For researchers

Is your paper here?

2,657 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.

35 matches for Navarro P, showing the first 20.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs1983546 rs12930096 rs12444261 rs1052536 rs1396515 rs1805128
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
Human molecular genetics · 2016 · PMID 26561523
12 pages+
rs2731439 rs7439150 rs7916868 rs11780978 rs9808651 rs12913259
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+
rs755291044 rs142916219 rs10889333 rs75331444 rs7412 rs71435601
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Nature communications · 2017 · PMID 28443625 · open access
12 pages+
rs6012558 rs4239436 rs6772896 rs765751 rs2645294 rs12679556
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
CHARGE Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS genetics · 2017 · PMID 28448500 · open access
12 pages+
rs1406948 rs10923724 rs2371767 rs7766106 rs10101061 rs7973683
Mapping the serum proteome to neurological diseases using whole genome sequencing
Nature communications · 2021 · PMID 34857772 · open access
12 pages+
rs67924081 rs28483039 rs11004802 rs217053 rs1921087 rs73070113
Genetic regulation of post-translational modification of two distinct proteins
Nature communications · 2022 · PMID 35332118 · open access
12 pages+
rs1671819 rs12892058 rs4131097 rs8022094 rs75757016 rs11622603
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
NBCS Investigators
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
12 pages+
rs4980383 rs10995187 rs10087804 rs9397436 rs3819405 rs34066050
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs6699943 rs6778977 rs7927901 rs2088627 rs7976280 rs30226
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs2762049 rs55824920 rs72798148 rs8019721 rs1724411 rs12467581
Efficient candidate drug target discovery through proteogenomics in a Scottish cohort
Communications biology · 2025 · PMID 40883583 · open access
12 pages+
rs2287331 rs72758637 rs7259861 rs56243392 rs903357 rs11591129
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
11 pages
rs1364063 rs4840086 rs9939609 rs10980926 rs7642134 rs17188434
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
rs434943 rs2106854 rs7968440 rs1938492 rs1019670 rs4817986
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
MAGIC investigators · GIANT Consortium
Nature genetics · 2010 · PMID 20581827
8 pages
rs1552224 rs5945326 rs11634397 rs231362 rs7957197 rs1470579
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
rs1635501 rs10183486 rs2153157 rs12294104 rs10852344 rs12461110
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs4140885 rs180242 rs17796783 rs17287293 rs11118555 rs13030174
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
UK BiLEVE
Nature communications · 2015 · PMID 26635082 · open access
8 pages
rs6681426 rs61067109 rs6441207 rs6856422 rs148274477 rs12149828

Showing 20 of 35 · 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.