For researchers
Is your paper here?
2,663 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.
9 matches for
Ding T.
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Manousaki D,
Dudding T,
Haworth S,
Hsu YH,
Liu CT,
Medina-Gómez C,
Voortman T,
van der Velde N,
Melhus H,
Robinson-Cohen C,
Cousminer DL,
Nethander M
and 41 more — show all
Vandenput L,
Noordam R,
Forgetta V,
Greenwood CMT,
Biggs ML,
Psaty BM,
Rotter JI,
Zemel BS,
Mitchell JA,
Taylor B,
Lorentzon M,
Karlsson M,
Jaddoe VVW,
Tiemeier H,
Campos-Obando N,
Franco OH,
Utterlinden AG,
Broer L,
van Schoor NM,
Ham AC,
Ikram MA,
Karasik D,
de Mutsert R,
Rosendaal FR,
den Heijer M,
Wang TJ,
Lind L,
Orwoll ES,
Mook-Kanamori DO,
Michaëlsson K,
Kestenbaum B,
Ohlsson C,
Mellström D,
de Groot LCPGM,
Grant SFA,
Kiel DP,
Zillikens MC,
Rivadeneira F,
Sawcer S,
Timpson NJ,
Richards JB
American journal of human genetics · 2017 · PMID 28757204
12 pages+
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci
Dudding T,
Haworth S,
Lind PA,
Sathirapongsasuti JF,
Tung JY,
Mitchell R,
Colodro-Conde L,
Medland SE,
Gordon S,
Elsworth B,
Paternoster L,
Franks PW
and 3 more — show all
23andMe Research Team
Nature communications · 2019 · PMID 30837455 · open access
12 pages+
Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci
Manousaki D,
Mitchell R,
Dudding T,
Haworth S,
Harroud A,
Forgetta V,
Shah RL,
Luan J,
Langenberg C,
Timpson NJ,
Richards JB
American journal of human genetics · 2020 · PMID 32059762
12 pages+
Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collective
Dack K,
Ludwig KU,
Stergiakouli E,
Sandy J,
Aryee S,
Davey Smith G,
Davies A,
Wren Y,
Sharp GC,
Humphries K,
Mangold E,
Goudswaard L
and 3 more — show all
Human molecular genetics · 2025 · PMID 41075272 · open access
12 pages+
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions
Wu C,
Kraft P,
Zhai K,
Chang J,
Wang Z,
Li Y,
Hu Z,
He Z,
Jia W,
Abnet CC,
Liang L,
Hu N
and 24 more — show all
Miao X,
Zhou Y,
Liu Z,
Zhan Q,
Liu Y,
Qiao Y,
Zhou Y,
Jin G,
Guo C,
Lu C,
Yang H,
Fu J,
Yu D,
Freedman ND,
Ding T,
Tan W,
Goldstein AM,
Wu T,
Shen H,
Ke Y,
Zeng Y,
Chanock SJ,
Taylor PR,
Lin D
Nature genetics · 2012 · PMID 22960999
3 pages
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Wang Z,
Dai J,
Hu N,
Miao X,
Abnet CC,
Yang M,
Freedman ND,
Chen J,
Burdette L,
Zhu X,
Chung CC,
Ren C
and 35 more — show all
Dawsey SM,
Wang M,
Ding T,
Du J,
Gao YT,
Zhong R,
Giffen C,
Pan W,
Koh WP,
Dai N,
Liao LM,
Yan C,
Qiao YL,
Jiang Y,
Shu XO,
Chen J,
Wang C,
Ma H,
Su H,
Zhang Z,
Wang L,
Wu C,
Xiang YB,
Hu Z,
Yuan JM,
Xie L,
Zheng W,
Zheng W,
Lin D,
Chanock SJ,
Shi Y,
Goldstein AM,
Jin G,
Taylor PR,
Shen H
Gut · 2017 · PMID 26701879 · open access
3 pages
The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages
Li S,
Weinstein G,
Zare H,
Teumer A,
Völker U,
Friedrich N,
Knol MJ,
Satizabal CL,
Petyuk VA,
Adams HHH,
Launer LJ,
Bennett DA
and 6 more — show all
Brain communications · 2020 · PMID 33345186 · open access
3 pages
Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer
Ferreiro-Iglesias A,
McKay JD,
Brenner N,
Virani S,
Lesseur C,
Gaborieau V,
Ness AR,
Hung RJ,
Liu G,
Diergaarde B,
Olshan AF,
Hayes N
and 40 more — show all
Weissler MC,
Schroeder L,
Bender N,
Pawlita M,
Thomas S,
Pring M,
Dudding T,
Kanterewicz B,
Ferris R,
Thomas S,
Brhane Y,
Díez-Obrero V,
Milojevic M,
Smith-Byrne K,
Mariosa D,
Johansson MJ,
Herrero R,
Boccia S,
Cadoni G,
Lacko M,
Holcátová I,
Ahrens W,
Lagiou P,
Lagiou A,
Polesel J,
Simonato L,
Merletti F,
Healy CM,
Hansen BT,
Nygård M,
Conway DI,
Wright S,
Macfarlane TV,
Robinson M,
Alemany L,
Agudo A,
Znaor A,
Amos CI,
Waterboer T,
Brennan P
Nature communications · 2021 · PMID 34642315 · open access
2 pages
Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008
Højfeldt SG,
Wolthers BO,
Tulstrup M,
Abrahamsson J,
Gupta R,
Harila-Saari A,
Heyman M,
Henriksen LT,
Jónsson ÒG,
Lähteenmäki PM,
Lund B,
Pruunsild K
and 3 more — show all
Nordic Society of Paediatric Haematology Oncology (NOPHO) group
British journal of haematology · 2019 · PMID 30450575
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.