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- 2017
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Mark
Familial associations of female breast cancer with other cancers
(
- Contribution to journal › Article
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Mark
Functional germline variants in driver genes of breast cancer
(
- Contribution to journal › Article
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Mark
Genetics of gallbladder cancer
(
- Contribution to journal › Letter
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Mark
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
(
- 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
-
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 risks for gallstones in the population of Sweden
(
- Contribution to journal › Article
- 2016
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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
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Mark
Cancer of unknown primary is associated with diabetes.
(
- Contribution to journal › Article
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Mark
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.
(
- Contribution to journal › Article
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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
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
(
- Contribution to journal › Article
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Mark
Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans
(
- Contribution to journal › Article
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Mark
Familial associations of monoclonal gammopathy of unknown significance with autoimmune diseases
(
- Contribution to journal › Letter
-
Mark
Polymorphisms within base and nucleotide excision repair pathways and risk of differentiated thyroid carcinoma
(
- 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
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
-
Mark
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
(
- Contribution to journal › Article
-
Mark
Origin of B-cell neoplasms in autoimmune disease
(
- 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
A review of the infection-associated cancers in North African countries
(
- Contribution to journal › Scientific review
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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
-
Mark
Search for familial clustering of cancer in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
- 2015
-
Mark
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
(
- Contribution to journal › Article
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Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
(
- Contribution to journal › Article
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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
Cancer risk and mortality in asthma patients: A Swedish national cohort study.
(
- Contribution to journal › Article
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Mark
Risk of Next Melanoma in Patients With Familial and Sporadic Melanoma by Number of Previous Melanomas.
(
- Contribution to journal › Article
-
Mark
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
(
- 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
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Mark
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.
(
- Contribution to journal › Article
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Mark
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
(
- 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
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Mark
Thalassemia and sickle cell anemia in Swedish immigrants : Genetic diseases have become global
(
- Contribution to journal › Article
- 2014
-
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
Cancer risk in amyloidosis patients in Sweden with novel findings on non-Hodgkin lymphoma and skin cancer
(
- Contribution to journal › Article
-
Mark
Hodgkin lymphoma after autoimmune diseases by age at diagnosis and histological subtype
(
- Contribution to journal › Article
-
Mark
Novel Genome-Wide Association Study-Based Candidate Loci for Differentiated Thyroid Cancer Risk
(
- Contribution to journal › Article
-
Mark
Repeat polymorphisms in ESR2 and AR and colorectal cancer risk and prognosis: results from a German population-based case-control study
(
- Contribution to journal › Article
-
Mark
Single Nucleotide Polymorphisms within Interferon Signaling Pathway Genes Are Associated with Colorectal Cancer Susceptibility and Survival.
(
- Contribution to journal › Article
-
Mark
Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors
(
- Contribution to journal › Article
-
Mark
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3
(
- Contribution to journal › Article
-
Mark
Cyclin D1 splice site variant triggers chromosomal aberrations in healthy humans.
(
- Contribution to journal › Letter
-
Mark
A coding IRAK2 variant compromises TLR signaling and is associated with colorectal cancer survival.
(
- Contribution to journal › Article
-
Mark
Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
(
- Contribution to journal › Article
-
Mark
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.
(
- Contribution to journal › Article
-
Mark
Toll-like receptor genetic variants and colorectal cancer.
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Autoimmune diseases associated with non-Hodgkin lymphoma: A nationwide cohort study.
(
- Contribution to journal › Article
-
Mark
Increased Risk of Hepatobiliary Cancers After Hospitalization for Autoimmune Disease
(
- Contribution to journal › Article
-
Mark
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
-
Mark
Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma.
(
- Contribution to journal › Letter
-
Mark
Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Risk of cancer in patients with medically diagnosed hay fever or allergic rhinitis.
(
- Contribution to journal › Article
-
Mark
Cancer in immigrants as a pointer to the causes of cancer.
(
- Contribution to journal › Article
-
Mark
Micronuclei in Cord Blood Lymphocytes and Associations with Biomarkers of Exposure to Carcinogens and Hormonally Active Factors, Gene Polymorphisms, and Gene Expression: The NewGeneris Cohort
(
- Contribution to journal › Article
- 2013
-
Mark
Do Reproductive Factors Influence T, N, and M Classes of Ductal and Lobular Breast Cancers? A Nation-Wide Follow-Up Study
(
- Contribution to journal › Article
-
Mark
Gender-Specific Effects of Genetic Variants within Th1 and Th17 Cell-Mediated Immune Response Genes on the Risk of Developing Rheumatoid Arthritis
(
- Contribution to journal › Article
-
Mark
Genome-wide investigation of gene-environment interactions in colorectal 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
Genetic Variants in Hormone-Related Genes and Risk of Breast Cancer
(
- Contribution to journal › Article
-
Mark
Subsequent brain tumors in patients with autoimmune disease.
(
- Contribution to journal › Article
-
Mark
Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome
(
- Contribution to journal › Article
-
Mark
Deciphering the 8q24.21 association for glioma
(
- Contribution to journal › Article
-
Mark
Subsequent leukaemia in autoimmune disease patients.
(
- Contribution to journal › Article
-
Mark
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
(
- Contribution to journal › Article
-
Mark
Genome-wide association study on differentiated thyroid cancer.
(
- Contribution to journal › Article
-
Mark
Association study identifying polymorphisms in CD47 and other extracellular matrix pathway genes as putative prognostic markers for colorectal cancer
(
- Contribution to journal › Article
-
Mark
Non-Hodgkin lymphoma in familial amyloid polyneuropathy patients in Sweden
(
- Contribution to journal › Letter
-
Mark
Genetic Polymorphisms in Host Innate Immune Sensor Genes and the Risk of Nasopharyngeal Carcinoma in North Africa
(
- Contribution to journal › Article
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Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
(
- Contribution to journal › Article
-
Mark
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
(
- Contribution to journal › Article
-
Mark
Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
(
- Contribution to journal › Article
-
Mark
Autoimmune diseases and subsequent urological cancers.
(
- Contribution to journal › Article
- 2012
-
Mark
Effect of autoimmune diseases on incidence and survival in subsequent multiple myeloma
(
- Contribution to journal › Article
-
Mark
Genetic variation in ALCAM and other chromosomal instability genes in breast cancer survival
(
- Contribution to journal › Article
-
Mark
A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer
(
- Contribution to journal › Article
-
Mark
Dectin-1 and DC-SIGN Polymorphisms Associated with Invasive Pulmonary Aspergillosis Infection
(
- Contribution to journal › Article
-
Mark
Ancestral susceptibility to colorectal cancer
(
- Contribution to journal › Article
-
Mark
Selected polymorphisms in sex hormone-related genes, circulating sex hormones and risk of endometrial cancer
(
- Contribution to journal › Article
-
Mark
Combined effect of low-penetrant SNPs on breast cancer risk.
(
- Contribution to journal › Article
-
Mark
Effect of autoimmune diseases on risk and survival in female cancers.
(
- Contribution to journal › Article
-
Mark
Effect of Type 2 Diabetes Predisposing Genetic Variants on Colorectal Cancer Risk.
(
- Contribution to journal › Article
-
Mark
Incidence and survival in non-hereditary amyloidosis in Sweden
(
- Contribution to journal › Article
-
Mark
Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer
(
- Contribution to journal › Article
-
Mark
Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer
(
- Contribution to journal › Article
-
Mark
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
(
- Contribution to journal › Article
-
Mark
Subsequent cancers in patients diagnosed with cancer of unknown primary (CUP): etiological insights?
(
- Contribution to journal › Article
- 2011
-
Mark
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Common Breast Cancer Susceptibility Loci Are Associated with Triple-Negative Breast Cancer
(
- Contribution to journal › Article
-
Mark
Preventable breast cancer is postmenopausal
(
- Contribution to journal › Article
-
Mark
Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome
(
- Contribution to journal › Article
-
Mark
Genetic variation in genes encoding for polymerase zeta subunits associates with breast cancer risk, tumour characteristics and survival
(
- Contribution to journal › Article