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.
4 matches for
Rashkin SR.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts
Rashkin SR,
Graff RE,
Kachuri L,
Thai KK,
Alexeeff SE,
Blatchins MA,
Cavazos TB,
Corley DA,
Emami NC,
Hoffman JD,
Jorgenson E,
Kushi LH
and 7 more — show all
Nature communications · 2020 · PMID 32887889 · open access
12 pages+
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden
Gabriel AAG,
Atkins JR,
Penha RCC,
Smith-Byrne K,
Gaborieau V,
Voegele C,
Abedi-Ardekani B,
Milojevic M,
Olaso R,
Meyer V,
Boland A,
Deleuze JF
and 21 more — show all
Zaridze D,
Mukeriya A,
Swiatkowska B,
Janout V,
Schejbalová M,
Mates D,
Stojšić J,
Ognjanovic M,
Witte JS,
Rashkin SR,
Kachuri L,
Hung RJ,
Kar S,
Brennan P,
Sertier AS,
Ferrari A,
Viari A,
Johansson M,
Amos CI,
Foll M,
McKay JD
ILCCO consortium
Journal of the National Cancer Institute · 2022 · PMID 35511172 · open access
7 pages
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility
Emami NC,
Cavazos TB,
Rashkin SR,
Cario CL,
Graff RE,
Tai CG,
Mefford JA,
Kachuri L,
Wan E,
Wong S,
Aaronson D,
Presti J
and 14 more — show all
Habel LA,
Shan J,
Ranatunga DK,
Chao CR,
Ghai NR,
Jorgenson E,
Sakoda LC,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Hoffmann TJ,
Van Den Eeden SK,
Witte JS
Cancer research · 2021 · PMID 33293427
1 page
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study
Rashkin SR,
Cleves M,
Shaw GM,
Nembhard WN,
Nestoridi E,
Jenkins MM,
Romitti PA,
Lou XY,
Browne ML,
Mitchell LE,
Olshan AF,
Lomangino K
and 3 more — show all
National Birth Defects Prevention Study
American journal of medical genetics. Part A · 2022 · PMID 35451555
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.