For researchers

Is your paper here?

2,681 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.

147 matches for To J, showing the first 20.

A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants
Diabetes Research on Patient Stratification (DIRECT)
Diabetes · 2017 · PMID 28490609 · open access
2 pages
rs1401735 rs1135314
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
rs17737404 rs11257600
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
kConFab Investigators · ABCTB Investigators and 2 more consortia
Nature genetics · 2020 · PMID 32424353 · open access
2 pages
rs17743054 rs11065822
Genome-wide association study identifies novel breast cancer susceptibility loci
SEARCH collaborators · kConFab and 1 more consortia
Nature · 2007 · PMID 17529967
1 page
rs3817198
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
CORGI Consortium · EPICOLON Consortium
Nature genetics · 2008 · PMID 18372905
1 page
rs16892766
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
1 page
rs10838738
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels
Human molecular genetics · 2010 · PMID 20167578
1 page
rs3093030
C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies
Blood · 2010 · PMID 20212171
1 page
rs3813948
Genome-wide association study of HPV seropositivity
Human molecular genetics · 2011 · PMID 21896673
1 page
rs9357152
Genetic determinants of serum testosterone concentrations in men
EMAS Study Group
PLoS genetics · 2011 · PMID 21998597 · open access
1 page
rs12150660
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Nature genetics · 2011 · PMID 22037553
1 page
rs10069690
A genome-wide association study of the Protein C anticoagulant pathway
PloS one · 2011 · PMID 22216198 · open access
1 page
rs867186
A genome-wide association search for type 2 diabetes genes in African Americans
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
rs7560163
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
MAGIC · DIAGRAM Consortium and 1 more consortia
PLoS genetics · 2012 · PMID 22693455 · open access
1 page
rs3802177
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study and 1 more consortia
Human molecular genetics · 2012 · PMID 22976474
1 page
rs9383938
Genome-wide association study of age at menarche in African-American women
Human molecular genetics · 2013 · PMID 23599027
1 page
rs10441737
Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes
FIND Consortium · FinnDiane Study Group and the GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2013 · PMID 24029427
1 page
rs4972593
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nature genetics · 2016 · PMID 27064256
1 page
rs3739821
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Age at Menarche

Showing 20 of 147 · page 7 of 8

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.