For researchers

Is your paper here?

2,657 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 Hosono N.

Genome-wide association study of hematological and biochemical traits in a Japanese population
Nature genetics · 2010 · PMID 20139978
12 pages+
rs7775698 rs2236496 rs2858942 rs2279434 rs11966072 rs11204538
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
Human molecular genetics · 2010 · PMID 20189936
5 pages
rs7833986 rs9825379 rs7571816 rs5742692 rs7678436
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
PLoS genetics · 2011 · PMID 21738478 · open access
5 pages
rs11018874 rs9373124 rs12988934 rs2516399 rs7275212
A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population
Gastroenterology · 2013 · PMID 23266558
4 pages
rs1487630 rs7765379 rs6478106 rs11894081
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population
Nature genetics · 2010 · PMID 20676098
2 pages
rs339331 rs9600079
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids
Nature genetics · 2011 · PMID 21460842
2 pages
rs12484776 Uterine Fibroids
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population
Human molecular genetics · 2011 · PMID 21750111
2 pages
rs3077 Chronic Hepatitis B
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations
GIANT consortium
Nature genetics · 2012 · PMID 22344221
2 pages
rs12149832 rs11671664
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 genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population
Nature genetics · 2009 · PMID 19915573
1 page
rs9263739
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 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
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
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

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.