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- 2024
-
Mark
Current and emerging sequencing-based tools for precision cancer medicine
(
- Contribution to journal › Scientific review
-
Mark
A Gradual Transition Toward Anaplasia in Wilms Tumor Through Tolerance to Genetic Damage
2024) In Modern Pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 37(1). p.100382-100382(
- Contribution to journal › Article
-
Mark
Weaponized genomics : potential threats to international and human security
(
- Contribution to journal › Letter
- 2023
-
Mark
Hallmark discoveries in the biology of Wilms tumour
2023) In Nature Reviews Urology(
- Contribution to journal › Scientific review
-
Mark
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer
(
- Contribution to journal › Article
-
Mark
Macrophage infiltration promotes regrowth in MYCN-amplified neuroblastoma after chemotherapy
(
- Contribution to journal › Article
-
Mark
Modelling evolution at the boundaries of solid tumours
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Systematic orientation of fresh rectal suction biopsies improves histopathological diagnostics in hirschsprung’s disease – a method description and preliminary report
(
- Contribution to journal › Article
-
Mark
Resolving the Pathogenesis of Anaplastic Wilms Tumors through Spatial Mapping of Cancer Cell Evolution
(
- Contribution to journal › Article
-
Mark
Wargaming cancer: a strategy for future precision oncology?
(
- Contribution to journal › Article
-
Mark
Building a precision medicine infrastructure at a national level: The Swedish experience
(
- Contribution to journal › Scientific review
-
Mark
Tumor biology, biomarkers, and liquid biopsy in pediatric renal tumors
(
- Contribution to journal › Scientific review
-
Mark
Inactivation of RB1, CDKN2A and TP53 have distinct effects on genomic stability at side-by-side comparison in karyotypically normal cells
(
- Contribution to journal › Article
-
Mark
SIX1 as a Novel Immunohistochemical Marker in the Differential Diagnosis of Rhabdomyosarcoma
(
- Contribution to journal › Article
-
Mark
Weaponized Genomics: New Threats to International Security and Human Rights
2023) In Nature Reviews. Genetics(
- Contribution to journal › Debate/Note/Editorial
- 2022
-
Mark
Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma : A potential treatment target in rare cases?
(
- Contribution to journal › Article
-
Mark
Differential Activation of Immune Effector Processes in Mature Compared to Immature Sacrococcygeal Teratomas
(
- Contribution to journal › Article
-
Mark
Clinically relevant treatment of PDX models reveals patterns of neuroblastoma chemoresistance
(
- Contribution to journal › Article
-
Mark
The immune cell atlas of human neuroblastoma
(
- Contribution to journal › Article
-
Mark
Implementing precision medicine in a regionally organized healthcare system in Sweden
(
- Contribution to journal › Letter
-
Mark
Next-Generation Biowarfare : Small in Scale, Sensational in Nature?
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Delineating the intra-patient heterogeneity of molecular alterations in treatment-naïve colorectal cancer with peritoneal carcinomatosis
(
- Contribution to journal › Article
-
Mark
Branching copy number evolution and parallel immune profiles across the regional tumor space of resected pancreatic cancer
(
- Contribution to journal › Article
-
Mark
Clinical-pathological features in placentas of pregnancies with SARS-CoV-2 infection and adverse outcome : case-series with and without congenital transmission
(
- Contribution to journal › Article
-
Mark
Histopathological dimensions differ between aganglionic and ganglionic bowel wall in children with Hirschsprung’s disease
(
- Contribution to journal › Article
-
Mark
Interleukin 4 promotes phagocytosis of murine leukemia cells counteracted by CD47 upregulation
(
- Contribution to journal › Article
-
Mark
Diagnostic Efficacy of Rectal Suction Biopsy with Regard to Weight in Children Investigated for Hirschsprung's Disease
(
- Contribution to journal › Article
- 2021
-
Mark
DEVOLUTION—A method for phylogenetic reconstruction of aneuploid cancers based on multiregional genotyping data
(
- Contribution to journal › Article
-
Mark
Tracing the evolution of aneuploid cancers by multiregional sequencing with CRUST
(
- Contribution to journal › Article
-
Mark
Intrauterine vertical SARS-CoV-2 infection : a case confirming transplacental transmission followed by divergence of the viral genome
(
- Contribution to journal › Article
-
Mark
Anti-tumor effects of rigosertib in high-risk neuroblastoma
(
- Contribution to journal › Article
-
Mark
Ultra high frequency ultrasonography to distinguish ganglionic from aganglionic bowel wall in Hirschsprung disease : A first report
(
- Contribution to journal › Article
-
Mark
Immune checkpoint inhibitors in Wilms' tumor and Neuroblastoma : What now?
(
- Contribution to journal › Article
-
Mark
HERA : a new era for health emergency preparedness in Europe?
(
- Contribution to journal › Letter
- 2020
-
Mark
Clonal competition within complex evolutionary hierarchies shapes AML over time
(
- Contribution to journal › Article
-
Mark
Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome
(
- Contribution to journal › Article
-
Mark
The Cellular Architectures of Hypospadias
(
- Contribution to journal › Letter
-
Mark
Therapeutic targeting of KSP in preclinical models of high-risk neuroblastoma
(
- Contribution to journal › Article
-
Mark
A dynamic mutational landscape associated with an inter-regionally diverse immune response in malignant rhabdoid tumour
(
- Contribution to journal › Article
-
Mark
Chemotherapy, host response and molecular dynamics in periampullary cancer : The CHAMP study
(
- Contribution to journal › Article
-
Mark
Extensive clonal branching shapes the evolutionary history of high-risk pediatric cancers
(
- Contribution to journal › Article
- 2019
-
Mark
Multidimensional intratumour heterogeneity in neuroblastoma
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Clonal evolution through genetic bottlenecks and telomere attrition : Potential threats to in vitro data reproducibility
(
- Contribution to journal › Scientific review
-
Mark
Changes in the Prevalence of Embryologic Remnants in Umbilical Cord With Gestational Age
(
- Contribution to journal › Article
-
Mark
The Iroquois homeobox proteins IRX3 and IRX5 have distinct roles in Wilms tumour development and human nephrogenesis
(
- Contribution to journal › Article
- 2018
-
Mark
Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers
(
- Contribution to journal › Article
-
Mark
Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer
(
- Contribution to journal › Article
-
Mark
Patient-derived xenograft models reveal intratumor heterogeneity and temporal stability in neuroblastoma
(
- Contribution to journal › Article
-
Mark
Neuroblastoma with flat genomic profile : A question of representativity?
(
- Contribution to journal › Article
- 2017
-
Mark
Cancer - An Insurgency of Clones
(
- Contribution to journal › Article
-
Mark
Mosaicism in health and disease — clones picking up speed
(
- Contribution to journal › Article
-
Mark
Neuroblastoma patient-derived xenograft cells cultured in stem-cell promoting medium retain tumorigenic and metastatic capacities but differentiate in serum
(
- Contribution to journal › Article
-
Mark
Respiratory chain complex III deficiency due to mutated BCS1L : A novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
(
- Contribution to journal › Article
-
Mark
Solide Kindertumoren : Ein Streifzug durch das Raritätenkabinett
(
- Contribution to journal › Article
- 2016
-
Mark
BCOR internal tandem duplication and YWHAE-NUTM2B/E fusion are mutually exclusive events in clear cell sarcoma of the kidney.
(
- Contribution to journal › Article
-
Mark
Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.
(
- Contribution to journal › Article
-
Mark
Comprehensive genetic analysis of a pediatric pleomorphic myxoid liposarcoma reveals near-haploidization and loss of the RB1 gene.
(
- Contribution to journal › Article
-
Mark
Gain of 1q as a prognostic biomarker in Wilms Tumors (WTs) treated with preoperative chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 trial : A SIOP renal tumours biology consortium study
(
- Contribution to journal › Article
-
Mark
The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement
(
- Contribution to journal › Article
-
Mark
Neuroblastoma patient-derived orthotopic xenografts reflect the microenvironmental hallmarks of aggressive patient tumours
(
- Contribution to journal › Article
-
Mark
Aberrant epigenetic regulation in clear cell sarcoma of the kidney featuring distinct DNA hypermethylation and EZH2 overexpression.
(
- Contribution to journal › Article
- 2015
-
Mark
Multiple mechanisms of MYCN dysregulation in Wilms tumour.
(
- Contribution to journal › Article
-
Mark
Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer.
(
- Contribution to journal › Article
-
Mark
Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing.
(
- Contribution to journal › Article
-
Mark
Neuroblastoma Patient-Derived Orthotopic Xenografts Retain Metastatic Patterns and Geno- and Phenotypes of Patient Tumours.
(
- Contribution to journal › Article
-
Mark
Activation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney.
(
- Contribution to journal › Article
-
Mark
Cytogenetic methods
2015) p.11-18(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Tumors of endocrine glands
2015) p.497-514(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2014
-
Mark
Regarding human cytomegalovirus in neuroblastoma.
(
- Contribution to journal › Letter
-
Mark
Reply to Duesberg: Stability of peritriploid and triploid states in neoplastic and nonneoplastic cells
(
- Contribution to journal › Letter
-
Mark
Clear cell sarcoma of the kidney demonstrates an embryonic signature indicative of a primitive nephrogenic origin.
(
- Contribution to journal › Article
-
Mark
Reply to Heng: Inborn aneuploidy and chromosomal instability
(
- Contribution to journal › Letter
-
Mark
Confined trisomy 8 mosaicism of meiotic origin: A rare cause of aneuploidy in childhood cancer.
(
- Contribution to journal › Article
-
Mark
A Comparison of Rectal Suction and Full Wall Biopsy in Hirschsprung’s Disease
(
- Contribution to journal › Article
-
Mark
Orthotopic Wilms tumor xenografts derived from cell lines reflect limited aspects of tumor morphology and clinical characteristics.
(
- Contribution to journal › Article
-
Mark
Evaluation of CITED1, SIX1, and CD56 Protein Expression for Identification of Blastemal Elements in Wilms Tumor.
(
- Contribution to journal › Article
- 2013
-
Mark
Intratumour diversity of chromosome copy numbers in neuroblastoma mediated by on-going chromosome loss from a polyploid state.
(
- Contribution to journal › Article
-
Mark
Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
(
- Contribution to journal › Article
-
Mark
Elevated tolerance to aneuploidy in cancer cells: estimating the fitness effects of chromosome number alterations by in silico modelling of somatic genome evolution.
(
- Contribution to journal › Article
-
Mark
Better Prognosis of Patients with Glioma Expressing FGF2-Dependent PDGFRA Irrespective of Morphological Diagnosis.
(
- Contribution to journal › Article
-
Mark
Absence of Epstein-Barr and Cytomegalovirus Infection in Neuroblastoma Cells by Standard Detection Methodologies.
(
- Contribution to journal › Article
-
Mark
snoRNPs Regulate Telomerase Activity in Neuroblastoma and Are Associated with Poor Prognosis.
(
- Contribution to journal › Article
-
Mark
Whole chromosome gain does not in itself confer cancer-like chromosomal instability.
(
- Contribution to journal › Article
- 2012
-
Mark
Copy Number Defects of G1-Cell Cycle Genes in Neuroblastoma are Frequent and Correlate with High Expression of E2F Target Genes and a Poor Prognosis
(
- Contribution to journal › Article
-
Mark
Oncogenic activation of FOXR1 by 11q23 intrachromosomal deletion-fusions in neuroblastoma
(
- Contribution to journal › Article
-
Mark
Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney
(
- Contribution to journal › Article
-
Mark
Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: A population-based survey.
(
- Contribution to journal › Article
-
Mark
Tumor-initiating cells in childhood neuroblastoma : Letter
(
- Contribution to journal › Letter
-
Mark
SIX1 protein expression selectively identifies blastemal elements in Wilms tumor.
(
- Contribution to journal › Article
-
Mark
Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity?
2012) In Journal of Pediatric Hematology/Oncology(
- Contribution to journal › Article
- 2011
-
Mark
Mutations in CEP57 cause mosaic variegated aneuploidy syndrome
(
- Contribution to journal › Article
-
Mark
Aneuploidy in cancer: Sudden or sequential?
(
- Contribution to journal › Article
-
Mark
Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.
(
- Contribution to journal › Article
-
Mark
Mechanisms of Whole Chromosome Gains in Tumors - Many Answers to a Simple Question.
(
- Contribution to journal › Article
-
Mark
Intratumor diversity and clonal evolution in cancer-a skeptical standpoint.
(
- Contribution to journal › Article
-
Mark
High-resolution genomic profiling of an adult Wilms' tumor: evidence for a pathogenesis distinct from corresponding pediatric tumors.
(
- Contribution to journal › Article
- 2010
-
Mark
Deletions of 16q in Wilms Tumors Localize to Blastemal-Anaplastic Cells and Are Associated with Reduced Expression of the IRXB Renal Tubulogenesis Gene Cluster.
(
- Contribution to journal › Article
-
Mark
Modeling the human 8p11-myeloproliferative syndrome in immunodeficient mice
(
- Contribution to journal › Article
-
Mark
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.
(
- Contribution to journal › Article
-
Mark
Genetic bottlenecks and the hazardous game of population reduction in cell line based research.
(
- Contribution to journal › Article
- 2009
-
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
Low frequency of EWSR1 rearrangements in neoplasms classified as high-risk wilms tumors.
(
- Contribution to journal › Article
- 2008
-
Mark
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12
(
- 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
High levels of HIF-2alpha highlight an immature neural crest-like neuroblastoma cell cohort located in a perivascular niche.
(
- 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
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
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
High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.
(
- 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
-
Mark
Classification of chromosome segregation errors in cancer.
(
- Contribution to journal › Article
- 2007
-
Mark
Defective chromosome segregation and telomere dysfunction in aggressive Wilms' tumors
(
- Contribution to journal › Article
-
Mark
Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma
(
- Contribution to journal › Article
-
Mark
Telomere dysfunction and telomerase activation in cancer - a pathological paradox?
(
- Contribution to journal › Article
-
Mark
Distinct mitotic segregation errors mediate chromosomal instability in aggressive urothelial cancers.
(
- Contribution to journal › Article
-
Mark
Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
(
- Contribution to journal › Article
-
Mark
Cancer stem cells: Differentiation block or developmental back-tracking?
(
- Contribution to journal › Letter
-
Mark
Distinct evolutionary mechanisms for genomic imbalances in high-risk and low-risk neuroblastomas
(
- Contribution to journal › Article
-
Mark
A case of Cornelia de Lange syndrome from Sudan
(
- Contribution to journal › Article
- 2006
-
Mark
Molecular cytogenetic characterization of the 11q13 amplicon in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
-
Mark
Cryptic terminal chromosome rearrangements in colorectal carcinoma cell lines detected by subtelomeric FISH analysis.
(
- Contribution to journal › Article
-
Mark
A del(X)(p11) carrying SRY sequences in an infant with ambiguous genitalia
(
- Contribution to journal › Article
-
Mark
Female genital mutilation of a karyotypic male presenting as a female with delayed puberty
(
- Contribution to journal › Article
- 2005
-
Mark
Statistical behavior of complex cancer karyotypes.
(
- Contribution to journal › Scientific review
-
Mark
Telomere-mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma
(
- Contribution to journal › Article
-
Mark
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
(
- Contribution to journal › Article
-
Mark
Mitotic instability in cancer - Is there method in the madness?
(
- Contribution to journal › Article
-
Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
(
- Contribution to journal › Article
-
Mark
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
(
- Contribution to journal › Article
-
Mark
Connecting mitotic instability and chromosome aberrations in cancer-can telomeres bridge the gap?
(
- Contribution to journal › Scientific review
- 2004
-
Mark
A model for karyotypic evolution in testicular germ cell tumors.
(
- Contribution to journal › Article
-
Mark
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
(
- Contribution to journal › Article
-
Mark
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas.
(
- Contribution to journal › Article
-
Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
-
Mark
Wilms tumors develop through two distinct karyotypic pathways.
(
- Contribution to journal › Article
-
Mark
Sudanesiska cytogenetiker - vision om en ny form av bistånd
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
(
- Contribution to journal › Article
-
Mark
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
(
- Contribution to journal › Article
-
Mark
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
(
- Contribution to journal › Article
- 2003
-
Mark
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Ring Y chromosome in an azoospermic male with short stature: additional evidence for a distinct ring Y syndrome in non-mosaic patients?
(
- Contribution to journal › Letter
-
Mark
Power law distribution of chromosome aberrations in cancer.
(
- Contribution to journal › Article
-
Mark
Ovarian Carcinoma Develops through Multiple Modes of Chromosomal Evolution.
(
- Contribution to journal › Article
-
Mark
Chromosome instability in cancer: how, when, and why?
(
- Contribution to journal › Scientific review
- 2002
-
Mark
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations and their prognostic impact in chondrosarcoma
(
- Contribution to journal › Article
-
Mark
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
(
- Contribution to journal › Article
-
Mark
Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances.
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.
(
- Contribution to journal › Article
-
Mark
Tumour morphology--interplay between chromosome aberrations and founder cell differentiation.
(
- Contribution to journal › Scientific review
-
Mark
Coping with complexity. multivariate analysis of tumor karyotypes.
(
- Contribution to journal › Article
- 2001
-
Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
(
- Contribution to journal › Article
-
Mark
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
(
- Contribution to journal › Article
-
Mark
Abnormal nuclear shape in solid tumors reflects mitotic instability
(
- Contribution to journal › Article
-
Mark
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH
(
- Contribution to journal › Article
-
Mark
PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms
(
- Contribution to journal › Article
-
Mark
Limitations of chromosome classification by multicolor karyotyping
(
- Contribution to journal › Article
-
Mark
Refined characterisation of chromosome aberrations in tumours by multicolour banding and electronic mapping resources
2001) In Methods in cell science: an official journal of the Society for In Vitro Biology 23(1-3). p.23-28(
- Contribution to journal › Article
-
Mark
ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization
(
- Contribution to journal › Article
- 2000
-
Mark
Putting chromosome aberrations on the map
(
- Contribution to journal › Article
-
Mark
Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study
(
- Contribution to journal › Article
-
Mark
Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia
(
- Contribution to journal › Article
-
Mark
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
(
- Contribution to journal › Article
-
Mark
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p
(
- Contribution to journal › Article
-
Mark
Chromosomal Instability and Genomic Amplification in Bone and Soft Tissue Tumours
2000)(
- Thesis › Doctoral thesis (compilation)
- 1999
-
Mark
Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics
(
- Contribution to journal › Article
-
Mark
Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics
(
- Contribution to journal › Article
-
Mark
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
(
- Contribution to journal › Article
-
Mark
Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours
(
- Contribution to journal › Article
- 1998
-
Mark
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization
(
- Contribution to journal › Article
-
Mark
Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma
(
- Contribution to journal › Article
-
Mark
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
(
- Contribution to journal › Article
-
Mark
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
(
- Contribution to journal › Article