For researchers

Is your paper here?

3,087 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.

17 matches for Tanabe K.

Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Nature genetics · 2017 · PMID 28604731 · open access
12 pages+
rs541594711 rs55986470 rs371681307 rs28458909 rs755927998 rs72827839
Item-level analyses reveal genetic heterogeneity in neuroticism
Nature communications · 2018 · PMID 29500382 · open access
12 pages+
rs998884 rs7077291 rs10811883 rs3742021 rs2160515 rs1360379
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
23andMe Research Team
Nature genetics · 2018 · PMID 29942085
12 pages+
rs1539844 rs274632 rs2407746 rs2921036 rs11496294 rs9829032
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs28522849 rs4687625 rs56306491 rs1115535 rs11646221 rs41293013
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Nature genetics · 2019 · PMID 30617256
12 pages+
rs10948363 rs9653111 rs183321458 rs539159088 rs11763230 rs7657553
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
12 pages+
rs62264767 rs17643634 rs78206187 rs12912299 rs72657797 rs10800992
Large-scale association analyses identify host factors influencing human gut microbiome composition
Nature genetics · 2021 · PMID 33462485
12 pages+
rs11110281 rs61841503 rs71348714 rs7574352 rs10209482 rs74348118
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs302317 rs77622099 rs619091 rs12652777 rs12476312 rs79445414
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
23andMe Research Team
Nature genetics · 2022 · PMID 35835914
12 pages+
rs17315269 rs77176363 rs7727558 rs729424 rs74743707 rs10488217
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
Nature genetics · 2017 · PMID 28530673 · open access
6 pages
rs36093924 rs7646501 rs10191758 rs12744310 rs12928404 rs16954078
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese
Nature communications · 2019 · PMID 31417091 · open access
6 pages
rs17011903 rs2467146 rs142502288 rs11057071 rs658839 rs7028900
A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine
Genetic Study Group of Investigation Committee on Ossification of the Spinal Ligaments
Nature genetics · 2014 · PMID 25064007
3 pages
rs374810 rs11045000 rs1979679
Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3
PloS one · 2013 · PMID 24023777 · open access
2 pages
rs12946942 Adolescent Idiopathic Scoliosis
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis
American journal of human genetics · 2015 · PMID 26211971
2 pages
rs4637667 Adolescent Idiopathic Scoliosis
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals
Regeneron Genetics Center · UKB Exome Sequencing Consortium
American journal of human genetics · 2021 · PMID 34115965 · open access
2 pages
rs769102632 rs1256764500
Genetic risk factors for COVID-19 and influenza are largely distinct
Colorado Center for Precision Medicine · Mayo Clinic Project Generation and 2 more consortia
Nature genetics · 2024 · PMID 39103650 · open access
1 page
rs2837112
Genome-Wide Association Study of Contrast Media Hypersensitivity in Japanese Patients
International heart journal · 2026 · PMID 42732936
1 page
rs2270190

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.