For researchers

Is your paper here?

2,655 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

16 matches for Eckardt KU.

Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms
GCKD Investigators
Journal of the American Society of Nephrology : JASN · 2018 · PMID 29545352
12 pages+
rs174560 rs1077989 rs2282377 rs850799 rs55888180 rs117935223
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
rs6785807 rs4445669 rs9298749 rs10957494 rs77819282 rs1045476
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs11062167 rs12736457 rs9932625 rs11071738 rs2634675 rs80576
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
rs12790943 rs74375025 rs6998967 rs73065147 rs147215801 rs35692677
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs2941487 rs148015593 rs12484809 rs62128132 rs2054576 rs12504795
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
GCKD Investigators
Nature genetics · 2020 · PMID 31959995
12 pages+
rs77289848 rs6889699 rs56768485 rs420332 rs34103191 rs10195357
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs3743140 rs3806155 rs7313668 rs76227980 rs41277236 rs78470967
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine
GCKD Investigators
Nature genetics · 2023 · PMID 37277652 · open access
12 pages+
rs10848574 rs2460451 rs7557590 rs114488830 rs61886489 rs2433228
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs34885433 rs17250977 rs6488140 rs147676117 rs952472 rs2800733
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs35658696 rs16826069 rs1127787 rs7572857 rs2233580 rs56200889
Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases
JCI insight · 2022 · PMID 35446786 · open access
4 pages
rs9646256 rs7224888 rs73338360 rs10738906
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Nature genetics · 2023 · PMID 37337107
3 pages
rs2075836 rs57917667 rs75413466
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
2 pages
rs56012466 rs141809766
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Nature communications · 2020 · PMID 32231244 · open access
1 page
rs17831251
Genetics of osteopontin in patients with chronic kidney disease: The German Chronic Kidney Disease study
GCKD investigators
PLoS genetics · 2022 · PMID 35385482 · open access
1 page
rs2731673
Meta-GWAS on PCSK9 concentrations reveals associations of novel loci outside the PCSK9 locus in White populations
Atherosclerosis · 2023 · PMID 37989062
1 page
rs184753872

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.