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Mark Wilkinson

Researcher at Syracuse University

Publications -  1079
Citations -  48295

Mark Wilkinson is an academic researcher from Syracuse University. The author has contributed to research in topics: Branching fraction & Caecilian. The author has an hindex of 87, co-authored 1014 publications receiving 38539 citations. Previous affiliations of Mark Wilkinson include University of Bristol & Royal Hallamshire Hospital.

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Journal ArticleDOI

Isolated torsion of the fallopian tube: two case reports.

B Sharma, +4 more
- 01 May 2003 - 
TL;DR: The patient had extensive pelvic endometriosis and an exploratory laparotomy was thought to be the most appropriate management, although the ureteric involvement was found to be extrinsic.
Posted Content

Strong constraints on the $K^0_{\mathrm{S}}\rightarrow\mu^{+}\mu^{-}$ branching fraction

Roel Aaij, +902 more
- 28 Jan 2020 - 
TL;DR: In this paper, a search for the decay of a proton-proton collision data with the LHCb experiment at a center-of-mass energy of $13.6\,\text{fb}^{-1}$ was performed.

Prompt and Nonprompt J/ψ Production and Nuclear Modification in p Pb Collisions at √s[subscript NN] = 8.16 TeV

Roel Aaij, +807 more
TL;DR: In this article, the double differential cross-sections of prompt and non-prompt J/ψ meson production are measured as a function of the Jψ transverse momentum and rapidity in the nucleon-nucleon center-of-mass frame.
Journal ArticleDOI

The Indole-3-Acetamide-Induced Arabidopsis Transcription Factor MYB74 Decreases Plant Growth and Contributes to the Control of Osmotic Stress Responses

Paloma Ortiz-García, +6 more
- 22 Jun 2022 - 
TL;DR: In this article , the authors investigated the transcriptional responses evoked by the exogenous application of IAM using comprehensive RNA-sequencing (RNA-seq) and reverse genetics approaches.
Posted ContentDOI

Semantic modelling of Common Data Elements for Rare Disease registries, and a prototype workflow for their deployment over registry data

R. Kaliyaperumal, +18 more
- 30 Jul 2021 - 
TL;DR: The European Platform on Rare Disease Registration (EU RD Platform) aims to address the fragmentation of European rare disease (RD) patient data, scattered among hundreds of independent and non-coordinating registries by establishing standards for integration and interoperability as discussed by the authors.