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Lipoprotein(a) beyond the kringle IV repeat polymorphism: The complexity of genetic variation in the LPA gene

Atherosclerosis, 2022-05, Vol.349, p.17-35

2022

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A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms[S]

Journal of lipid research, 2017-09, Vol.58 (9), p.1834-1844

2017

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Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model

Genome Biology, 2024-06, Vol.25 (1), p.167-25, Article 167

2024

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A comprehensive map of single-base polymorphisms in the hypervariable LPA kringle IV type 2 copy number variation region[S]

Journal of lipid research, 2019-01, Vol.60 (1), p.186-199

2019

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The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat

Journal of lipid research, 2022-12, Vol.63 (12), p.100306, Article 100306

2022

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Lysis reagents, cell numbers, and calculation method influence high-throughput measurement of HDL-mediated cholesterol efflux capacity

Journal of lipid research, 2021-01, Vol.62, p.100125-100125, Article 100125

2021

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FURIN Expression in Vascular Endothelial Cells Is Modulated by a Coronary Artery Disease-Associated Genetic Variant and Influences Monocyte Transendothelial Migration

Journal of the American Heart Association, 2020-02, Vol.9 (4), p.e014333-e014333

2020

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Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR

Genome medicine, 2024-10, Vol.16 (1), p.117-20, Article 117

2024

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A genome-wide analysis of DNA methylation identifies a novel association signal for Lp(a) concentrations in the LPA promoter

PloS one, 2020-04, Vol.15 (4), p.e0232073

2020

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Genetic determinants of complement activation in the general population

Cell reports (Cambridge), 2024-01, Vol.43 (1), p.113611-113611, Article 113611

2024

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Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals

Genome medicine, 2020-08, Vol.12 (1), p.1-13, Article 74

2020

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Lost in the space of bioinformatic tools: A constantly updated survival guide for genetic epidemiology. The GenEpi Toolbox

Atherosclerosis, 2010-04, Vol.209 (2), p.321-335

2010

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Mechanistic insights into lipoprotein(a): from infamous to ‘inflammous’

European heart journal, 2020-06, Vol.41 (24), p.2272-2274

2020

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Evaluating the Causal Relation of ApoA-IV with Disease-Related Traits - A Bidirectional Two-sample Mendelian Randomization Study

Scientific reports, 2017-08, Vol.7 (1), p.8734-13, Article 8734

2017

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When the genome bluffs: a tandem duplication event during generation of a novel Agmo knockout mouse model fools routine genotyping

Cell & bioscience, 2021-03, Vol.11 (1), p.54-54, Article 54

2021

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Sex-Specific Association of the Putative Fructose Transporter SLC2A9 Variants With Uric Acid Levels Is Modified by BMI

Diabetes care, 2008-08, Vol.31 (8), p.1662-1667

2008

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Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working population

PLoS genetics, 2010-12, Vol.6 (12), p.e1001239-e1001239

2010

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Genome-Wide Association Analysis of High-Density Lipoprotein Cholesterol in the Population-Based KORA Study Sheds New Light on Intergenic Regions

Circulation. Cardiovascular genetics, 2008-10, Vol.1 (1), p.10-20

2008

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A systematic evaluation of short tandem repeats in lipid candidate genes: riding on the SNP-wave

PloS one, 2014-07, Vol.9 (7), p.e102113

2014

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SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays

PloS one, 2013-03, Vol.8 (3), p.e59508-e59508

2013

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Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation

PloS one, 2012-04, Vol.7 (4), p.e35015-e35015

2012

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Polymorphisms in the gene regions of the adaptor complex LAMTOR2/LAMTOR3 and their association with breast cancer risk

PloS one, 2013-01, Vol.8 (1), p.e53768-e53768

2013

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An optimized procedure for the design and evaluation of Ecotilling assays

BMC genomics, 2008-10, Vol.9 (1), p.510-510, Article 510

2008

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Plasmid-normalized quantification of relative mitochondrial DNA copy number

Scientific reports, 2018-10, Vol.8 (1), p.15347-11, Article 15347

2018

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The TMEM189 gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogens

Proceedings of the National Academy of Sciences - PNAS, 2020-04, Vol.117 (14), p.7792-7798

2020

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Lipoprotein(a) beyond the kringle IV repeat polymorphism: The complexity of genetic variation in the LPA gene

A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms[S]

Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model

A comprehensive map of single-base polymorphisms in the hypervariable LPA kringle IV type 2 copy number variation region[S]

The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat

Lysis reagents, cell numbers, and calculation method influence high-throughput measurement of HDL-mediated cholesterol efflux capacity

FURIN Expression in Vascular Endothelial Cells Is Modulated by a Coronary Artery Disease-Associated Genetic Variant and Influences Monocyte Transendothelial Migration

Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR

A genome-wide analysis of DNA methylation identifies a novel association signal for Lp(a) concentrations in the LPA promoter

Genetic determinants of complement activation in the general population

Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals

Lost in the space of bioinformatic tools: A constantly updated survival guide for genetic epidemiology. The GenEpi Toolbox

Mechanistic insights into lipoprotein(a): from infamous to ‘inflammous’

Evaluating the Causal Relation of ApoA-IV with Disease-Related Traits - A Bidirectional Two-sample Mendelian Randomization Study

When the genome bluffs: a tandem duplication event during generation of a novel Agmo knockout mouse model fools routine genotyping

Sex-Specific Association of the Putative Fructose Transporter SLC2A9 Variants With Uric Acid Levels Is Modified by BMI

Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working population

Genome-Wide Association Analysis of High-Density Lipoprotein Cholesterol in the Population-Based KORA Study Sheds New Light on Intergenic Regions

A systematic evaluation of short tandem repeats in lipid candidate genes: riding on the SNP-wave

SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays

Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation

Polymorphisms in the gene regions of the adaptor complex LAMTOR2/LAMTOR3 and their association with breast cancer risk

An optimized procedure for the design and evaluation of Ecotilling assays

Plasmid-normalized quantification of relative mitochondrial DNA copy number

The TMEM189 gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogens

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