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Alex Bloemendal

Showing results (11-20 of 16) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 15, 2022
Inferring gene regulation from stochastic transcriptional variation across single cells at steady stateAnika Gupta, Jorge D Martin-Rufino, Thouis R Jones, et al.
Nature Communications|July 12, 2019
Paternal-age-related de novo mutations and risk for five disordersJacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, et al.
Nature|February 7, 2024
Convergence of coronary artery disease genes onto endothelial cell programsGavin R Schnitzler, Helen Kang, Shi Fang, et al.
Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2025
Scalable automated reanalysis of genomic data in research and clinical rare disease cohortsMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
Nature Medicine|June 24, 2026
Automated reanalysis of genomic data for rare disease diagnostics at scaleMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
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Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2022
Inferring gene regulation from stochastic transcriptional variation across single cells at steady stateAnika Gupta, Jorge D Martin-Rufino, Thouis R Jones, et al.
Nature Communications|July 12, 2019
Paternal-age-related de novo mutations and risk for five disordersJacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, et al.
Nature|February 7, 2024
Convergence of coronary artery disease genes onto endothelial cell programsGavin R Schnitzler, Helen Kang, Shi Fang, et al.
Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2025
Scalable automated reanalysis of genomic data in research and clinical rare disease cohortsMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
Nature Medicine|June 24, 2026
Automated reanalysis of genomic data for rare disease diagnostics at scaleMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
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