For researchers

Is your paper here?

2,662 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.

44 matches for Ma H, showing the first 20.

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels
Nature communications · 2015 · PMID 26068415
3 pages
rs12297049 rs2540641 rs16844839
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 study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Nature communications · 2016 · PMID 27005778 · open access
3 pages
rs74249229 rs73066442 rs2921604
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma
Nature communications · 2016 · PMID 27501781 · open access
3 pages
rs7216064 rs2495239 EGFR Mutation-Positive Lung Adenocarcinoma
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
Eurogout Consortium · Eurogout Consortium
Annals of the rheumatic diseases · 2017 · PMID 27899376 · open access
3 pages
rs4766566 rs11758351 rs1871744
Development and evaluation of a polygenic risk score for lung cancer in never-smoking women: A large-scale prospective Chinese cohort study
International journal of cancer · 2024 · PMID 37846649
3 pages
rs11928222 rs9275164 rs11196063
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
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
rs12296850 Lung Squamous Cell Carcinoma
Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians
Human molecular genetics · 2014 · PMID 25035420
2 pages
rs2483280 rs7433306
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788
Twelve Loci Associated With Bone Density in Middle-aged and Elderly Chinese: The Shanghai Changfeng Study
The Journal of clinical endocrinology and metabolism · 2023 · PMID 36228083
2 pages
rs422623 rs17522056
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Nature genetics · 2011 · PMID 21725308
1 page
rs753955
Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review
Gastroenterology · 2012 · PMID 22001864
1 page
Crohn's Disease
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Lancet (London, England) · 2012 · PMID 22607825 · open access
1 page
Cholesterol (LDL, HDL and Total)
Common variants on chromosome 9p21 are associated with normal tension glaucoma
PloS one · 2012 · PMID 22792221 · open access
1 page
rs523096
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations
Nature genetics · 2013 · PMID 23708190
1 page
rs1531070
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
Splicing variant of <i>WDFY4</i> augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis
Annals of the rheumatic diseases · 2018 · PMID 29331962
1 page
rs7919656
A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia
Journal of human genetics · 2018 · PMID 30266950
1 page
rs10988217

Showing 20 of 44 · page 2 of 3

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.