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.

89 matches for Nalls M, showing the first 20.

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
rs10929547 rs6430549 rs2060597 rs592423 rs4535497
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs60401382 rs72934589 rs76110445 rs12415501 Cardioembolic Stroke
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors
Circulation. Cardiovascular genetics · 2010 · PMID 20884846
4 pages
rs675209 rs13129697 rs1106766 Gout
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans
Human molecular genetics · 2012 · PMID 23001564 · open access
4 pages
rs412658 rs1317082 rs3027234 Telomere Length and Epigenetic Age Acceleration
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
rs2107595 rs879324 rs13407662 Ischaemic Stroke
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
rs7894407 rs72848980 rs7909791 rs7214628
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
rs10908557 rs6885307 rs2347867 rs2721195
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
rs9308788 rs141962517 rs75535814 rs113809930
Multiple loci are associated with white blood cell phenotypes
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
rs1449263 rs10980800 rs2517510
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
rs1481012 rs4475146 Gout
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
BioBank Japan Project · CHARGE Consortium
Human molecular genetics · 2013 · PMID 23446634
3 pages
rs762516 rs13008603 rs13339636
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
International Parkinson's Disease Genomics Consortium · 23andMe Research Team
Nature genetics · 2017 · PMID 28892059
3 pages
rs4653767 rs143918452 rs9468199
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
3 pages
rs11196033 rs2912063 rs844396
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease
Molecular psychiatry · 2023 · PMID 37198259 · open access
3 pages
rs117807585 rs9394766 rs74825460
Genome-wide association studies of the PR interval in African Americans
Candidate-gene Association Resource (CARe) Consortium
PLoS genetics · 2011 · PMID 21347284 · open access
2 pages
rs6798015 rs10865355
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
rs17178006 rs6581612
Genetic variation associated with circulating monocyte count in the eMERGE Network
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
2 pages
rs2124440 Monocyte Count
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878

Showing 20 of 89 · page 3 of 5

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.