For researchers

Is your paper here?

2,661 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.

90 matches for Field J, showing the first 20.

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs57737646 rs7315236 rs699465 rs10414501 rs77951490 rs78863347
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10180829 rs10071837 rs4899520 rs75823898 rs112226333 rs2553033
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs759831202 rs952170 rs11167778 rs1338668 rs749804194 rs9976784
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs227756 rs2277886 rs2524074 rs2609334 rs3743369 rs507903
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs10813745 rs587204 rs655559 rs4963744 rs61875182 rs10185713
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
rs67507374 rs62523081 rs11925442 rs138917529 rs721156 rs11767259
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18587394
11 pages
rs3764147 rs2301436 rs9286879 rs1551398 rs7927894 rs11175593
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
11 pages
rs11154801 rs12212193 rs7522462 rs9282641 rs10466829 rs2119704
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
11 pages
rs62105306 rs17057164 rs149352150 rs56330886 rs112778462 rs378854
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Alcohol Genome-wide Association (AlcGen) Consortium · Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study and 5 more consortia
Nature genetics · 2011 · PMID 22001757
9 pages
rs13030978 rs6834314 rs2954021 rs1976403 rs1883415 rs7923609
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Nature human behaviour · 2019 · PMID 31358974
9 pages
rs2277499 rs10496076 rs71414193 rs57281063 rs227179 rs4794015
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
rs17287293 rs11118555 rs13030174 rs826838 rs11578508 rs4140885
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
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
rs5931180 rs12382607 rs4328011 rs139036121 rs5933079 rs181497961
Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits
BMC medical genetics · 2011 · PMID 21943158 · open access
7 pages
rs10199768 rs1803274 rs4698036 rs17091905 rs11754288 rs508487
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
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
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
6 pages
rs1526692 rs719700 rs1410656 rs13107347 rs17767445 Vitamin D Deficiency and the GC Gene
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
Frontiers of medicine · 2021 · PMID 32889700
6 pages
rs465498 rs1200399 rs2517873 rs4573350 rs1264308 rs17038564

Showing 20 of 90 · page 2 of 5

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.