For researchers

Is your paper here?

2,677 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.

62 matches for Nakamura Y, showing the first 20.

Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count
Human molecular genetics · 2010 · PMID 20172861
1 page
rs2072910
A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese
Nature genetics · 2010 · PMID 20601957
1 page
rs10965235
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population
Nature genetics · 2010 · PMID 20711176
1 page
rs873549
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations
Nature genetics · 2010 · PMID 20871597
1 page
rs2736100
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population
Human molecular genetics · 2010 · PMID 20876614
1 page
rs2131877
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus
Human molecular genetics · 2011 · PMID 21196492
1 page
rs2097677
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population
Human Disease Genomics Working Group · RA Clinical and Genetic Study Consortium
Human molecular genetics · 2011 · PMID 21505073
1 page
rs2075876
HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease
Gastroenterology · 2011 · PMID 21699788
1 page
rs2006996
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese
Human molecular genetics · 2012 · PMID 22180457
1 page
rs10509373
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese
PLoS genetics · 2012 · PMID 22291604 · open access
1 page
rs340630
Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese
PloS one · 2012 · PMID 22558069 · open access
1 page
rs4985726
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene
Psychiatric genetics · 2013 · PMID 23142968
1 page
rs7527939
Genome-wide association study of breast cancer in the Japanese population
PloS one · 2013 · PMID 24143190 · open access
1 page
rs12922061
Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics
The Journal of allergy and clinical immunology · 2014 · PMID 24280104
1 page
rs10411428
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
Aneurysm Consortium; Vascular Research Consortium of New Zealand
Journal of the American Heart Association · 2016 · PMID 27418160 · open access
1 page
rs595244
SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway
Breast cancer research and treatment · 2017 · PMID 28429243
1 page
rs2900478
A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study
Scientific reports · 2018 · PMID 29367735 · open access
1 page
rs144504271
Genomewide Association Study of Leisure-Time Exercise Behavior in Japanese Adults
Medicine and science in sports and exercise · 2018 · PMID 30102679 · open access
1 page
rs10252228
Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21
Cancer science · 2018 · PMID 30281874 · open access
1 page
rs7849280

Showing 20 of 62 · page 3 of 4

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.