For researchers

Is your paper here?

2,649 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 Miao X.

Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
Human molecular genetics · 2015 · PMID 25429064
12 pages+
rs2401171 rs7250071 rs11170624 rs16848425 rs12459943 rs611203
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies
Genome medicine · 2024 · PMID 38872215 · open access
12 pages+
rs73039433 rs75128197 rs56270678 rs371061408 rs6507877 rs11213825
Genetic architecture of bone marrow fat fraction implies its involvement in osteoporosis risk
Nature communications · 2025 · PMID 40796918 · open access
12 pages+
rs1962515 rs12025977 rs2378715 rs79260952 rs117210562 rs11712037
Genome-wide association analysis of left ventricular imaging-derived phenotypes identifies 72 risk loci and yields genetic insights into hypertrophic cardiomyopathy
Nature communications · 2023 · PMID 38036550 · open access
7 pages
rs35630683 rs79548216 rs9428227 rs62253183 rs7928419 rs9462210
Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations
Nature genetics · 2011 · PMID 21642993
6 pages
rs11066015 rs10052657 rs10058728 rs8030672 rs2274223 Oesophageal Cancer
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions
Nature genetics · 2012 · PMID 22960999
3 pages
rs4822983 rs4785204 Oesophageal Cancer
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Gut · 2017 · PMID 26701879 · open access
3 pages
rs80142782 rs13361707 Non-Cardia Gastric Cancer
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease
Proceedings of the National Academy of Sciences of the United States of America · 2009 · PMID 19196962
2 pages
rs2742234 Hirschsprung Disease
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Human molecular genetics · 2010 · PMID 20460270
2 pages
rs17095355 Biliary Atresia
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations
Nature genetics · 2011 · PMID 22158540
2 pages
rs372883 Pancreatic Cancer
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
American journal of human genetics · 2012 · PMID 23103227
2 pages
rs2494938 rs2285947
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
Identification of specific susceptibility loci for the early-onset colorectal cancer
Genome medicine · 2023 · PMID 36869385 · open access
2 pages
rs138234416 rs13197175
A genome wide association study identifies common variants associated with lipid levels in the Chinese population
PloS one · 2013 · PMID 24386095 · open access
1 page
rs2043085

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.