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- 2024
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Mark
Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
- 2022
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Mark
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
(
- Contribution to journal › Letter
- 2021
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Mark
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population
(
- Contribution to journal › Article
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Mark
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations
(
- Contribution to journal › Article
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Mark
Search for AL amyloidosis risk factors using Mendelian randomization
(
- Contribution to journal › Article
- 2020
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Mark
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
(
- Contribution to journal › Article
- 2019
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Mark
Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population
(
- Contribution to journal › Article
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Mark
Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS) : comparison with multiple myeloma
2019) In Leukemia(
- Contribution to journal › Letter
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Mark
Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
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Mark
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes
(
- Contribution to journal › Article
- 2018
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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
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Mark
Genetic variation associated with chromosomal aberration frequency : A genome-wide association study
2018) In Environmental and Molecular Mutagenesis(
- Contribution to journal › Article
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Mark
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
(
- Contribution to journal › Article
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Mark
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia
(
- Contribution to journal › Article
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Mark
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology
(
- Contribution to journal › Article
- 2017
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Mark
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
(
- Contribution to journal › Article
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Mark
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts
(
- Contribution to journal › Letter
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Mark
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
(
- Contribution to journal › Article
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Mark
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci
(
- Contribution to journal › Article
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Mark
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
(
- Contribution to journal › Article
- 2016
-
Mark
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
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Mark
Runs of homozygosity and inbreeding in thyroid cancer
(
- Contribution to journal › Article
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Mark
Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.
(
- Contribution to journal › Article
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Mark
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
(
- Contribution to journal › Article
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Mark
Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
(
- Contribution to journal › Article
- 2015
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Mark
Inbreeding and homozygosity in breast cancer survival.
(
- 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
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
The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A.
(
- Contribution to journal › Article
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Mark
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
(
- Contribution to journal › Article
- 2014
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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
Novel Genome-Wide Association Study-Based Candidate Loci for Differentiated Thyroid Cancer Risk
(
- Contribution to journal › Article
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Mark
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
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Mark
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
(
- Contribution to journal › Article
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Mark
Defining the role of common variation in the genomic and biological architecture of adult human height.
(
- Contribution to journal › Article
- 2013
-
Mark
Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease
(
- Contribution to journal › Article
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Mark
Genome-wide association study on differentiated thyroid cancer.
(
- 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
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
(
- Contribution to journal › Article
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Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
(
- Contribution to journal › Article
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Mark
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
(
- Contribution to journal › Article
- 2012
-
Mark
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk
(
- Contribution to journal › Article
- 2011
-
Mark
Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome
(
- Contribution to journal › Article