For researchers

Is your paper here?

2,651 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.

13 matches for Gulcher JR.

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 pages
rs12526453 rs17114036 rs3798220 rs3825807 rs1231206 rs12936587
Genetic correction of PSA values using sequence variants associated with PSA levels
Science translational medicine · 2010 · PMID 21160077
4 pages
rs401681 rs17632542 rs10788160 rs11067228
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Nature genetics · 2008 · PMID 18264098
3 pages
rs5945572 rs721048 Prostate Cancer
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Nature genetics · 2009 · PMID 19767754
3 pages
rs16902094 rs8102476 rs11228565
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Nature genetics · 2012 · PMID 22267200
3 pages
rs2439302 rs116909374 Thyroid Cancer
Variants conferring risk of atrial fibrillation on chromosome 4q25
Nature · 2007 · PMID 17603472
2 pages
rs10033464 Atrial Fibrillation
Multiple genetic loci for bone mineral density and fractures
The New England journal of medicine · 2008 · PMID 18445777
2 pages
rs4870044 Spine Bone Mineral Density
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
Nature genetics · 2009 · PMID 19198613
2 pages
rs944289 Thyroid Cancer
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia
A genetic risk factor for periodic limb movements in sleep
The New England journal of medicine · 2007 · PMID 17634447
1 page
rs3923809
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Nature · 2008 · PMID 18385739
1 page
Lung Cancer
New sequence variants associated with bone mineral density
Nature genetics · 2009 · PMID 19079262
1 page
rs1038304
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
rs4105144

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.