For researchers
Is your paper here?
2,662 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.
10 matches for
Pui CH.
Clinical Pharmacogenetics Implementation Consortium Guideline for Thiopurine Dosing Based on TPMT and NUDT15 Genotypes: 2018 Update
Relling MV,
Schwab M,
Whirl-Carrillo M,
Suarez-Kurtz G,
Pui CH,
Stein CM,
Moyer AM,
Evans WE,
Klein TE,
Antillon-Klussmann FG,
Caudle KE,
Kato M
and 3 more — show all
Clinical pharmacology and therapeutics · 2019 · PMID 30447069
5 pages
Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia
Diouf B,
Crews KR,
Lew G,
Pei D,
Cheng C,
Bao J,
Zheng JJ,
Yang W,
Fan Y,
Wheeler HE,
Wing C,
Delaney SM
and 13 more — show all
Komatsu M,
Paugh SW,
McCorkle JR,
Lu X,
Winick NJ,
Carroll WL,
Loh ML,
Hunger SP,
Devidas M,
Pui CH,
Dolan ME,
Relling MV,
Evans WE
JAMA · 2015 · PMID 25710658
2 pages
Genome-wide analysis links NFATC2 with asparaginase hypersensitivity
Fernandez CA,
Smith C,
Yang W,
Mullighan CG,
Qu C,
Larsen E,
Bowman WP,
Liu C,
Ramsey LB,
Chang T,
Karol SE,
Loh ML
and 9 more — show all
Blood · 2015 · PMID 25987655
2 pages
Clinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia
Liu C,
Yang W,
Devidas M,
Cheng C,
Pei D,
Smith C,
Carroll WL,
Raetz EA,
Bowman WP,
Larsen EC,
Maloney KW,
Martin PL
and 12 more — show all
Mattano LA Jr,
Winick NJ,
Mardis ER,
Fulton RS,
Bhojwani D,
Howard SC,
Jeha S,
Pui CH,
Hunger SP,
Evans WE,
Loh ML,
Relling MV
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2016 · PMID 27114598
2 pages
Genome-Wide Study Links PNPLA3 Variant With Elevated Hepatic Transaminase After Acute Lymphoblastic Leukemia Therapy
Liu Y,
Fernandez CA,
Smith C,
Yang W,
Cheng C,
Panetta JC,
Kornegay N,
Liu C,
Ramsey LB,
Karol SE,
Janke LJ,
Larsen EC
and 13 more — show all
Winick N,
Carroll WL,
Loh ML,
Raetz EA,
Hunger SP,
Devidas M,
Yang JJ,
Mullighan CG,
Zhang J,
Evans WE,
Jeha S,
Pui CH,
Relling MV
Clinical pharmacology and therapeutics · 2017 · PMID 28090653
2 pages
Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk
Vijayakrishnan J,
Qian M,
Studd JB,
Yang W,
Kinnersley B,
Law PJ,
Broderick P,
Raetz EA,
Allan J,
Pui CH,
Vora A,
Evans WE
and 14 more — show all
Moorman A,
Yeoh A,
Yang W,
Li C,
Bartram CR,
Mullighan CG,
Zimmerman M,
Hunger SP,
Schrappe M,
Relling MV,
Stanulla M,
Loh ML,
Houlston RS,
Yang JJ
Nature communications · 2019 · PMID 31767839 · open access
2 pages
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia
Yang JJ,
Cheng C,
Devidas M,
Cao X,
Campana D,
Yang W,
Fan Y,
Neale G,
Cox N,
Scheet P,
Borowitz MJ,
Winick NJ
and 11 more — show all
Martin PL,
Bowman WP,
Camitta B,
Reaman GH,
Carroll WL,
Willman CL,
Hunger SP,
Evans WE,
Pui CH,
Loh M,
Relling MV
Blood · 2012 · PMID 23007406
1 page
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia
Karol SE,
Yang W,
Van Driest SL,
Chang TY,
Kaste S,
Bowton E,
Basford M,
Bastarache L,
Roden DM,
Denny JC,
Larsen E,
Winick N
and 16 more — show all
Carroll WL,
Cheng C,
Pei D,
Fernandez CA,
Liu C,
Smith C,
Loh ML,
Raetz EA,
Hunger SP,
Scheet P,
Jeha S,
Pui CH,
Evans WE,
Devidas M,
Mattano LA Jr,
Relling MV
Blood · 2015 · PMID 26265699
1 page
Genome-Wide Association Study of Susceptibility Loci for TCF3-PBX1 Acute Lymphoblastic Leukemia in Children
Lee SHR,
Qian M,
Yang W,
Diedrich JD,
Raetz E,
Yang W,
Dong Q,
Devidas M,
Pei D,
Yeoh A,
Cheng C,
Pui CH
and 7 more — show all
Journal of the National Cancer Institute · 2021 · PMID 32882024
1 page
Class II Human Leukocyte Antigen Variants Associate With Risk of Pegaspargase Hypersensitivity
Liu Y,
Yang W,
Smith CA,
Cheng C,
Karol SE,
Larsen EC,
Winick N,
Carroll WL,
Loh ML,
Raetz EA,
Hunger SP,
Winter SS
and 8 more — show all
Clinical pharmacology and therapeutics · 2021 · PMID 33768542
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.