Submissions from 2018
Sox2 conditional mutation in mouse causes ataxic symptoms, cerebellar vermis hypoplasia, and postnatal defects of Bergmann glia., Valentina Cerrato, Sara Mercurio, Ketty Leto, Elisa Fucà, Eriola Hoxha, Sara Bottes, Miriam Pagin, Marco Milanese, Chew Yee Ngan, Giulia Concina, Sergio Ottolenghi, Chia-Lin Wei, Giambattista Bonanno, Giulio Pavesi, Filippo Tempia, Annalisa Buffo, and Silvia K Nicolis
Functional Interrogation of Primary Human T Cells via CRISPR Genetic Editing., Xin Chen, Lina Kozhaya, Cihan Tastan, Lindsey Placek, Mikail Dogan, Meghan Horne, Rebecca Abblett, Ece Karhan, Martin Vaeth, Stefan Feske, and Derya Unutmaz
Identification of a novel gene regulating amygdala-mediated fear extinction., Ozge Gunduz-Cinar, Emma Brockway, Lauren Lederle, Troy Wilcox, Lindsay R Halladay, Ying Ding, Hyunjung Oh, Erica F Busch, Katie Kaugars, Shaun Flynn, Aaron Limoges, Olena Bukalo, Kathryn P MacPherson, Sophie Masneuf, Courtney Pinard, Etienne Sibille, Elissa J Chesler, and Andrew Holmes
DNA methylomes of bovine gametes and in vivo produced preimplantation embryos., Z Jiang, Jianan Lin, H Dong, X Zheng, S L Marjani, J Duan, Zhengqing Ouyang, J Chen, and X C Tian
A FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency., Yang Kong, Lihong Zhao, Jeremy R. Charette, Wanda L. Hicks, Lisa Stone, Patsy M. Nishina, and Juergen K. Naggert
Harmonising phenomics information for a better interoperability in the rare disease field., Sylvie Maiella, Annie Olry, Marc Hanauer, Valérie Lanneau, Halima Lourghi, Bruno Donadille, Charlotte Rodwell, Sebastian Köhler, Dominik Seelow, Simon Jupp, Helen Parkinson, Tudor Groza, Michael Brudno, Peter N Robinson, and Ana Rath
The Tandem Duplicator Phenotype Is a Prevalent Genome-Wide Cancer Configuration Driven by Distinct Gene Mutations., Francesca Menghi, Floris P Barthel, Vinod Yadav, Ming Tang, Bo Ji, Zhonghui Tang, Gregory W. Carter, Yijun Ruan, Ralph Scully, Roel G W Verhaak, Jos Jonkers, and Edison T Liu
Immunomodulatory interventions in myocardial infarction and heart failure: a systematic review of clinical trials and meta-analysis of IL-1 inhibition., Mona Panahi, Angelos Papanikolaou, Azam Torabi, Ji-Gang Zhang, Habib Khan, Ali Vazir, Muneer G. Hasham, John G F Cleland, Nadia Rosenthal, Sian E Harding, and Susanne Sattler
Extracellular vesicles in DLBCL provide abundant clues to aberrant transcriptional programming and genomic alterations., Sarah C Rutherford, Angela A Fachel, Sheng Li, Seema Sawh, Ashlesha Muley, Jennifer Ishii, Ashish Saxena, Pilar M Dominguez, Eloisi Caldas Lopes, Xabier Agirre, Nyasha Chambwe, Fabian Correa, Yanwen Jiang, Kristy L Richards, Doron Betel, and Rita Shaknovich
Unpackaging the genetics of mammalian fertility: Strategies to identify the "reproductive genome"., John C Schimenti and Mary Ann Handel
IL-1 receptor antagonist controls transcriptional signature of inflammation in patients with metastatic breast cancer., Te-Chia Wu, Kangling Xu, Jan Martinek, Robyn R Young, Romain Banchereau, Joshy George, Jacob Turner, Kyung In Kim, Sandra Zurawski, Xuan Wang, Derek Blankenship, Hannah M Brookes, Florentina Marches, Gerlinde Obermoser, Elizabeth Lavecchio, Maren K Levin, Sookyoung Bae, Cheng-Han Chung, Jennifer L Smith, Alma-Martina Cepika, Kyp L Oxley, George J Snipes, Jacques Banchereau, Virginia Pascual, Joyce O'Shaughnessy, and Karolina Palucka
Two-phase differential expression analysis for single cell RNA-seq., Zhijin Wu, Yi Zhang, Michael L. Stitzel, and Hao Wu
Submissions from 2017
ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID)., Jayson Lian, Mario Cuk, Sascha Kahlfuss, Lina Kozhaya, Martin Vaeth, Frédéric Rieux-Laucat, Capucine Picard, Melina J Benson, Antonia Jakovcevic, Karmen Bilic, Iva Martinac, Peter Stathopulos, Imre Kacskovics, Thomas Vraetz, Carsten Speckmann, Stephan Ehl, Thomas Issekutz, Derya Unutmaz, and Stefan Feske