For researchers

Is your paper here?

2,662 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.

22 matches for Beekman M, showing the first 20.

Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs13393800 rs6920372 rs6485978 rs4332428 rs1562975 rs17807185
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs6060717 rs11989744 rs4646404 rs319564 rs2179129 rs16996700
The impact of low-frequency and rare variants on lipid levels
ENGAGE Consortium
Nature genetics · 2015 · PMID 25961943
12 pages+
rs72959041 rs7759633 rs9988450 rs419132 rs9638182 rs115400054
Genome-Wide Association Study on Immunoglobulin G Glycosylation Patterns
Frontiers in immunology · 2018 · PMID 29535710 · open access
12 pages+
rs11622829 rs10134589 rs7153297 rs11158592 rs7804185 rs6764279
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
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+
rs56288844 rs149520992 rs6987444 rs2852151 rs9385532 rs12083537
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs73923006 rs6797002 rs7603972 rs17205972 rs7596872 rs55940034
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
Genome-wide characterization of circulating metabolic biomarkers
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team and 1 more consortia
Nature · 2024 · PMID 38448586 · open access
12 pages+
rs3754053 rs236984 rs4310508 rs12037485 rs111705570 rs79683221
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers
PLoS genetics · 2013 · PMID 23382691 · open access
10 pages
rs11710456 rs7652995 rs4878639 rs6583437 rs2072209 rs2186369
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
PLoS genetics · 2013 · PMID 23408906 · open access
10 pages
rs9497965 rs7860634 rs7240777 rs10799824 rs9472138 rs11755845
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
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
rs7214628 rs7894407 rs72848980 rs7909791
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
American journal of human genetics · 2020 · PMID 32109421 · open access
4 pages
rs59294613 rs73624724 rs932827 rs4691895
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels
Nature communications · 2015 · PMID 26068415
3 pages
rs12297049 rs2540641 rs16844839
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Nature communications · 2016 · PMID 27005778 · open access
3 pages
rs74249229 rs73066442 rs2921604
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Human molecular genetics · 2014 · PMID 24688116 · open access
2 pages
rs2149954 Human Lifespan and Longevity
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Nature communications · 2018 · PMID 29343764 · open access
2 pages
rs10745742 Vitamin D Deficiency and the GC Gene
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Nature genetics · 2023 · PMID 37770635
2 pages
rs62555371 rs10899970

Showing 20 of 22 · 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.