For researchers

Is your paper here?

2,682 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.

47 matches for Hu Y, showing the first 20.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
rs10182181 rs1412239 rs1421085 rs538656 rs1514177 rs3101336
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+
rs13072744 rs3755206 rs3771381 rs1865760 rs11970475 rs10448080
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci
Human molecular genetics · 2017 · PMID 28199695 · open access
12 pages+
rs149082847 rs35488337 rs6673928 rs1127348 rs971891 rs34119525
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Human molecular genetics · 2017 · PMID 28334899
12 pages+
rs2188380 rs2144300 rs11984636 rs3786247 rs11208004 rs2244608
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs5758651 rs34149579 rs12236219 rs284860 rs1131877 rs2277598
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
12 pages+
rs755157567 rs374450628 rs2540913 rs17052130 rs534057083 rs149371331
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
Blood Cell Consortium
BMC genomics · 2021 · PMID 34107879 · open access
12 pages+
rs9659479 rs2768762 rs11240092 rs28873209 rs11264765 rs16848876
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology
NeuroImage · 2021 · PMID 34560273
12 pages+
rs10508465 rs12621130 rs12666168 rs4272702 rs56192920 rs10118690
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
Nature genetics · 2022 · PMID 35710981
12 pages+
rs9295131 rs10462068 rs12222671 rs1274653 rs17512836 rs62088028
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+
rs72818736 rs181112261 rs77572134 rs7728240 rs6117251 rs73039433
Genetic architecture of bone marrow fat fraction implies its involvement in osteoporosis risk
Nature communications · 2025 · PMID 40796918 · open access
12 pages+
rs79260952 rs12195627 rs117210562 rs11712037 rs10753536 rs10761756
Cross-ancestry analysis of gestational diabetes mellitus identifies novel loci, drug targets and biological pathways
Frontiers in endocrinology · 2026 · PMID 42109742 · open access
12 pages+
rs78020513 rs117423971 rs9350269 rs11738345 rs141621067 rs112667651
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person
Nature communications · 2016 · PMID 26835600 · open access
10 pages
rs9479402 rs12736689 rs55694368 rs12927162 rs12965577 rs11545787
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs9505301 rs9818981 rs2410767 rs10439607 rs10217651 rs35200015
Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects
PLoS genetics · 2012 · PMID 23028341 · open access
8 pages
rs2071278 rs3763317 rs241428 rs11575839 rs2857009 rs3753394
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
8 pages
rs62250980 rs7928419 rs9462210 rs117742247 rs35630683 rs79548216
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Brain : a journal of neurology · 2022 · PMID 35511193 · open access
6 pages
rs3744027 rs6503417 rs12149643 rs73191849 rs13403122 Cerebral Small Vessel Disease

Showing 20 of 47 · page 1 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.