Trainee Paper Spotlight

Trainee Author: Janson White, PhD Senior Fellow Department of Pediatrics, University of Washington (Photo courtesy White) White JJ, et al. WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. AJHG. 2018 Jan 4;102(1):27-43. This study was selected for the Trainee Paper Spotlight because it uses extensive genetic and genomic studies to identify new pathogenic... Read More

Trainee Author: Kevin Gillinder, PhD Research Fellow Australian Centre for Blood Diseases, Monash University, Australia (Photo courtesy Gillinder) Gillinder KR, et al. Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability. NAR. 2017 Feb 17;45(3):1130-1143 This is the first study to show neomorphic functions in a zinc finger binding... Read More

Trainee Author: Alina Kurolap, RN, MSc PhD Student, Medical Sciences Technion – Israel Institute of Technology, the Ruth and Bruce Rappaport Faculty of Medicine (Photo courtesy Kurolap) Kurolap A, Armbruster A, et al. Loss of glycine transporter 1 causes a subtype of glycine encephalopathy with arthrogryposis and mildly elevated cerebrosipinal fluid glycine. AJHG. 2016 Nov... Read More

Trainee Author: Zafar Iqbal, PhD Researcher Oslo University Hospital, Oslo, Norway (Photo courtesy Iqbal) Riazuddin S, Hussain M, Razzaq A, Iqbal Z, et al. Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability. Molecular Psychiatry (2017) 22, 1604-1614 This multi-investigator exome sequencing project aims to discover pathogenic mutations for... Read More

  Trainee Author: Ryan Collins, AB PhD Candidate, Program in Bioinformatics and Integrative Genomics Harvard Medical School (Photo courtesy Collins) Collins RL et al. Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome. Genome Biology. 2017 Mar 6; 18 (1): 36 This study expands our understanding of the... Read More