. IFC-
1 p.
|
artikel
|
| 39 |
Emergence of clonal hematopoiesis in the majority of patients with acquired aplastic anemia
|
Babushok, Daria V.
|
|
2015
|
|
4 |
p. 115-128
14 p.
|
artikel
|
| 40 |
Erratum to “5-hydroxymethylcytosine in cancer: Significance in diagnosis and therapy” [Cancer Genet 208 (2015):167–177]
|
Vasanthakumar, Aparna
|
|
2016
|
|
4 |
p. 177-
1 p.
|
artikel
|
| 41 |
Errors in the interpretation of copy number variations due to the use of public databases as a reference
|
Bastida-Lertxundi, Nerea
|
|
2014
|
|
4 |
p. 164-167
4 p.
|
artikel
|
| 42 |
Establishment and characterization of a novel acute myeloid leukemia cell line, JIH-4, carrying a t(16;21)(p11.2;q22) and expressing the FUS-ERG fusion
|
Jiang, Hui
|
|
2011
|
|
4 |
p. 219-223
5 p.
|
artikel
|
| 43 |
Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: the proposal of a formula
|
Valli, Roberto
|
|
2011
|
|
4 |
p. 216-218
3 p.
|
artikel
|
| 44 |
Genetic anticipation of familial breast cancer with or without BRCA mutation in the Korean population
|
Noh, Jae Myoung
|
|
2014
|
|
4 |
p. 160-163
4 p.
|
artikel
|
| 45 |
Germline and somatic mutations in meningiomas
|
Smith, Miriam J.
|
|
2015
|
|
4 |
p. 107-114
8 p.
|
artikel
|
| 46 |
Identification of differentially expressed genes in gastric cancer by high density cDNA microarray
|
Zhang, Song-Nan
|
|
2012
|
|
4 |
p. 147-155
9 p.
|
artikel
|
| 47 |
Increased yield of actionable mutations using multi-gene panels to assess hereditary cancer susceptibility in an ethnically diverse clinical cohort
|
Ricker, Charité
|
|
2016
|
|
4 |
p. 130-137
8 p.
|
artikel
|
| 48 |
In Memoriam: Warren G. Sanger, PhD (October 6, 1945–February 5, 2015)
|
Sanmann, Jennifer N.
|
|
2015
|
|
4 |
p. 105-106
2 p.
|
artikel
|
| 49 |
Isolated trisomy 2 in bone marrows of patients with suspected hematopoietic malignancies
|
Aypar, Umut
|
|
2014
|
|
4 |
p. 124-127
4 p.
|
artikel
|
| 50 |
Jumping translocation of chromosome 1q associated with good clinical outcome in a case of Burkitt leukemia
|
Bessenyei, Beata
|
|
2011
|
|
4 |
p. 207-210
4 p.
|
artikel
|
| 51 |
Loss of heterozygosity in tumor tissue in hormonal receptor genes is associated with poor prognostic criteria in breast cancer
|
Iobagiu, Cristina
|
|
2015
|
|
4 |
p. 135-142
8 p.
|
artikel
|
| 52 |
Molecular studies reveal a MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotype
|
Ney Garcia, Daniela Ribeiro
|
|
2015
|
|
4 |
p. 143-147
5 p.
|
artikel
|
| 53 |
MYC and MYCN amplification can be reliably assessed by aCGH in medulloblastoma
|
Bourdeaut, Franck
|
|
2013
|
|
4 |
p. 124-129
6 p.
|
artikel
|
| 54 |
Myelofibrosis in Philadelphia chromosome–negative myeloproliferative neoplasms is associated with aberrant karyotypes
|
Hauck, Gesa
|
|
2013
|
|
4 |
p. 116-123
8 p.
|
artikel
|
| 55 |
Partial trisomy of chromosome 13 as a single cytogenetic abnormality in an Italian case of nasal NK/T lymphoma
|
Uccella, Silvia
|
|
2012
|
|
4 |
p. 186-189
4 p.
|
artikel
|
| 56 |
Philadelphia Chromosome Symposium: commemoration of the 50th anniversary of the discovery of the Ph chromosome
|
Chandra, H. Sharat
|
|
2011
|
|
4 |
p. 171-179
9 p.
|
artikel
|
| 57 |
Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study
|
Gromowski, Tomasz
|
|
2014
|
|
4 |
p. 128-132
5 p.
|
artikel
|
| 58 |
Profiling of potential driver mutations in sarcomas by targeted next generation sequencing
|
Andersson, Carola
|
|
2016
|
|
4 |
p. 154-160
7 p.
|
artikel
|
| 59 |
Promoter length polymorphism in UGT1A1 and the risk of sporadic colorectal cancer
|
Hiljadnikova Bajro, Marija
|
|
2012
|
|
4 |
p. 163-167
5 p.
|
artikel
|
| 60 |
Prostate cancer in Cowden syndrome: somatic loss and germline mutation of the PTEN gene
|
Barbosa, Mafalda
|
|
2011
|
|
4 |
p. 224-225
2 p.
|
artikel
|
| 61 |
Reduced membranous MET expression is linked to bladder cancer progression
|
Kluth, Martina
|
|
2014
|
|
4 |
p. 147-152
6 p.
|
artikel
|
| 62 |
Successful treatment of acute promyelocytic leukemia with a t(X;17)(p11.4;q21) and BCOR-RARA fusion gene
|
Ichikawa, Satoshi
|
|
2015
|
|
4 |
p. 162-163
2 p.
|
artikel
|
| 63 |
Table of Contents
|
|
|
2015
|
|
4 |
p. A1-A2
nvt p.
|
artikel
|
| 64 |
Table of Contents
|
|
|
2016
|
|
4 |
p. A3-
1 p.
|
artikel
|
| 65 |
Table of Contents
|
|
|
2012
|
|
4 |
p. A1-A2
nvt p.
|
artikel
|
| 66 |
Table of Contents
|
|
|
2013
|
|
4 |
p. A1-
1 p.
|
artikel
|
| 67 |
Table of Contents
|
|
|
2011
|
|
4 |
p. A1-A2
nvt p.
|
artikel
|
| 68 |
Table of Contents
|
|
|
2014
|
|
4 |
p. A1-
1 p.
|
artikel
|
| 69 |
The molecular basis of adrenocortical cancer
|
Lehmann, Tomasz
|
|
2012
|
|
4 |
p. 131-137
7 p.
|
artikel
|
| 70 |
Translocation t(7;19)(q22;q13)—a recurrent chromosome aberration in pseudomyogenic hemangioendothelioma?
|
Trombetta, Domenico
|
|
2011
|
|
4 |
p. 211-215
5 p.
|
artikel
|
| 71 |
Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome
|
Ponti, Giovanni
|
|
2012
|
|
4 |
p. 177-181
5 p.
|
artikel
|
| 72 |
Unknown partner for USP6 and unusual SS18 rearrangement detected by fluorescence in situ hybridization in a solid aneurysmal bone cyst
|
Geiersbach, Katherine
|
|
2011
|
|
4 |
p. 195-202
8 p.
|
artikel
|
| 73 |
Whole exome sequencing identifies driver mutations in asymptomatic computed tomography-detected lung cancers with normal karyotype
|
Belloni, Elena
|
|
2015
|
|
4 |
p. 152-155
4 p.
|
artikel
|
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