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.

23 matches for McMahon G, showing the first 20.

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
rs2274465 rs6747380 rs6758290 rs4369815 rs17236969 rs17233066
Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs56044892 rs12410444 rs12754946 rs1008078 rs17372140 rs78365243
Genome-wide associations for birth weight and correlations with adult disease
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
rs35261542 rs28510415 rs700059 rs3753639 rs62466330 rs6016377
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+
rs1173470 rs1956589 rs10805858 rs10821523 rs12878369 rs2184513
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
rs10853531 rs11145488 rs12511037 rs1649081 rs16949788 rs10089517
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
10 pages
rs6440008 rs10960765 rs58979150 rs11041426 rs72917317 rs10899501
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
rs2506142 rs4081947 rs6791480 rs6693567 rs10155855 rs10218452
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Bone Mineral Density in Childhood Study (BMDCS) · Early Genetics and Lifecourse Epidemiology (EAGLE) consortium and 2 more consortia
Human molecular genetics · 2016 · PMID 26604143
8 pages
rs12041852 rs13253111 rs13387838 rs17024393 rs3829849 rs7550711
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 association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
23andMe Research Team
Human molecular genetics · 2018 · PMID 29659830 · open access
5 pages
rs4927012 rs12474669 rs847158 rs10790969 rs1080014
Genome-wide association study identifies loci affecting blood copper, selenium and zinc
Human molecular genetics · 2013 · PMID 23720494
4 pages
rs1175550 rs2769264 rs2120019 Zinc
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci
Nature genetics · 2013 · PMID 23817569 · open access
4 pages
rs10497813 rs17388568 rs7720838 rs6021270
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
4 pages
rs1487441 rs9858213 rs13401104 rs3789044
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
rs4851266 rs9320913 rs1056667
Genome-wide meta-analysis identifies new susceptibility loci for migraine
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
rs11759769 rs12134493 rs4379368
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
3 pages
rs6885307 rs2347867 rs2721195
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
rs9811920 rs12193446
Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position
American journal of human genetics · 2012 · PMID 22341974
1 page
rs7559271
Common variants at 12q15 and 12q24 are associated with infant head circumference
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
rs1042725
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans
Molecular vision · 2013 · PMID 23401653 · open access
1 page
rs17084051

Showing 20 of 23 · 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.