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.

22 matches for Boutin T, showing the first 20.

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
rs12142240 rs2236918 rs704795 rs930036 rs6856693 rs11738223
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
NEIGHBORHOOD Consortium
Human molecular genetics · 2017 · PMID 28073927
12 pages+
rs6107845 rs2157719 rs114503346 rs10753787 rs72759609 rs8015152
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants
Genome medicine · 2017 · PMID 28270201 · open access
12 pages+
rs571835655 rs755546258 rs72742734 rs554379257 rs184469050 rs7952436
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2018 · PMID 29760442 · open access
12 pages+
rs3808520 rs7026684 rs10980623 rs7040970 rs7308752 rs11553764
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
rs61653296 rs7187540 rs77692990 rs75902664 rs7976167 rs10873612
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Understanding Society Scientific Group · International Consortium for Blood Pressure and 2 more consortia
Nature genetics · 2019 · PMID 30578418 · open access
12 pages+
rs2009598 rs9708177 rs139055942 rs6848906 rs533030436 rs181718607
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs6779998 rs4441471 rs6574652 rs74748843 rs7966357 rs6473252
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs11781985 rs72782806 rs861536 rs10438961 rs6707386 rs98270
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters
International Glaucoma Genetics Consortium · NEIGHBORHOOD consortium and 1 more consortia
Communications biology · 2019 · PMID 31798171 · open access
12 pages+
rs28503222 rs61045038 rs7868669 rs4074178 rs62014490 rs2393730
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs17712080 rs28540500 rs67234920 rs76611452 rs2642608 rs10226357
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs7178801 rs76480089 rs1634517 rs62193063 rs9807908 rs3742564
Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants
Communications biology · 2020 · PMID 33311554 · open access
12 pages+
rs4537621 rs149879035 rs12778515 rs72940171 rs9375452 rs72823422
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs17256082 rs12784552 rs142484519 rs118164457 rs7063597 rs3752435
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
rs28734123 rs7151849 rs10040811 rs13270541 rs16852778 rs1878825
A genome-wide association analysis reveals new pathogenic pathways in gout
FAST Study Group · Japan Gout Genomics Consortium and 3 more consortia
Nature genetics · 2024 · PMID 39406924
12 pages+
rs6129802 rs4790 rs12673242 rs75712687 rs12510411 rs259848
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs5931180 rs12382607 rs4328011 rs139036121 rs5933079 rs181497961
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Nature communications · 2017 · PMID 29030599 · open access
3 pages
rs34831921 rs55730499 Human Lifespan and Longevity
Insights into the genetic basis of retinal detachment
UK Biobank Eye & Vision Consortium · 23andMe Research Team
Human molecular genetics · 2020 · PMID 31816047 · open access
2 pages
rs562698611 rs10765567
Genetic Landscape of the ACE2 Coronavirus Receptor
GenOMICC Consortium† · IMI-DIRECT Consortium†
Circulation · 2022 · PMID 35387486 · open access
2 pages
rs5992134 rs3094087
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Age at Menarche

Showing 20 of 22 · page 1 of 2

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.