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Andrea Rommal

Researcher at Muhlenberg College

Publications -  5
Citations -  285

Andrea Rommal is an academic researcher from Muhlenberg College. The author has contributed to research in topics: Bell test experiments & Randomness. The author has an hindex of 4, co-authored 4 publications receiving 234 citations.

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Experimentally generated randomness certified by the impossibility of superluminal signals

TL;DR: 1,024 random bits that are uniformly distributed to within 10−12 and unpredictable assuming the impossibility of superluminal communication are generated and certified using a loophole-free Bell test and a protocol is described that is optimized for devices that are characterized by a low per-trial violation of Bell inequalities.
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Experimentally Generated Random Numbers Certified by the Impossibility of Superluminal Signaling

TL;DR: In this paper, the authors exploit the phenomenon of quantum nonlocality in a loophole-free photonic Bell test experiment for the generation of randomness that cannot be predicted within any physical theory.
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AdS-Sliced Flavor Branes and Adding Flavor to the Janus Solution

TL;DR: In this article, the authors have implemented D7 flavor branes in anti-de Sitter-sliced coordinates with the ansatz that the brane fluctuates only in the warped ($\ensuremath{\mu}$) direction in this slicing.
Journal Article

Experimentally Generated Random Numbers Certified by the Impossibility of Superluminal Signaling

TL;DR: This poster presents a probabilistic procedure for inferring the stationary phase of proton-proton collisions and shows direct AFM correspondence between the stationary and the moving parts of the electron.
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Disordered network structure and function in dystonia: pathological connectivity vs. adaptive responses.

TL;DR: In this paper , a network mapping algorithm based on resting-state functional MRI (rs-fMRI), a method that is readily implemented on conventional MRI scanners, was used to identify similar disease topographies in hereditary dystonia associated with the DYT1 or DYTs6 mutations and in sporadic patients lacking these mutations.