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.

18 matches for Highland HM.

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs5758651 rs34149579 rs12236219 rs284860 rs1131877 rs2277598
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
Blood Cell Consortium
BMC genomics · 2021 · PMID 34107879 · open access
12 pages+
rs76676074 rs9659479 rs2768762 rs11240092 rs28873209 rs11264765
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+
rs7856817 rs11626768 rs180705493 rs2811468 rs532566544 rs5752963
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
rs181676594 rs6974288 rs3846663 rs12939051 rs58458113 rs58223766
Large-scale genome-wide analyses of stuttering
23andMe Research Team
Nature genetics · 2025 · PMID 40721530 · open access
12 pages+
rs192857772 rs35713684 rs76347047 rs62337988 rs58120907 rs558002155
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
Scientific reports · 2017 · PMID 29213071 · open access
7 pages
rs73017364 rs12035622 rs55863869 rs35760656 rs12271931 rs12626657
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Early Growth Genetics Consortium
Human molecular genetics · 2019 · PMID 31504550
5 pages
rs6567160 rs4077678 rs10493544 rs114670539 rs74583214
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
5 pages
rs5400 rs17853166 rs75619922 rs7225887 rs56381411
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
HGG advances · 2022 · PMID 35399580 · open access
3 pages
rs6817771 rs9922708 rs3751813
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
American journal of human genetics · 2019 · PMID 31178129
2 pages
rs145119400 rs11646213
Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy
Scientific reports · 2018 · PMID 29618737 · open access
1 page
rs7545860
Genetic analyses of diverse populations improves discovery for complex traits
Nature · 2019 · PMID 31217584
1 page
Obesity and Body Weight
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
1 page
rs28450540
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study
Diabetologia · 2022 · PMID 34951656
1 page
rs6975024
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
1 page
rs62033408

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.