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.

16 matches for Parra EJ.

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
rs35255404 rs231889 rs10066990 rs10851885 rs11039221 rs111449836
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+
rs3211938 rs151235402 rs73339979 rs114139997 rs10184673 rs117139027
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs7819706 rs1473781 rs6876198 rs3743140 rs3806155 rs7313668
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+
rs3967200 rs7156625 rs12463674 rs12136856 rs4282339 rs823114
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · open access
12 pages+
rs1123573 rs111837807 rs7528026 rs17713054 rs7949972 rs12046291
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs11466334 rs12555274 rs13094957 rs76675804 rs2056857 rs72802365
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
rs6974288 rs3846663 rs12939051 rs58458113 rs58223766 rs117525671
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs17791513 rs6813195 rs17106184 rs849135 rs2261181 rs9936385
A large Canadian cohort provides insights into the genetic architecture of human hair colour
Communications biology · 2021 · PMID 34737440 · open access
7 pages
rs77381714 rs72932523 rs144104266 rs116895175 rs3940272 rs79912986
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs139120857 rs5942972 rs7063103 rs62603531 rs151113194 rs762517
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Early Growth Genetics Consortium
Human molecular genetics · 2019 · PMID 31504550
5 pages
rs6567160 rs4077678 rs10493544 rs114670539 rs74583214
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
Scientific reports · 2016 · PMID 26780889 · open access
3 pages
rs8102280 rs138534124 rs2238675
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations
BMC genetics · 2019 · PMID 31315583 · open access
3 pages
rs35395 rs10160510 rs112332856
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
HGG advances · 2022 · PMID 35399580 · open access
3 pages
rs9922708 rs3751813 rs6817771
Genome-wide association study of warfarin maintenance dose in a Brazilian sample
Pharmacogenomics · 2015 · PMID 26265036
1 page
rs4918798
Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry
PeerJ · 2017 · PMID 29109912 · open access
1 page
rs76930569

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.