Division of Clinical Genetics
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- 2020
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Mark
Why classical cytogenetics still matters in acute myeloid leukemia
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Deep sequencing of myxoinflammatory fibroblastic sarcoma
(
- Contribution to journal › Article
-
Mark
Genomic and transcriptomic features of dermatofibrosarcoma protuberans : Unusual chromosomal origin of the COL1A1-PDGFB fusion gene and synergistic effects of amplified regions in tumor development
(
- Contribution to journal › Article
-
Mark
Clonal competition within complex evolutionary hierarchies shapes AML over time
(
- Contribution to journal › Article
-
Mark
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
(
- Contribution to journal › Article
-
Mark
Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
(
- Contribution to journal › Article
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Mark
A century of Hereditas : from local publication to international journal
(
- Contribution to journal › Article
-
Mark
Abstract CT074: Pre-existing ESR1 mutations in early-stage primary breast cancer predict failure of endocrine therapy and poor survival
(
- Contribution to journal › Published meeting abstract
-
Mark
Adherent Intestinal Cells From Atlantic Salmon Show Phagocytic Ability and Express Macrophage-Specific Genes
(
- Contribution to journal › Article
-
Mark
Microphthalmia-associated transcription factor-dependent melanoma cell adhesion molecule activation promotes peritoneal metastasis of ovarian cancer
(
- Contribution to journal › Article
-
Mark
The reversal of human phylogeny : Homo left Africa as erectus, came back as sapiens sapiens
(
- Contribution to journal › Scientific review
-
Mark
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
(
- Contribution to journal › Article
-
Mark
Transcriptomic profiling of T-cell populations in non-muscle invasive and muscle invasive bladder cancer.
2020) The Society for Immunotherapy of Cancer's (SITC) 35th annual meeting In Journal for ImmunoTherapy of Cancer 8(Suppl. 3).(
- Contribution to journal › Published meeting abstract
-
Mark
Cancer risks associated with germline PALB2 pathogenic variants : An international study of 524 families
(
- Contribution to journal › Article
- 2019
-
Mark
Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors : an international survey
(
- Contribution to journal › Article
-
Mark
A novel human in vitro papillomavirus type 16 positive tonsil cancer cell line with high sensitivity to radiation and cisplatin
(
- Contribution to journal › Article
-
Mark
PRDM10 -rearranged Soft Tissue Tumor : A Clinicopathologic Study of 9 Cases
(
- Contribution to journal › Article
-
Mark
Changes in the Prevalence of Embryologic Remnants in Umbilical Cord With Gestational Age
(
- Contribution to journal › Article
-
Mark
Multidimensional intratumour heterogeneity in neuroblastoma
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Generation of an induced pluripotent stem cell line (CSC-46) from a patient with Parkinson's disease carrying a novel p.R301C mutation in the GBA gene
(
- Contribution to journal › Article
-
Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- Contribution to journal › Article
-
Mark
Genetic testing and surveillance guidelines in hereditary pheochromocytoma and paraganglioma
(
- Contribution to journal › Scientific review
-
Mark
Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition
(
- Contribution to journal › Article
-
Mark
Clonal evolution through genetic bottlenecks and telomere attrition : Potential threats to in vitro data reproducibility
(
- Contribution to journal › Scientific review
-
Mark
Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas
(
- Thesis › Doctoral thesis (compilation)
-
Mark
The Iroquois homeobox proteins IRX3 and IRX5 have distinct roles in Wilms tumour development and human nephrogenesis
(
- Contribution to journal › Article
-
Mark
Genetic predisposition to B-cell acute lymphoblastic leukemia at 14q11.2 is mediated by a CEBPE promoter polymorphism
(
- Contribution to journal › Article
-
Mark
Aberrant receptor tyrosine kinase signaling in lipofibromatosis : a clinicopathological and molecular genetic study of 20 cases
(
- Contribution to journal › Article
-
Mark
A stroke gene panel for whole-exome sequencing
(
- Contribution to journal › Article
-
Mark
Hereditary colorectal cancer diagnostics in southern Sweden : retrospective evaluation and future considerations with emphasis on Lynch syndrome
(
- Contribution to journal › Article
-
Mark
The WNT5A Agonist Foxy5 Reduces the Number of Colonic Cancer Stem Cells in a Xenograft Mouse Model of Human Colonic Cancer
(
- Contribution to journal › Article
-
Mark
Gene fusion involving the insulin-like growth factor 1 receptor in an ALK-negative inflammatory myofibroblastic tumour
(
- Contribution to journal › Article
-
Mark
Identification of targetable lesions in anaplastic thyroid cancer by genome profiling
(
- Contribution to journal › Article
-
Mark
Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene
(
- Contribution to journal › Article
-
Mark
Vi måste ta ställning till den nya gentekniken
2019) In Svenska Dagbladet, Stockholm(
- Contribution to specialist publication or newspaper › Newspaper article
-
Mark
Immune effector monocyte–neutrophil cooperation induced by the primary tumor prevents metastatic progression of breast cancer
2019) In Proceedings of the National Academy of Sciences of the United States of America 116(43). p.21704-21714(
- Contribution to journal › Article
-
Mark
Genetic Characterization and Identification of Novel Treatment Targets in Anaplastic Thyroid Carcinoma
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study
(
- Contribution to journal › Article
-
Mark
PAX5 is part of a functional transcription factor network targeted in lymphoid leukemia
(
- Contribution to journal › Article
-
Mark
Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile
(
- Contribution to journal › Article
-
Mark
Genetic profiling of a chondroblastoma-like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1-FGFR1 gene fusion
(
- Contribution to journal › Article
-
Mark
Outcome of Children With Hypodiploid Acute Lymphoblastic Leukemia : A Retrospective Multinational Study
(
- Contribution to journal › Article
-
Mark
Arrayed molecular barcoding identifies TNFSF13 as a positive regulator of acute myeloid leukemia-initiating cells
(
- Contribution to journal › Article
-
Mark
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : An ENIGMA resource to support clinical variant classification
(
- Contribution to journal › Article
-
Mark
Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
FLT3
N676K
drives acute myeloid leukemia in a xenograft model of KMT2A-MLLT3 leukemogenesis
(
- Contribution to journal › Letter
-
Mark
Idiopathic ventricular fibrillation – Long term prognosis in relation to clinical findings and ECG patterns in a Swedish cohort
(
- Contribution to journal › Article
-
Mark
Identification of two abundant Aerococcus urinae cell wall-anchored proteins
(
- Contribution to journal › Article
-
Mark
Most gene fusions in cancer are stochastic events
(
- Contribution to journal › Article
-
Mark
A urinary extracellular vesicle microRNA biomarker discovery pipeline; from automated extracellular vesicle enrichment by acoustic trapping to microRNA sequencing
(
- Contribution to journal › Article
-
Mark
Recombinant dermatan sulfate is a potent activator of heparin cofactor II-dependent inhibition of thrombin
(
- Contribution to journal › Article
-
Mark
Att inte debattera är inte ett alternativ
2019) In Svenska Dagbladet, Stockholm(
- Contribution to specialist publication or newspaper › Newspaper article
-
Mark
Cellular alterations identified in pluripotent stem cell-derived midbrain spheroids generated from a female patient with progressive external ophthalmoplegia and parkinsonism who carries a novel variation (p.Q811R) in the POLG1 gene
(
- Contribution to journal › Article
-
Mark
Disseqt-distribution-based modeling of sequence space time dynamics
(
- Contribution to journal › Article
- 2018
-
Mark
Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study : experiences from re-contacting mutation carriers and relatives
(
- Contribution to journal › Article
-
Mark
Inflammatory leiomyosarcoma is a distinct tumor characterized by near-haploidization, few somatic mutations, and a primitive myogenic gene expression signature
(
- Contribution to journal › Article
-
Mark
Isolated myelosarcoma is characterized by recurrent NFE2 mutations and concurrent preleukemic clones in the bone marrow
(
- Contribution to journal › Letter
-
Mark
Novel subgroups of adult-onset diabetes and their association with outcomes : A data-driven cluster analysis of six variables
(
- Contribution to journal › Article
-
Mark
Generation of an induced pluripotent stem cell line (CSC-44) from a Parkinson's disease patient carrying a compound heterozygous mutation (c.823C > T and EX6 del) in the PARK2 gene
(
- Contribution to journal › Article
-
Mark
Utvidgad anlagsbärartestning kan bredda fosterdiagnostiken - Recessiva sjukdomsanlag kan kartläggas hos friska personer inför planerad graviditet
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Identification and characterization of candidate therapeutic targets in acute myeloid leukemia
2018)(
- Thesis › Doctoral thesis (compilation)
-
Mark
PREPL deficiency : Delineation of the phenotype and development of a functional blood assay
(
- Contribution to journal › Article
-
Mark
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
(
- Contribution to journal › Article
-
Mark
Generation of an induced pluripotent stem cell line (CSC-41) from a Parkinson's disease patient carrying a p.G2019S mutation in the LRRK2 gene
(
- Contribution to journal › Article
-
Mark
Interleukin 4 induces apoptosis of acute myeloid leukemia cells in a Stat6 dependent manner
(
- Contribution to journal › Article
-
Mark
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant : Breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
(
- Contribution to journal › Article
-
Mark
BRCAsearch : written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer
(
- Contribution to journal › Article
-
Mark
Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer
(
- Contribution to journal › Article
-
Mark
A field guide for cancer diagnostics using cell-free DNA : From principles to practice and clinical applications
(
- Contribution to journal › Scientific review
-
Mark
Generation of a human induced pluripotent stem cell line (CSC-40) from a Parkinson's disease patient with a PINK1 p.Q456X mutation
(
- Contribution to journal › Article
-
Mark
Generation of an integration-free induced pluripotent stem cell line (CSC-43J) from a patient with sporadic Parkinson's disease
(
- Contribution to journal › Article
-
Mark
Generation of a human induced pluripotent stem cell line (CSC-42) from a patient with sporadic form of Parkinson's disease
(
- Contribution to journal › Article
-
Mark
Use of the BOADICEA Web Application in clinical practice : appraisals by clinicians from various countries
(
- Contribution to journal › Article
-
Mark
Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Discontinuation of tyrosine kinase inhibitor therapy in chronic myeloid leukaemia (EURO-SKI) : a prespecified interim analysis of a prospective, multicentre, non-randomised, trial
(
- Contribution to journal › Article
-
Mark
Montelukast, a CysLT1 receptor antagonist, reduces colon cancer stemness and tumor burden in a mouse xenograft model of human colon cancer
(
- Contribution to journal › Article
-
Mark
Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers
(
- Contribution to journal › Article
-
Mark
Studies of Ligands and Receptors Regulating Acute Myeloid Leukemia
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years
(
- Contribution to journal › Article
-
Mark
Transcriptional landscape of B cell precursor acute lymphoblastic leukemia based on an international study of 1,223 cases
2018) In Proceedings of the National Academy of Sciences of the United States of America 115(50). p.11711-11720(
- Contribution to journal › Article
-
Mark
Microenvironmental control of breast cancer subtype elicited through paracrine platelet-derived growth factor-CC signaling
(
- Contribution to journal › Article
-
Mark
Inferior survival for patients with malignant peripheral nerve sheath tumors defined by aberrant TP53
(
- Contribution to journal › Article
-
Mark
Gastrointestinal microbiota contributes to the development of murine transfusion-related acute lung injury
(
- Contribution to journal › Article
-
Mark
Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Patient-derived xenograft models reveal intratumor heterogeneity and temporal stability in neuroblastoma
(
- Contribution to journal › Article
-
Mark
A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families 11 Medical and Health Sciences 1112 Oncology and Carcinogenesis 11 Medical and Health Sciences 1117 Public Health and Health Services
(
- Contribution to journal › Article
-
Mark
Neuroblastoma with flat genomic profile : A question of representativity?
(
- Contribution to journal › Article
-
Mark
Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis : A single center experience of 296 cases
(
- Contribution to journal › Article
-
Mark
Intact glucose uptake despite deteriorating signaling in adipocytes with high-fat feeding
(
- Contribution to journal › Article
-
Mark
Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer
(
- Contribution to journal › Article
-
Mark
De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged leukemia
(
- Contribution to journal › Article
-
Mark
CD36 defines primitive chronic myeloid leukemia cells less responsive to imatinib but vulnerable to antibody-based therapeutic targeting
(
- Contribution to journal › Article
- 2017
-
Mark
Distinct global binding patterns of the Wilms' tumor gene 1 (WT1) -KTS and +KTS isoforms in leukemic cells
(
- Contribution to journal › Article
-
Mark
Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
(
- Contribution to journal › Article
-
Mark
Mosaicism in health and disease — clones picking up speed
(
- Contribution to journal › Article
-
Mark
Near-haploid and low hypodiploid acute lymphoblastic leukemia - two distinct subtypes but consistently poor prognosis
(
- Contribution to journal › Article
-
Mark
Cancer - An Insurgency of Clones
(
- Contribution to journal › Article
-
Mark
Pediatric T-cell acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
-
Mark
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS and neurological symptoms
(
- Contribution to journal › Article
-
Mark
Frequent low-level mutations of Protein Kinase D2 in angiolipoma
(
- Contribution to journal › Article
-
Mark
Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer
(
- Contribution to journal › Article
-
Mark
New oncogenic subtypes in pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
-
Mark
Transgenic expression of human cytokines in immunodeficient mice does not facilitate myeloid expansion of BCR-ABL1 transduced human cord blood cells
(
- Contribution to journal › Article
-
Mark
In-depth genetic analysis of sclerosing epithelioid fibrosarcoma reveals recurrent genomic alterations and potential treatment targets
(
- Contribution to journal › Article
-
Mark
Agonistic targeting of TLR1/TLR2 induces p38 MAPK-dependent apoptosis and NFκB-dependent differentiation of AML cells
(
- Contribution to journal › Article
-
Mark
Functional screen of MSI2 interactors identifies an essential role for SYNCRIP in myeloid leukemia stem cells
(
- 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
Molecular Interrogation and Functional Studies of Acute Leukemia
2017)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Frequent miRNA-convergent fusion gene events in breast cancer
(
- Contribution to journal › Article
-
Mark
Somatic Genetic Variation in Children: from Mosaicism to Cancer
2017)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic anticipation in Swedish Lynch syndrome families
(
- Contribution to journal › Article
-
Mark
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Primary cells in BCR/FGFR1-positive 8p11 myeloproliferative syndrome are sensitive to dovitinib, ponatinib, and dasatinib
(
- Contribution to journal › Article
-
Mark
Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines
(
- Contribution to journal › Article
-
Mark
Nollutsläpp i basindustrin - förutsättningar för en ny industripolitik
2017) In IMES/EESS report(
- Book/Report › Report
-
Mark
Evolution of antigenic diversity in the tick-transmitted bacterium Borrelia afzelii : a role for host specialization?
(
- Contribution to journal › Article
-
Mark
Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS Cohort
(
- Contribution to journal › Article
-
Mark
From Mendel to Medical Genetics
(
- Contribution to journal › Scientific review
-
Mark
Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2
(
- Contribution to journal › Article
-
Mark
FNA Cytology of Soft Tissue and Bone Tumors
(
- Book/Report › Book
-
Mark
Pathogenetic Mechanisms in Soft Tissue Tumors
2017)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Soft tissue angiofibroma : Clinicopathologic, immunohistochemical and molecular analysis of 14 cases
(
- Contribution to journal › Article
-
Mark
Loss of the tumor suppressor gene AIP mediates the browning of human brown fat tumors
(
- Contribution to journal › Article
-
Mark
Solide Kindertumoren : Ein Streifzug durch das Raritätenkabinett
(
- Contribution to journal › Article
-
Mark
Scattered genomic amplification in dedifferentiated liposarcoma
(
- 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
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
(
- Contribution to journal › Article
-
Mark
Incidence and prognostic significance of isolated trisomies in adult acute myeloid leukemia : A population-based study from the Swedish AML registry
(
- Contribution to journal › Article
-
Mark
Increased proportion of mature NK cells is associated with successful imatinib discontinuation in chronic myeloid leukemia
(
- Contribution to journal › Article
-
Mark
Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
- 2016
-
Mark
The clinical value of genetic analyses of bone and soft tissue tumors
(
- Thesis › Doctoral thesis (compilation)
-
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
An update of a classical textbook.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.
(
- Contribution to journal › Article
-
Mark
Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p.
(
- Contribution to journal › Article
-
Mark
Familial aggregation of stroke amongst young patients in Lund Stroke Register.
(
- Contribution to journal › Article
-
Mark
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
2016) In Nature Genetics(
- 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
Patterns and Frequencies of Acquired and Constitutional Uniparental Isodisomies in Pediatric and Adult B-Cell Precursor Acute Lymphoblastic Leukemia.
(
- Contribution to journal › Article
-
Mark
Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes.
(
- Contribution to journal › Scientific review
-
Mark
FN1-EGF gene fusions are recurrent in calcifying aponeurotic fibroma.
(
- Contribution to journal › Article
-
Mark
Primary Pseudomyogenic Hemangioendothelioma of Bone.
(
- Contribution to journal › Article
-
Mark
L1 syndrome diagnosis complemented with functional analysis of L1CAM variants located to the two N-terminal Ig-like domains.
2016) In Clinical Genetics(
- 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
-
Mark
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
(
- Contribution to journal › Article
-
Mark
The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes
(
- Contribution to journal › Article
-
Mark
Genomic profiling and directed ex vivo drug analysis of an unclassifiable myelodysplastic/myeloproliferative neoplasm progressing into acute myeloid leukemia
(
- Contribution to journal › Article
-
Mark
The genomic landscape of core-binding factor acute myeloid leukemias
(
- Contribution to journal › Letter
-
Mark
Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations
(
- Contribution to journal › Article
-
Mark
A New Method for Endoscopic Sampling of Submucosal Tissue in the Gastrointestinal Tract : A Comparison of the Biopsy Forceps and a New Drill Instrument
(
- 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
Rare novel variants in the ZIC3 gene cause X-linked heterotaxy
(
- Contribution to journal › Article
-
Mark
Neuroblastoma patient-derived orthotopic xenografts reflect the microenvironmental hallmarks of aggressive patient tumours
(
- Contribution to journal › Article
-
Mark
Single nucleotide polymorphism array analysis of clonal evolution in younger adult acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
(
- Contribution to journal › Article
-
Mark
Clonal conversion of B lymphoid leukemia reveals cross-lineage transfer of malignant states
(
- Contribution to journal › Article
-
Mark
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
(
- Contribution to journal › Article
-
Mark
IL1RAP antibodies block IL-1-induced expansion of candidate CML stem cells and mediate cell killing in xenograft models
(
- 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
Leukemic stem cell quantification in newly diagnosed chronic myeloid leukemia patients predicts response to nilotinib therapy
(
- Contribution to journal › Article
-
Mark
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic
(
- Contribution to journal › Article
-
Mark
Core Circadian Clock Genes Regulate Leukemia Stem Cells in AML
(
- Contribution to journal › Article
-
Mark
Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia
(
- Contribution to journal › Article
-
Mark
Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Global binding pattern of the Wilms' tumor gene 1 (WT1) +17AA -KTS isoform in leukemic cells
2016) American Association for Cancer Research (AACR) 107th Annual Meeting 2016 In Cancer Research 76(14 Suppl.).(
- Contribution to journal › Published meeting abstract
-
Mark
High hyperdiploid childhood acute lymphoblastic leukemia : Chromosomal gains as the main driver event
(
- Contribution to journal › Article
-
Mark
Cancer in first-degree relatives of women with early-onset breast cancer: a comparison of self-reported and cancer registry data
(
- Contribution to journal › Published meeting abstract
-
Mark
PKC activation sensitizes basal-like breast cancer cell lines to Smac mimetics
(
- Contribution to journal › Article
- 2015
-
Mark
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
(
- Contribution to journal › Article
-
Mark
Multiple mechanisms of MYCN dysregulation in Wilms tumour.
(
- Contribution to journal › Article
-
Mark
Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
(
- Contribution to journal › Article
-
Mark
IL1RAP expression as a measure of leukemic stem cell burden at diagnosis of chronic myeloid leukemia predicts therapy outcome.
(
- Contribution to journal › Article
-
Mark
Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer.
(
- Contribution to journal › Article
-
Mark
Molecular Genetic Characterization of Acute Lymphoblastic Leukemia with a Poor Prognosis
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Pharmacologically relevant doses of valproate upregulate CD20 expression in three diffuse large B-cell lymphoma patients in vivo.
(
- Contribution to journal › Article
-
Mark
Ciliary neurotrophic factor has intrinsic and extrinsic roles in regulating B cell differentiation and bone structure.
(
- Contribution to journal › Article
-
Mark
Chromosome gains drive childhood ALL.
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A.
(
- Contribution to journal › Article
-
Mark
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.
(
- Contribution to journal › Article
-
Mark
A certified plasmid reference material for the standardisation of BCR-ABL1 mRNA quantification by real time quantitative PCR.
(
- Contribution to journal › Article
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Mark
Antibodies targeting human IL1RAP (IL1R3) show therapeutic effects in xenograft models of acute myeloid leukemia.
(
- Contribution to journal › Article
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Mark
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
(
- Contribution to journal › Article
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Mark
Methylated RASSF1A in malignant peripheral nerve sheath tumors identifies neurofibromatosis type 1 patients with inferior prognosis.
(
- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
2015) In European Journal of Human Genetics(
- Contribution to journal › Article
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Mark
Neuroblastoma Patient-Derived Orthotopic Xenografts Retain Metastatic Patterns and Geno- and Phenotypes of Patient Tumours.
(
- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
(
- Contribution to journal › Article
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Mark
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
(
- Contribution to journal › Article
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Mark
Ebf1 heterozygosity results in increased DNA damage in pro-B cells and their synergistic transformation by Pax5 haploinsufficiency.
(
- Contribution to journal › Article
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Mark
The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013.
(
- Contribution to journal › Article
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Mark
Ikaros and leukaemia.
(
- Contribution to journal › Scientific review
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Mark
RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.
(
- Contribution to journal › Article
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Mark
Acute Traumatic Brain Injury Mortality in the elderly.
(
- Contribution to journal › Article
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Mark
Activation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney.
(
- Contribution to journal › Article
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Mark
Laboratory recommendations for scoring deep molecular responses following treatment for chronic myeloid leukemia.
(
- Contribution to journal › Scientific review
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Mark
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.
(
- Contribution to journal › Article
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Mark
Protein expression of BIRC5, TK1, and TOP2A in malignant peripheral nerve sheath tumours - A prognostic test after surgical resection.
(
- Contribution to journal › Article
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Mark
The emerging complexity of gene fusions in cancer.
(
- Contribution to journal › Scientific review
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Mark
Dasatinib induces fast and deep responses in newly diagnosed chronic myeloid leukaemia patients in chronic phase: clinical results from a randomised phase-2 study (NordCML006)
(
- Contribution to journal › Article
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Mark
Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing.
(
- Contribution to journal › Article
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Mark
A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients
(
- Contribution to journal › Article
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Mark
The gynecological surveillance of women with Lynch syndrome in Sweden.
(
- Contribution to journal › Article
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Mark
Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
(
- Contribution to journal › Article
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Mark
Prognostic significance of high hyperdiploid and tri-/tetraploid adult acute myeloid leukemia.
(
- Contribution to journal › Article
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Mark
The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.
(
- Contribution to journal › Article
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Mark
Failure matters: unsuccessful cytogenetics and unperformed cytogenetics are associated with a poor prognosis in a population-based series of acute myeloid leukaemia.
(
- Contribution to journal › Article
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Mark
Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.
(
- Contribution to journal › Article
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Mark
The DEK oncoprotein and its emerging roles in gene regulation.
(
- Contribution to journal › Scientific review
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Mark
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
(
- Contribution to journal › Article
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Mark
Non-fibrosing sclerosing epithelioid fibrosarcoma: An unusual variant.
2015) In Histopathology(
- Contribution to journal › Letter
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Mark
Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Lenalidomide induces ubiquitination and degradation of CK1α in del(5q) MDS
(
- Contribution to journal › Article
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Mark
A short history of chromosome rearrangements and gene fusions in cancer
2015) p.3-11(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Soft tissue tumors
2015) p.583-614(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Chronic myeloid leukemia
2015) p.153-174(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Cytogenetic methods
2015) p.11-18(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Tumors of bone
2015) p.566-582(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Tumors of endocrine glands
2015) p.497-514(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Preface to the Fourth Edition
2015)(
- Chapter in Book/Report/Conference proceeding › Foreword/Postscript
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Mark
How it all began : Cancer cytogenetics before sequencing
2015) p.1-10(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Cancer cytogenetics : Chromosomal and Molecular Genetic Aberrations of Tumor Cells
Heim, Sverre LU and Mitelman, Felix LU (2015)
- Book/Report › Anthology (editor)
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Mark
Cytogenetic nomenclature
2015) p.19-25(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Acute lymphoblastic leukemia
2015) p.198-251(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Nonrandom chromosome abnormalities in cancer : An overview
2015) p.26-41(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Acute myeloid leukemia
2015) p.62-125(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Tumors of the skin
2015) p.555-565(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Increasing age at first full-time pregnancy correlates to use of oral contraceptives before age 20 in women with a family history of breast cancer
2015) 106th Annual Meeting of the American Association for Cancer Research(
- Contribution to conference › Abstract
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Mark
Omission of doxorubicin from the treatment of stage II-III, intermediate-risk Wilms' tumour (SIOP WT 2001) : an open-label, non-inferiority, randomised controlled trial
(
- Contribution to journal › Article
- 2014
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Mark
t(6;9)(p22; q34)/DEK-NUP214-rearranged pediatric myeloid leukemia: an international study of 62 patients
(
- Contribution to journal › Article
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Mark
Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in Non-Hodgkin Lymphoma
(
- Contribution to journal › Letter
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Mark
IKAROS and LEUKEMIA
(
- Thesis › Doctoral thesis (compilation)
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Mark
Detecting dic(9;20)(p13.2;p11.2)-positive B-cell precursor acute lymphoblastic leukemia in a clinical setting using fluorescence in situ hybridization
(
- Contribution to journal › Letter
-
Mark
Genetic Characterization of Pediatric T-cell Acute Lymphoblastic Leukemia
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Csnk1a1 inhibition has p53-dependent therapeutic efficacy in acute myeloid leukemia
(
- Contribution to journal › Article
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Mark
Regarding human cytomegalovirus in neuroblastoma.
(
- Contribution to journal › Letter
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Mark
Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
(
- Contribution to journal › Article
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Mark
Primary mesenchymal stem cells in human transplanted lungs are CD90/CD105 perivascularly located tissue-resident cells.
(
- Contribution to journal › Article
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Mark
Identification, Validation and Implementation of Blastemal Biomarkers in Wilms Tumour
(
- Thesis › Doctoral thesis (compilation)
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Mark
Incidence and prognostic significance of karyotypic subgroups in older patients with acute myeloid leukemia: the Swedish population-based experience.
(
- Contribution to journal › Article
-
Mark
Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study
(
- Contribution to journal › Article
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Mark
Feasibility of targeted next-generation sequencing of the TP53 and ATM genes in chronic lymphocytic leukemia
(
- Contribution to journal › Letter
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Mark
Permanent activation of HMGA2 in lipomas mimics its temporal physiological activation linked to the gain of adipose tissue
(
- Contribution to journal › Article
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Mark
Clear cell sarcoma of the kidney demonstrates an embryonic signature indicative of a primitive nephrogenic origin.
(
- Contribution to journal › Article
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Mark
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
(
- Contribution to journal › Article
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Mark
Myoepithelioma of bone with a novel FUS-POU5F1 fusion gene
(
- Contribution to journal › Article
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Mark
Evolving techniques for gene fusion detection in soft tissue tumours.
(
- Contribution to journal › Scientific review
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Mark
Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011.
(
- Contribution to journal › Article
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Mark
HIF-1α can act as a tumor suppressor gene in murine Acute Myeloid Leukemia.
(
- Contribution to journal › Article
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Mark
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma.
(
- Contribution to journal › Article