For researchers

Is your paper here?

2,671 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.

32 matches for Le N, showing the first 20.

Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor
Testicular Cancer Consortium
Nature genetics · 2017 · PMID 28604732 · open access
12 pages+
rs3755605 rs55873183 rs61408740 rs12912292 rs60180747 rs58521262
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Nature genetics · 2019 · PMID 30617256
12 pages+
rs150820726 rs141864196 rs10948363 rs9653111 rs183321458 rs539159088
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
rs7806224 rs7948789 rs80032242 rs9423279 rs10044618 rs10233018
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs76181804 rs9290877 rs9594366 rs16856530 rs62283809 rs10854002
Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk
International journal of molecular sciences · 2023 · PMID 37108169 · open access
12 pages+
rs13358188 rs146072725 rs17587821 rs188290902 rs189257688 rs554596237
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs12113633 rs62169409 rs4140952 rs7629500 rs61758556 rs240471
A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer
BMC cancer · 2019 · PMID 30738427 · open access
10 pages
rs2327990 rs7582977 rs13402783 rs11692570 rs1372330 rs17082301
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
9 pages
rs1400482 rs1879586 rs7207826 rs11651755 rs688187 rs7902587
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility
Nature communications · 2015 · PMID 25903422 · open access
7 pages
rs12564022 rs7769061 rs34394770 rs8128234 rs7709212 rs3747517
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
rs1656404 rs4793501 rs10882165 rs17183295 rs11145465 Myopia
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
ABCTB Investigators · AOCS Study Group & Australian Cancer Study (Ovarian Cancer) and 5 more consortia
Cancer discovery · 2016 · PMID 27432226
6 pages
rs2628317 rs17762342 rs739704 rs3802173 rs1469713 rs9657608
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs1173771 rs13139571 rs6015450 rs11191548 rs7129220
Unraveling shared susceptibility loci and Mendelian genetic associations linking educational attainment with multiple neuropsychiatric disorders
Frontiers in psychiatry · 2023 · PMID 38250258 · open access
5 pages
rs35926495 rs76025409 rs73073015 rs4839923 rs1879581
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
4 pages
rs1746048 rs6725887 rs1122608 Coronary Artery Disease
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
CHARGE Hematology Working Group
Diabetes · 2014 · PMID 24647736 · open access
4 pages
rs11667918 rs1046875 rs3755157 Type 2 Diabetes
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals
Communications biology · 2019 · PMID 30993211 · open access
4 pages
rs16856823 rs4966024 rs11202346 rs1549287
Multiple newly identified loci associated with prostate cancer susceptibility
UK Genetic Prostate Cancer Study Collaborators · British Association of Urological Surgeons' Section of Oncology and 1 more consortia
Nature genetics · 2008 · PMID 18264097
3 pages
rs2660753 rs9364554 rs7931342
Two common single nucleotide polymorphisms in the gene encoding beta-carotene 15,15'-monoxygenase alter beta-carotene metabolism in female volunteers
FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2009 · PMID 19103647
3 pages
rs7501331 rs12934922 Vitamin A (beta-carotene conversion)
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542

Showing 20 of 32 · page 1 of 2

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.