For researchers

Is your paper here?

2,663 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.

26 matches for Tabara Y, showing the first 20.

Interethnic analyses of blood pressure loci in populations of East Asian and European descent
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
rs6590816 rs6712094 rs2270860 rs1004467 rs4684242 rs4980389
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population
European journal of human genetics : EJHG · 2019 · PMID 30659259 · open access
12 pages+
rs2135116 rs4673546 rs61997624 rs2242508 rs774211 rs2538054
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs186568031 rs117267808 rs4711389 rs75536691 rs7787720 rs1955163
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs17205972 rs7596872 rs55940034 rs2303655 rs55897749 rs72934583
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs7063597 rs3752435 rs4317621 rs4731113 rs4674280 rs138245006
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+
rs17105330 rs8079564 rs4813853 rs7015100 rs7522427 rs9907557
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs12789028 rs11466334 rs12555274 rs13094957 rs76675804 rs2056857
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
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
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
Nature genetics · 2011 · PMID 21572416
4 pages
rs35444 rs17249754 rs6825911 Blood Pressure
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
CHARGE Hematology Working Group
Diabetes · 2014 · PMID 24647736 · open access
4 pages
rs11667918 rs1046875 rs3755157 Type 2 Diabetes
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Human molecular genetics · 2014 · PMID 24861553
4 pages
rs2535633 rs11030104 rs574367 rs591166
Genetic determinants and an epistasis of <i>LILRA3</i> and HLA-B*52 in Takayasu arteritis
Proceedings of the National Academy of Sciences of the United States of America · 2018 · PMID 30498034
3 pages
rs1713450 rs4817988 Takayasu Arteritis
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs6011998 rs112407396 rs72485816
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
rs150607032 rs190975828 rs192018195
Meta-analysis identifies common variants associated with body mass index in east Asians
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
2 pages
rs9356744 rs261967
A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2
Human molecular genetics · 2014 · PMID 24105470
2 pages
rs10937273 Adiponectin Levels

Showing 20 of 26 · 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.