For researchers

Is your paper here?

2,663 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+
rs9820353 rs7619708 rs142680548 rs2078179 rs2507971 rs68191221
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+
rs11030102 rs4145878 rs4782285 rs532352152 rs184622626 rs62036624
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+
rs284860 rs1131877 rs2277598 rs295322 rs62623713 rs11555762
Genomic atlas of the human plasma proteome
Nature · 2018 · PMID 29875488
12 pages+
rs41552714 rs76258418 rs342702 rs1432688 rs365299 rs9287090
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+
rs73158427 rs60255247 rs11159091 rs11623535 rs848445 rs4904503
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+
rs71490394 rs12497779 rs74053129 rs12634907 rs35505 rs268717
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+
rs2252281 rs6088528 rs6087579 rs113445505 rs34468415 rs12671694
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
rs73065147 rs147215801 rs35692677 rs113139575 rs162890 rs141493439
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+
rs149670286 rs34888828 rs62585312 rs2760215 rs60388273 rs17550549
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income
Nature communications · 2019 · PMID 31844048 · open access
12 pages+
rs1352890 rs12119149 rs9342115 rs6028085 rs248686 rs952594
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+
rs3804139 rs61210140 rs386869 rs6824723 rs55982282 rs3181215
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs7748918 rs12980879 rs11891215 rs117327684 rs2239196 rs73289263
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs1227734 rs35524242 rs56084311 rs5744249 rs2922996 rs12802112
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+
rs11718848 rs11537816 rs16859180 rs1449592 rs13196885 rs576629818
A cross-platform approach identifies genetic regulators of human metabolism and health
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
12 pages+
rs17756732 rs3119311 rs9382940 rs12492717 rs1014680 rs10899134
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+
rs547260160 rs35111391 rs8061527 rs4975528 rs916216189 rs551864820
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+
rs10133655 rs10148645 rs12880477 rs13055900 rs149096129 rs7957274
Rare and common genetic determinants of metabolic individuality and their effects on human health
Nature medicine · 2022 · PMID 36357675 · open access
12 pages+
rs9332172 rs13149149 rs1043011 rs11188148 rs191860149 rs1163548

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.