For researchers

Is your paper here?

2,676 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.

43 matches for Davey Smith G, showing the first 20.

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
Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure
International Consortium for Blood Pressure
American journal of human genetics · 2018 · PMID 30220432
12 pages+
rs12727980 rs6750228 rs183131780 rs35924503 rs6768627 rs112607182
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
rs9366778 rs10734564 rs10221267 rs1724889 rs2168443 rs4579095
Evidence for causal effects of lifetime smoking on risk for depression and schizophrenia: a Mendelian randomisation study
Psychological medicine · 2020 · PMID 31689377 · open access
12 pages+
rs112282219 rs317021 rs13153393 rs421983 rs11948770 rs10282292
Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis
PLoS medicine · 2020 · PMID 32203549 · open access
12 pages+
rs75225803 rs838777 rs13042367 rs17008972 rs28567061 rs9943778
Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study
BMJ (Clinical research ed.) · 2020 · PMID 32376654 · open access
12 pages+
rs61971082 rs661878 rs9477762 rs28629903 rs2246623 rs8048855
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
Nature communications · 2020 · PMID 32769997 · open access
12 pages+
rs6721104 rs10186921 rs62174422 rs6717283 rs4571283 rs77994712
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs139689864 rs117008454 rs8104447 rs55861089 rs17860955 rs176694
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs187207161 rs767105335 rs77357563 rs2306899 rs2273171 rs4846567
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
arcOGEN Consortium · HUNT All-In Pain and 2 more consortia
Cell · 2021 · PMID 34450027 · open access
12 pages+
rs747952496 rs3993110 rs781661531 rs7967762 rs10842226 rs116112221
Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation
PLoS biology · 2022 · PMID 35213538 · open access
12 pages+
rs614944 rs116598794 rs12067569 rs34034398 rs545103933 rs143387210
The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture
Human molecular genetics · 2025 · PMID 39574169 · open access
12 pages+
rs17083097 rs2322967 rs56101873 rs6811457 rs1927629 rs56115627
Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collective
Human molecular genetics · 2025 · PMID 41075272 · open access
12 pages+
rs2210119 rs72823645 rs79482068 rs2600519 rs10483604 rs13385292
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs9505301 rs9818981 rs2410767 rs10439607 rs10217651 rs35200015
The identification of distinct protective and susceptibility mechanisms for hip osteoarthritis: findings from a genome-wide association study meta-analysis of minimum joint space width and Mendelian randomisation cluster analyses
EBioMedicine · 2023 · PMID 37619450 · open access
10 pages
rs12511230 rs34687269 rs10933424 rs7711053 rs34717890 rs61648765
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Nature genetics · 2025 · PMID 40962958
9 pages
rs7708883 rs4462678 rs9959583 rs4131786 rs1435746 rs7100410
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances
Human molecular genetics · 2013 · PMID 23704328 · open access
8 pages
rs1799922 rs10740993 rs997154 rs1994969 rs11796357 rs4937076
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment
PLoS genetics · 2014 · PMID 24945404 · open access
7 pages
rs2450083 rs3920498 rs7776725 rs17536328 rs2235529 rs798943
Whole-genome sequence-based analysis of thyroid function
UK0K Consortium
Nature communications · 2015 · PMID 25743335 · open access
7 pages
rs12410532 rs310763 rs6923866 rs3008034 rs112817873 rs11103377

Showing 20 of 43 · page 1 of 3

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.