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- 2024
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Mark
Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
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Mark
Vector integration and fate in the hemophilia dog liver multi-years following AAV-FVIII gene transfer
2024) In Blood(
- Contribution to journal › Article
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Mark
Deciphering the genetics and mechanisms of predisposition to multiple myeloma
(
- Contribution to journal › Article
- 2023
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Mark
Molecular evaluation and vector integration analysis of HCC complicating AAV gene therapy for hemophilia B
(
- Contribution to journal › Article
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Mark
Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression?
(
- Contribution to journal › Article
- 2022
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Mark
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
(
- Contribution to journal › Letter
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Mark
Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia : a CRuCIAL study
(
- Contribution to journal › Letter
- 2021
-
Mark
Familial Risks between Pernicious Anemia and Other Autoimmune Diseases in the Population of Sweden
(
- Contribution to journal › Article
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Mark
Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium
(
- Contribution to journal › Article
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Mark
Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years
(
- Contribution to journal › Article
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Mark
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population
(
- Contribution to journal › Article
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Mark
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations
(
- Contribution to journal › Article
- 2020
-
Mark
Performance of individual and joint risk stratification by an environmental risk score and a genetic risk score in a colorectal cancer screening setting
(
- Contribution to journal › Article
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Mark
Familial associations for rheumatoid autoimmune diseases
(
- Contribution to journal › Article
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Mark
Familial associations for Addison’s disease and between Addison’s disease and other autoimmune diseases
(
- Contribution to journal › Article
-
Mark
Familial risks between giant cell arteritis and Takayasu arteritis and other autoimmune diseases in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Familial associations between autoimmune hepatitis and primary biliary cholangitis and other autoimmune diseases
(
- Contribution to journal › Article
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Mark
Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis
(
- Contribution to journal › Article
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Mark
Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1
(
- Contribution to journal › Article
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Mark
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
(
- Contribution to journal › Article
-
Mark
Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium
2020)(
- Working paper/Preprint › Preprint in preprint archive
- 2019
-
Mark
Quantification and detection of genetic risk factors in the familial aggregation of cancer : Habilitation thesis
2019)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk
(
- Contribution to journal › Article
-
Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
(
- Contribution to journal › Article
-
Mark
The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism : Association study and meta-analysis
(
- Contribution to journal › Article
-
Mark
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma
(
- Contribution to journal › Article
-
Mark
Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population
(
- Contribution to journal › Article
-
Mark
Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS) : comparison with multiple myeloma
2019) In Leukemia(
- Contribution to journal › Letter
-
Mark
Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
-
Mark
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes
(
- Contribution to journal › Article
-
Mark
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
(
- Contribution to journal › Article
- 2018
-
Mark
Clinical landscape of cancer metastases
(
- Contribution to journal › Article
-
Mark
Genetic Risk Score Is Associated With Prevalence of Advanced Neoplasms in a Colorectal Cancer Screening Population
(
- Contribution to journal › Article
-
Mark
Familial risks of acute myeloid leukemia, myelodysplastic syndromes, and myeloproliferative neoplasms
(
- Contribution to journal › Letter
-
Mark
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance : a genome-wide genetic interaction study
(
- Contribution to journal › Article
-
Mark
Genetic variation associated with chromosomal aberration frequency : A genome-wide association study
2018) In Environmental and Molecular Mutagenesis(
- Contribution to journal › Article
-
Mark
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
(
- Contribution to journal › Article
-
Mark
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology
(
- Contribution to journal › Article
- 2017
-
Mark
Risk of second cancer in Hodgkin lymphoma survivors and influence of family history
(
- Contribution to journal › Article
-
Mark
The impact of methylation quantitative trait loci (mQTLs) on active smoking-related DNA methylation changes
(
- Contribution to journal › Article
-
Mark
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
(
- Contribution to journal › Article
-
Mark
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
(
- Contribution to journal › Article
-
Mark
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci
(
- Contribution to journal › Article
- 2016
-
Mark
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
-
Mark
Runs of homozygosity and inbreeding in thyroid cancer
(
- Contribution to journal › Article
- 2015
-
Mark
Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches.
(
- Contribution to journal › Article
-
Mark
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
(
- Contribution to journal › Article
-
Mark
Inbreeding and homozygosity in breast cancer survival.
(
- Contribution to journal › Article
-
Mark
The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A.
(
- Contribution to journal › Article
- 2014
-
Mark
Metastatic sites and survival in lung cancer.
(
- Contribution to journal › Article
- 2013
-
Mark
Comparison of survival of patients with metastases from known versus unknown primaries: survival in metastatic cancer
(
- Contribution to journal › Article
-
Mark
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
(
- Contribution to journal › Article
- 2012
-
Mark
Colorectal cancer patients : what do they die of?
(
- Contribution to journal › Article
-
Mark
Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants
(
- Contribution to journal › Article
- 2011
-
Mark
Influence of family size and birth order on risk of cancer: a population-based study
(
- Contribution to journal › Article
-
Mark
What Do Prostate Cancer Patients Die Of?
(
- Contribution to journal › Article
-
Mark
Determinants of unfavorable presentation of primary cutaneous melanoma
(
- Contribution to journal › Letter
-
Mark
QTL explaining variation in production traits and udder health in the Danish Holstein population
(
- Contribution to journal › Article
- 2010
-
Mark
Tumor location and patient characteristics of colon and rectal adenocarcinomas in relation to survival and TNM classes
(
- Contribution to journal › Article
- 2006
-
Mark
Confirmation of quantitative trait loci for somatic cell score on bovine chromosome 18 in the German Holstein
(
- Contribution to journal › Article
- 2005
-
Mark
Combined line-cross and half-sib QTL analysis of crosses between outbred lines
(
- Contribution to journal › Article
- 2004
-
Mark
Investigation of obesity candidate genes on porcine fat deposition quantitative trait loci regions
(
- Contribution to journal › Article
-
Mark
Multiple quantitative trait loci mapping with cofactors and application of alternative variants of the false discovery rate in an enlarged granddaughter design
(
- Contribution to journal › Article
- 2003
-
Mark
Combined analysis of data from two granddaughter designs : A simple strategy for QTL confirmation and increasing experimental power in dairy cattle
(
- Contribution to journal › Article
- 2001
-
Mark
A mammary gland EST showing linkage disequilibrium to a milk production QTL on bovine Chromosome 14
(
- Contribution to journal › Article
-
Mark
A whole genome scan for differences in recombination rates among three Bos taurus breeds
(
- Contribution to journal › Article