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- 2014
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Mark
Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
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- Contribution to journal › Article
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Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.
(
- Contribution to journal › Article
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A coding IRAK2 variant compromises TLR signaling and is associated with colorectal cancer survival.
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- 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
Cyclin D1 splice site variant triggers chromosomal aberrations in healthy humans.
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- Contribution to journal › Letter
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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
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- Contribution to journal › Article
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Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer
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- Contribution to journal › Article
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Risk of cancer in patients with medically diagnosed hay fever or allergic rhinitis.
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- Contribution to journal › Article
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Autoimmune diseases associated with non-Hodgkin lymphoma: A nationwide cohort study.
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- Contribution to journal › Article
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Increased Risk of Hepatobiliary Cancers After Hospitalization for Autoimmune Disease
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- Contribution to journal › Article
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Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
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- 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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Cancer in immigrants as a pointer to the causes of cancer.
(
- Contribution to journal › Article
- 2013
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Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
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- 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
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
(
- Contribution to journal › Article
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Mark
Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
(
- Contribution to journal › Article
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Mark
Gender-Specific Effects of Genetic Variants within Th1 and Th17 Cell-Mediated Immune Response Genes on the Risk of Developing Rheumatoid Arthritis
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- 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
Genome-wide investigation of gene-environment interactions in colorectal 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
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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
Deciphering the 8q24.21 association for glioma
(
- Contribution to journal › Article
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Mark
Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome
(
- Contribution to journal › Article
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Mark
Subsequent leukaemia in autoimmune disease patients.
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- Contribution to journal › Article
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Mark
Subsequent brain tumors in patients with autoimmune disease.
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- Contribution to journal › Article
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Mark
Autoimmune diseases and subsequent urological cancers.
(
- Contribution to journal › Article
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Mark
Association study identifying polymorphisms in CD47 and other extracellular matrix pathway genes as putative prognostic markers for colorectal cancer
(
- Contribution to journal › Article
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Mark
Non-Hodgkin lymphoma in familial amyloid polyneuropathy patients in Sweden
(
- Contribution to journal › Letter
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Mark
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
(
- Contribution to journal › Article
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Mark
Genome-wide association study on differentiated thyroid cancer.
(
- Contribution to journal › Article
- 2012
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Mark
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
(
- Contribution to journal › Article
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Mark
Incidence and survival in non-hereditary amyloidosis in Sweden
(
- Contribution to journal › Article
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Mark
Genetic variation in ALCAM and other chromosomal instability genes in breast cancer survival
(
- Contribution to journal › Article
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Mark
Effect of autoimmune diseases on incidence and survival in subsequent multiple myeloma
(
- Contribution to journal › Article
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Mark
Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer
(
- Contribution to journal › Article
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Mark
Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer
(
- Contribution to journal › Article
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Mark
A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer
(
- Contribution to journal › Article
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Mark
Dectin-1 and DC-SIGN Polymorphisms Associated with Invasive Pulmonary Aspergillosis Infection
(
- Contribution to journal › Article
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Mark
Ancestral susceptibility to colorectal cancer
(
- Contribution to journal › Article
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Mark
Selected polymorphisms in sex hormone-related genes, circulating sex hormones and risk of endometrial cancer
(
- Contribution to journal › Article
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Mark
Combined effect of low-penetrant SNPs on breast cancer risk.
(
- Contribution to journal › Article
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Mark
Subsequent cancers in patients diagnosed with cancer of unknown primary (CUP): etiological insights?
(
- Contribution to journal › Article
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Mark
Effect of Type 2 Diabetes Predisposing Genetic Variants on Colorectal Cancer Risk.
(
- Contribution to journal › Article
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Mark
Effect of autoimmune diseases on risk and survival in female cancers.
(
- Contribution to journal › Article
- 2011
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Mark
Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin
(
- Contribution to journal › Article
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Mark
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
(
- Contribution to journal › Article
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Mark
Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome
(
- Contribution to journal › Article
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Mark
Genetic variation in genes encoding for polymerase zeta subunits associates with breast cancer risk, tumour characteristics and survival
(
- Contribution to journal › Article
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Mark
Preventable breast cancer is postmenopausal
(
- Contribution to journal › Article