Publication > Page 35
  • 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

    link out icon
  • 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

    link out icon
  • 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

    link out icon
  • 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

    link out icon
  • Nature Methods  ·  December 22, 2022

    Efficient combinatorial targeting of RNA transcripts in single cells with Cas13 RNA Perturb-seq.

    Hans-Hermann Wessels, Alejandro Méndez-Mancilla, Yuhan Hao, Efthymia Papalexi, William M. Mauck III, Lu Lu, John A. Morris, Eleni P. Mimitou, Peter Smibert, Neville E. Sanjana & Rahul Satija

    link out icon
  • Nature Biotechnology  ·  December 19, 2022

    Nanobody-tethered transposition enables multifactorial chromatin profiling at single-cell resolution.

    Tim Stuart, Stephanie Hao, Bingjie Zhang, Levan Mekerishvili, Dan A. Landau, Silas Maniatis, Rahul Satija & Ivan Raimondi

    link out icon
  • Nature.  ·  December 14, 2022

    Recurrent repeat expansions in human cancer genomes.

    Graham S. Erwin*, Gamze Gürsoy*, Rashid Al-Abri, Ashwini Suriyaprakash, EgorDolzhenko, Kevin Zhu, Christian R. Hoerner, Shannon M. White, Lucia Ramirez, Ananya Vadlakonda, Alekhya Vadlakonda, Konor von Kraut, Julia Park, Charlotte M. Brannon,Daniel A. Sumano, Raushun A. Kirtikar, Alicia A. Erwin, Thomas J. Metzner, Ryan K. C.Yuen, Alice C. Fan, John T. Leppert, Michael A. Eberle, Mark Gerstein, Michael P. Snyder

    link out icon
  • JCO Precision Oncology  ·  December 8, 2022

    Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care.

    Edwin Cuppen, Olivier Elemento, Richard Rosenquist, Svetlana Nikic, Maarten IJzerman, Isabelle Durand Zaleski, Geert Frederix, Lars-Åke Levin, Charles G Mullighan, Reinhard Buettner, Trevor J Pugh, Sean Grimmond, Carlos Caldas, Fabrice Andre, Ilse Custers, Elias Campo, Hans van Snellenberg, Anna Schuh, Hidewaki Nakagawa, Christof von Kalle, Torsten Haferlach, Stefan Fröhling, Vaidehi Jobanputra

    link out icon
  • Nature Neuroscience  ·  December 8, 2022

    Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes.

    Jack Humphrey, Sanan Venkatesh, Rahat Hasan, Jake T. Herb, Katia de Paiva Lopes, Fahri Küçükali, Marta Byrska-Bishop, Uday S. Evani, Giuseppe Narzisi, Delphine Fagegaltier, NYGC ALS Consortium, Kristel Sleegers, Hemali Phatnani, David A. Knowles, Pietro Fratta & Towfique Raj

    link out icon
  • Nature  ·  November 30, 2022

    Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer.

    Andrew L. H. Webster, Mathijs A. Sanders, Krupa Patel, Ralf Dietrich, Raymond J. Noonan, Francis P. Lach, Ryan R. White, Audrey Goldfarb, Kevin Hadi, Matthew M. Edwards, Frank X. Donovan, Remco M. Hoogenboezem, Moonjung Jung, Sunandini Sridhar, Tom F. Wiley, Olivier Fedrigo, Huasong Tian, Joel Rosiene, Thomas Heineman, Jennifer A. Kennedy, Lorenzo Bean, Rasim O. Rosti, Rebecca Tryon, Ashlyn-Maree Gonzalez, Allana Rosenberg, Ji-Dung Luo, Thomas S. Carroll, Sanjana Shroff, Michael Beaumont, Eunike Velleuer, Jeff C. Rastatter, Susanne I. Wells, Jordi Surrallés, Grover Bagby, Margaret L. MacMillan, John E. Wagner, Maria Cancio, Farid Boulad, Theresa Scognamiglio, Roger Vaughan, Kristin G. Beaumont, Amnon Koren, Marcin Imielinski, Settara C. Chandrasekharappa, Arleen D. Auerbach, Bhuvanesh Singh, David I. Kutler, Peter J. Campbell & Agata Smogorzewska

    link out icon
Decorative image color fade left Decorative image color fade right Decorative image color fade