For researchers

Is your paper here?

2,660 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.

61 matches for Melander O, 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
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Nature · 2010 · PMID 20881960 · open access
12 pages+
rs822552 rs12694997 rs7853377 rs7532866 rs4605213 rs4640244
Seventy-five genetic loci influencing the human red blood cell
Nature · 2012 · PMID 23222517
12 pages+
rs901683 rs10849023 rs3892630 rs4953318 rs243070 rs10207392
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
rs1544935 rs1870634 rs2891168 rs56131196 rs72689147 rs2487928
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
rs12247028 rs6779380 rs4691707 rs12705390 rs2898290 rs7076398
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
rs60848348 rs1454934 rs36004974 rs577676 rs11598047 rs10800507
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs34878803 rs13213986 rs7383287 rs11632038 rs116826541 rs139244745
Multi-ethnic genome-wide association study for atrial fibrillation
Nature genetics · 2018 · PMID 29892015
12 pages+
rs10027347 rs10165883 rs1044258 rs10479177 rs10760361 rs10842383
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
rs62491354 rs4598218 rs72816333 rs10823136 rs2400509 rs7555285
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Understanding Society Scientific Group · International Consortium for Blood Pressure and 2 more consortia
Nature genetics · 2019 · PMID 30578418 · open access
12 pages+
rs6797165 rs2366264 rs12506184 rs162366 rs11187844 rs2084600
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+
rs924981 rs35636653 rs1078442 rs4918943 rs10096421 rs57126710
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
HPAP Consortium · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2020 · PMID 32541925 · open access
12 pages+
rs113036477 rs144052331 rs9479 rs7227272 rs6011155 rs9852406
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs36106412 rs142444346 rs887945 rs11579145 rs77255899 rs11225452
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs149165710 rs145441283 rs187207161 rs767105335 rs77357563 rs2306899
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Biobank Japan · EPIC-CVD and 1 more consortia
Nature genetics · 2022 · PMID 36474045 · open access
12 pages+
rs192425087 rs2492304 rs66778572 rs8124182 rs2215614 rs72836800
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1533104 rs580585 rs1046521 rs1393202 rs183623967 rs35404821
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
rs11007929 rs1155349 rs9463706 rs13206305 rs3807095 rs729639
A genome-wide association analysis reveals new pathogenic pathways in gout
FAST Study Group · Japan Gout Genomics Consortium and 3 more consortia
Nature genetics · 2024 · PMID 39406924
12 pages+
rs185746473 rs28529426 rs55692900 rs8557 rs9493650 rs11689277
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
rs149780392 rs3794752 rs62233286 rs7095308 rs73048654 rs143445113
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
rs848189 rs61750827 rs17309887 rs12211167 rs34216626 rs2030653

Showing 20 of 61 · page 1 of 4

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.