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- 2023
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Mark
Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia
(
- Contribution to journal › Article
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Mark
Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
(
- Contribution to journal › Article
- 2022
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Mark
Complement C4 copy number variation is linked to SSA/Ro and SSB/La autoantibodies in systemic inflammatory autoimmune diseases
(
- Contribution to journal › Article
- 2021
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Mark
Contributions of de novo variants to systemic lupus erythematosus
(
- Contribution to journal › Article
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Mark
Mutational patterns and clonal evolution from diagnosis to relapse in pediatric acute lymphoblastic leukemia
(
- Contribution to journal › Article
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Mark
Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus
(
- Contribution to journal › Article
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Mark
Variants in BANK1 are associated with lupus nephritis of European ancestry
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- Contribution to journal › Article
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Mark
Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing
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- Contribution to journal › Article
- 2020
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Mark
High genetic risk score is associated with early disease onset, damage accrual and decreased survival in systemic lupus erythematosus
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- Contribution to journal › Article
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Mark
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment
(
- Contribution to journal › Article
- 2019
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Mark
Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus
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- Contribution to journal › Article
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Mark
A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
(
- Contribution to journal › Article
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Mark
Genetic variations in A20 DUB domain provide a genetic link to citrullination and neutrophil extracellular traps in systemic lupus erythematosus
(
- Contribution to journal › Article
- 2018
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Mark
DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus
(
- Contribution to journal › Article
- 2017
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Mark
Novel risk genes for systemic lupus erythematosus predicted by random forest classification
(
- Contribution to journal › Article
- 2016
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Mark
PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia
(
- Contribution to journal › Article
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Mark
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
(
- Contribution to journal › Article
- 2015
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Mark
GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb.
(
- Contribution to journal › Article
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Mark
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus.
(
- Contribution to journal › Article
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Mark
Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors.
(
- Contribution to journal › Article
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Mark
New genetic loci link adipose and insulin biology to body fat distribution.
(
- Contribution to journal › Article
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Mark
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
(
- Contribution to journal › Article
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Mark
Genetic studies of body mass index yield new insights for obesity biology.
(
- Contribution to journal › Article
- 2014
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Mark
A Central Role for GRB10 in Regulation of Islet Function in Man.
(
- 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
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- 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
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Mark
Association of STAT4 Polymorphism with Severe Renal Insufficiency in Lupus Nephritis.
(
- Contribution to journal › Article
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Mark
HLA-DRB1*04/*13 alleles are associated with vascular disease and antiphospholipid antibodies in systemic lupus erythematosus
(
- Contribution to journal › Article
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Mark
Coronary Heart Disease in Systemic Lupus Erythematosus Is Associated With Interferon Regulatory Factor-8 Gene Variants
(
- Contribution to journal › Article
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Mark
Association of Genes in the NF-kappa B Pathway with Antibody-Positive Primary Sjogren's Syndrome
(
- Contribution to journal › Article
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Mark
Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations
(
- Contribution to journal › Article
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Mark
Higher Magnesium Intake Is Associated with Lower Fasting Glucose and Insulin, with No Evidence of Interaction with Select Genetic Loci, in a Meta-Analysis of 15 CHARGE Consortium Studies
(
- Contribution to journal › Article
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Mark
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
(
- Contribution to journal › Article
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Mark
Large-scale association analysis identifies new risk loci for coronary artery disease
(
- Contribution to journal › Article
- 2012
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Mark
Association between genetic variants in the tumour necrosis factor/lymphotoxin alpha/lymphotoxin beta locus and primary Sjogren's syndrome in Scandinavian samples
(
- Contribution to journal › Article
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Mark
Identification of the BCAR1-CFDP1-TMEM170A Locus as a Determinant of Carotid Intima-Media Thickness and Coronary Artery Disease Risk
(
- Contribution to journal › Article
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Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- Contribution to journal › Article
- 2011
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Mark
Salt-inducible kinase 1 influences Na+,K+-ATPase activity in vascular smooth muscle cells and associates with variations in blood pressure.
(
- Contribution to journal › Article
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Mark
A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE
(
- Contribution to journal › Article
-
Mark
Total Zinc Intake May Modify the Glucose-Raising Effect of a Zinc Transporter (SLC30A8) Variant A 14-Cohort Meta-analysis
(
- Contribution to journal › Article
-
Mark
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes
(
- Contribution to journal › Article
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Mark
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile
(
- Contribution to journal › Article
- 2010
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Mark
Gene Variants In Fam167A-Blk And Tnfsf4 Are Associated With Primary Sjogren'S Syndrome
(
- Contribution to journal › Published meeting abstract
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Mark
Niemann-Pick C1 Modulates Hepatic Triglyceride Metabolism and Its Genetic Variation Contributes to Serum Triglyceride Levels
(
- Contribution to journal › Article
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Mark
A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus
(
- Contribution to journal › Article
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Mark
Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
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Mark
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
(
- Contribution to journal › Article
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Mark
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
(
- Contribution to journal › Article
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Mark
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
(
- Contribution to journal › Article