For researchers

Is your paper here?

2,660 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.

45 matches for Butterworth AS, showing the first 20.

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Cell · 2016 · PMID 27863252 · open access
12 pages+
rs139459946 rs11562010 rs11723763 rs1830951 rs26578 rs144861591
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
SpiroMeta Consortium · GoT2D Consortium and 3 more consortia
American journal of human genetics · 2017 · PMID 28552196 · open access
12 pages+
rs28376121 rs3116614 rs2061456 rs42377 rs1975474 rs28721484
Association analyses based on false discovery rate implicate new loci for coronary artery disease
EPIC-CVD Consortium · CARDIoGRAMplusC4D and 1 more consortia
Nature genetics · 2017 · PMID 28714975
12 pages+
rs142695226 rs10857147 rs7678555 rs6909752 rs7500448 rs1964272
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+
rs9891146 rs13447324 rs5758651 rs34149579 rs12236219 rs284860
Genomic atlas of the human plasma proteome
Nature · 2018 · PMID 29875488
12 pages+
rs10762481 rs9274954 rs76665138 rs12493107 rs357253 rs5753231
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
rs62491354 rs4598218 rs72816333 rs10823136 rs2400509 rs7555285
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
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
rs2236180 rs10836366 rs1985511 rs11205354 rs1215 rs34093919
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs924981 rs35636653 rs1078442 rs4918943 rs10096421 rs57126710
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
rs7597336 rs12790943 rs74375025 rs6998967 rs73065147 rs147215801
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs699465 rs10414501 rs77951490 rs78863347 rs9271585 rs4807003
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income
Nature communications · 2019 · PMID 31844048 · open access
12 pages+
rs12614880 rs13402908 rs240702 rs62166490 rs27565 rs2068428
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs1571967 rs61962202 rs674451 rs117524719 rs117871957 rs118131223
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs182056137 rs466477 rs4979859 rs601081 rs6940880 rs7504089
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs36106412 rs142444346 rs887945 rs11579145 rs77255899 rs11225452
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+
rs149165710 rs145441283 rs187207161 rs767105335 rs77357563 rs2306899
A cross-platform approach identifies genetic regulators of human metabolism and health
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
12 pages+
rs10024263 rs2234633 rs2608920 rs4253272 rs731165 rs74095612
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
12 pages+
rs61047863 rs189305788 rs781930992 rs968218067 rs114310641 rs890565237
Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci
BMC medicine · 2021 · PMID 34503513 · open access
12 pages+
rs2199312 rs2199314 rs2366638 rs28361366 rs73008767 rs954730
Rare and common genetic determinants of metabolic individuality and their effects on human health
Nature medicine · 2022 · PMID 36357675 · open access
12 pages+
rs41348645 rs11229660 rs7214014 rs12729167 rs6017949 rs148100514

Showing 20 of 45 · 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.