For researchers

Is your paper here?

2,655 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.

14 matches for Soler Artigas M.

New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
rs2544536 rs7098573 rs12627254 rs6533183 rs1102077 rs17009288
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs112481526 rs28455634 rs12672003 rs35306827 rs2336147 rs10866641
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
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Nature genetics · 2025 · PMID 40962958
8 pages
rs4749820 rs4462678 rs9959583 rs4131786 rs1435746 rs7100410
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study
The Lancet. Respiratory medicine · 2019 · PMID 30552067 · open access
7 pages
rs144829310 rs11603634 rs1986009 rs10519068 rs7305461 rs703816
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
6 pages
rs4372354 rs2047409 rs9274600 rs2532349 rs61784651 rs11729080
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs1173771 rs13139571 rs6015450 rs11191548 rs7129220
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality
ADHD Group of the Psychiatric Genomics Consortium, International Cannabis Consortium
Molecular psychiatry · 2020 · PMID 30610198
5 pages
rs113551349 rs797267 rs56319043 rs2782639 ADHD (Attention Deficit Hyperactivity Disorder)
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
rs1036429 rs2798641 rs12447804 rs6903823
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Nature genetics · 2014 · PMID 24929828
4 pages
rs1430193 rs6923462 rs2863171 rs6501431
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
4 pages
rs76857496 rs6537401 rs114142727 rs2311059
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
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
American journal of respiratory and critical care medicine · 2012 · PMID 22837378
1 page
rs8031948
A Genome-Wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos
American journal of respiratory and critical care medicine · 2018 · PMID 29394082
1 page
rs138712481

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.