For researchers
Is your paper here?
2,661 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
Weinshilboum R.
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies
Tamm R,
Mägi R,
Tremmel R,
Winter S,
Mihailov E,
Smid A,
Möricke A,
Klein K,
Schrappe M,
Stanulla M,
Houlston R,
Weinshilboum R
and 5 more — show all
Clinical pharmacology and therapeutics · 2017 · PMID 27770449
4 pages
Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder
Amare AT,
Schubert KO,
Tekola-Ayele F,
Hsu YH,
Sangkuhl K,
Jenkins G,
Whaley RM,
Barman P,
Batzler A,
Altman RB,
Arolt V,
Brockmöller J
and 25 more — show all
Chen CH,
Domschke K,
Hall-Flavin DK,
Hong CJ,
Illi A,
Ji Y,
Kampman O,
Kinoshita T,
Leinonen E,
Liou YJ,
Mushiroda T,
Nonen S,
Skime MK,
Wang L,
Kato M,
Liu YL,
Praphanphoj V,
Stingl JC,
Bobo WV,
Tsai SJ,
Kubo M,
Klein TE,
Weinshilboum RM,
Biernacka JM,
Baune BT
Frontiers in psychiatry · 2018 · PMID 29559929 · open access
3 pages
SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway
Dudenkov TM,
Ingle JN,
Buzdar AU,
Robson ME,
Kubo M,
Ibrahim-Zada I,
Batzler A,
Jenkins GD,
Pietrzak TL,
Carlson EE,
Barman P,
Goetz MP
and 7 more — show all
Breast cancer research and treatment · 2017 · PMID 28429243
1 page
Genetic predictors of chemotherapy-related amenorrhea in women with breast cancer
Ruddy KJ,
Schaid DJ,
Partridge AH,
Larson NB,
Batzler A,
Häberle L,
Dittrich R,
Widschwendter P,
Fink V,
Bauer E,
Schwitulla J,
Rübner M
and 12 more — show all
Ekici AB,
Aivazova-Fuchs V,
Stewart EA,
Beckmann MW,
Ginsburg E,
Wang L,
Weinshilboum RM,
Couch FJ,
Janni W,
Rack B,
Vachon C,
Fasching PA
Fertility and sterility · 2019 · PMID 31371054
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.