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- 2017
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Mark
Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism
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- Contribution to journal › Article
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Mark
Genetics of gallbladder cancer
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- Contribution to journal › Letter
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Mark
Surveillance Bias in Cancer Risk after Unrelated Medical Conditions : Example Urolithiasis
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- Contribution to journal › Article
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Mark
Familial associations of lymphoma and myeloma with autoimmune diseases
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- Contribution to journal › Article
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Mark
Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts : Comparison with myeloma
(
- Contribution to journal › Article
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Mark
Familial associations of male breast cancer with other cancers
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- Contribution to journal › Article
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Mark
Direct evidence for a polygenic etiology in familial multiple myeloma
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- Contribution to journal › Article
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Mark
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
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- Contribution to journal › Article
- 2016
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Mark
Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.
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- Contribution to journal › Article
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Mark
Survival in familial and non-familial breast cancer by age and stage at diagnosis.
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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
Cancer of unknown primary is associated with diabetes.
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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
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
Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans
(
- 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
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
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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
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
A review of the infection-associated cancers in North African countries
(
- Contribution to journal › Scientific review
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Mark
The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias : Etiologic Implications
(
- Contribution to journal › Article
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Mark
Search for familial clustering of cancer in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
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Mark
Polymorphisms within base and nucleotide excision repair pathways and risk of differentiated thyroid carcinoma
(
- 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
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
- 2015
-
Mark
Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells.
(
- Contribution to journal › Article
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Mark
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
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- Contribution to journal › Article
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Mark
Subsequent Type 2 Diabetes in Patients with Autoimmune Disease.
(
- 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
Inbreeding and homozygosity in breast cancer survival.
(
- Contribution to journal › Article
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Mark
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.
(
- Contribution to journal › Article
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Mark
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.
(
- Contribution to journal › Article
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Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
(
- Contribution to journal › Article
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Mark
Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.
(
- Contribution to journal › Article
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Mark
Cancer risk in patients with type 2 diabetes mellitus and their relatives.
(
- Contribution to journal › Article
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Mark
Risk of Next Melanoma in Patients With Familial and Sporadic Melanoma by Number of Previous Melanomas.
(
- Contribution to journal › Article
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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
Thalassemia and sickle cell anemia in Swedish immigrants : Genetic diseases have become global
(
- Contribution to journal › Article
- 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
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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
Novel Genome-Wide Association Study-Based Candidate Loci for Differentiated Thyroid Cancer Risk
(
- 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
GWAS-Identified Common Variants for Obesity Are Not Associated with the Risk of Developing Colorectal Cancer
(
- 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
Toll-like receptor genetic variants and colorectal cancer.
(
- Contribution to journal › Debate/Note/Editorial