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.

12 matches for Granell R.

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
12 pages+
rs167769 rs17637472 rs2855812 rs1420101 rs2952156 rs17806299
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
rs11644510 rs34004019 rs12939457 rs12509403 rs62257549 rs11677002
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct
23andMe Research Team · eQTLGen Consortium and 1 more consortia
American journal of human genetics · 2019 · PMID 30929738
12 pages+
rs3122929 rs62623446 rs1612986 rs4491851 rs117097909 rs1861245
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
rs4337253 rs62321845 rs57380671 rs227728 rs9600261 rs6806825
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
Australian Asthma Genetics Consortium Collaborators
The Journal of allergy and clinical immunology · 2014 · PMID 24388013
8 pages
rs4833095 rs1438673 rs10197862 rs1837253 rs72699186 rs17294280
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
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
AAGC
Nature genetics · 2013 · PMID 23817571
7 pages
rs6906021 rs3771175 rs17616434 rs17454584 rs1059513 rs6932730
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
7 pages
rs7559046 rs7521390 rs73739621 rs2918302 rs3017289 rs61907712
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 study identifies five loci associated with lung function
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
3 pages
rs12899618 rs10516526 rs12504628
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants
EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium
The Journal of allergy and clinical immunology · 2014 · PMID 24315451
3 pages
rs3751972 rs2016444 rs12500579
Genome-wide association study of preserved ratio impaired spirometry (PRISm)
The European respiratory journal · 2024 · PMID 38097206 · open access
3 pages
rs1233604 rs11623779 rs9649071

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.