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- 2024
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Mark
Human Leukocyte Antigen Signatures as Pathophysiological Discriminants of Microscopic Colitis Subtypes
(
- Contribution to journal › Article
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Mark
Predicting type 2 diabetes via machine learning integration of multiple omics from human pancreatic islets
(
- Contribution to journal › Article
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Mark
MERTK in the rat trigeminal system : a potential novel target for cluster headache?
(
- Contribution to journal › Article
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Mark
Identification of Quantitative Trait Nucleotides and Development of Diagnostic Markers for Nine Fatty Acids in the Peanut
(
- Contribution to journal › Article
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Mark
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
(
- Contribution to journal › Article
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Mark
KnockoffHybrid : A knockoff framework for hybrid analysis of trio and population designs in genome-wide association studies
(
- Contribution to journal › Article
- 2023
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Mark
Functional genomics approaches to dissect causal DNA variations in obesity and type 2 diabetes
2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Engineered allele substitution at PPARGC1A rs8192678 alters human white adipocyte differentiation, lipogenesis, and PGC-1α content and turnover
(
- Contribution to journal › Article
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Mark
Precision medicine in complex diseases - : Molecular subgrouping for improved prediction and treatment stratification
(
- Contribution to journal › Scientific review
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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
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Mark
Periodontitis and NAFLD-related diseases : A bidirectional two-sample Mendelian randomization study
2023) In Oral Diseases(
- Contribution to journal › Article
- 2022
-
Mark
Genetics of Diabetes Subtypes. Characterization of novel cluster-based diabetes subtypes.
2022) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic Predisposition to Sporadic and Familial Multiple Myeloma
2022) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Iam hiQ-a novel pair of accuracy indices for imputed genotypes
(
- Contribution to journal › Article
-
Mark
Genetic predisposition for Multiple Myeloma. Identification and functional characterization of risk variants
2022) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
(
- Contribution to journal › Article
-
Mark
Genetic Variants Associated with Neuropeptide Y Autoantibody Levels in Newly Diagnosed Individuals with Type 1 Diabetes
(
- Contribution to journal › Article
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Mark
Genome-Wide Association Study of Salt Tolerance-Related Traits during Germination and Seedling Development in an Intermedium-Spike Barley Collection
(
- Contribution to journal › Article
- 2021
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Mark
Pleiotropy-guided transcriptome imputation from normal and tumor tissues identifies candidate susceptibility genes for breast and ovarian cancer
(
- Contribution to journal › Article
- 2020
-
Mark
Neutrophil mediators and their receptors in the pathogenesis and prognosis of cardiovascular disease
2020) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
The Parkinson's Disease Genome-Wide Association Study Locus Browser
2020) In Movement Disorders(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies novel single nucleotide polymorphisms having age-specific effect on prostate-specific antigen levels
(
- Contribution to journal › Article
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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
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Mark
Transcriptome-wide association study reveals candidate causal genes for lung cancer
(
- Contribution to journal › Article
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Mark
An integrative phenotype–genotype approach using phenotypic characteristics from the UAE national diabetes study identifies HSD17B12 as a candidate gene for obesity and type 2 diabetes
(
- Contribution to journal › Article
- 2019
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Mark
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
(
- Contribution to journal › Article
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Mark
A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals
(
- Contribution to journal › Article
- 2018
-
Mark
Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines
(
- Contribution to journal › Article
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Mark
Bivariate genome-wide association study of depressive symptoms with type 2 diabetes and quantitative glycemic traits
(
- Contribution to journal › Article
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Mark
Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA
(
- Contribution to journal › Article
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Mark
Chemotherapy-induced peripheral neuropathy : Evidence from genome-wide association studies and replication within multiple myeloma patients
(
- Contribution to journal › Article
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Mark
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
(
- Contribution to journal › Article
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Mark
Genetic modifiers of radon-induced lung cancer risk : a genome-wide interaction study in former uranium miners
(
- 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
-
Mark
Bortezomib-induced peripheral neuropathy : A genome-wide association study on multiple myeloma patients
(
- Contribution to journal › Article
- 2017
-
Mark
Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study
(
- Contribution to journal › Article
-
Mark
Genetics of complex disease
2017)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
(
- Contribution to journal › Article
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Mark
Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy : Replication of the Reported Candidate Susceptibility Loci
(
- Contribution to journal › Article
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Mark
The complex genetics of gait speed : Genome-wide meta-analysis approach
(
- Contribution to journal › Article
- 2016
-
Mark
Brief Report : IRF4 Newly Identified as a Common Susceptibility Locus for Systemic Sclerosis and Rheumatoid Arthritis in a Cross-Disease Meta-Analysis of Genome-Wide Association Studies
(
- Contribution to journal › Article
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Mark
Runs of homozygosity and inbreeding in thyroid cancer
(
- Contribution to journal › Article
- 2014
-
Mark
Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes
(
- Contribution to journal › Article
- 2013
-
Mark
Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women
(
- Contribution to journal › Article
- 2010
-
Mark
The role of genetic variation and DNA methylation in human glucose metabolism and type 2 diabetes
(
- Thesis › Doctoral thesis (compilation)