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1. Is ‘likely pathogenic’ really 90% likely? Reclassification data in ClinVar

   Authors:Steven M. Harrison and Heidi L. Rehm

   Content type:Comment

   21 November 2019

2. Neoantigens and genome instability: impact on immunogenomic phenotypes and immunotherapy response

   Authors:Elaine R. Mardis

   Content type:Review

   20 November 2019

3. Artificial intelligence in clinical and genomic diagnostics

   Authors:Raquel Dias and Ali Torkamani

   Content type:Review

   19 November 2019

4. Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension

   Authors:Na Zhu, Michael W. Pauciulo, Carrie L. Welch, Katie A. Lutz, Anna W. Coleman, Claudia Gonzaga-Jauregui, Jiayao Wang, Joseph M. Grimes, Lisa J. Martin, Hua He, Yufeng Shen, Wendy K. Chung and William C. Nichols

   Content type:Research

   14 November 2019

5. From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

   Authors:Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, Claudia M. B. Carvalho, Malin Kvarnung, Giedre Grigelioniene, Britt-Marie Anderlid, Olof Bjerin, Peter Gustavsson, Anna Hammarsjö, Patrik Georgii-Hemming, Erik Iwarsson, Maria Johansson-Soller, Kristina Lagerstedt-Robinson, Agne Lieden, Måns Magnusson…

   Content type:Research

   7 November 2019