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.

25 matches for Prins B, showing the first 20.

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
rs7095607 rs7872188 rs10515750 rs113745635 rs11658500 rs1458979
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
BIOS Consortium · Understanding Society Scientific Group
Hypertension (Dallas, Tex. : 1979) · 2017 · PMID 28739976
12 pages+
rs35783704 rs73075659 rs73099903 rs36047283 rs871524 rs337100
Genomic atlas of the human plasma proteome
Nature · 2018 · PMID 29875488
12 pages+
rs35179000 rs10920578 rs4613561 rs112493023 rs3826667 rs11003118
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+
rs61653296 rs7187540 rs77692990 rs75902664 rs7976167 rs10873612
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 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+
rs72698571 rs2246469 rs56288844 rs149520992 rs6987444 rs2852151
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
European journal of human genetics : EJHG · 2019 · PMID 30679814 · open access
12 pages+
rs13111293 rs34991781 rs75013985 rs6489973 rs3757868 rs432256
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
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs7178801 rs76480089 rs1634517 rs62193063 rs9807908 rs3742564
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+
rs10025456 rs8032301 rs1624825 rs145502455 rs273592 rs11937432
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 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
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Alcohol Genome-wide Association (AlcGen) Consortium · Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study and 5 more consortia
Nature genetics · 2011 · PMID 22001757
10 pages
rs13030978 rs7267979 rs6834314 rs2954021 rs1976403 rs1883415
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs35658696 rs16826069 rs1127787 rs7572857 rs2233580 rs56200889
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs75619922 rs7225887 rs56381411 rs3784634 rs5400 rs17853166
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Genome biology · 2018 · PMID 30012220 · open access
4 pages
rs11588271 rs116202356 rs3746435 rs11848785
Discovery and fine mapping of serum protein loci through transethnic meta-analysis
LifeLines Cohort Study
American journal of human genetics · 2012 · PMID 23022100
3 pages
rs204999 rs11078597 rs4561508
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia
Translational psychiatry · 2018 · PMID 30470734 · open access
2 pages
rs6598475 rs17616243

Showing 20 of 25 · 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.