Z
Zhiyong Zhang
Researcher at Weizmann Institute of Science
Publications - 39
Citations - 294
Zhiyong Zhang is an academic researcher from Weizmann Institute of Science. The author has contributed to research in topics: Magnetic field & Two-dimensional nuclear magnetic resonance spectroscopy. The author has an hindex of 8, co-authored 36 publications receiving 233 citations. Previous affiliations of Zhiyong Zhang include Shanghai Jiao Tong University & Xiamen University.
Papers
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High-Resolution 2D J-Resolved Spectroscopy in Inhomogeneous Fields with Two Scans
TL;DR: A scheme via spatially encoded intermolecular zero-quantum coherences was proposed for high-resolution 2D J-resolved spectra in inhomogeneous fields with high acquisition efficiency and can obtain chemical shifts and J multiplicity patterns directly.
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High-Resolution Two-Dimensional J-Resolved NMR Spectroscopy for Biological Systems
TL;DR: An NMR approach based on intermolecular double-quantum coherences to recover high-resolution two-dimensional (2D) J-resolved spectra from inhomogeneous magnetic fields, such as those created by susceptibility variations in intact biological tissues are proposed.
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Spatially encoded ultrafast high-resolution 2D homonuclear correlation spectroscopy in inhomogeneous fields
TL;DR: Two new pulse sequences tracking the differences of the precession frequencies of two coupled spins are proposed to ultrafast achieve high-resolution 2D correlation spectroscopy (COSY and TOCSY) in inhomogeneous fields in a single scan.
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Single-scan MRI with exceptional resilience to field heterogeneities.
TL;DR: Cross-term spatio-temporal encoding (xSPEN) as discussed by the authors is a single-shot two-dimensional MRI method that relies on spatiotemporal encoding to encode the image being sought.
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Robust Single-Shot T 2 Mapping via Multiple Overlapping-Echo Acquisition and Deep Neural Network
TL;DR: The results of simulation, phantom, and in vivo human brain experiments show the great performance of the proposed single-shot quantitative T2 mapping method, MOLED-4, which may be extended to other ultrafast quantitative parameter mappings and potentially lead to new dynamic MRI with high efficiency to catch quantitative variation of tissue properties.