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Adina Weinberger

Researcher at Weizmann Institute of Science

Publications -  62
Citations -  10515

Adina Weinberger is an academic researcher from Weizmann Institute of Science. The author has contributed to research in topics: Microbiome & Promoter. The author has an hindex of 30, co-authored 52 publications receiving 7169 citations.

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Personalized Nutrition by Prediction of Glycemic Responses

TL;DR: A machine-learning algorithm is devised that integrates blood parameters, dietary habits, anthropometrics, physical activity, and gut microbiota measured in an 800-person cohort and shows that it accurately predicts personalized postprandial glycemic response to real-life meals, and a blinded randomized controlled dietary intervention based on this algorithm resulted in significantly lower postpr andial responses and consistent alterations to gut microbiota configuration.
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Artificial sweeteners induce glucose intolerance by altering the gut microbiota

TL;DR: It is demonstrated that consumption of commonly used NAS formulations drives the development of glucose intolerance through induction of compositional and functional alterations to the intestinal microbiota, thereby calling for a reassessment of massive NAS usage.
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The human tumor microbiome is composed of tumor type–specific intracellular bacteria

Deborah Nejman, +71 more
- 29 May 2020 - 
TL;DR: A comprehensive analysis of the tumor microbiome was undertaken, studying 1526 tumors and their adjacent normal tissues across seven cancer types, finding that each tumor type has a distinct microbiome composition and that breast cancer has a particularly rich and diverse microbiome.
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Inferring gene regulatory logic from high-throughput measurements of thousands of systematically designed promoters

TL;DR: A method for obtaining parallel, highly accurate gene expression measurements from thousands of designed promoters is devised and applied to measure the effect of systematic changes in the location, number, orientation, affinity and organization of transcription-factor binding sites and nucleosome-disfavoring sequences.