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- 2024
-
Mark
Burden of malignant mesothelioma in China during 1990-2019 and the projections through 2029
2024) In Journal of the National Cancer Center(
- Contribution to journal › Article
-
Mark
Critical survival periods in prostate cancer in Sweden explored by conditional survival analysis
(
- 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
-
Mark
Deciphering the genetics and mechanisms of predisposition to multiple myeloma
(
- Contribution to journal › Article
-
Mark
Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
- 2023
-
Mark
Re: Mark N. Brook, Holly Ní Raghallaigh, Koveela Govindasami, et al. Family History of Prostate Cancer and Survival Outcomes in the UK Genetic Prostate Cancer Study. Eur Urol 2023;83:257-66
(
- Contribution to journal › Letter
-
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
Autoimmune diseases as comorbidities for liver, gallbladder, and biliary duct cancers in Sweden
(
- Contribution to journal › Article
-
Mark
Personal comorbidities and their subsequent risks for liver, gallbladder and bile duct cancers
(
- Contribution to journal › Article
-
Mark
Population-Attributable Fractions of Personal Comorbidities for Liver, Gallbladder, and Bile Duct Cancers
(
- Contribution to journal › Article
- 2022
-
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
Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia : a CRuCIAL study
(
- Contribution to journal › Letter
-
Mark
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
(
- Contribution to journal › Letter
-
Mark
Functional dissection of inherited non-coding variation influencing multiple myeloma risk
(
- Contribution to journal › Article
- 2021
-
Mark
Familial Risks between Pernicious Anemia and Other Autoimmune Diseases in the Population of Sweden
(
- Contribution to journal › Article
-
Mark
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population
(
- 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 and proportions describing population landscape of familial cancer
(
- 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
Characterization of rare germline variants in familial multiple myeloma
(
- Contribution to journal › Letter
-
Mark
Second Primary Cancers After Kidney Cancers, and Kidney Cancers as Second Primary Cancers
(
- Contribution to journal › Article
-
Mark
Types of second primary cancer influence overall survival in cutaneous melanoma
(
- Contribution to journal › Article
-
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
- 2020
-
Mark
Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1
(
- Contribution to journal › Article
-
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
Second primary cancers in non-Hodgkin lymphoma : Family history and survival
(
- Contribution to journal › Article
-
Mark
Autoimmune diseases and hematological malignancies : exploring the underlying mechanisms from epidemiological evidence
(
- Contribution to journal › Scientific review
-
Mark
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
(
- 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
Second primary cancers in melanoma patients critically shorten survival
(
- 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
Genetic predisposition for multiple myeloma
(
- Contribution to journal › Scientific review
-
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
Loci associated with genomic damage levels in chronic kidney disease patients and controls
(
- 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
Epistatic effect of TLR3 and cGAS-STING-IKKε-TBK1-IFN signaling variants on colorectal cancer risk
(
- 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
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
Familial Associations of Colon and Rectal Cancers With Other Cancers
(
- 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
Second primary cancer after female breast cancer : Familial risks and cause of death
(
- Contribution to journal › Article
-
Mark
Associations between autoimmune conditions and hepatobiliary cancer risk among elderly US adults
(
- 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
Familial Clustering, Second Primary Cancers and Causes of Death in Penile, Vulvar and Vaginal Cancers
(
- Contribution to journal › Article
-
Mark
Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk
(
- Contribution to journal › Article
-
Mark
Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival
(
- Contribution to journal › Article
- 2018
-
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 between Urolithiasis and Cancer
(
- Contribution to journal › Article
-
Mark
Response : Methods for second primary cancers evaluation have to be standardized (IJC-17-2354)
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Bortezomib-induced peripheral neuropathy : A genome-wide association study on multiple myeloma patients
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia
(
- 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
The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression
(
- Contribution to journal › Article
-
Mark
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology
(
- Contribution to journal › Article
-
Mark
Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma
(
- Contribution to journal › Letter
-
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
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
Familial risks of acute myeloid leukemia, myelodysplastic syndromes, and myeloproliferative neoplasms
(
- Contribution to journal › Letter
-
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
Familial risks of second primary cancers and mortality in ovarian cancer patients
(
- Contribution to journal › Article
-
Mark
Importance of tumor location and histology in familial risk of upper gastrointestinal cancers : A nationwide cohort study
(
- 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
Short article : Influence of regulatory NLRC5 variants on colorectal cancer survival and 5-fluorouracil-based chemotherapy
(
- 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 variation associated with chromosomal aberration frequency : A genome-wide association study
2018) In Environmental and Molecular Mutagenesis(
- Contribution to journal › Article
-
Mark
RE : Familial Cancer Clustering of Urothelial Cancer: A Population-Based Case-Control Study
(
- Contribution to journal › Debate/Note/Editorial
-
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
HLA and KIR Associations of Cervical Neoplasia
(
- Contribution to journal › Article
-
Mark
Familial risks of ovarian cancer by age at diagnosis, proband type and histology
(
- Contribution to journal › Article
-
Mark
Clinical landscape of cancer metastases
(
- 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
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
(
- Contribution to journal › Article
-
Mark
Familial risk of pleural mesothelioma increased drastically in certain occupations : A nationwide prospective cohort study
(
- 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
Familial risks in urolithiasis in the population of Sweden
(
- Contribution to journal › Article
-
Mark
Familial Urinary Bladder Cancer with Other Cancers
(
- Contribution to journal › Article
- 2017
-
Mark
Common cancers share familial susceptibility : Implications for cancer genetics and counselling
(
- 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 Associations Between Prostate Cancer and Other Cancers
(
- Contribution to journal › Article
-
Mark
Concordant and discordant familial cancer : Familial risks, proportions and population impact
(
- Contribution to journal › Article
-
Mark
Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study
(
- Contribution to journal › Article
-
Mark
Direct evidence for a polygenic etiology in familial multiple myeloma
(
- Contribution to journal › Article
-
Mark
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1
(
- Contribution to journal › Article
-
Mark
Risk of second primary cancers in women diagnosed with endometrial cancer in German and Swedish cancer registries
(
- 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
Functional germline variants in driver genes of breast 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
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
Risk of other Cancers in Families with Melanoma : Novel Familial Links
(
- 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
Other cancers in lung cancer families are overwhelmingly smoking-related cancers
(
- Contribution to journal › Article
-
Mark
Familial associations of colorectal cancer with other cancers
(
- Contribution to journal › Article
-
Mark
Genetics of gallbladder cancer
(
- Contribution to journal › Letter
-
Mark
Low expression of hexokinase-2 is associated with false-negative FDG–positron emission tomography in multiple myeloma
(
- Contribution to journal › Article
-
Mark
Inherited variants in genes somatically mutated in thyroid cancer
(
- Contribution to journal › Article
-
Mark
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
(
- Contribution to journal › Article
-
Mark
Risk of second cancer in Hodgkin lymphoma survivors and influence of family history
(
- 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
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
- 2016
-
Mark
Risk of Second Primary Cancers in Multiple Myeloma Survivors in German and Swedish Cancer Registries.
(
- Contribution to journal › Article
-
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
TERT promoter mutations in melanoma survival.
(
- Contribution to journal › Article
-
Mark
Cancer of unknown primary is associated with diabetes.
(
- 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
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
Genetic factors influencing the risk of multiple myeloma bone disease.
(
- 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
Location of metastases in cancer of unknown primary are not random and signal familial clustering.
(
- 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
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
-
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
Patterns of metastasis in colon and rectal cancer
(
- 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
The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias : Etiologic Implications
(
- Contribution to journal › Article
-
Mark
Metastatic spread in patients with gastric cancer
(
- Contribution to journal › Article
-
Mark
Origin of B-cell neoplasms in autoimmune disease
(
- Contribution to journal › Article
-
Mark
Age-Dependent Metastatic Spread and Survival : Cancer of Unknown Primary as a Model
(
- 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
Predictive and prognostic clinical variables in cancer patients treated with adenoviral oncolytic immunotherapy
(
- Contribution to journal › Article
-
Mark
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
-
Mark
Search for familial clustering of cancer in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
- 2015
-
Mark
Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells.
(
- 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
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
Population Landscape of Familial Cancer.
(
- Contribution to journal › Article
-
Mark
Frequent DPH3 promoter mutations in skin cancers.
(
- 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
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
(
- 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
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
(
- Contribution to journal › Article
-
Mark
Joint occurrence of Merkel cell carcinoma and non-Hodgkin lymphomas in four Nordic countries
(
- Contribution to journal › Article
-
Mark
Cancer risk and mortality in asthma patients: A Swedish national cohort study.
(
- Contribution to journal › Article
-
Mark
Cancer risk in patients with type 2 diabetes mellitus and their relatives.
(
- 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
Incorporation of Detailed Family History from the Swedish Family-Cancer Database into the Prostate Cancer Prevention Trial Risk Calculator.
(
- 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
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
Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.
(
- Contribution to journal › Article
-
Mark
Special section editorial: Cancer incidence in five continents including Africa.
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Case-control estimation of the impact of oncolytic adenovirus on the survival of patients with refractory solid tumors.
(
- Contribution to journal › Article
-
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
Risk of Next Melanoma in Patients With Familial and Sporadic Melanoma by Number of Previous Melanomas.
(
- 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 Cancer of Unknown Primary after Hospitalization for Autoimmune Diseases.
(
- Contribution to journal › Article
-
Mark
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
(
- Contribution to journal › Article
-
Mark
TERT promoter mutations in clear cell renal cell carcinoma
(
- 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
The risk of contralateral breast cancer in daughters of women with and without breast cancer.
2015) In Clinical Genetics(
- Contribution to journal › Article
-
Mark
Thalassemia and sickle cell anemia in Swedish immigrants : Genetic diseases have become global
(
- Contribution to journal › Article
- 2014
-
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
Risk of Kaposi Sarcoma Among Immigrants to Sweden
(
- 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
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
Novel Genome-Wide Association Study-Based Candidate Loci for Differentiated Thyroid Cancer Risk
(
- 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
Causes of death in patients with extranodal cancer of unknown primary: searching for the primary site
(
- Contribution to journal › Article
-
Mark
Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma.
(
- 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
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Mark
Single Nucleotide Polymorphisms within Interferon Signaling Pathway Genes Are Associated with Colorectal Cancer Susceptibility and Survival.
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- Contribution to journal › Article
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Mark
Inherited genetic susceptibility to multiple myeloma
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- Contribution to journal › Scientific review
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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
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- Contribution to journal › Article
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Mark
Age-time risk patterns of solid cancers in 60 901 non-Hodgkin lymphoma survivors from Finland, Norway and Sweden
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- Contribution to journal › Article
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Mark
Risk of subsequent cancers in renal cell carcinoma survivors with a family history.
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- Contribution to journal › Article
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Mark
TERT promoter mutations in cancer development.
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- Contribution to journal › Article
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Mark
Collection and Use of Family History in Oncology Clinics.
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- Contribution to journal › Letter
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Mark
Special section editorial.
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- Contribution to journal › Debate/Note/Editorial
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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
Risk factors for cancers of unknown primary site: Results from the prospective EPIC cohort
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- Contribution to journal › Article
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Mark
Familial melanoma by histology and age: Joint data from five Nordic countries.
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- Contribution to journal › Article
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Mark
Metastatic sites and survival in lung cancer.
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- 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
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- Contribution to journal › Article
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Mark
Autoimmune diseases associated with non-Hodgkin lymphoma: A nationwide cohort study.
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- Contribution to journal › Article
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Mark
Increased Risk of Hepatobiliary Cancers After Hospitalization for Autoimmune Disease
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- Contribution to journal › Article
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Mark
Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma.
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- Contribution to journal › Letter
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Mark
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
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- Contribution to journal › Article
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Mark
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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Mark
Multiple primary (even in situ) melanomas in a patient pose significant risk to family members.
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- Contribution to journal › Article
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Mark
Foreword: Euro-Mediterranean partnership and EUNAM.
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- Contribution to journal › Article
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Mark
Emigration flows from North Africa to Europe.
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- Contribution to journal › Article
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Mark
Immigrant health, our health.
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- Contribution to journal › Article
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Mark
Prevalence of overweight and obesity in adults from North Africa.
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- Contribution to journal › Article
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Mark
Overview on health research ethics in Egypt and North Africa.
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- Contribution to journal › Article
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Mark
Consanguinity and genetic diseases in North Africa and immigrants to Europe.
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- Contribution to journal › Article
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Mark
Cancer in immigrants as a pointer to the causes of cancer.
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- Contribution to journal › Article
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Mark
The population impact of familial cancer, a major cause of cancer
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- 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
Functional TLR5 Genetic Variants Affect Human Colorectal Cancer Survival
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- Contribution to journal › Article
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Mark
Variants at the 9p21 locus and melanoma risk
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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
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- Contribution to journal › Article
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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
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
Prostate cancer incidence and survival in immigrants to Sweden
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- Contribution to journal › Article
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Mark
Genome-wide investigation of gene-environment interactions in colorectal cancer
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- Contribution to journal › Article
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Mark
Ethnic differences in breast cancer risk and survival: A study on immigrants in Sweden
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- Contribution to journal › Article
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Mark
TERT Promoter Mutations in Familial and Sporadic Melanoma
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- Contribution to journal › Article
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Mark
Somatic Mutations in Exocrine Pancreatic Tumors: Association with Patient Survival
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- 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
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- Contribution to journal › Article
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Mark
Comparison of survival of patients with metastases from known versus unknown primaries: survival in metastatic cancer
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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
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- Contribution to journal › Article
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Mark
Risk of thyroid cancer in first-degree relatives of patients with non-medullary thyroid cancer by histology type and age at diagnosis: a joint study from five Nordic countries
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- Contribution to journal › Article
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Mark
Genetic Variants in Hormone-Related Genes and Risk of Breast Cancer
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- Contribution to journal › Article
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Mark
Deciphering the 8q24.21 association for glioma
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- 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
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- 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