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Collection: Highlights from infectious disease genomics

Disease Neurogenomics: Special issue

Genomic Technologies: Special issue

Featured Video: Identification of a molecular cause of a developmental disorder

A study by Smits and colleagues has pinpointed specific regions of the DLG2 gene expressed in brain cells that upon deletion appear to be associated with developmental delay and intellectual disability phenotypes. This research improves our understanding of the molecular causes of neurodevelopmental disorders and fundamental knowledge about the DLG2 gene – see the video abstract for a graphic summary of the paper.

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1. CONTENT TYPE:RESEARCH

     |  29 November 2017

   Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience

   Authors:Perry G. Ridge, Celeste M. Karch, Simon Hsu, Ivan Arano, Craig C. Teerlink, Mark T. W. Ebbert, Josue D. Gonzalez Murcia, James M. Farnham, Anna R. Damato, Mariet Allen, Xue Wang, Oscar Harari, Victoria M. Fernandez, Rita Guerreiro, Jose Bras, John Hardy…
2. CONTENT TYPE:RESEARCH

     |  28 November 2017

   A novel Ruminococcus gnavus clade enriched in inflammatory bowel disease patients

   Authors:Andrew Brantley Hall, Moran Yassour, Jenny Sauk, Ashley Garner, Xiaofang Jiang, Timothy Arthur, Georgia K. Lagoudas, Tommi Vatanen, Nadine Fornelos, Robin Wilson, Madeline Bertha, Melissa Cohen, John Garber, Hamed Khalili, Dirk Gevers, Ashwin N. Ananthakrishnan…
3. CONTENT TYPE:RESEARCH

     |  28 November 2017

   Predicting cancer type from tumour DNA signatures

   Authors:Kee Pang Soh, Ewa Szczurek, Thomas Sakoparnig and Niko Beerenwinkel
4. CONTENT TYPE:RESEARCH

     |  27 November 2017

   A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder

   Authors:Renato Polimanti, Ananda B. Amstadter, Murray B. Stein, Lynn M. Almli, Dewleen G. Baker, Laura J. Bierut, Bekh Bradley, Lindsay A. Farrer, Eric O. Johnson, Anthony King, Henry R. Kranzler, Adam X. Maihofer, John P. Rice, Andrea L. Roberts, Nancy L. Saccone, Hongyu Zhao…
5. CONTENT TYPE:REVIEW

     |  27 November 2017

   Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications

   Authors:Amy B. Wilfert, Arvis Sulovari, Tychele N. Turner, Bradley P. Coe and Evan E. Eichler

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