For researchers

Is your paper here?

2,673 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.

121 matches for Morris A, showing the first 20.

Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
Communications biology · 2022 · PMID 35393509 · open access
2 pages
rs2980766 rs13039863
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Biobank Japan Project
Communications biology · 2024 · PMID 39702642 · open access
2 pages
rs202213319 rs117371763
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Science (New York, N.Y.) · 2007 · PMID 17434869
1 page
Obesity and Body Weight
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
DIAGRAM · MuTHER
Nature genetics · 2011 · PMID 21874001
1 page
rs4812829
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
rs9470794
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
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations
Journal of lipid research · 2017 · PMID 28298293 · open access
1 page
rs10883511
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
iPSYCH-SSI-Broad Group
Nature communications · 2017 · PMID 28537267 · open access
1 page
rs12700667
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
rs60780116
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Understanding Society Scientific Group
Wellcome open research · 2018 · PMID 30175238 · open access
1 page
rs1448044
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes
Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Acta ophthalmologica · 2018 · PMID 30178632 · open access
1 page
rs11018670
Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity
Nutrients · 2018 · PMID 30453627 · open access
1 page
rs9957425
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions
Clinical pharmacology and therapeutics · 2019 · PMID 31066027 · open access
1 page
rs192543598
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
Diabetes · 2020 · PMID 32917775
1 page
rs791600
Blood copper and risk of cardiometabolic diseases: a Mendelian randomization study
Human molecular genetics · 2022 · PMID 34523676 · open access
1 page
rs17564336
Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration
EBioMedicine · 2021 · PMID 34864618 · open access
1 page
rs12678747
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37291194 · open access
1 page
rs60453193

Showing 20 of 121 · page 6 of 7

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.