For researchers

Is your paper here?

2,681 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.

37 matches for Lettre G, showing the first 17.

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Identification of ten loci associated with height highlights new biological pathways in human growth
Diabetes Genetics Initiative · FUSION and 4 more consortia
Nature genetics · 2008 · PMID 18391950
3 pages
rs4896582 rs1492820 rs10946808
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
Multiple loci are associated with white blood cell phenotypes
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
rs1449263 rs10980800 rs2517510
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
BioBank Japan Project · CHARGE Consortium
Human molecular genetics · 2013 · PMID 23446634
3 pages
rs762516 rs13008603 rs13339636
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18245381
2 pages
rs11886868 Blood Cell Counts
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
rs17428471 rs17080102
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol
Journal of the American Heart Association · 2018 · PMID 30369316 · open access
2 pages
rs141622900 rs77069344
DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18667698
1 page
Blood Cell Counts
Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A
Science (New York, N.Y.) · 2008 · PMID 19056937
1 page
Blood Cell Counts
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
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
PLoS genetics · 2011 · PMID 21347282 · open access
1 page
rs7801190
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116
An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level
Science (New York, N.Y.) · 2013 · PMID 24115442
1 page
Blood Cell Counts
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
1 page
rs28450540

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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.