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.

116 matches for Lin MR, showing the first 20.

Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
3 pages
rs964184 rs2304130 rs10105606
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits
Circulation. Cardiovascular genetics · 2012 · PMID 22399527
3 pages
rs8060686 rs268 Metabolic Syndrome
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
rs4851266 rs9320913 rs1056667
Genome-wide meta-analysis identifies new susceptibility loci for migraine
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
rs11759769 rs12134493 rs4379368
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Nature communications · 2016 · PMID 27005778 · open access
3 pages
rs74249229 rs73066442 rs2921604
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
rs12599112 rs11940694 Alcohol Consumption
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
rs3783347 rs6072275 rs4869272
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Nature genetics · 2009 · PMID 19060910
2 pages
rs3764261 rs2650000
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease
JAMA · 2009 · PMID 19567438
2 pages
rs7553007 rs4537545
Genome-wide association study reveals multiple loci associated with primary tooth development during infancy
PLoS genetics · 2010 · PMID 20195514 · open access
2 pages
rs8079702 Tooth Eruption Timing
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups
PLoS genetics · 2010 · PMID 20421936 · open access
2 pages
rs17700144 rs17150703
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
2 pages
rs6943555 Alcohol Consumption
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation
PLoS genetics · 2012 · PMID 22829776 · open access
2 pages
rs17496332 rs1573036
Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA
Australian Asthma Genetics Consortium Collaborators
PloS one · 2012 · PMID 23028483 · open access
2 pages
rs13408661 rs9268516
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
PLoS genetics · 2012 · PMID 23284291 · open access
2 pages
rs7764819 rs11654749
A novel common variant in DCST2 is associated with length in early life and height in adulthood
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
2 pages
rs1380294 rs905938
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
rs9902453 rs7800944
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
rs16851483 rs2121279
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788

Showing 20 of 116 · page 5 of 6

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.