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Is your paper here?

2,676 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+
rs4149081 rs2216405 rs2652822 rs662138 rs9393903 rs7760535
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+
rs1983546 rs12930096 rs12444261 rs1052536 rs1396515 rs1805128
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+
rs139699952 rs187270959 rs150571318 rs149302195 rs75234242 rs117026595
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+
rs3811978 rs11063028 rs1580278 rs2431115 rs13426680 rs6780171
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+
rs16942713 rs78986840 rs56411466 rs12361687 rs72658302 rs7327286
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+
rs11202345 rs584425 rs188917216 rs34861762 rs4897160 rs2941487
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
GCKD Investigators
Nature genetics · 2020 · PMID 31959995
12 pages+
rs820503 rs61898064 rs77289848 rs6889699 rs56768485 rs420332
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+
rs56881390 rs77631946 rs2010871 rs940922629 rs117047468 rs11758358
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+
rs11196296 rs3825801 rs79495865 rs1871045 rs80102379 rs7819706
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+
rs473913 rs1126742 rs4149128 rs55672373 rs2972516 rs12887044
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs60128210 rs244080 rs2534653 rs4932747 rs6073369 rs11576244
A genetic map of human metabolism across the allele frequency spectrum
Nature genetics · 2025 · PMID 41044249 · open access
12 pages+
rs7631792 rs79077117 rs12158430 rs148387942 rs397092 rs73954926
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
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.