For researchers

Is your paper here?

2,676 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.

46 matches for Butterworth A, 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+
rs111527163 rs1887639 rs7716229 rs2078064 rs11671005 rs35304300
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+
rs13447324 rs5758651 rs34149579 rs12236219 rs284860 rs1131877
Genomic atlas of the human plasma proteome
Nature · 2018 · PMID 29875488
12 pages+
rs55636108 rs61985370 rs112206797 rs71426155 rs72732234 rs28383228
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+
rs10823136 rs2400509 rs7555285 rs76719272 rs72683923 rs34413141
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+
rs1215 rs34093919 rs1978968 rs79898473 rs1800888 rs7752448
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+
rs16942713 rs78986840 rs56411466 rs12361687 rs72658302 rs7327286
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
rs12790943 rs74375025 rs6998967 rs73065147 rs147215801 rs35692677
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+
rs11202345 rs584425 rs188917216 rs34861762 rs4897160 rs2941487
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income
Nature communications · 2019 · PMID 31844048 · open access
12 pages+
rs974295 rs2732596 rs79550344 rs72819191 rs12463 rs2842192
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+
rs62037423 rs73101498 rs75865061 rs868868 rs991057 rs10998648
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs58018068 rs6627558 rs7818560 rs9521533 rs9912487 rs10081968
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs139689864 rs117008454 rs8104447 rs55861089 rs17860955 rs176694
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+
rs187207161 rs767105335 rs77357563 rs2306899 rs2273171 rs4846567
A cross-platform approach identifies genetic regulators of human metabolism and health
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
12 pages+
rs2608920 rs4253272 rs731165 rs74095612 rs2306386 rs4143279
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+
rs968218067 rs114310641 rs890565237 rs755157567 rs374450628 rs2540913
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+
rs56051693 rs56113838 rs56195705 rs56247501 rs56249653 rs56280069
Rare and common genetic determinants of metabolic individuality and their effects on human health
Nature medicine · 2022 · PMID 36357675 · open access
12 pages+
rs118154869 rs140404849 rs779696952 rs12202038 rs111730788 rs116906529

Showing 20 of 46 · 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.