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- 2017
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Mark
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci
(
- Contribution to journal › Article
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Mark
Concordant and discordant familial cancer : Familial risks, proportions and population impact
(
- Contribution to journal › Article
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Mark
Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy : Replication of the Reported Candidate Susceptibility Loci
(
- Contribution to journal › Article
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Mark
Familial Associations Between Prostate Cancer and Other Cancers
(
- Contribution to journal › Article
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Mark
Familial risks for gallstones in the population of Sweden
(
- Contribution to journal › Article
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Mark
Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach
(
- Contribution to journal › Letter
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Mark
Other cancers in lung cancer families are overwhelmingly smoking-related cancers
(
- Contribution to journal › Article
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Mark
Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism
(
- Contribution to journal › Article
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Mark
Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study
(
- Contribution to journal › Article
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Mark
Familial associations of female breast cancer with other cancers
(
- Contribution to journal › Article
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Mark
Risk of second primary cancers in women diagnosed with endometrial cancer in German and Swedish cancer registries
(
- Contribution to journal › Article
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Mark
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts
(
- Contribution to journal › Letter
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Mark
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1
(
- Contribution to journal › Article
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Mark
Direct evidence for a polygenic etiology in familial multiple myeloma
(
- Contribution to journal › Article
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Mark
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
(
- Contribution to journal › Article
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Mark
Genetics of gallbladder cancer
(
- Contribution to journal › Letter
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Mark
Low expression of hexokinase-2 is associated with false-negative FDG–positron emission tomography in multiple myeloma
(
- Contribution to journal › Article
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Mark
Inherited variants in genes somatically mutated in thyroid cancer
(
- Contribution to journal › Article
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Mark
Risk of second cancer in Hodgkin lymphoma survivors and influence of family history
(
- Contribution to journal › Article
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Mark
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
(
- Contribution to journal › Article
-
Mark
Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts : Comparison with myeloma
(
- Contribution to journal › Article
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Mark
Familial associations of lymphoma and myeloma with autoimmune diseases
(
- Contribution to journal › Article
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Mark
Familial associations of colorectal cancer with other cancers
(
- Contribution to journal › Article
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Mark
Surveillance Bias in Cancer Risk after Unrelated Medical Conditions : Example Urolithiasis
(
- Contribution to journal › Article
-
Mark
Familial associations of male breast cancer with other cancers
(
- Contribution to journal › Article
- 2016
-
Mark
Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.
(
- Contribution to journal › Article
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Mark
Survival in familial and non-familial breast cancer by age and stage at diagnosis.
(
- Contribution to journal › Article
-
Mark
Familial risk of non-Hodgkin lymphoma by sex, relationship, age at diagnosis and histology: a joint study from five Nordic countries.
(
- Contribution to journal › Article
-
Mark
Mapping of deletion breakpoints at the CDKN2A locus in melanoma: detection of MTAP-ANRIL fusion transcripts.
(
- Contribution to journal › Article
-
Mark
Genetic factors influencing the risk of multiple myeloma bone disease.
(
- Contribution to journal › Article
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Mark
Search for familial clustering of multiple myeloma with any cancer.
(
- Contribution to journal › Article
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Mark
Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.
(
- Contribution to journal › Article
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Mark
Cancer of unknown primary is associated with diabetes.
(
- Contribution to journal › Article
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Mark
Location of metastases in cancer of unknown primary are not random and signal familial clustering.
(
- Contribution to journal › Article
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Mark
Metastatic spread in patients with gastric cancer
(
- Contribution to journal › Article
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Mark
Patterns of metastasis in colon and rectal cancer
(
- Contribution to journal › Article
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Mark
Origin of B-cell neoplasms in autoimmune disease
(
- Contribution to journal › Article
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Mark
The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias : Etiologic Implications
(
- Contribution to journal › Article
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Mark
Pedigree based DNA sequencing pipeline for germline genomes of cancer families
(
- Contribution to journal › Article
-
Mark
Runs of homozygosity and inbreeding in thyroid cancer
(
- Contribution to journal › Article
-
Mark
Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
(
- Contribution to journal › Article
-
Mark
A comprehensive meta-analysis of case-control association studies to evaluate polymorphisms associated with the risk of differentiated thyroid carcinoma
(
- Contribution to journal › Article
-
Mark
The epidemiology of metastases in neuroendocrine tumors
(
- Contribution to journal › Article
-
Mark
Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression
(
- Contribution to journal › Article
-
Mark
Polymorphisms within base and nucleotide excision repair pathways and risk of differentiated thyroid carcinoma
(
- Contribution to journal › Article
-
Mark
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.
(
- Contribution to journal › Article
-
Mark
Risk of Second Primary Cancers in Multiple Myeloma Survivors in German and Swedish Cancer Registries.
(
- Contribution to journal › Article
-
Mark
Predictive and prognostic clinical variables in cancer patients treated with adenoviral oncolytic immunotherapy
(
- Contribution to journal › Article
-
Mark
Age-Dependent Metastatic Spread and Survival : Cancer of Unknown Primary as a Model
(
- Contribution to journal › Article
-
Mark
Familial associations of monoclonal gammopathy of unknown significance with autoimmune diseases
(
- Contribution to journal › Letter
-
Mark
Search for familial clustering of cancer in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
-
Mark
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
-
Mark
TERT promoter mutations in melanoma survival.
(
- Contribution to journal › Article
- 2015
-
Mark
Population Landscape of Familial Cancer.
(
- Contribution to journal › Article
-
Mark
TERT promoter mutations and telomere length in adult malignant gliomas and recurrences.
(
- Contribution to journal › Article
-
Mark
Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches.
(
- Contribution to journal › Article
-
Mark
Frequent DPH3 promoter mutations in skin cancers.
(
- 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
-
Mark
Joint occurrence of Merkel cell carcinoma and non-Hodgkin lymphomas in four Nordic countries
(
- Contribution to journal › Article
-
Mark
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
(
- Contribution to journal › Article
-
Mark
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
(
- Contribution to journal › Article
-
Mark
Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.
(
- Contribution to journal › Article
-
Mark
Cancer risk in patients with type 2 diabetes mellitus and their relatives.
(
- Contribution to journal › Article
-
Mark
Incorporation of Detailed Family History from the Swedish Family-Cancer Database into the Prostate Cancer Prevention Trial Risk Calculator.
(
- Contribution to journal › Article
-
Mark
Smoking and body mass index as risk factors for subtypes of cancer of unknown primary.
(
- Contribution to journal › Letter
-
Mark
Cancer Risk in Relatives of Testicular Cancer Patients by Histology Type and Age at Diagnosis: A Joint Study from Five Nordic Countries.
(
- Contribution to journal › Article
-
Mark
Distribution and risk of the second discordant primary cancers combined after a specific first primary cancer in German and Swedish cancer registries.
(
- Contribution to journal › Article
-
Mark
Histological concordance in familial central nervous system tumors: Evidence from nationwide Swedish Family-Cancer Database.
(
- Contribution to journal › Article
-
Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
(
- Contribution to journal › Article
-
Mark
TERT promoter mutations: a novel independent prognostic factor in primary glioblastomas.
(
- Contribution to journal › Article
-
Mark
Mutations in TERT promoter and FGFR3 and telomere length in bladder cancer
(
- Contribution to journal › Article
-
Mark
Special section editorial: Cancer incidence in five continents including Africa.
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
(
- Contribution to journal › Article
-
Mark
Telomere length in circulating lymphocytes: Association with chromosomal aberrations.
(
- Contribution to journal › Letter
-
Mark
A simple-to-use method incorporating genomic markers into prostate cancer risk prediction tools facilitated future validation.
(
- Contribution to journal › Article
-
Mark
Risk of Next Melanoma in Patients With Familial and Sporadic Melanoma by Number of Previous Melanomas.
(
- Contribution to journal › Article
-
Mark
Case-control estimation of the impact of oncolytic adenovirus on the survival of patients with refractory solid tumors.
(
- Contribution to journal › Article
-
Mark
Risk of Cancer of Unknown Primary after Hospitalization for Autoimmune Diseases.
(
- Contribution to journal › Article
-
Mark
The risk of contralateral breast cancer in daughters of women with and without breast cancer.
2015) In Clinical Genetics(
- Contribution to journal › Article
-
Mark
Cancer incidence, trends, and survival among immigrants to Sweden: a population-based study.
2015) In European Journal of Cancer Prevention(
- Contribution to journal › Article
-
Mark
Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells.
(
- Contribution to journal › Article
-
Mark
Subsequent Type 2 Diabetes in Patients with Autoimmune Disease.
(
- Contribution to journal › Article
-
Mark
The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells
(
- Contribution to journal › Letter
-
Mark
Inbreeding and homozygosity in breast cancer survival.
(
- Contribution to journal › Article
-
Mark
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.
(
- Contribution to journal › Article
-
Mark
Thalassemia and sickle cell anemia in Swedish immigrants : Genetic diseases have become global
(
- Contribution to journal › Article
-
Mark
TERT promoter mutations in clear cell renal cell carcinoma
(
- Contribution to journal › Article
-
Mark
Cancer risk and mortality in asthma patients: A Swedish national cohort study.
(
- Contribution to journal › Article
- 2014
-
Mark
Hodgkin lymphoma after autoimmune diseases by age at diagnosis and histological subtype
(
- Contribution to journal › Article
-
Mark
Risk of Kaposi Sarcoma Among Immigrants to Sweden
(
- Contribution to journal › Article
-
Mark
Effect of multiplicity, laterality, and age at onset of breast cancer on familial risk of breast cancer: a nationwide prospective cohort study
(
- Contribution to journal › Article
-
Mark
Novel Genome-Wide Association Study-Based Candidate Loci for Differentiated Thyroid Cancer Risk
(
- Contribution to journal › Article
-
Mark
Causes of death in patients with extranodal cancer of unknown primary: searching for the primary site
(
- Contribution to journal › Article
-
Mark
Cancer risk in amyloidosis patients in Sweden with novel findings on non-Hodgkin lymphoma and skin cancer
(
- Contribution to journal › Article
-
Mark
A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer
(
- Contribution to journal › Article
-
Mark
GWAS-Identified Common Variants for Obesity Are Not Associated with the Risk of Developing Colorectal Cancer
(
- Contribution to journal › Article
-
Mark
Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome.
(
- Contribution to journal › Article
-
Mark
Effect of a Detailed Family History of Melanoma on Risk for Other Tumors: A Cohort Study Based on the Nationwide Swedish Family-Cancer Database
(
- Contribution to journal › Article
-
Mark
Inherited genetic susceptibility to multiple myeloma
(
- Contribution to journal › Scientific review