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- 2016
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Mark
Evidence of Inbreeding in Hodgkin Lymphoma
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- Contribution to journal › Article
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Mark
Origin of B-cell neoplasms in autoimmune disease
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- 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
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- Contribution to journal › Article
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Mark
Pedigree based DNA sequencing pipeline for germline genomes of cancer families
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- Contribution to journal › Article
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Mark
Runs of homozygosity and inbreeding in thyroid cancer
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- Contribution to journal › Article
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Mark
Search for familial clustering of multiple myeloma with any cancer.
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- 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.
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- Contribution to journal › Article
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Mark
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.
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- Contribution to journal › Article
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Mark
Genetic factors influencing the risk of multiple myeloma bone disease.
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- Contribution to journal › Article
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Mark
Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans
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- Contribution to journal › Article
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Mark
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
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- Contribution to journal › Article
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Mark
Familial associations of monoclonal gammopathy of unknown significance with autoimmune diseases
(
- Contribution to journal › Letter
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Mark
Polymorphisms within base and nucleotide excision repair pathways and risk of differentiated thyroid carcinoma
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- 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
Search for familial clustering of cancer in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
- 2015
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Mark
Inbreeding and homozygosity in breast cancer survival.
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- Contribution to journal › Article
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Mark
Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells.
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- Contribution to journal › Article
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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
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Mark
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.
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- Contribution to journal › Article
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Mark
Subsequent Type 2 Diabetes in Patients with Autoimmune Disease.
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- Contribution to journal › Article
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Mark
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
(
- Contribution to journal › Article
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Mark
Cancer risk and mortality in asthma patients: A Swedish national cohort study.
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- Contribution to journal › Article
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Mark
Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.
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- Contribution to journal › Article
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Mark
Cancer risk in patients with type 2 diabetes mellitus and their relatives.
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- Contribution to journal › Article
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Mark
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
(
- 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.
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- Contribution to journal › Article
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Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
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- Contribution to journal › Article
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Mark
Thalassemia and sickle cell anemia in Swedish immigrants : Genetic diseases have become global
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- Contribution to journal › Article
- 2014
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Mark
Novel Genome-Wide Association Study-Based Candidate Loci for Differentiated Thyroid Cancer Risk
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- Contribution to journal › Article
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Mark
GWAS-Identified Common Variants for Obesity Are Not Associated with the Risk of Developing Colorectal Cancer
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- Contribution to journal › Article
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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
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Mark
Hodgkin lymphoma after autoimmune diseases by age at diagnosis and histological subtype
(
- Contribution to journal › Article
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Mark
Cancer risk in amyloidosis patients in Sweden with novel findings on non-Hodgkin lymphoma and skin cancer
(
- Contribution to journal › Article
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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
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Mark
Single Nucleotide Polymorphisms within Interferon Signaling Pathway Genes Are Associated with Colorectal Cancer Susceptibility and Survival.
(
- Contribution to journal › Article
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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
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Mark
Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma.
(
- Contribution to journal › Letter
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Mark
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
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Mark
Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors
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- Contribution to journal › Article
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Mark
Autoimmune diseases associated with non-Hodgkin lymphoma: A nationwide cohort study.
(
- Contribution to journal › Article
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Mark
Increased Risk of Hepatobiliary Cancers After Hospitalization for Autoimmune Disease
(
- Contribution to journal › Article
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Mark
Cyclin D1 splice site variant triggers chromosomal aberrations in healthy humans.
(
- Contribution to journal › Letter
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Mark
Cancer in immigrants as a pointer to the causes of cancer.
(
- Contribution to journal › Article
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Mark
Risk of cancer in patients with medically diagnosed hay fever or allergic rhinitis.
(
- Contribution to journal › Article
- 2013
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Mark
Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
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- 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
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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
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma
(
- Contribution to journal › Article
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Mark
Genetic Variants in Hormone-Related Genes and Risk of Breast Cancer
(
- Contribution to journal › Article
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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