For researchers

Is your paper here?

2,663 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.

16 matches for Nethander M.

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
American journal of human genetics · 2017 · PMID 28757204
12 pages+
rs117865811 rs116970203 rs117300835 rs2277458 rs148189294 rs1607741
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
American journal of human genetics · 2018 · PMID 29304378
12 pages+
rs71569047 rs10450586 rs34406563 rs7112229 rs11606709 rs4647728
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+
rs12083537 rs67129560 rs4752829 rs12749227 rs4845623 rs9271608
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+
rs3211938 rs151235402 rs73339979 rs114139997 rs10184673 rs117139027
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+
rs17105330 rs8079564 rs4813853 rs7015100 rs7522427 rs9907557
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Communications biology · 2023 · PMID 37402774 · open access
11 pages
rs34814687 rs13204469 rs11030009 rs55963900 rs143348825 rs1101560
An atlas of genetic determinants of forearm fracture
Estonian Biobank Research Team · DBDS Genomic Consortium
Nature genetics · 2023 · PMID 37919453 · open access
10 pages
rs9482773 rs4792909 rs1891002 rs80107551 rs4389863 rs1467561
Femoral neck width genetic risk score is a novel independent risk factor for hip fractures
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024 · PMID 38477772 · open access
8 pages
rs75495843 rs149882987 rs30224 rs7636776 rs17779649 rs59932020
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs139120857 rs5942972 rs7063103 rs62603531 rs151113194 rs762517
Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization
Arthritis & rheumatology (Hoboken, N.J.) · 2023 · PMID 37096546
7 pages
rs17138656 rs7143806 rs34136735 rs34498262 rs2957124 rs13042961
Genetic Variants Associated with Circulating Parathyroid Hormone
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
3 pages
rs35194449 rs4074995 rs4443100
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
Nature communications · 2021 · PMID 33510174 · open access
3 pages
rs2899611 rs11236213 rs34464763
Genetic Variants Associated with Circulating Fibroblast Growth Factor 23
Journal of the American Society of Nephrology : JASN · 2018 · PMID 30217807
2 pages
rs11741640 rs2769071
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
PLoS genetics · 2018 · PMID 30261039 · open access
1 page
rs12310519
The HUNT study identifies host genetic factors reproducibly associated with human gut microbiota composition
Nature genetics · 2026 · PMID 41688637 · open access
1 page
rs4556017
Genome-wide association analyses highlight the role of the intestinal molecular environment in human gut microbiota variation
Nature genetics · 2026 · PMID 41688638 · open access
1 page
rs2279628

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.