For researchers

Is your paper here?

2,676 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.

176 matches for An K, showing the first 20.

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
1 page
rs10838738
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility
Nature genetics · 2009 · PMID 19578366 · open access
1 page
rs4809324
Common genetic variants associate with serum phosphorus concentration
Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
1 page
rs947583
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels
GEFOS Consortium
Human molecular genetics · 2010 · PMID 20705733
1 page
rs17251221
CUBN is a gene locus for albuminuria
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Kidney Function
A variant in MCF2L is associated with osteoarthritis
arcOGEN Consortium
American journal of human genetics · 2011 · PMID 21871595
1 page
rs11842874
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval
Heart rhythm · 2012 · PMID 22342860
1 page
rs7219669
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer
PLoS genetics · 2012 · PMID 22383897 · open access
1 page
rs9485372
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function
Human molecular genetics · 2012 · PMID 22494929
1 page
rs10028213
Genome-wide association study confirming association of HLA-DP with protection against chronic hepatitis B and viral clearance in Japanese and Korean
PloS one · 2012 · PMID 22737229 · open access
1 page
rs9277535
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
1 page
rs11177
Genome-wide meta-analyses of smoking behaviors in African Americans
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
rs2036527
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
American journal of respiratory and critical care medicine · 2012 · PMID 22837378
1 page
rs8031948
Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3
Nature genetics · 2012 · PMID 22863731
1 page
rs312691
Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility
PloS one · 2012 · PMID 22952805 · open access
1 page
rs9268145
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
1 page
rs10498633
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25
COLUMBUS Consortium
Nature communications · 2014 · PMID 25327703 · open access
1 page
rs140068132
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
iPSYCH-SSI-Broad Group
Nature communications · 2017 · PMID 28537267 · open access
1 page
rs12700667
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528
Genome-wide association study identifies the common variants in CYP3A4 and CYP3A5 responsible for variation in tacrolimus trough concentration in Caucasian kidney transplant recipients
The pharmacogenomics journal · 2018 · PMID 29160300
1 page
rs35599367

Showing 20 of 176 · page 8 of 9

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.