For researchers

Is your paper here?

2,673 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.

32 matches for Kronenberg F, showing the first 20.

Biological, clinical and population relevance of 95 loci for blood lipids
Nature · 2010 · PMID 20686565 · open access
12 pages+
rs1042034 rs439401 rs2929282 rs9686661 rs11613352 rs2412710
Human metabolic individuality in biomedical and pharmaceutical research
CARDIoGRAM
Nature · 2011 · PMID 21886157
12 pages+
rs4253252 rs4149081 rs2216405 rs2652822 rs662138 rs9393903
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs17460657 rs347272 rs164133 rs545833 rs10919070 rs12079745
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
rs6795744 rs228611 rs3750082 rs10491967 rs11666497 rs1800615
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms
Journal of lipid research · 2017 · PMID 28512139 · open access
12 pages+
rs4252109 rs151181359 rs12204009 rs12207325 rs145470851 rs147402310
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
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Nature genetics · 2018 · PMID 30297969
12 pages+
rs4281707 rs80147536 rs67254669 rs234853 rs184509201 rs3772071
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+
rs6779998 rs4441471 rs6574652 rs74748843 rs7966357 rs6473252
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
rs35692677 rs113139575 rs162890 rs141493439 rs557338857 rs1145078
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+
rs11781985 rs72782806 rs861536 rs10438961 rs6707386 rs98270
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
GCKD Investigators
Nature genetics · 2020 · PMID 31959995
12 pages+
rs1165187 rs3949301 rs6666886 rs11854689 rs7159760 rs1706821
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs10928512 rs187479321 rs6493583 rs72729623 rs115726216 rs144242131
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+
rs9899520 rs75307421 rs3780012 rs4267865 rs57634870 rs11196296
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+
rs61886489 rs2433228 rs7549167 rs10912836 rs61987136 rs1442937
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1683935 rs71474196 rs72798545 rs1523539 rs7307263 rs11716527
A genetic map of human metabolism across the allele frequency spectrum
Nature genetics · 2025 · PMID 41044249 · open access
12 pages+
rs34569561 rs35483388 rs62114505 rs8018486 rs12933886 rs1814728
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs762517 rs12012576 rs139120857 rs5942972 rs7063103 rs62603531
A genome-wide perspective of genetic variation in human metabolism
Nature genetics · 2010 · PMID 20037589
6 pages
rs211718 rs8396 rs174547 rs2014355 rs2286963 Blood Metabolite Levels
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels

Showing 20 of 32 · page 1 of 2

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.