Division of Clinical Genetics
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- 2009
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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
The utility of fluorescence in situ hybridization (FISH) in the diagnosis of myxoid soft tissue neoplasms
(
- Contribution to journal › Article
-
Mark
An improved method for detecting and delineating genomic regions with altered gene expression in cancer
(
- Contribution to journal › Article
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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
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
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
Mechanisms and Consequences of Chromosomal Instability in Malignant tumours
(
- Thesis › Doctoral thesis (monograph)
-
Mark
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives
(
- Contribution to journal › Article
-
Mark
Genetics in clinical practice: general practitioners' educational priorities in European countries
(
- 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
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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
CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome
(
- Contribution to journal › Article
-
Mark
What is ideal genetic counselling? A survey of current international guidelines
(
- 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
Characterization Of Non-Small Cell Lung Cancer Using Tiling Resolution Bacterial Artificial Chromosome Microarrays
(
- Contribution to journal › Published meeting abstract
-
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
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors
(
- 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
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
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
EuroGentest: DNA-based testing for heritable disorders in Europe
(
- 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
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
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
The hypermethylome of pediatric acute lymphoblastic leukemia
(
- Contribution to journal › Published meeting abstract
-
Mark
The FLT3 inhibitor PKC412 in combination with cytostatic drugs in vitro in acute myeloid leukemia
(
- 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
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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
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
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
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
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
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Mark
Heterogeneous genetic profiles in soft tissue myoepitheliomas
(
- Contribution to journal › Article
-
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
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
Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.
(
- Contribution to journal › Article
-
Mark
Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region.
(
- Contribution to journal › Article
-
Mark
High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.
(
- Contribution to journal › Article
-
Mark
Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype-phenotype correlation and a comprehensive review of previously published cases.
(
- Contribution to journal › Article
-
Mark
A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1.
(
- Contribution to journal › Article
-
Mark
When the genome plays dice: circumvention of the spindle assembly checkpoint and near-random chromosome segregation in multipolar cancer cell mitoses.
(
- Contribution to journal › Article
-
Mark
Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.
(
- Contribution to journal › Article
-
Mark
Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors.
(
- Contribution to journal › Article
-
Mark
The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1.
(
- Contribution to journal › Article
-
Mark
BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias.
(
- Contribution to journal › Article
-
Mark
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
(
- Contribution to journal › Article
-
Mark
Regulatory Issues for Genetic Testing in Clinical Practice.
(
- 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
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
Recurrent and multiple bladder tumors show conserved expression profiles.
(
- Contribution to journal › Article
-
Mark
Binomial mitotic segregation of MYCN-carrying double minutes in neuroblastoma illustrates the role of randomness in oncogene amplification.
(
- Contribution to journal › Article
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Mark
An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera
(
- Contribution to journal › Article
-
Mark
Exit of pediatric pre-B acute lymphoblastic leukaemia cells from the bone marrow to the peripheral blood is not associated with cell maturation or alterations in gene expression.
(
- Contribution to journal › Article
-
Mark
Classification of chromosome segregation errors in cancer.
(
- Contribution to journal › Article
-
Mark
Delection of the SCN gene cluster on 2q24.4 is associated with severe epilepsy an array-based genotype-phenotype correlation and a comprehensive review of previously published area
(
- Contribution to journal › Article
- 2007
-
Mark
Reduced high-frequency QRS components in electrocardiogram leads facing an area of the heart with intraventricular conduction delay due to bundle branch block.
(
- Contribution to journal › Article
-
Mark
Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).
(
- Contribution to journal › Article
-
Mark
High-frequency electrocardiogram analysis in the ability to predict reversible perfusion defects during adenosine myocardial perfusion imaging.
(
- Contribution to journal › Article
-
Mark
Successful treatment of a child with t(15;19)-positive tumor.
(
- Contribution to journal › Article
-
Mark
Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations
(
- Contribution to journal › Article
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Mark
Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome.
(
- Contribution to journal › Article
-
Mark
Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma
(
- Contribution to journal › Article
-
Mark
The molecular signature of MDS stem cells supports a stem-cell origin of 5q - myelodysplastic syndromes
(
- Contribution to journal › Article
-
Mark
Cytogenetic evolution patterns in CML post-SCT.
(
- Contribution to journal › Article
-
Mark
Distinct mitotic segregation errors mediate chromosomal instability in aggressive urothelial cancers.
(
- Contribution to journal › Article
-
Mark
Threshold-free high-power methods for the ontological analysis of genome-wide gene expression studies
(
- Contribution to journal › Article
-
Mark
A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families
(
- Contribution to journal › Article
-
Mark
Defective chromosome segregation and telomere dysfunction in aggressive Wilms' tumors
(
- Contribution to journal › Article
-
Mark
Generation of human cortical neurons from a new immortal fetal neural stem cell line.
(
- Contribution to journal › Article
-
Mark
Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias.
(
- Contribution to journal › Article
-
Mark
Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer
(
- Contribution to journal › Article
-
Mark
Telomere dysfunction and telomerase activation in cancer - a pathological paradox?
(
- Contribution to journal › Article
-
Mark
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
(
- Contribution to journal › Article
-
Mark
Proposals for standardized Protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes
(
- Contribution to journal › Article
-
Mark
Tiling resolution array CGH of dic(7;9)(p11 approximately 13;p11 approximately 13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2 approximately 12.1 and 9p13.1.
(
- Contribution to journal › Article
-
Mark
Response to letter by the ISCN standing committee
(
- Contribution to journal › Letter
-
Mark
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3
(
- Contribution to journal › Article
-
Mark
High-resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization.
(
- Contribution to journal › Article
-
Mark
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature
(
- Contribution to journal › Scientific review
-
Mark
Report of an international survey of molecular genetic testing laboratories
(
- Contribution to journal › Article
-
Mark
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera
(
- Contribution to journal › Article
-
Mark
Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status.
(
- Contribution to journal › Article
-
Mark
Bladder cancer, a two phased disease?
(
- Contribution to journal › Scientific review
-
Mark
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
(
- Contribution to journal › Article
-
Mark
On the Origin of Syn- and Metachronous Urothelial Carcinomas.
(
- Contribution to journal › Scientific review
-
Mark
Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies
(
- Contribution to journal › Article
-
Mark
Establishment of a cell line from a chemotherapy resistant diffuse large B-cell lymphoma
(
- Contribution to journal › Letter
-
Mark
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes
(
- Contribution to journal › Article
-
Mark
Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
(
- Contribution to journal › Scientific review
-
Mark
Cytogenetic findings in pediatric renal cell carcinoma
(
- Contribution to journal › Article
-
Mark
Fusion genes in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma
(
- Contribution to journal › Letter
-
Mark
Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
(
- Contribution to journal › Article
-
Mark
Germline E-cadherin mutations in familial lobular breast cancer
(
- Contribution to journal › Article
-
Mark
Study of ATP-release from acoustically levitated eryhrocytes
(
- Contribution to journal › Published meeting abstract
-
Mark
Brister i genetisk kunskap i vården?
2007) p.109-109(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Study of ATP-release from acoustically levitated eryhrocytes
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
THE ANDROGEN RECEPTOR GGN POLYMORPHISM. Genetic and functional analyses.
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region
(
- Contribution to journal › Article
-
Mark
Microarray analysis of gliomas reveals chromosomal position-associated gene expression patterns and identifies potential immunotherapy targets.
(
- Contribution to journal › Article
-
Mark
Cancer stem cells: Differentiation block or developmental back-tracking?
(
- Contribution to journal › Letter
-
Mark
Etisk argumentation och klinisk verklighet kan med fördel förenas.
(
- Contribution to journal › Article
-
Mark
Papillomavirus type 16 E6/E7 and human telomerase reverse transcriptase in esophageal cell immortalization and early transformation
(
- Contribution to journal › Article
-
Mark
Genetic variant of the human homologous recombination-associated gene RMI1 (S455N) impacts the risk of AML/MDS and malignant melanoma.
(
- Contribution to journal › Article
-
Mark
Distinct evolutionary mechanisms for genomic imbalances in high-risk and low-risk neuroblastomas
(
- Contribution to journal › Article
-
Mark
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
(
- Contribution to journal › Article
-
Mark
Deregulation of the Wilms' tumour gene 1 protein (WT1) by BCR/ABL1 mediates resistance to imatinib in human leukaemia cells
(
- Contribution to journal › Article
-
Mark
A case of Cornelia de Lange syndrome from Sudan
(
- Contribution to journal › Article
-
Mark
The impact of translocations and gene fusions on cancer causation.
(
- Contribution to journal › Scientific review
- 2006
-
Mark
Comparison of ST-Segment Deviation to Scintigraphically Quantified Myocardial Ischemia During Acute Coronary Occlusion Induced by Percutaneous Transluminal Coronary Angioplasty.
(
- Contribution to journal › Article
-
Mark
Cross-platform classification in microarray-based leukemia diagnostics
(
- Contribution to journal › Article
-
Mark
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
(
- Contribution to journal › Article
-
Mark
Human short-term repopulating cells have enhanced telomerase reverse transcriptase expression.
(
- Contribution to journal › Article
-
Mark
Education in medical genetics for non-genetic health care providers in sweden.
(
- Contribution to journal › Article
-
Mark
Re: Wilting et al. Increased gene copy numbers at chromosome 20q are frequent in both squamous cell carcinomas and adenocarcinomas of the cervix. J Pathol 2006; 209:220-230.
(
- Contribution to journal › Letter
-
Mark
High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.
(
- Contribution to journal › Article
-
Mark
Handy book on cancer genetics risk assessment
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters
(
- Contribution to journal › Article
-
Mark
Serial changes in the high-frequency ECG during the first year following acute myocardial infarction.
(
- Contribution to journal › Article
-
Mark
A gene fusion network in human neoplasia.
(
- Contribution to journal › Article
-
Mark
The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
(
- Contribution to journal › Article
-
Mark
Fine-needle aspiration of neurilemoma (schwannoma). A clinicocytopathologic study of 116 patients
(
- Contribution to journal › Article
-
Mark
Molecular cytogenetic characterization of the 11q13 amplicon in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
-
Mark
Fusion of the Tumor-Suppressor Gene CHEK2 and the Gene for the Regulatory Subunit B of Protein Phosphatase 2 PPP2R2A in Childhood Teratoma.
(
- Contribution to journal › Article
-
Mark
Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias
(
- Contribution to journal › Letter
-
Mark
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
(
- Contribution to journal › Article
-
Mark
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2 : implications for formation and pathogenetic outcome of the idic(7)(p11.2)
(
- Contribution to journal › Article
-
Mark
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)
(
- Contribution to journal › Article
-
Mark
Detection of cell cycle- and differentiation stage-dependent human telomerase reverse transcriptase expression in single living cancer cells.
(
- Contribution to journal › Article
-
Mark
Trisomy 19 as the sole chromosomal abnormality in proliferative chronic myelomonocytic leukemia
2006) In Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis 30(8). p.1043-1047(
- Contribution to journal › Article
-
Mark
Cryptic terminal chromosome rearrangements in colorectal carcinoma cell lines detected by subtelomeric FISH analysis.
(
- Contribution to journal › Article
-
Mark
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.
(
- Contribution to journal › Letter
-
Mark
Deregulation of cyclin D2 by juxtaposition with T-cell receptor alpha/delta locus in t(12;14)(p13;q11)-positive childhood T-cell acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement.
(
- Contribution to journal › Article
-
Mark
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
(
- Contribution to journal › Article
-
Mark
Genetic education for non-geneticist health professionals
(
- Contribution to journal › Article
-
Mark
Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours
(
- Contribution to journal › Article
-
Mark
Comparison of EASI-derived 12-lead electrocardiograms versus paramedic-acquired 12-lead electrocardiograms using Mason-Likar limb lead configuration in patients with chest pain
(
- Contribution to journal › Article
-
Mark
C2028T polymorphism in exon 12 and dinucleotide repeat polymorphism in intron 13 of the HIF-1 alpha gene define HIF-1 alpha protein expression in non-small cell lung cancer
(
- Contribution to journal › Article
-
Mark
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities
(
- Contribution to journal › Letter
-
Mark
Prognostic significance of chromosome aberrations in high-grade soft tissue sarcomas
(
- Contribution to journal › Article
-
Mark
Molecular characterization of early-stage bladder carcinomas by expression profiles, FGFR3 mutation status, and loss of 9q.
(
- Contribution to journal › Article
-
Mark
Determination of the ability of high-frequency ECG to estimate left ventricular mass in humans, determined by magnetic resonance imaging.
(
- Contribution to journal › Article
-
Mark
Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2
(
- Contribution to journal › Article
-
Mark
New Probabilistic network models and algorithms for oncogenesis
(
- Contribution to journal › Article
-
Mark
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Gene copy number changes in dermatofibrosarcoma protuberans - a fine-resolution study using array comparative genomic hybridization
(
- Contribution to journal › Article
-
Mark
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
(
- Contribution to journal › Article
-
Mark
Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15)
(
- Contribution to journal › Article
-
Mark
MOLECULAR PROFILING OF UROTHELIAL CARCINOMA
2006) In Lund University Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
(
- Contribution to journal › Letter
-
Mark
Cytogenetic aberrations in immortalization of esophageal epithelial cells
(
- Contribution to journal › Article
-
Mark
A del(X)(p11) carrying SRY sequences in an infant with ambiguous genitalia
(
- Contribution to journal › Article
-
Mark
Independent component analysis reveals new and biologically significant structures in micro array data
(
- Contribution to journal › Article
-
Mark
Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma
(
- Contribution to journal › Article
-
Mark
Increased expression of cyclin A1 protein is associated with all-trans retinoic acid-induced apoptosis.
(
- Contribution to journal › Article
-
Mark
Meta- and synchronous urothelial carcinomas with divergent genomic profiles show highly similar gene-expression profiles
(
- Contribution to journal › Published meeting abstract
-
Mark
Molecular and functional studies of the BCR/ABL1 fusion gene
2006)(
- Thesis › Doctoral thesis (compilation)
-
Mark
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42
(
- Contribution to journal › Article
-
Mark
Mechanisms underlying neoplasia-associated genomic rearrangements
2006) p.327-337(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Female genital mutilation of a karyotypic male presenting as a female with delayed puberty
(
- Contribution to journal › Article
-
Mark
High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
(
- Contribution to journal › Article
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Mark
MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia
(
- Contribution to journal › Letter
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Mark
Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy
(
- Contribution to journal › Article
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Mark
Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes
(
- Contribution to journal › Article
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Mark
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene
(
- Contribution to journal › Letter
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Mark
Analysis of promoter regions of co-expressed genes identified by microarray analysis
(
- Contribution to journal › Article
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Mark
Cytogenetic abnormalities in 106 oral squamous cell carcinomas
(
- Contribution to journal › Article
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Mark
ECA Permanent working group for cytogenetics and society: Cytogenetic guidelines and quality assurance. A common framework for quality assessment for constitutional and acquired cytogenetic investigations
(
- Contribution to journal › Article
- 2005
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Mark
Telomere-mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma
(
- Contribution to journal › Article
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Mark
The parental origin of trisomy 14 in hyperdiploid childhood ALL
(
- Contribution to journal › Letter
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Mark
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Clear cell hidradenoma of the skin - a third tumor type with a t(11;19)-associated TORC1-MAML2 gene fusion
(
- Contribution to journal › Article
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Mark
Prevalence of Stroke and Vascular Risk Factors among First-Degree Relatives of Stroke Patients and Control Subjects.
(
- Contribution to journal › Article
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Mark
Statistical behavior of complex cancer karyotypes.
(
- Contribution to journal › Scientific review
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Mark
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene
(
- Contribution to journal › Article
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Mark
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
(
- Contribution to journal › Article
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Mark
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer.
(
- Contribution to journal › Article
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Mark
Amplification and overexpression of Aurora kinase A (AURKA) in immortalized human ovarian epithelial (HOSE) cells
(
- Contribution to journal › Article
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Mark
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma
(
- Contribution to journal › Article
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Mark
Mitotic instability in cancer - Is there method in the madness?
(
- Contribution to journal › Article
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Mark
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
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Mark
Genetic education and nongenetic health professionals: Educational providers and curricula in Europe.
(
- Contribution to journal › Article
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Mark
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
(
- Contribution to journal › Article
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Mark
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.
(
- Contribution to journal › Article
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Mark
Culturing of human tumor cells for use in immune gene tumor therapy
2005) World Federation of Neuro-Oncology Second Quadrennial Meeting and the Sixth Meeting of the European Association for Neuro-Oncology In Neuro-Oncology 7(3). p.371-371(
- Contribution to journal › Published meeting abstract
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Mark
Core-needle biopsy performed by the cytopathologist : a technique to complement fine-needle aspiration of soft tissue and bone lesions
(
- Contribution to journal › Article
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Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
(
- Contribution to journal › Article
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Mark
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
(
- Contribution to journal › Article
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Mark
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses)
(
- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
(
- Contribution to journal › Article
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Mark
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
(
- Contribution to journal › Article
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Mark
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
(
- Contribution to journal › Article
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Mark
Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Trisomies in Hematologic Malignancies
2005) In Lund University Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Fusion of the HMGA2 and NFIB genes in lipoma
(
- Contribution to journal › Article
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Mark
Ny kunskap om arv och ärftlighet ger nya aspekter på hjärtsjukdom
(
- Contribution to journal › Article
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Mark
Gene Expression Studies of Hematologic Malignacies
2005)(
- Thesis › Doctoral thesis (compilation)
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Mark
Connecting mitotic instability and chromosome aberrations in cancer-can telomeres bridge the gap?
(
- Contribution to journal › Scientific review
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Mark
Karyotypic evolution and tumor progression in head and neck squamous cell carcinomas.
(
- Contribution to journal › Article
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Mark
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations
(
- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of chromosome aberrations in soft tissue and bone tumors
2005)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Immortalization of human extravillous cytotrophoblasts by human papilloma virus gene E6E7: sequential cytogenetic and molecular genetic characterization.
(
- Contribution to journal › Article
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Mark
Book review: Genetic predisposition of cancer, 2nd ed.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
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Mark
Euploidy in somatic cells from R6/2 transgenic Huntington's disease mice
(
- Contribution to journal › Article
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Mark
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
(
- Contribution to journal › Article
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Mark
Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt
(
- Contribution to journal › Article
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Mark
Genetic Characterization of Bone and Soft Tissue Tumors
2005)(
- Thesis › Doctoral thesis (compilation)
- 2004
-
Mark
Identification of genes differentially regulated by the P210 BCR/ABL1 fusion oncogene using cDNA microarrays.
(
- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion).
(
- Contribution to journal › Article
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Mark
Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells
(
- Contribution to journal › Article
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Mark
Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.
(
- Contribution to journal › Article
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Mark
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
(
- Contribution to journal › Article
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Mark
Activation of the GLI Oncogene through Fusion with the beta-Actin Gene (ACTB) in a Group of Distinctive Pericytic Neoplasms: Pericytoma with t(7;12).
(
- Contribution to journal › Article
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Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
(
- Contribution to journal › Article
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Mark
Approximate geodesic distances reveal biologically relevant structures in microarray data
(
- Contribution to journal › Article
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Mark
Vascular endothelial growth factor gene polymorphisms and pre-eclampsia
(
- Contribution to journal › Article
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Mark
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
(
- Contribution to journal › Article
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Mark
Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells
(
- Contribution to journal › Article
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Mark
Abstracts from the Ninth Annual Meeting of the Society for Neuro-Oncology
(
- Contribution to journal › Article
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Mark
Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
(
- Contribution to journal › Article
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Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
(
- Contribution to journal › Article
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Mark
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
(
- Contribution to journal › Article
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Mark
Pearson correlation analysis of micro-array data allows for the identification of genetic targets for early B-cell factor.
(
- Contribution to journal › Article
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Mark
Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo
(
- Contribution to journal › Article
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Mark
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
(
- Contribution to journal › Article
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Mark
A model for karyotypic evolution in testicular germ cell tumors.
(
- Contribution to journal › Article
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Mark
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
(
- Contribution to journal › Article
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Mark
Tumor karyotype predicts clinical outcome in colorectal cancer patients
(
- Contribution to journal › Article
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Mark
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma
(
- Contribution to journal › Article
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Mark
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
(
- Contribution to journal › Article
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Mark
An excess of chromosome 1 breakpoints in male infertility.
(
- Contribution to journal › Article
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Mark
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
(
- Contribution to journal › Article
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Mark
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
(
- Contribution to journal › Article
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Mark
Reduced high-frequency QRS components in patients with ischemic heart disease compared to normal subjects
(
- Contribution to journal › Article
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Mark
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
(
- Contribution to journal › Article
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Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
(
- Contribution to journal › Article