For researchers

Is your paper here?

2,685 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.

662 matches for Er J, showing the first 20.

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
8 pages
rs7953528 rs163879 rs1864325 rs7084921 rs344081 rs3905706
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs4140885 rs180242 rs17796783 rs17287293 rs11118555 rs13030174
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease
The American journal of clinical nutrition · 2013 · PMID 23824729
8 pages
rs2275565 rs7130284 rs154657 rs234709 rs548987 rs12780845
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
Australian Asthma Genetics Consortium Collaborators
The Journal of allergy and clinical immunology · 2014 · PMID 24388013
8 pages
rs4833095 rs1438673 rs10197862 rs1837253 rs72699186 rs17294280
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Bone Mineral Density in Childhood Study (BMDCS) · Early Genetics and Lifecourse Epidemiology (EAGLE) consortium and 2 more consortia
Human molecular genetics · 2016 · PMID 26604143
8 pages
rs12041852 rs13253111 rs13387838 rs17024393 rs3829849 rs7550711
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
SUMMIT Consortium · BioBank Japan Project
American journal of human genetics · 2016 · PMID 27588450 · open access
8 pages
rs35716097 rs5020545 rs62435145 rs57989581 rs8096658 rs1511299
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
PLoS genetics · 2017 · PMID 28498854 · open access
8 pages
rs115795127 rs7651190 rs11563582 rs62434120 rs113866309 rs76987554
Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants
Nature communications · 2017 · PMID 28537254 · open access
8 pages
rs12118303 rs118086960 rs559406 rs34517439 rs2944542 rs61871342
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 1 more consortia
Nature genetics · 2019 · PMID 30478444
8 pages
rs11591402 rs1427829 rs3001723 rs1592757 rs4275621 rs2243517
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
INVENT Consortium; MEGASTROKE Consortium of the International Stroke Genetics Consortium (ISGC)
Circulation · 2019 · PMID 30586737
8 pages
rs58204830 rs7135039 rs35458154 rs2238109 rs9390460 rs55954186
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology
INVENT Consortium · MEGASTROKE Consortium of the International Stroke Genetics Consortium
Blood · 2019 · PMID 30642921
8 pages
rs1755685 rs7946992 rs10761784 rs7935829 rs569557 rs2480952
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
rs79624003 rs55809639 rs4847240 rs4660303 rs7298909 rs56204645
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
8 pages
rs12012576 rs6527977 rs139120857 rs5942972 rs7063103 rs62603531
Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample
The American journal of psychiatry · 2023 · PMID 37282553
8 pages
rs28470433 rs13130101 rs35942385 rs13146907 rs144228648 rs147759217
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs12382607 rs4328011 rs139036121 rs5933079 rs181497961 rs111410539
Human milk oligosaccharides are associated with maternal genetics and respiratory health of human milk-fed children
Nature communications · 2024 · PMID 39232002 · open access
8 pages
rs73061656 rs485186 rs546308 rs16982241 rs1132054 rs4015
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 pages
rs12526453 rs17114036 rs3798220 rs3825807 rs1231206 rs12936587
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
Diabetes · 2011 · PMID 21386085 · open access
7 pages
rs173539 rs11820589 rs301 rs11823543 rs2954033 rs1919128
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource and 3 more consortia
Nature genetics · 2013 · PMID 23535732
7 pages
rs3850699 rs1894292 rs2273669 rs1270884 rs11650494 rs1218582

Showing 20 of 662 · page 10 of 34

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.