For researchers

Is your paper here?

2,660 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.

73 matches for Rice K, showing the first 13.

Common genetic variants associate with serum phosphorus concentration
Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
1 page
rs947583
Genome-wide association analysis identifies multiple loci related to resting heart rate
Human molecular genetics · 2010 · PMID 20639392
1 page
rs9398652
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3
Human molecular genetics · 2011 · PMID 21216879
1 page
rs700752
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
Annals of neurology · 2011 · PMID 21681796
1 page
rs1055129
A genome-wide association search for type 2 diabetes genes in African Americans
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
rs7560163
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies
CARDIoGRAM Consortium
Circulation. Cardiovascular genetics · 2013 · PMID 23247143
1 page
rs12564445
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
Genetic epidemiology · 2013 · PMID 23650146
1 page
rs4253399
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
American journal of human genetics · 2016 · PMID 26805783
1 page
rs117672662
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans
American journal of respiratory and critical care medicine · 2016 · PMID 26977737
1 page
rs116791765
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Nature communications · 2018 · PMID 30258056 · open access
1 page
rs34113929
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
1 page
rs11265618
Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
TOPMed Longevity and Healthy Aging Working Group · from the NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
PloS one · 2021 · PMID 34214102 · open access
1 page
rs185725127

Showing 13 of 73 · page 4 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.