For researchers

Is your paper here?

2,662 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.

153 matches for Martin NG, showing the first 20.

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
rs56288844 rs149520992 rs6987444 rs2852151 rs9385532 rs12083537
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
rs231889 rs10066990 rs10851885 rs11039221 rs111449836 rs12722725
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
rs7841320 rs10028756 rs9557376 rs3846449 rs4650206 rs8192726
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+
rs1727284 rs442467 rs11135030 rs11210887 rs12053870 rs1264322
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci
23andMe Research Team
Nature communications · 2019 · PMID 30837455 · open access
12 pages+
rs12232497 rs11710258 rs8058904 rs4683148 rs62351974 rs73156502
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs1543238 rs4940525 rs2976178 rs1268176 rs3774726 rs9879531
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs57737646 rs7315236 rs699465 rs10414501 rs77951490 rs78863347
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
12 pages+
rs11246003 rs7412010 rs149934734 rs35417544 rs62323682 rs4821939
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
NEIGHBORHOOD consortium · UK Biobank Eye and Vision Consortium
Nature genetics · 2020 · PMID 31959993
12 pages+
rs2881425 rs17339357 rs66716938 rs4864858 rs75265191 rs56031192
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs2358483 rs149142 rs78155705 rs62005276 rs639016 rs34322452
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · open access
12 pages+
rs7959830 rs4083463 rs13050142 rs7657200 rs4887113 rs7004112
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Nature communications · 2020 · PMID 32242144 · open access
12 pages+
rs72997623 rs11732896 rs12794714 rs8121940 rs10832254 rs12278461
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
rs747657 rs2273699 rs7533482 rs75883022 rs79356439 rs72834823
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs6667536 rs12540035 rs9819278 rs2491422 rs62391632 rs66819623
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression
23andMe Research Team
Nature human behaviour · 2021 · PMID 33859377
12 pages+
rs17708090 rs10821130 rs1554269 rs10193760 rs72813408 rs7567451
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs2336147 rs10866641 rs67712855 rs748455 rs78308718 rs6875495
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs41272475 rs2844466 rs140353819 rs540836853 rs2736609 rs9438982
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs202219817 rs35499210 rs759831202 rs952170 rs11167778 rs1338668
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs4483592 rs1947066 rs144839021 rs1625595 rs197439 rs68049022
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs12566345 rs1921907 rs210280 rs4696931 rs6727028 rs7070947

Showing 20 of 153 · page 2 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.