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- 2024
-
Mark
Deciphering the genetics and mechanisms of predisposition to multiple myeloma
(
- Contribution to journal › Article
-
Mark
Critical survival periods in prostate cancer in Sweden explored by conditional survival analysis
(
- Contribution to journal › Article
-
Mark
Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
-
Mark
Large differencies in age-specific survival in multiple myeloma in the nordic countries
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Age-specific survival in acute myeloid leukemia in the Nordic countries through a half century
(
- Contribution to journal › Debate/Note/Editorial
- 2023
-
Mark
Personal comorbidities and their subsequent risks for liver, gallbladder and bile duct cancers
(
- Contribution to journal › Article
-
Mark
Autoimmune diseases as comorbidities for liver, gallbladder, and biliary duct cancers in Sweden
(
- Contribution to journal › Article
-
Mark
Are population level familial risks and germline genetics meeting each other?
(
- Contribution to journal › Scientific review
-
Mark
Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression?
(
- Contribution to journal › Article
-
Mark
Germline variants of the genes involved in NF-kB activation are associated with the risk of COPD and lung cancer development
(
- Contribution to journal › Article
-
Mark
Population-Attributable Fractions of Personal Comorbidities for Liver, Gallbladder, and Bile Duct Cancers
(
- Contribution to journal › Article
- 2022
-
Mark
Functional dissection of inherited non-coding variation influencing multiple myeloma risk
(
- Contribution to journal › Article
-
Mark
Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia : a CRuCIAL study
(
- Contribution to journal › Letter
-
Mark
Familial Risks for Liver, Gallbladder and Bile Duct Cancers and for Their Risk Factors in Sweden, a Low-Incidence Country
(
- Contribution to journal › Article
-
Mark
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
(
- Contribution to journal › Letter
- 2021
-
Mark
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations
(
- Contribution to journal › Article
-
Mark
Bladder and upper urinary tract cancers as first and second primary cancers
2021) In Cancer Reports(
- Contribution to journal › Article
-
Mark
Family history of early onset acute lymphoblastic leukemia is suggesting genetic associations
(
- Contribution to journal › Article
-
Mark
Types of second primary cancer influence overall survival in cutaneous melanoma
(
- Contribution to journal › Article
-
Mark
Search for AL amyloidosis risk factors using Mendelian randomization
(
- Contribution to journal › Article
-
Mark
Second primary cancers after liver, gallbladder and bile duct cancers, and these cancers as second primary cancers
(
- Contribution to journal › Article
-
Mark
Familial risks and proportions describing population landscape of familial cancer
(
- Contribution to journal › Article
-
Mark
Family history of head and neck cancers
(
- Contribution to journal › Article
-
Mark
Second primary cancers after gastric cancer, and gastric cancer as second primary cancer
(
- Contribution to journal › Article
-
Mark
Familial Risks between Pernicious Anemia and Other Autoimmune Diseases in the Population of Sweden
(
- Contribution to journal › Article
-
Mark
Second Primary Cancers After Kidney Cancers, and Kidney Cancers as Second Primary Cancers
(
- Contribution to journal › Article
-
Mark
Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium
(
- Contribution to journal › Article
-
Mark
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population
(
- Contribution to journal › Article
-
Mark
Characterization of rare germline variants in familial multiple myeloma
(
- Contribution to journal › Letter
- 2020
-
Mark
Second Primary Cancers in Patients with Invasive and In Situ Squamous Cell Skin Carcinoma, Kaposi Sarcoma, and Merkel Cell Carcinoma : Role for Immune Mechanisms?
(
- Contribution to journal › Article
-
Mark
Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1
(
- Contribution to journal › Article
-
Mark
Second primary cancers in non-Hodgkin lymphoma : Family history and survival
(
- Contribution to journal › Article
-
Mark
Epistatic effect of TLR3 and cGAS-STING-IKKε-TBK1-IFN signaling variants on colorectal cancer risk
(
- Contribution to journal › Article
-
Mark
Rate differences between first and second primary cancers may outline immune dysfunction as a key risk factor
(
- Contribution to journal › Article
-
Mark
Incidence differences between first primary cancers and second primary cancers following skin squamous cell carcinoma as etiological clues
(
- Contribution to journal › Article
-
Mark
Familial associations between autoimmune hepatitis and primary biliary cholangitis and other autoimmune diseases
(
- Contribution to journal › Article
-
Mark
Association between tumor characteristics and second primary cancers with cutaneous melanoma survival : A nationwide cohort study
(
- Contribution to journal › Article
-
Mark
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
(
- Contribution to journal › Article
-
Mark
Influence of family history on risk of second primary cancers and survival in patients with squamous cell skin cancer
(
- Contribution to journal › Article
-
Mark
Second primary cancers in melanoma patients critically shorten survival
(
- Contribution to journal › Article
-
Mark
Loci associated with genomic damage levels in chronic kidney disease patients and controls
(
- Contribution to journal › Article
-
Mark
Search for multiple myeloma risk factors using Mendelian randomization
(
- 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
-
Mark
Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Familial associations for rheumatoid autoimmune diseases
(
- Contribution to journal › Article
-
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
- 2019
-
Mark
Second primary cancer after female breast cancer : Familial risks and cause of death
(
- Contribution to journal › Article
-
Mark
Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients
(
- Contribution to journal › Letter
-
Mark
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma
(
- Contribution to journal › Article
-
Mark
Second cancers and causes of death in patients with testicular cancer in Sweden
(
- Contribution to journal › Article
-
Mark
Second primary cancers in patients with acute lymphoblastic, chronic lymphocytic and hairy cell leukaemia
(
- 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
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
(
- Contribution to journal › Article
-
Mark
Impact of family history of cancer on risk and mortality of second cancers in patients with prostate cancer
(
- Contribution to journal › Article
-
Mark
Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
-
Mark
Comparison of Familial Clustering of Anogenital and Skin Cancers Between In Situ and Invasive Types
(
- 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
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes
(
- Contribution to journal › Article
-
Mark
Familial Clustering, Second Primary Cancers and Causes of Death in Penile, Vulvar and Vaginal Cancers
(
- Contribution to journal › Article
-
Mark
Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival
(
- Contribution to journal › Article
- 2018
-
Mark
Risk of second primary cancer following myeloid neoplasia and risk of myeloid neoplasia as second primary cancer : a nationwide, observational follow up study in Sweden
(
- Contribution to journal › Article
-
Mark
Chemotherapy-induced peripheral neuropathy : Evidence from genome-wide association studies and replication within multiple myeloma patients
(
- Contribution to journal › Article
-
Mark
Multiple myeloma : family history and mortality in second primary cancers
(
- Contribution to journal › Letter
-
Mark
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
(
- Contribution to journal › Article
-
Mark
Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma
(
- Contribution to journal › Letter
-
Mark
Borderline Ovarian Tumors Share Familial Risks with Themselves and Invasive Cancers
2018) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 27(11). p.1358-1363(
- Contribution to journal › Article
-
Mark
Familial risks of ovarian cancer by age at diagnosis, proband type and histology
(
- 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
Familial risks of second primary cancers and mortality in ovarian cancer patients
(
- Contribution to journal › Article
-
Mark
Familial risks in and between stone diseases : Sialolithiasis, urolithiasis and cholelithiasis in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology
(
- Contribution to journal › Article
-
Mark
Familial Associations in Testicular Cancer with Other Cancers
(
- Contribution to journal › Article
-
Mark
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family
(
- Contribution to journal › Article
-
Mark
Familial Ovarian Cancer Clusters with Other Cancers
(
- Contribution to journal › Article
-
Mark
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
(
- Contribution to journal › Article
-
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
Second primary cancers in non-Hodgkin lymphoma : Bidirectional analyses suggesting role for immune dysfunction
(
- Contribution to journal › Article
-
Mark
Prostate cancer survivors : Risk and mortality in second primary cancers
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations in multiple myeloma are associated with shifts in serum immunoglobulin isotypes distribution and levels
(
- Contribution to journal › Letter
-
Mark
Genetic variation of acquired structural chromosomal aberrations
(
- Contribution to journal › Article
-
Mark
Short article : Influence of regulatory NLRC5 variants on colorectal cancer survival and 5-fluorouracil-based chemotherapy
(
- Contribution to journal › Article
-
Mark
Levels of DNA damage (Micronuclei) in patients suffering from chronic kidney disease. Role of GST polymorphisms
(
- Contribution to journal › Article
-
Mark
Coding variants in NOD-like receptors : An association study on risk and survival of colorectal cancer
(
- Contribution to journal › Article
-
Mark
Familial Urinary Bladder Cancer with Other Cancers
(
- Contribution to journal › Article
-
Mark
Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer
(
- Contribution to journal › Article
-
Mark
Familial risks in urolithiasis in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Familial Risks between Urolithiasis and Cancer
(
- Contribution to journal › Article
-
Mark
SNPs related to vitamin D and breast cancer risk : A case-control study
(
- Contribution to journal › Article
-
Mark
Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study
(
- Contribution to journal › Article
-
Mark
Bortezomib-induced peripheral neuropathy : A genome-wide association study on multiple myeloma patients
(
- Contribution to journal › Article
- 2017
-
Mark
Functional germline variants in driver genes of breast cancer
(
- 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
-
Mark
Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy : Replication of the Reported Candidate Susceptibility Loci
(
- Contribution to journal › Article
-
Mark
Familial risks for gallstones in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach
(
- Contribution to journal › Letter
-
Mark
Genetics of gallbladder cancer
(
- Contribution to journal › Letter
-
Mark
Direct evidence for a polygenic etiology in familial multiple myeloma
(
- Contribution to journal › Article
-
Mark
Familial associations of female breast cancer with other cancers
(
- Contribution to journal › Article
-
Mark
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
(
- Contribution to journal › Article
-
Mark
Familial associations of lymphoma and myeloma with autoimmune diseases
(
- 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
-
Mark
Inherited variants in genes somatically mutated in thyroid cancer
(
- Contribution to journal › Article
-
Mark
Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism
(
- Contribution to journal › Article
-
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
-
Mark
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts
(
- Contribution to journal › Letter
-
Mark
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
(
- 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
-
Mark
Survival in familial and non-familial breast cancer by age and stage at diagnosis.
(
- Contribution to journal › Article
-
Mark
Cancer of unknown primary is associated with diabetes.
(
- Contribution to journal › Article
-
Mark
Genetic factors influencing the risk of multiple myeloma bone disease.
(
- Contribution to journal › Article
-
Mark
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
(
- 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
Origin of B-cell neoplasms in autoimmune disease
(
- Contribution to journal › Article
-
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
-
Mark
The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias : Etiologic Implications
(
- Contribution to journal › Article
-
Mark
Polymorphisms within base and nucleotide excision repair pathways and risk of differentiated thyroid carcinoma
(
- Contribution to journal › Article
-
Mark
Search for familial clustering of cancer in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
-
Mark
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.
(
- Contribution to journal › Article
-
Mark
Search for familial clustering of multiple myeloma with any cancer.
(
- Contribution to journal › Article
-
Mark
Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.
(
- Contribution to journal › Article
-
Mark
Familial associations of monoclonal gammopathy of unknown significance with autoimmune diseases
(
- Contribution to journal › Letter
-
Mark
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
- 2015
-
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
Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells.
(
- Contribution to journal › Article
-
Mark
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
(
- Contribution to journal › Article
-
Mark
Subsequent Type 2 Diabetes in Patients with Autoimmune Disease.
(
- 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
-
Mark
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
(
- Contribution to journal › Article
-
Mark
Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.
(
- Contribution to journal › Article
-
Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
(
- 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
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
(
- Contribution to journal › Article
-
Mark
Thalassemia and sickle cell anemia in Swedish immigrants : Genetic diseases have become global
(
- 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
- 2014
-
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
-
Mark
Cancer risk in amyloidosis patients in Sweden with novel findings on non-Hodgkin lymphoma and skin 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
Novel Genome-Wide Association Study-Based Candidate Loci for Differentiated Thyroid Cancer Risk
(
- Contribution to journal › Article
-
Mark
Toll-like receptor genetic variants and colorectal cancer.
(
- Contribution to journal › Debate/Note/Editorial
-
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
Cyclin D1 splice site variant triggers chromosomal aberrations in healthy humans.
(
- Contribution to journal › Letter
-
Mark
Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma.
(
- Contribution to journal › Letter
-
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
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
Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors
(
- Contribution to journal › Article
-
Mark
A coding IRAK2 variant compromises TLR signaling and is associated with colorectal cancer survival.
(
- 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
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
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
-
Mark
Cancer in immigrants as a pointer to the causes of cancer.
(
- Contribution to journal › Article
-
Mark
Hodgkin lymphoma after autoimmune diseases by age at diagnosis and histological subtype
(
- Contribution to journal › Article
- 2013
-
Mark
Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
(
- Contribution to journal › Article
-
Mark
Genetic Polymorphisms in Host Innate Immune Sensor Genes and the Risk of Nasopharyngeal Carcinoma in North Africa
(
- 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
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
Subsequent brain tumors in patients with autoimmune disease.
(
- Contribution to journal › Article
-
Mark
Deciphering the 8q24.21 association for glioma
(
- 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
Subsequent leukaemia in autoimmune disease patients.
(
- Contribution to journal › Article
-
Mark
Genetic Variants in Hormone-Related Genes and Risk of Breast Cancer
(
- 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
Autoimmune diseases and subsequent urological cancers.
(
- Contribution to journal › Article
-
Mark
Non-Hodgkin lymphoma in familial amyloid polyneuropathy patients in Sweden
(
- Contribution to journal › Letter
-
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
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma
(
- 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
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
(
- Contribution to journal › Article
- 2012
-
Mark
Incidence and survival in non-hereditary amyloidosis in Sweden
(
- Contribution to journal › Article
-
Mark
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
(
- 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
Genetic variation in ALCAM and other chromosomal instability genes in breast cancer survival
(
- Contribution to journal › Article
-
Mark
Effect of autoimmune diseases on incidence and survival in subsequent multiple myeloma
(
- 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
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
Subsequent cancers in patients diagnosed with cancer of unknown primary (CUP): etiological insights?
(
- Contribution to journal › Article
-
Mark
Ancestral susceptibility to colorectal cancer
(
- Contribution to journal › Article
- 2011
-
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
-
Mark
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Searching for the Missing Heritability of Complex Diseases
(
- Contribution to journal › Letter
-
Mark
Preventable breast cancer is postmenopausal
(
- 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
-
Mark
Common Breast Cancer Susceptibility Loci Are Associated with Triple-Negative Breast Cancer
(
- 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
Association of genetic polymorphisms in ESR2, HSD17B1, ABCB1, and SHBG genes with colorectal cancer risk
(
- Contribution to journal › Article
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Mark
TLR-3 polymorphism is an independent prognostic marker for stage II colorectal cancer
(
- Contribution to journal › Article
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Mark
Familial risks of age-related macular degeneration.
(
- Contribution to journal › Letter
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Mark
A candidate CpG SNP approach identifies a breast cancer associated ESR1-SNP.
(
- Contribution to journal › Article
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Mark
5-Fluorouracil-based chemotherapy for colorectal cancer and MTHFR/MTRR genotypes.
(
- Contribution to journal › Article
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Mark
Survival in common cancers defined by risk and survival of family members
(
- Contribution to journal › Scientific review
- 2010
-
Mark
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
(
- Contribution to journal › Article
-
Mark
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study
(
- Contribution to journal › Article
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Mark
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility
(
- Contribution to journal › Article
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Mark
Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus
(
- Contribution to journal › Article
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Mark
Re: Underlying Genetic Models Of Inheritance In Established Type 2 Diabetes Associations
(
- Contribution to journal › Letter
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Mark
Breast and prostate cancer: familial associations
(
- Contribution to journal › Letter
- 2009
-
Mark
Polymorphisms in telomere-associated genes, breast cancer susceptibility and prognosis
(
- Contribution to journal › Article
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Mark
Survival in non-Hodgkin's lymphoma by histology and family history.
(
- Contribution to journal › Article
- 2008
-
Mark
Risk of familial breast cancer is not increased after pregnancy
(
- Contribution to journal › Article
-
Mark
Survival in ovarian cancer patients by histology and family history
(
- Contribution to journal › Article
-
Mark
Survival in breast cancer is familial
(
- Contribution to journal › Article
-
Mark
Survival in familial pancreatic cancer
(
- Contribution to journal › Article
-
Mark
Survival in bladder and renal cell cancers is familial
(
- Contribution to journal › Article
-
Mark
Concordance of survival in family members with prostate cancer
(
- Contribution to journal › Article
- 2007
-
Mark
Incidence and familial risks in pituitary adenoma and associated tumors
(
- Contribution to journal › Article
-
Mark
Risks for familial and contralateral breast cancer interact multiplicatively and cause a high risk
(
- Contribution to journal › Article
-
Mark
Risks of breast, endometrial, and ovarian cancers after twin births
(
- Contribution to journal › Article