Publication > Page 25
  • Communications Medicine  ·  May 9, 2024

    A comprehensive AI model development framework for consistent Gleason grading.

    Xinmi Huo, Kok Haur Ong, Kah Weng Lau, Laurent Gole, David M. Young, Char Loo Tan, Xiaohui Zhu, Chongchong Zhang, Yonghui Zhang, Longjie Li, Hao Han, Haoda Lu…Haotian Cao, Xiaozhen Yu, Yabin Shi, Ziling Huang, Gabriel Marini, Jun Xu, Bingxian Liu, Bingxian Chen, Qiang Wang, Kun Gui, Wenzhao Shi, Yingying Sun, Wanyuan Chen, Dalong Cao, Stephan J. Sanders, Hwee Kuan Lee, Susan Swee-Shan Hue, Weimiao Yu & Soo Yong Tan

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  • Nature  ·  May 8, 2024

    Mapping genotypes to chromatin accessibility profiles in single cells.

    Franco Izzo, Robert M. Myers, Saravanan Ganesan, Levan Mekerishvili, Sanjay Kottapalli, Tamara Prieto, Elliot O. Eton, Theo Botella, Andrew J. Dunbar, Robert L. Bowman, Jesus Sotelo, Catherine Potenski, Eleni P. Mimitou, Maximilian Stahl, Sebastian El Ghaity-Beckley, JoAnn Arandela, Ramya Raviram, Daniel C. Choi, Ronald Hoffman, Ronan Chaligné, Omar Abdel-Wahab, Peter Smibert, Irene M. Ghobrial, Joseph M. Scandura, Bridget Marcellino, Ross L. Levine & Dan A. Landau

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  • JAMA Psychiatry  ·  April 17, 2024

    Examining Sex Differences in Autism Heritability.

    Sven Sandin, Benjamin H K Yip, Weiyao Yin, Lauren A Weiss, Joseph D Dougherty, Stuart Fass, John N Constantino, Zhu Hailin, Tychele N Turner, Natasha Marrus, David H Gutmann, Stephan J Sanders, Benjamin Christoffersson

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  • Nature Reviews Genetics  ·  April 12, 2024

    SIMPLE-seq to decode DNA methylation dynamics in single cells.

    Dongsheng Bai & Chenxu Zhu

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  • Acta Neuropathologica  ·  April 10, 2024

    Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer’s disease.

    Prabesh Bhattarai, Tamil Iniyan Gunasekaran, … Andrew F. Teich, Dennis W. Dickson, Scott Holley, Michael Greicius, Clifton L. Dalgard, Michael Zody, Richard Mayeux, Caghan Kizil & Badri N. Vardarajan

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  • Cancer Cell  ·  April 2, 2024

    Mutant IDH inhibitors induce lineage differentiation in IDH-mutant oligodendroglioma.

    Avishay Spitzer, Simon Gritsch, Masashi Nomura, Alexander Jucht, Jerome Fortin, Ramya Raviram, Hannah R Weisman, L Nicolas Gonzalez Castro, Nicholas Druck, Rony Chanoch-Myers, John J Y Lee, Ravindra Mylvaganam, Rachel Lee Servis, Jeremy Man Fung, Christine K Lee, Hiroaki Nagashima, Julie J Miller, Isabel Arrillaga-Romany, David N Louis, Hiroaki Wakimoto, Will Pisano, Patrick Y Wen, Tak W Mak, Marc Sanson, Mehdi Touat, Dan A Landau, Keith L Ligon, Daniel P Cahill, Mario L Suvà, Itay Tirosh

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  • NPJ Genomic Medicine  ·  March 27, 2024

    Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action.

    Vaidehi Jobanputra, Brock Schroeder, Heidi L. Rehm, Wei Shen, Elizabeth Spiteri, Ghunwa Nakouzi, Stacie Taylor, Christian R. Marshall, Linyan Meng, Stephen F. Kingsmore, Katarzyna Ellsworth, Euan Ashley & Ryan J. Taft on behalf of the Medical Genome Initiative

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  • Science Advances  ·  March 22, 2024

    Childhood cancer mutagenesis caused by transposase-derived PGBD5.

    Makiko Yamada, Ross R Keller, Rodrigo Lopez Gutierrez, Daniel Cameron, Hiromichi Suzuki, Reeti Sanghrajka, Jake Vaynshteyn, Jeffrey Gerwin, Francesco Maura, William Hooper, Minita Shah, Nicolas Robine, Phillip Demarest, N Sumru Bayin, Luz Jubierre Zapater, Casie Reed, Steven Hébert, Ignas Masilionis, Ronan Chaligne, Nicholas D Socci, Michael D Taylor, Claudia L Kleinman, Alexandra L Joyner, G Praveen Raju, Alex Kentsis

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  • NPJ Genomic Medicine  ·  March 22, 2024

    Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.

    Marta Viggiano, Fabiola Ceroni, Paola Visconti, Annio Posar, Maria Cristina Scaduto, Laura Sandoni, Irene Baravelli, Cinzia Cameli, Magali J. Rochat, Alessandra Maresca, Alessandro Vaisfeld, Davide Gentilini, Luciano Calzari, Valerio Carelli, Michael C. Zody, Elena Maestrini & Elena Bacchelli

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