M
Muhammad Ramzan
Researcher at Islamia University
Publications - 240
Citations - 3285
Muhammad Ramzan is an academic researcher from Islamia University. The author has contributed to research in topics: Quantum decoherence & Quantum entanglement. The author has an hindex of 21, co-authored 218 publications receiving 1976 citations. Previous affiliations of Muhammad Ramzan include Umm al-Qura University & Information Technology University.
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Quantum Stackelberg duopoly in the presence of correlated noise
TL;DR: In this article, the influence of correlated amplitude damping, depolarizing and phase damping channels on the quantum Stackelberg duopoly was investigated and the authors showed that the game becomes a leader advantage game when the channel is highly decohered.
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A note on some perfect fluid Kantowski-Sachs and Bianchi type III space-times and their conformal vector fields in f(R) theory of gravity
TL;DR: In this paper, the authors find conformal vector fields of perfect fluid Kantowski-Sachs and Bianchi type III space-times in the f(R) theory of gravity using direct integration technique.
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Quantum Monty Hall Problem under Decoherence
TL;DR: In this article, the effect of decoherence on quantum Monty Hall problem under the influence of amplitude damping, depolarizing, and dephasing channels was studied, and it was shown that there is a Nash equilibrium of the game in case of depolarising channel for Alice's quantum strategy.
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Role of Renewable Energy Consumption and Technological Innovation to Achieve Carbon Neutrality in Spain: Fresh Insights From Wavelet Coherence and Spectral Causality Approaches
Yawen Zhao,Muhammad Ramzan,Tomiwa Sunday Adebayo,Seun Damola Oladipupo,Ibrahim Adeshola,Ephraim Bonah Agyekum +5 more
TL;DR: In this paper, the authors applied the wavelet tools to assess the interconnection between CO2 and globalization, technological innovation, economic growth, and renewable energy consumption in Spain, and revealed that the association amongst the series evolves over frequency and time.
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Synthesis and Biological Evaluation of Some New N4-Aryl Substituted 5-Chloroisatin-3-thiosemicarbazones
TL;DR: Structural-activity relationship studies revealed that electronic effects of the substituents about the phenyl ring at N4 of the thiosemicarbazone moiety played an important role in enhancing the urease inhibitory potential of some of the synthesized compounds.