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.

21 matches for Aben KK, showing the first 20.

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
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+
rs2277598 rs295322 rs62623713 rs11555762 rs9891146 rs13447324
Multi-population GWAS meta-analysis identifies bladder cancer susceptibility loci and highlights genetic regulation of smoking-related risk
UROMOL Consortium
Nature communications · 2026 · PMID 42706231 · open access
12 pages+
rs72826305 rs112204664 rs7076867 rs7937265 rs6910215 rs7145592
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
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
9 pages
rs1879586 rs7207826 rs11651755 rs688187 rs7902587 rs9886651
Genetic correction of PSA values using sequence variants associated with PSA levels
Science translational medicine · 2010 · PMID 21160077
4 pages
rs401681 rs17632542 rs10788160 rs11067228
Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights
UROMOL Consortium
European urology · 2023 · PMID 37210288
4 pages
rs1414253 rs411482 rs4743687 rs17863783
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Nature genetics · 2008 · PMID 18264098
3 pages
rs5945572 rs721048 Prostate Cancer
Many sequence variants affecting diversity of adult human height
Nature genetics · 2008 · PMID 18391951
3 pages
rs3748069 rs12198986 rs6830062
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Nature genetics · 2009 · PMID 19767754
3 pages
rs16902094 rs8102476 rs11228565
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Nature genetics · 2009 · PMID 19079260
2 pages
rs6499640 rs7647305
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Nature genetics · 2009 · PMID 19648920
2 pages
rs2294008 Bladder Cancer
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Nature genetics · 2010 · PMID 20622881
2 pages
rs7025486 Abdominal Aortic Aneurysm
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
rs8102137 rs798766
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Nature · 2008 · PMID 18385739
1 page
Lung Cancer
Two newly identified genetic determinants of pigmentation in Europeans
Nature genetics · 2008 · PMID 18488028
1 page
rs1408799
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
rs4105144
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Human molecular genetics · 2011 · PMID 21357676
1 page
rs6968865
Mutations in BRIP1 confer high risk of ovarian cancer
Nature genetics · 2011 · PMID 21964575
1 page
rs34289250

Showing 20 of 21 · 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.