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.

16 matches for Lo K.

Hundreds of variants clustered in genomic loci and biological pathways affect human height
Nature · 2010 · PMID 20881960 · open access
12 pages+
rs11830103 rs822552 rs12694997 rs7853377 rs7532866 rs4605213
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+
rs2854207 rs9650315 rs7870753 rs2278483 rs4735677 rs310421
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs13011109 rs2820443 rs12955983 rs6737082 rs2821248 rs10840060
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs284860 rs1131877 rs2277598 rs295322 rs62623713 rs11555762
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs6897196 rs75211492 rs76738175 rs922 rs10423120 rs10493441
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs4700436 rs6595714 rs72843867 rs7356611 rs7810260 rs79709502
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+
rs10928512 rs187479321 rs6493583 rs72729623 rs115726216 rs144242131
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+
rs1887200 rs11904581 rs6139109 rs1442883 rs973730 rs6020177
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs762517 rs12012576 rs139120857 rs5942972 rs7063103 rs62603531
Multiomics analyses prioritize disease genes and pathways in hidradenitis suppurativa
The Journal of investigative dermatology · 2026 · PMID 41548865
5 pages
rs116212806 rs11545042 rs3129879 rs150315199 Hidradenitis Suppurativa
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
UK NIHR BioResource Rare Diseases Consortium · UK PAH Cohort Study Consortium and 1 more consortia
The Lancet. Respiratory medicine · 2019 · PMID 30527956 · open access
4 pages
rs2856830 rs13266183 rs10103692 Pulmonary Arterial Hypertension
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
rs2121279 rs16851483
Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration
Nature genetics · 2015 · PMID 25774636 · open access
2 pages
rs4733781 Tuberculosis
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol
Journal of the American Heart Association · 2018 · PMID 30369316 · open access
2 pages
rs141622900 rs77069344
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
rs4105144

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.