For researchers

Is your paper here?

2,665 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.

27 matches for Han X, showing the first 20.

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+
rs2277598 rs295322 rs62623713 rs11555762 rs9891146 rs13447324
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
rs4650206 rs8192726 rs3025312 rs17234745 rs7833370 rs6545765
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
rs1727284 rs442467 rs11135030 rs11210887 rs12053870 rs1264322
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
Combined analysis of keratinocyte cancers identifies novel genome-wide loci
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
12 pages+
rs144984465 rs11707807 rs9557210 rs138501911 rs6714430 rs35540156
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Human molecular genetics · 2019 · PMID 31809533
12 pages+
rs787540 rs4858678 rs742127 rs74891390 rs11639803 rs35285683
Using Mendelian randomization to evaluate the causal relationship between serum C-reactive protein levels and age-related macular degeneration
European journal of epidemiology · 2020 · PMID 31900758
12 pages+
rs4788867 rs117211511 rs1353792 rs149523036 rs111435864 rs62491814
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
NEIGHBORHOOD consortium · UK Biobank Eye and Vision Consortium
Nature genetics · 2020 · PMID 31959993
12 pages+
rs2881425 rs17339357 rs66716938 rs4864858 rs75265191 rs56031192
Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study
JAMA ophthalmology · 2020 · PMID 32352494
12 pages+
rs117010584 rs568613 rs144364340 rs11024110 rs2180231 rs3814212
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs9819278 rs2491422 rs62391632 rs66819623 rs8141610 rs56233426
Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging
International Glaucoma Genetics Consortium
JAMA ophthalmology · 2022 · PMID 35446358
12 pages+
rs10137741 rs11142375 rs4849047 rs7585194 rs2910770 rs62283793
Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease
Nature communications · 2022 · PMID 35668104 · open access
12 pages+
rs74178014 rs60376022 rs6845515 rs148325200 rs2415038 rs6078899
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
23andMe Research Team · International Glaucoma Genetics Consortium
Nature genetics · 2023 · PMID 37386247 · open access
12 pages+
rs10139172 rs955934 rs10947614 rs73250939 rs67349114 rs11187315
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Nature genetics · 2018 · PMID 30054594
10 pages
rs12699251 rs10505100 rs61861119 rs73174345 rs11710139 rs9284802
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
23andMe Research team · Esophageal cancer consortium
Gut · 2022 · PMID 34187846 · open access
8 pages
rs2145318 rs2597301 rs1431196 rs2106353 rs761777 rs9372625
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
23andMe Research Team
The Journal of investigative dermatology · 2022 · PMID 34813871
5 pages
rs112761681 rs9322309 rs6737159 rs7943603 rs1888621
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Nature genetics · 2010 · PMID 20081858 · open access
4 pages
rs11920090 rs7944584 rs11605924 Fasting Blood Glucose
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
4 pages
rs10940767 rs4676893 rs7282609 Gastroesophageal Reflux Disease

Showing 20 of 27 · 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.