For researchers

Is your paper here?

2,663 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.

35 matches for Havulinna AS, showing the first 15.

Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
FinnGen · Estonian Biobank research team and 1 more consortia
Nature communications · 2026 · PMID 42178310 · open access
8 pages
rs58238559 rs10773287 rs2021095 rs6733156 rs4148211 rs2788095
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs151113194 rs762517 rs12012576 rs139120857 rs5942972 rs7063103
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
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs12415501 rs60401382 rs72934589 rs76110445 Cardioembolic Stroke
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure
FinnGen
Nature communications · 2023 · PMID 36653343 · open access
5 pages
rs11868207 rs7995158 rs791903 rs4636903 Otosclerosis
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
Nature genetics · 2008 · PMID 18193044
4 pages
rs4846914 rs17145738 rs12130333 rs12654264
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
4 pages
rs1746048 rs6725887 rs1122608 Coronary Artery Disease
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population
Circulation. Cardiovascular genetics · 2017 · PMID 29237677 · open access
4 pages
rs198379 rs11105298 rs3753584 rs12406089
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Wellcome Trust Case Control Consortium · Procardis Consortia and 1 more consortia
PLoS genetics · 2009 · PMID 19557161 · open access
3 pages
rs987237 rs7826222 rs2605100
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits
Circulation. Cardiovascular genetics · 2012 · PMID 22399527
3 pages
rs8060686 rs268 Metabolic Syndrome
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
1 page
rs10838738
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval
Heart rhythm · 2012 · PMID 22342860
1 page
rs7219669
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis
Circulation. Cardiovascular genetics · 2017 · PMID 29212897
1 page
rs1560833

Showing 15 of 35 · page 2 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.