Genome-wide investigation of an ID cohort reveals de novo 3′UTR variants affecting gene expression

Understanding Neurodevelopmental Disorders: The Promise of Regulatory Variation in the 3′UTRome

(2018) Kai A. Wanke et al.   BIOLOGICAL PSYCHIATRY

AMD1 mRNA employs ribosome stalling as a mechanism for molecular memory formation

(2018) Martina M. Yordanova et al.   NATURE

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders

(2017) P Devanna et al.   MOLECULAR PSYCHIATRY

Identification and characterization of new isoforms of human fas apoptotic inhibitory molecule (FAIM)

(2017) Elena Coccia et al.   PLoS One

Genomic diagnosis for children with intellectual disability and/or developmental delay

(2017) Kevin M. Bowling et al.   Genome Medicine

Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability

(2016) Glen R. Monroe et al.   GENETICS IN MEDICINE

Genetic studies in intellectual disability and related disorders

(2015) Lisenka E. L. M. Vissers et al.   NATURE REVIEWS GENETICS

Large-scale discovery of novel genetic causes of developmental disorders

(2014) T. W. Fitzgerald et al.   NATURE

Genome sequencing identifies major causes of severe intellectual disability

(2014) Christian Gilissen et al.   NATURE

De Novo Mutations in Moderate or Severe Intellectual Disability

(2014) Fadi F. Hamdan et al.   PLoS Genetics

AMD1 is essential for ESC self-renewal and is translationally down-regulated on differentiation to neural precursor cells

(2012) D. Zhang et al.   GENES & DEVELOPMENT

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

(2012) Anita Rauch et al.   LANCET

Genetics of Early Onset Cognitive Impairment

(2010) Hans Hilger Ropers   Annual Review of Genomics and Human Genetics

BEDTools: a flexible suite of utilities for comparing genomic features

(2010) Aaron R. Quinlan et al.   BIOINFORMATICS