For researchers
Is your paper here?
2,657 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.
7 matches for
Cavallari LH.
Genome-wide association study of warfarin maintenance dose in a Brazilian sample
Parra EJ,
Botton MR,
Perini JA,
Krithika S,
Bourgeois S,
Johnson TA,
Tsunoda T,
Pirmohamed M,
Wadelius M,
Limdi NA,
Cavallari LH,
Burmester JK
and 5 more — show all
Pharmacogenomics · 2015 · PMID 26265036
1 page
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Pharmacogenetics-Guided Warfarin Dosing: 2017 Update
Johnson JA,
Caudle KE,
Gong L,
Whirl-Carrillo M,
Stein CM,
Scott SA,
Lee MT,
Gage BF,
Kimmel SE,
Perera MA,
Anderson JL,
Pirmohamed M
and 4 more — show all
Clinical pharmacology and therapeutics · 2017 · PMID 28198005
1 page
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C19 and Proton Pump Inhibitor Dosing
Lima JJ,
Thomas CD,
Barbarino J,
Desta Z,
Van Driest SL,
El Rouby N,
Johnson JA,
Cavallari LH,
Shakhnovich V,
Thacker DL,
Scott SA,
Schwab M
and 8 more — show all
Clinical pharmacology and therapeutics · 2021 · PMID 32770672
1 page
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2D6, OPRM1, and COMT Genotypes and Select Opioid Therapy
Crews KR,
Monte AA,
Huddart R,
Caudle KE,
Kharasch ED,
Gaedigk A,
Dunnenberger HM,
Leeder JS,
Callaghan JT,
Samer CF,
Klein TE,
Haidar CE
and 9 more — show all
Clinical pharmacology and therapeutics · 2021 · PMID 33387367
1 page
Meta-analysis of genome-wide association studies of stable warfarin dose in patients of African ancestry
Asiimwe IG,
Blockman M,
Cavallari LH,
Cohen K,
Cupido C,
Dandara C,
Davis BH,
Jacobson B,
Johnson JA,
Lamorde M,
Limdi NA,
Morgan J
and 15 more — show all
Mouton JP,
Muyambo S,
Nakagaayi D,
Ndadza A,
Okello E,
Perera MA,
Schapkaitz E,
Sekaggya-Wiltshire C,
Semakula JR,
Tatz G,
Waitt C,
Yang G,
Zhang EJ,
Jorgensen AL,
Pirmohamed M
Blood advances · 2024 · PMID 39163621 · 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.