For researchers

Is your paper here?

2,671 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.

145 matches for He G, showing the first 20.

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
International IBD Genetics Consortium (IIBDGC)
Nature · 2012 · PMID 23128233 · open access
12 pages+
rs2823286 rs10486483 rs16967103 rs2945412 rs10065637 rs483905
Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs9993613 rs3020418 rs3767627 rs7692995 rs17556750 rs9392918
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
rs6026748 rs11128722 rs6891344 rs6271 rs2493134 rs12940887
The effect of host genetics on the gut microbiome
Nature genetics · 2016 · PMID 27694959
12 pages+
rs11606643 rs199545687 rs10969143 rs12137699 rs16913594 rs1889714
Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota
Nature genetics · 2016 · PMID 27723756
12 pages+
rs11877825 rs938295 rs13096731 rs9831278 rs35275482 rs11915634
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
NEIGHBORHOOD Consortium
Human molecular genetics · 2017 · PMID 28073927
12 pages+
rs2487048 rs6107845 rs2157719 rs114503346 rs10753787 rs72759609
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
American journal of human genetics · 2017 · PMID 28757204
12 pages+
rs4423214 rs3819817 rs117865811 rs116970203 rs117300835 rs2277458
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Nature genetics · 2017 · PMID 28991256
12 pages+
rs13261217 rs2381759 rs61041384 rs6846161 rs10510653 rs2383377
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease
Circulation research · 2018 · PMID 29212778 · open access
12 pages+
rs17114046 rs61848342 rs944172 rs7116641 rs11637783 rs17612693
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Nature communications · 2018 · PMID 29773799 · open access
12 pages+
rs9393800 rs707938 rs1799949 rs291269 rs1516883 rs144048300
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Profile Study · Australian Prostate Cancer BioResource (APCB) and 7 more consortia
Nature genetics · 2018 · PMID 29892016
12 pages+
rs11135910 rs11691517 rs17321482 rs76551843 rs2427345 rs6091758
Elucidating the genetic basis of social interaction and isolation
Nature communications · 2018 · PMID 29970889 · open access
12 pages+
rs74338595 rs10992800 rs12472555 rs111610257 rs36030660 rs139920
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
Alzheimer’s Disease Neuroimaging Initiative · Pediatric Imaging, Neurocognition and Genetics Study
Molecular psychiatry · 2020 · PMID 30279459 · open access
12 pages+
rs58499557 rs6675690 rs1861979 rs57246240 rs12218858 rs1419859
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+
rs12195240 rs7809303 rs4674916 rs35375873 rs378421 rs10490159
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+
rs7806224 rs7948789 rs80032242 rs9423279 rs10044618 rs10233018
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs1080066 rs73313052 rs9375477 rs117461235 rs68175985 rs71471500
Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma
Nature communications · 2020 · PMID 32296059 · open access
12 pages+
rs56375023 rs10912564 rs2066844 rs72833417 rs13077048 rs4842921
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
rs75570604 rs55797833 rs10873172 rs32578 rs72930659 rs4904871
The Genetic Makeup of the Electrocardiogram
Cell systems · 2020 · PMID 32916098
12 pages+
rs11665344 rs61367953 rs1200130 rs1088450 rs12652726 rs73195040
The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study
Communications biology · 2020 · PMID 33097823 · open access
12 pages+
rs61812150 rs67551338 rs244711 rs117543413 rs55838622 rs8019890

Showing 20 of 145 · page 1 of 8

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.