For researchers

Is your paper here?

2,665 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.

70 matches for Hveem K, showing the first 20.

Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs12907966 rs2421628 rs33959890 rs35189630 rs4793875 rs56000694
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs147660927 rs7209222 rs9272456 rs4515883 rs6743072 rs35073727
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
rs67507374 rs62523081 rs11925442 rs138917529 rs721156 rs11767259
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
rs12138773 rs4705908 rs10988863 rs4312054 rs6023002 rs705699
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs7431106 rs61946067 rs28986300 rs16948230 rs6801151 rs78201023
Genetic architecture reconciles linkage and association studies of complex traits
Estonian Biobank Research Team · Lifelines Cohort Study
Nature genetics · 2024 · PMID 39375568
12 pages+
rs12900485 rs4639527 rs2012284 rs2482398 rs17239055 rs1799993
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+
rs188987157 rs147030877 rs72797166 rs848189 rs61750827 rs17309887
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs7572753 rs11911487 rs1152620 rs2738292 rs11726937 rs55658362
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
rs543874 rs10150332 rs2241423 rs2287019 rs12444979 rs206936
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs10861661 rs201596848 rs900399 rs7157785 rs3927680 rs7946
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators and 4 more consortia
Nature genetics · 2012 · PMID 22885922 · open access
10 pages
rs2075423 rs10203174 rs1496653 rs7955901 rs7177055 rs7640539
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
rs7130753 rs17607589 rs11236814 rs11204896 rs35469349 rs16922576
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
rs6040436 rs10486660 rs7783810 rs12529634 rs140691414 rs1434836
An atlas of genetic determinants of forearm fracture
Estonian Biobank Research Team · DBDS Genomic Consortium
Nature genetics · 2023 · PMID 37919453 · open access
10 pages
rs1467561 rs55730604 rs113061374 rs755760 rs3957282 rs9482773
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
BSTOP study group · Estonian Biobank research team
Nature communications · 2025 · PMID 40021644 · open access
9 pages
rs8107351 rs13137072 rs56007024 rs3825765 rs75826800 rs7108441
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
MAGIC investigators · GIANT Consortium
Nature genetics · 2010 · PMID 20581827
8 pages
rs1552224 rs5945326 rs11634397 rs231362 rs7957197 rs1470579
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs5931180 rs12382607 rs4328011 rs139036121 rs5933079 rs181497961
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
7 pages
rs7559046 rs7521390 rs73739621 rs2918302 rs3017289 rs61907712

Showing 20 of 70 · page 2 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.