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.
2 matches for
Stephens OW.
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
Mitchell JS,
Li N,
Weinhold N,
Försti A,
Ali M,
van Duin M,
Thorleifsson G,
Johnson DC,
Johnson DC,
Chen B,
Halvarsson BM,
Gudbjartsson DF
and 47 more — show all
Kuiper R,
Stephens OW,
Bertsch U,
Broderick P,
Campo C,
Einsele H,
Gregory WA,
Gullberg U,
Henrion M,
Hillengass J,
Hoffmann P,
Jackson GH,
Johnsson E,
Jöud M,
Kristinsson SY,
Lenhoff S,
Lenive O,
Mellqvist UH,
Migliorini G,
Nahi H,
Nelander S,
Nickel J,
Nöthen MM,
Rafnar T,
Ross FM,
da Silva Filho MI,
Swaminathan B,
Thomsen H,
Turesson I,
Vangsted A,
Vogel U,
Waage A,
Walker BA,
Wihlborg AK,
Broyl A,
Davies FE,
Thorsteinsdottir U,
Langer C,
Hansson M,
Kaiser M,
Sonneveld P,
Stefansson K,
Morgan GJ,
Goldschmidt H,
Hemminki K,
Nilsson B,
Houlston RS
Nature communications · 2016 · PMID 27363682 · open access
9 pages
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
Went M,
Sud A,
Försti A,
Halvarsson BM,
Weinhold N,
Kimber S,
van Duin M,
Thorleifsson G,
Holroyd A,
Johnson DC,
Johnson DC,
Li N
and 58 more — show all
Orlando G,
Law PJ,
Ali M,
Chen B,
Mitchell JS,
Gudbjartsson DF,
Kuiper R,
Stephens OW,
Bertsch U,
Broderick P,
Campo C,
Bandapalli OR,
Einsele H,
Gregory WA,
Gullberg U,
Hillengass J,
Hoffmann P,
Jackson GH,
Jöckel KH,
Johnsson E,
Kristinsson SY,
Mellqvist UH,
Nahi H,
Easton D,
Pharoah P,
Dunning A,
Peto J,
Canzian F,
Swerdlow A,
Eeles RA,
Kote-Jarai Z,
Muir K,
Pashayan N,
Nickel J,
Nöthen MM,
Rafnar T,
Ross FM,
da Silva Filho MI,
Thomsen H,
Turesson I,
Vangsted A,
Andersen NF,
Waage A,
Walker BA,
Wihlborg AK,
Broyl A,
Davies FE,
Thorsteinsdottir U,
Langer C,
Hansson M,
Goldschmidt H,
Kaiser M,
Sonneveld P,
Stefansson K,
Morgan GJ,
Hemminki K,
Nilsson B,
Houlston RS
PRACTICAL consortium
Nature communications · 2018 · PMID 30213928 · open access
5 pages
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.