For researchers

Is your paper here?

2,661 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.

131 matches for Wareham NJ, showing the first 20.

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 meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
Nature communications · 2021 · PMID 33510174 · open access
3 pages
rs34464763 rs2899611 rs11236213
Causal associations between cardiorespiratory fitness and type 2 diabetes
Nature communications · 2023 · PMID 37400433 · open access
3 pages
rs142556838 rs11062107 rs17695155
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
GIANT Consortium
PLoS genetics · 2009 · PMID 20011104 · open access
2 pages
rs1648707 Adiponectin Levels
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
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 central role for GRB10 in regulation of islet function in man
PLoS genetics · 2014 · PMID 24699409 · open access
2 pages
rs12549902 rs11187144
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
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
Nature communications · 2015 · PMID 26416764 · open access
2 pages
rs1351592 rs11031006
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis
PLoS medicine · 2016 · PMID 27898682 · open access
2 pages
rs7678928 rs75950518
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Nature communications · 2018 · PMID 29343764 · open access
2 pages
rs10745742 Vitamin D Deficiency and the GC Gene
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
American journal of human genetics · 2019 · PMID 31178129
2 pages
rs145119400 rs11646213
Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations
Diabetes care · 2021 · PMID 33203707 · open access
2 pages
rs117885456 rs13028225
Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation
Estonian Biobank Research Team
Nature communications · 2024 · PMID 38494474 · open access
2 pages
rs1016819 rs2077522
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Science (New York, N.Y.) · 2007 · PMID 17434869
1 page
Obesity and Body Weight
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
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
Genetic loci influencing kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383145
1 page
rs3127573
CUBN is a gene locus for albuminuria
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Kidney Function

Showing 20 of 131 · page 6 of 7

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.