Division of Clinical Genetics
701 – 800 of 1291
- show: 100
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2010
-
Mark
Comparison of high-frequency QRS components and ST-segment elevation to detect and quantify acute myocardial ischemia.
(
- Contribution to journal › Article
-
Mark
Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
2010) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 19. p.2859-2868(
- Contribution to journal › Article
-
Mark
Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.
(
- Contribution to journal › Article
-
Mark
Characterization of an alternative transcript of the human CREB3L2 gene.
(
- Contribution to journal › Article
- 2009
-
Mark
Characterization of a Hotspot Region on Chromosome 12 for Amplification in Ring Chromosomes in Atypical Lipomatous Tumors
(
- Contribution to journal › Article
-
Mark
Balanced and Unbalanced Rearrangement of Chromosome Arm 6q in Chondromyxoid Fibroma (CMF): Delineation of Breakpoints and Analysis of Candidate Target Genes
2009) 98th Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology In Laboratory Investigation 89(S1). p.21-21(
- Contribution to journal › Published meeting abstract
-
Mark
ISCN (2009): Important revisions and new additions to molecular methods for copy number detection for cytogenetic analysis
(
- Contribution to journal › Published meeting abstract
-
Mark
t(19;22)(q13;q12) Translocation Leading to the Novel Fusion Gene EWSRI-ZNF444 in Soft Tissue Myoepithelial Carcinoma
(
- Contribution to journal › Article
-
Mark
Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia
(
- Contribution to journal › Article
-
Mark
Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden
(
- Contribution to journal › Article
-
Mark
No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies
(
- Contribution to journal › Article
-
Mark
Expression of P190 and P210 BCR/ABL1 in normal human CD34(+) cells induces similar gene expression profiles and results in a STAT5-dependent expansion of the erythroid lineage
(
- Contribution to journal › Article
-
Mark
Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union
(
- Contribution to journal › Article
-
Mark
Molecular Characterization Of The 12Q13.3-14.1 Recurrent Breakpoint Region On Ring Chromosomes 12 In Atypical Lipomatous Tumors
2009) 3rd Marie Curie-Genome Architecture in Relation to Disease Meeting (MC-GARD) In Cellular Oncology 31(2). p.113-113(
- Contribution to journal › Published meeting abstract
-
Mark
Comparison of cisplatin sensitivity and the 18F fluoro-2-deoxy 2 glucose uptake with proliferation parameters and gene expression in squamous cell carcinoma cell lines of the head and neck
(
- Contribution to journal › Article
-
Mark
Germline and somatic NF1 mutations in sporadic and NF1-associated malignant peripheral nerve sheath tumours
(
- Contribution to journal › Article
-
Mark
Clinical Variability of Waardenburg-Shah Syndrome in Patients With Proximal 13q Deletion Syndrome Including the Endothelin-B Receptor Locus
(
- Contribution to journal › Article
-
Mark
Cancer Chromosomes: From Meaningless Noise to Proof of Principle.
(
- Contribution to journal › Published meeting abstract
-
Mark
Relapsed Childhood High Hyperdiploid Acute Lymphoblastic Leukemia: Genome-Wide Screening Reveals the Presence of Preleukemic Ancestral Clones and the Secondary Nature of Microdeletions and RTK-RAS Mutations
(
- Contribution to journal › Published meeting abstract
-
Mark
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors
(
- Contribution to journal › Article
-
Mark
Cytogenetic Analysis of 101 Giant Cell Tumors of Bone: Nonrandom Patterns of Telomeric Associations and Other Structural Aberrations
(
- Contribution to journal › Article
-
Mark
Bone Marrow Multipotent Mesenchymal Stroma Cells Act as Pericyte-like Migratory Vehicles in Experimental Gliomas.
(
- Contribution to journal › Article
-
Mark
High-resolution imaging of mitotic instability
(
- Contribution to journal › Published meeting abstract
-
Mark
HIF-2 alpha maintains an undifferentiated state in neural crest-like human neuroblastoma tumor-initiating cells
(
- Contribution to journal › Article
-
Mark
Telomere length in neuroblastoma: a prognostic factor?
(
- Contribution to journal › Published meeting abstract
-
Mark
High-resolution imaging of mitotic instability
(
- Contribution to journal › Published meeting abstract
-
Mark
Clonal chromosome aberrations in a sialoblastoma
(
- Contribution to journal › Letter
-
Mark
t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia
(
- Contribution to journal › Article
-
Mark
Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
(
- Contribution to journal › Article
-
Mark
The expression of pluripotency marker Oct 3/4 in prostate cancer and benign prostate hyperplasia.
(
- Contribution to journal › Article
-
Mark
The DNA methylome of pediatric acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
The t(X;7)(q22;q34) in paediatric T-cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination with the T-cell receptor beta locus.
(
- Contribution to journal › Article
-
Mark
False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.
(
- Contribution to journal › Article
-
Mark
Smoking as a risk factor for myelodysplastic syndromes and acute myeloid leukemia and its relation to cytogenetic findings: A case-control study.
2009) In Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis Nov 17. p.788-791(
- Contribution to journal › Article
-
Mark
Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.
(
- Contribution to journal › Article
-
Mark
B-cell precursor t(8;14)(q11;q32)-positive acute lymphoblastic leukemia in children is strongly associated with Down syndrome or with a concomitant Philadelphia chromosome.
(
- Contribution to journal › Article
-
Mark
Characterization of the human CREB3L2 gene promoter
(
- Contribution to journal › Article
-
Mark
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.
(
- Contribution to journal › Article
-
Mark
Translocation-related sarcomas.
(
- Contribution to journal › Article
-
Mark
MiRNA expression in urothelial carcinomas: Important roles of miR-10a, miR-222, miR-125b, miR-7 and miR-452 for tumor stage and metastasis, and frequent homozygous losses of miR-31.
(
- Contribution to journal › Article
-
Mark
Low-grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases.
(
- Contribution to journal › Article
-
Mark
Tiling resolution array-based comparative genomic hybridisation analyses of acute lymphoblastic leukaemias in children with Down syndrome reveal recurrent gain of 8q and deletions of 7p and 9p.
(
- Contribution to journal › Article
-
Mark
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.
(
- Contribution to journal › Article
-
Mark
High hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone.
(
- Contribution to journal › Article
-
Mark
Low frequency of EWSR1 rearrangements in neoplasms classified as high-risk wilms tumors.
(
- Contribution to journal › Article
-
Mark
Bidirectionality and transcriptional activity of the EWSR1 promoter region
(
- Contribution to journal › Article
-
Mark
Association between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study.
(
- Contribution to journal › Article
-
Mark
Mild hypothermia does not attenuate platelet aggregation and may even increase ADP-stimulated platelet aggregation after clopidogrel treatment
(
- Contribution to journal › Article
-
Mark
HAMLET, a tumoricidal molecular complex from human milk
2009) 6th International Symposium on the Intraductal Approach to Breast Cancer In BMC Proceedings 3(Suppl 5). p.11-11(
- Contribution to journal › Published meeting abstract
- 2008
-
Mark
Genetics in clinical practice: general practitioners' educational priorities in European countries
(
- Contribution to journal › Article
-
Mark
Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease
(
- Contribution to journal › Article
-
Mark
Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study
(
- Contribution to journal › Article
-
Mark
Mesenchymal Stromal Cells (MSC) Isolated from Human Osteosarcomas Show a High Progenitor Cell Frequency, Typical MSC Morphology, Surface Marker Profile, and Differentiation Capacity, and They Are Considerably Affected by Tyrosine Kinase Inhibitors in Vitro
(
- Contribution to journal › Published meeting abstract
-
Mark
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors
(
- Contribution to journal › Article
-
Mark
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12
(
- Contribution to journal › Article
-
Mark
Gene expression analysis of BCR/ABL1-dependent transcriptional response reveals enrichment for genes involved in negative feedback regulation.
(
- Contribution to journal › Article
-
Mark
An improved method for detecting and delineating genomic regions with altered gene expression in cancer
(
- Contribution to journal › Article
-
Mark
Mechanisms and Consequences of Chromosomal Instability in Malignant tumours
(
- Thesis › Doctoral thesis (monograph)
-
Mark
A Novel Fusion 5'Aff3/3'Bcl2 Originated From A T(2;18)(Q11.2-Q21.33) Translocation In Follicular Lymphoma
2008) 10th Congress of the Italian-Society-of-Experimental-Hematology In Haematologica-The Hematology Journal 93. p.27-27(
- Contribution to journal › Published meeting abstract
-
Mark
The utility of fluorescence in situ hybridization (FISH) in the diagnosis of myxoid soft tissue neoplasms
(
- Contribution to journal › Article
-
Mark
Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale
(
- Contribution to journal › Article
-
Mark
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Tumor Specific Migration Of Bone-Marrow Derived Rat Mesenchymal Stem Cells In The Invasive N29 Rat Brain Tumor Model
2008) 8th Congress of the European-Association-for-Neuro-Oncology (EANO) In Neuro-Oncology 10(6). p.1066-1066(
- Contribution to journal › Published meeting abstract
-
Mark
EuroGentest: DNA-based testing for heritable disorders in Europe
(
- Contribution to journal › Article
-
Mark
The hypermethylome of pediatric acute lymphoblastic leukemia
(
- Contribution to journal › Published meeting abstract
-
Mark
CANCER-RELATED GENE REGULATION MECHANISMS
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Fusion of the COL1A1 and USP6 genes in a benign bone tumor.
(
- Contribution to journal › Article
-
Mark
The Fatty Acid Amide Hydrolase (FAAH) Pro129Thr Polymorphism is not Associated with Severe Obesity in Greek Subjects
(
- Contribution to journal › Article
-
Mark
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
(
- Contribution to journal › Article
-
Mark
The FLT3 inhibitor PKC412 in combination with cytostatic drugs in vitro in acute myeloid leukemia
(
- Contribution to journal › Article
-
Mark
Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72
(
- Contribution to journal › Article
-
Mark
Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation
(
- Contribution to journal › Article
-
Mark
What is ideal genetic counselling? A survey of current international guidelines
(
- Contribution to journal › Article
-
Mark
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives
(
- Contribution to journal › Article
-
Mark
Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays
(
- Contribution to journal › Article
-
Mark
Tissue microarray based analysis of prognostic markers in invasive bladder cancer: Much effort to no avail?
(
- Contribution to journal › Article
-
Mark
Female haemophilia A caused by skewed X inactivation
(
- Contribution to journal › Letter
-
Mark
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival
(
- Contribution to journal › Article
-
Mark
CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome
(
- Contribution to journal › Article
-
Mark
Detection of a t(1;22)(q23;q 12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma
(
- Contribution to journal › Article
-
Mark
Characterization Of Non-Small Cell Lung Cancer Using Tiling Resolution Bacterial Artificial Chromosome Microarrays
(
- Contribution to journal › Published meeting abstract
-
Mark
A novel fusion 5 ' AFF3/3 ' BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma
(
- Contribution to journal › Article
-
Mark
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-Cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature
(
- Contribution to journal › Scientific review
-
Mark
Deep-seated ordinary and atypical lipomas - Histopathology, cytogenetics, clinical features, and outcome in 215 tumours of the extremity and trunk wall
(
- Contribution to journal › Article
-
Mark
High levels of HIF-2alpha highlight an immature neural crest-like neuroblastoma cell cohort located in a perivascular niche.
(
- Contribution to journal › Article
-
Mark
Array based genetic profiling of bone and soft tissue tumors
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Molecular screening for new fusion genes in cancer
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Heterogeneous genetic profiles in soft tissue myoepitheliomas
(
- Contribution to journal › Article
-
Mark
Glial Progenitor-Like Phenotype in Low-Grade Glioma and Enhanced CD133-Expression and Neuronal Lineage Differentiation Potential in High-Grade Glioma
(
- Contribution to journal › Article
-
Mark
Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region.
(
- Contribution to journal › Article
-
Mark
Promoter analysis of epigenetically controlled genes in bladder cancer.
(
- Contribution to journal › Article
-
Mark
Selection of Influential Genetic Markers Among a Large Number of Candidates Based on Effect Estimation Rather than Hypothesis Testing: An Approach for Genome-Wide Association Studies.
(
- Contribution to journal › Article
-
Mark
Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.
(
- Contribution to journal › Article
-
Mark
Glial progenitor-like phenotype in low-grade glioma and enhanced CD133-expression and neuronal lineage differentiation potential in high-grade glioma.
2008) 8th Congress of the European-Association-for-Neuro-Oncology (EANO) In Neuro-Oncology 10(6). p.1107-1107(
- Contribution to journal › Published meeting abstract
-
Mark
POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands.
(
- Contribution to journal › Article
-
Mark
FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.
(
- Contribution to journal › Article
-
Mark
Increased sensitivity to bleomycin in upper aerodigestive tract mucosa of head and neck squamous cell carcinoma patients.
(
- Contribution to journal › Article
-
Mark
Recurrent and multiple bladder tumors show conserved expression profiles.
(
- Contribution to journal › Article