For researchers
Is your paper here?
2,676 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.
29 matches for
Smith C,
showing the first 9.
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits
Zheng JS,
Arnett DK,
Lee YC,
Shen J,
Parnell LD,
Smith CE,
Richardson K,
Li D,
Borecki IB,
Ordovás JM,
Lai CQ
PloS one · 2013 · PMID 24204828 · open access
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 and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci
Tanskanen T,
van den Berg L,
Välimäki N,
Aavikko M,
Ness-Jensen E,
Hveem K,
Wettergren Y,
Bexe Lindskog E,
Tõnisson N,
Metspalu A,
Silander K,
Orlando G
and 48 more — show all
Law PJ,
Tuupanen S,
Gylfe AE,
Hänninen UA,
Cajuso T,
Kondelin J,
Sarin AP,
Pukkala E,
Jousilahti P,
Salomaa V,
Ripatti S,
Palotie A,
Järvinen H,
Renkonen-Sinisalo L,
Lepistö A,
Böhm J,
Mecklin JP,
Al-Tassan NA,
Palles C,
Martin L,
Barclay E,
Tenesa A,
Farrington SM,
Timofeeva MN,
Meyer BF,
Wakil SM,
Campbell H,
Smith CG,
Idziaszczyk S,
Maughan TS,
Kaplan R,
Kerr R,
Kerr D,
Buchanan DD,
Win AK,
Hopper J,
Jenkins MA,
Newcomb PA,
Gallinger S,
Conti D,
Schumacher FR,
Casey G,
Cheadle JP,
Dunlop MG,
Tomlinson IP,
Houlston RS,
Palin K,
Aaltonen LA
International journal of cancer · 2018 · PMID 28960316
1 page
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A<sub>1c</sub> With Implications for Glycemic Status in U.S. Hispanics/Latinos
Moon JY,
Louie TL,
Jain D,
Sofer T,
Schurmann C,
Below JE,
Lai CQ,
Aviles-Santa ML,
Talavera GA,
Smith CE,
Petty LE,
Bottinger EP
and 13 more — show all
Chen YI,
Taylor KD,
Daviglus ML,
Cai J,
Wang T,
Tucker KL,
Ordovás JM,
Hanis CL,
Loos RJF,
Schneiderman N,
Rotter JI,
Kaplan RC,
Qi Q
Diabetes care · 2019 · PMID 31213470
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
Comparative Genetic Analysis of Psoriatic Arthritis and Psoriasis for the Discovery of Genetic Risk Factors and Risk Prediction Modeling
Soomro M,
Stadler M,
Dand N,
Bluett J,
Jadon D,
Jalali-Najafabadi F,
Duckworth M,
Ho P,
Marzo-Ortega H,
Helliwell PS,
Ryan AW,
Kane D
and 17 more — show all
Korendowych E,
Simpson MA,
Packham J,
McManus R,
Gabay C,
Lamacchia C,
Nissen MJ,
Brown MA,
Verstappen SMM,
Van Staa T,
Barker JN,
Smith CH,
FitzGerald O,
McHugh N,
Warren RB,
Bowes J,
Barton A
BADBIR Study Group · BSTOP study group
Arthritis & rheumatology (Hoboken, N.J.) · 2022 · PMID 35507331 · open access
1 page
Genome-wide association analyses highlight the role of the intestinal molecular environment in human gut microbiota variation
Dekkers KF,
Pertiwi K,
Baldanzi G,
Lundmark P,
Hammar U,
Moksnes MR,
Coward E,
Nethander M,
Salih GA,
Miari M,
Nguyen D,
Sayols-Baixeras S
and 23 more — show all
Eklund AC,
Holm JB,
Nielsen HB,
Volpiano CG,
Méric G,
Thangam M,
Hakaste L,
Tuomi T,
Ahlqvist E,
Smith CA,
Allen M,
Reimann F,
Gribble FM,
Ohlsson C,
Hveem K,
Melander O,
Nilsson PM,
Engström G,
Smith JG,
Michaëlsson K,
Ärnlöv J,
Orho-Melander M,
Fall T
Nature genetics · 2026 · PMID 41688638 · 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.