Publication > Page 35
  • Nature Scientific Reports.  ·  January 30, 2023

    Privacy-preserving cancer type prediction with homomorphic encryption.

    Sarkar E, Chielle E, Gursoy G, Chen L, Gerstein M, Maniatakos M.

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  • BMC  ·  January 25, 2023

    Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis.

    Kristina L. Buschur, Craig Riley, Aabida Saferali, Peter Castaldi, Grace Zhang, Francois Aguet, Kristin G. Ardlie, Peter Durda, W. Craig Johnson, Silva Kasela, Yongmei Liu, Ani Manichaikul, Stephen S. Rich, Jerome I. Rotter, Josh Smith, Kent D. Taylor, Russell P. Tracy, Tuuli Lappalainen, R. Graham Barr, Frank Sciurba, Craig P. Hersh & Panayiotis V. Benos

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  • PLOS Genetics  ·  January 19, 2023

    Using epigenomics to understand cellular responses to environmental influences in diseases.

    Julia J. Wattacheril, Srilakshmi Raj, David A. Knowles, John M. Greally

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  • IEEE Explore.  ·  January 18, 2023

    A generalizable physiological model for detection of Delayed Cerebral Ischemia using Federated Learning.

    Ahmed Elhussein, Murad Megjhani, Daniel Nametz, Miriam Weiss, Jude Savarraj, Soon Bin Kwon, David J. Roh, Saachin Agarwal, Sander Connolly, Angela Velazquez, Jan Claassen, Huimahn Choi, Gerrit Schubert, Soojin Park, Gamze Gürsoy

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  • Schizophrenia Research  ·  January 14, 2023

    Genetic insights into childhood-onset schizophrenia: The yield of clinical exome sequencing.

    Anna Alkelai, Lior Greenbaum, Shahar Shohat, Gundula Povysil, Ayan Malakar, Zhong Ren, Joshua E Motelow, Tanya Schechter, Benjamin Draiman, Eti Chitrit-Raveh, Daniel Hughes, Vaidehi Jobanputra, Sagiv Shifman, David B Goldstein, Yoav Kohn

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  • medRxiv  ·  January 10, 2023

    The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change.

    Heidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, Pinar Bayrak-Toydemir, Hunter Best, Rhonda Brandon, Jillian G Buchan, Elizabeth C. Chao, Elaine Chen, Jacob Clifford, Ana S A Cohen, Laura K Conlin, Soma Das, Kyle W Davis, Daniela del Gaudio, Florencia Del Viso, Christina DiVincenzo, Marcia Eisenberg, Lucia Guidugli, Monia B Hammer, Steven M Harrison, Kathryn E Hatchell, Lindsay Havens Dyer, Lily U Hoang, James M. Holt, Vaidehi Jobanputra, Izabela D Karbassi, Hutton M Kearney, Melissa A. Kelly, Jacob M. Kelly, Michelle L Kluge, Timothy Komala, Paul Kruszka, Lynette Lau, Matthew S. Lebo, Christian R Marshall, Dianalee McKnight, Kirsty McWalter, Yan Meng, Narasimhan Nagan, Christian S Neckelmann, Nir Neerman, Zhiyv Niu, Vitoria K Paolillo, Sarah A Paolucci, Denise Perry, Tina Pesaran, Kelly Radtke, Kristen J Rasmussen, Kyle Retterer, Carol J Saunders, Elizabeth Spiteri, Christine Stanley, Anna Szuto, Ryan J Taft, Isabelle Thiffault, Brittany C Thomas, Amanda Thomas-Wilson, Erin Thorpe, Timothy J Tidwell, Meghan C Towne, Hana Zouk, Medical Genome Initiative

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  • Biomolecules  ·  January 9, 2023

    Genetic Predisposition to Neurological Complications in Patients with COVID-19.

    Nikhil Shri Sahajpal, Alex R Hastie, Maximilian Schieck, Ashis K Mondal, Marc Felde, Caspar I van der Made, Janet S Chou, Adrienne G Randolph, Thomas Illi, Michael C Zody, Catherine A Brownstein, Alan H Beggs, Alexander Hoischen, Alka Chaubey, Ravindra Kolhe; COVID19hostgenomesv Consortium

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  • Nature Biotechnology  ·  January 2, 2023

    Integration of whole transcriptome spatial profiling with protein markers.

    Nir Ben-Chetrit, Xiang Niu, Ariel D. Swett, Jesus Sotelo, Maria S. Jiao, Caitlin M. Stewart, Catherine Potenski, Paulius Mielinis, Patrick Roelli, Marlon Stoeckius & Dan A. Landau

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  • Cold Spring Harbor Molecular Case Studies  ·  December 28, 2022

    Whole-genome characterization of myoepithelial carcinomas of the soft tissue.

    Joanna Cyrta, Joel Rosiene, Rohan Bareja, Sarah Kudman, Wael Al Zoughbi, Samaneh Motanagh, David C Wilkes, Kenneth Eng, Tuo Zhang, Evan Sticca, Susan Mathew, Mark A Rubin, Andrea Sboner, Olivier Elemento, Brian P Rubin, Marcin Imielinski, Juan Miguel Mosquera

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  • American Journal of Medical Genetics  ·  December 23, 2022

    Detection of mosaic variants using genome sequencing in a large pediatric cohort.

    Jacqueline A. Odgis, Katie M. Gallagher, Atteeq U. Rehman, Priya N. Marathe, Katherine E. Bonini, Monisha Sebastin, Miranda Di Biase, Kaitlyn Brown, Nicole R. Kelly, Michelle A. Ramos, Amanda Thomas-Wilson, Saurav Guha, Volkan Okur, Mythily Ganapathi, Lama Elkhoury, Lisa Edelmann, Randi E. Zinberg, Noura S. Abul-Husn, George A. Diaz, John M. Greally, Sabrina A. Suckiel, Vaidehi Jobanputra, Carol R. Horowitz, Eimear E. Kenny, Melissa P. Wasserstein, Bruce D. Gelb

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