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.
24 matches for
Klarin D,
showing the first 4.
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease
Klarin D,
Zhu QM,
Emdin CA,
Chaffin M,
Horner S,
McMillan BJ,
Leed A,
Weale ME,
Spencer CCA,
Aguet F,
Segrè AV,
Ardlie KG
and 4 more — show all
CARDIoGRAMplusC4D Consortium
Nature genetics · 2017 · PMID 28714974 · open access
1 page
Heritability of Atrial Fibrillation
Weng LC,
Choi SH,
Klarin D,
Smith JG,
Loh PR,
Chaffin M,
Roselli C,
Hulme OL,
Lunetta KL,
Dupuis J,
Benjamin EJ,
Newton-Cheh C
and 3 more — show all
Circulation. Cardiovascular genetics · 2017 · PMID 29237688
1 page
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
Bellomo TR,
Bone WP,
Chen BY,
Gawronski KAB,
Zhang D,
Park J,
Levin M,
Tsao N,
Klarin D,
Lynch J,
Assimes TL,
Gaziano JM
and 10 more — show all
Frontiers in genetics · 2021 · PMID 35186008 · open access
1 page
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Iglesias MJ,
Sanchez-Rivera L,
Ibrahim-Kosta M,
Naudin C,
Munsch G,
Goumidi L,
Farm M,
Smith PM,
Thibord F,
Kral-Pointner JB,
Hong MG,
Suchon P
and 31 more — show all
Germain M,
Schrottmaier W,
Dusart P,
Boland A,
Kotol D,
Edfors F,
Koprulu M,
Pietzner M,
Langenberg C,
Damrauer SM,
Johnson AD,
Klarin DM,
Smith NL,
Smadja DM,
Holmström M,
Magnusson M,
Silveira A,
Uhlén M,
Renné T,
Martinez-Perez A,
Emmerich J,
Deleuze JF,
Antovic J,
Soria Fernandez JM,
Assinger A,
Schwenk JM,
Souto Andres JC,
Morange PE,
Butler LM,
Trégouët DA,
Odeberg J
Nature communications · 2023 · PMID 37286573 · open access
1 page
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.