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.

47 matches for Starr J, showing the first 20.

New gene functions in megakaryopoiesis and platelet formation
Nature · 2011 · PMID 22139419
12 pages+
rs342275 rs4731120 rs6995402 rs7149242 rs2297067 rs397969
Seventy-five genetic loci influencing the human red blood cell
Nature · 2012 · PMID 23222517
12 pages+
rs3916164 rs10445033 rs901683 rs10849023 rs3892630 rs4953318
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
Human molecular genetics · 2016 · PMID 26561523
12 pages+
rs11859517 rs2710804 rs76289367 rs12777 rs2057655 rs2731439
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
BIOS Consortium · Understanding Society Scientific Group
Hypertension (Dallas, Tex. : 1979) · 2017 · PMID 28739976
12 pages+
rs35783704 rs73075659 rs73099903 rs36047283 rs871524 rs337100
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
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs7633520 rs11716820 rs7646366 rs28433345 rs10798879 rs71324996
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
rs4886640 rs7125196 rs259983 rs11725969 rs1894400 rs34063670
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs28888764 rs28522849 rs4687625 rs56306491 rs1115535 rs11646221
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
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
rs6785807 rs4445669 rs9298749 rs10957494 rs77819282 rs1045476
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
rs12749227 rs4845623 rs9271608 rs72698571 rs2246469 rs56288844
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs72834327 rs116376114 rs114846969 rs6029549 rs556107 rs117753190
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
PRACTICAL consortium
Nature communications · 2019 · PMID 31089142 · open access
12 pages+
rs61336918 rs77776598 rs16969681 rs75686861 rs10849438 rs12143541
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
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
Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs10861661 rs201596848 rs900399 rs7157785 rs3927680 rs7946
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
PLoS genetics · 2013 · PMID 23408906 · open access
10 pages
rs9497965 rs7860634 rs7240777 rs10799824 rs9472138 rs11755845
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
rs4938021 rs3756290 rs782212 rs12903563 rs12961969 rs35688236
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
rs7968440 rs1938492 rs1019670 rs4817986 rs6010044 rs10226084
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
rs10852344 rs12461110 rs16991615 rs1635501 rs10183486 rs2153157

Showing 20 of 47 · 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.