For researchers

Is your paper here?

2,657 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.

24 matches for Concas MP, showing the first 20.

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
rs4332760 rs41393947 rs10879211 rs1346720 rs55684140 rs4693773
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
rs2852151 rs9385532 rs12083537 rs67129560 rs4752829 rs12749227
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs114846969 rs6029549 rs556107 rs117753190 rs6489786 rs217358
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+
rs6589750 rs271679 rs16942713 rs78986840 rs56411466 rs12361687
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+
rs4766898 rs56106601 rs11202345 rs584425 rs34861762 rs4897160
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs17099893 rs7803297 rs11214037 rs922000 rs3784192 rs3794809
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+
rs114876144 rs145437104 rs3134988 rs7575245 rs269781 rs4741016
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
rs61734651 rs11881070 rs11152089 rs143796236 rs222835 rs11643684
Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits
Nature communications · 2022 · PMID 35585065 · open access
12 pages+
rs336614 rs199469 rs283917 rs61912249 rs1632926 rs11035710
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs17060733 rs13226149 rs1811677 rs55756479 rs1061056 rs12109259
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs11570441 rs11656344 rs11030613 rs11769128 rs11955611 rs11991223
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs72825047 rs11195260 rs10793848 rs2066626 rs2762049 rs55824920
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations
Frontiers in genetics · 2023 · PMID 37359372 · open access
12 pages+
rs117316296 rs141214468 rs191921656 rs117992346 rs140150162 rs148223916
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+
rs41394446 rs56295994 rs4480763 rs1457553 rs3765618 rs57917116
Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
rs2600895 rs143437464 rs186044114 rs485073 rs55925547 rs996347
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
10 pages
rs6440008 rs10960765 rs58979150 rs11041426 rs72917317 rs10899501
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
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
rs1740397 rs3809761 rs13297008 rs62330021 rs9971729
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
3 pages
rs6885307 rs2347867 rs2721195
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Nature communications · 2017 · PMID 29030599 · open access
3 pages
rs34831921 rs55730499 Human Lifespan and Longevity

Showing 20 of 24 · 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.