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.

31 matches for Ho MH, showing the first 20.

A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry
ECLIPSE Investigators · COPDGene Investigators
BMC genetics · 2015 · PMID 26634245 · open access
12 pages+
rs28381684 rs6842889 rs737693 rs72983513 rs34684276 rs1813903
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
rs7095607 rs7872188 rs10515750 rs113745635 rs11658500 rs1458979
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
Nature communications · 2018 · PMID 30061609 · open access
12 pages+
rs252746 rs143246821 rs916888 rs963406 rs79294353 rs111898810
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+
rs12811814 rs6539952 rs12945803 rs4952564 rs4721442 rs2304340
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
SpiroMeta Consortium · International COPD Genetics Consortium
Nature genetics · 2019 · PMID 30804561 · open access
12 pages+
rs629619 rs72626215 rs35584079 rs12466981 rs4523894 rs9273404
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs2296740 rs2371340 rs403407 rs4953150 rs56357145 rs7960340
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+
rs62454414 rs6541092 rs661857 rs2967516 rs17160476 rs6667222
Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models
Nature genetics · 2023 · PMID 37069358
12 pages+
rs326479 rs62191107 rs11607392 rs2896630 rs9562541 rs13101469
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
Nature genetics · 2026 · PMID 41565855
12 pages+
rs924150 rs8089099 rs4791806 rs41522747 rs340121 rs2609260
Genome-Wide Gene-by-Smoking Interaction Study of Chronic Obstructive Pulmonary Disease
American journal of epidemiology · 2021 · PMID 33106845
6 pages
rs4973115 rs12519165 rs9605481 rs11727524 rs57062879 rs979453
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians
American journal of human genetics · 2013 · PMID 23273568
5 pages
rs6705628 rs4852324 rs6804441 rs34330 rs729302
Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns
COPDGene Investigators
American journal of respiratory and critical care medicine · 2014 · PMID 25006744
5 pages
rs17486278 rs17368659 rs56113850 rs379123 rs11852372
Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution
COPDGene and ECLIPSE Investigators
American journal of respiratory and critical care medicine · 2017 · PMID 27669027
4 pages
rs138544659 rs2645694 rs75755010 rs35374984
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease
American journal of physiology. Lung cellular and molecular physiology · 2021 · PMID 33909500
4 pages
rs2523989 rs11938093 rs13195509 rs11155242
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis
NETT Genetics, ICGN, ECLIPSE and COPDGene Investigators
The Lancet. Respiratory medicine · 2014 · PMID 24621683
3 pages
rs4416442 rs4846480 Chronic Obstructive Pulmonary Disease (COPD)
A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes
NETT Genetics, ECLIPSE, and COPDGene Investigators
American journal of respiratory and critical care medicine · 2015 · PMID 26030696
3 pages
rs55676755 rs75200691 rs74834049
A genome-wide analysis of the response to inhaled β2-agonists in chronic obstructive pulmonary disease
ECLIPSE and COPDGene Investigators · COPDGene Investigators—clinical centers
The pharmacogenomics journal · 2016 · PMID 26503814 · open access
3 pages
rs140948272 rs114132812 rs10056066
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
COPDGene Investigators · ECLIPSE Investigators and 5 more consortia
Nature genetics · 2017 · PMID 28166215
3 pages
rs17035917 rs17707300 rs11727735
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
rs11863726 rs2562181 rs35837297
Genome-wide association study of preserved ratio impaired spirometry (PRISm)
The European respiratory journal · 2024 · PMID 38097206 · open access
3 pages
rs11623779 rs9649071 rs1233604

Showing 20 of 31 · 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.