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List of works by Eric M. Morrow

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

scientific article

A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene

article

Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait

scientific article published on 06 June 2013

An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma.

scientific article

Ascertainment and gender in autism spectrum disorders

scientific article published in June 2014

Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study

scientific article published on 20 January 2020

Autism and brain development

scientific article

BKca channel in autism and mental retardation

scientific article published in June 2007

Brief Report: Factors Influencing Healthcare Satisfaction in Adults with Autism Spectrum Disorder

scientific article published on 7 March 2017

Characterization of Medication Use in a Multicenter Sample of Pediatric Inpatients with Autism Spectrum Disorder

scientific article published on 17 May 2017

Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development

scientific article

Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy

scientific article

Common genetic variants, acting additively, are a major source of risk for autism

scientific article

Complex Neurological Phenotype in Female Carriers of NHE6 Mutations

scientific article published on 06 March 2019

Creating Patient-Specific Neural Cells for the In Vitro Study of Brain Disorders

scientific article

Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.

scientific article published on November 1997

DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism

scientific article

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

scientific article

Distribution of disease-associated copy number variants across distinct disorders of cognitive development

scientific article published on April 2013

Executive function in probands with autism with average IQ and their unaffected first-degree relatives

scientific article

Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein

scientific article

Female Autism Phenotypes Investigated at Different Levels of Language and Developmental Abilities

scientific article

Functional Assessment In Vivo of the Mouse Homolog of the Human Ala-9-Ser NHE6 Variant

scientific article published on 01 November 2019

Further clinical and molecular delineation of the 15q24 microdeletion syndrome

scientific article (publication date: February 2012)

GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates

scientific article published on 30 August 2019

Genes for endosomal NHE6 and NHE9 are misregulated in autism brains.

scientific article published on 19 March 2013

Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome

scientific article

Genetic control of postnatal human brain growth

scientific article published on 24 November 2016

Genetic influences on cognitive endophenotypes in schizophrenia

scientific article

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Genetics in autism diagnosis: adding molecular subtypes to neurobehavioral diagnoses ⬇️

scientific article published on May 1, 2011

Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing

scientific article

Genomic Copy Number Variation in Disorders of Cognitive Development ⬇️

scientific article published on November 1, 2010

Graph Metrics of Structural Brain Networks in Individuals with Schizophrenia and Healthy Controls: Group Differences, Relationships with Intelligence, and Genetics

scientific article published in February 2016

Identifying autism loci and genes by tracing recent shared ancestry

scientific article

Inaugural Christianson Syndrome Association conference: families meeting for the first time

scientific article published on 23 May 2014

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

scientific article

Intellectual disability is associated with increased runs of homozygosity in simplex autism

scientific article published on 03 July 2013

Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders ⬇️

scientific article published on September 1, 2012

Live-cell Microscopy and Fluorescence-based Measurement of Luminal pH in Intracellular Organelles

scientific article published on 21 August 2017

Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification

scientific article published on 12 August 2019

Loss of Christianson Syndrome Na<sup>+</sup>/H<sup>+</sup> Exchanger 6 (NHE6) Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in Neurons

scientific article published on 15 September 2021

Methods for study of neuronal morphogenesis: ex vivo RNAi electroporation in embryonic murine cerebral cortex

scientific article

MicroRNAs in copy number variants in schizophrenia: misregulation of genome-wide gene expression programs

scientific article published in January 2015

Misexpression of basic helix-loop-helix genes in the murine cerebral cortex affects cell fate choices and neuronal survival.

scientific article published in July 2000

Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome

scientific article published on 17 January 2017

Modeling developmental neuropsychiatric disorders with iPSC technology: challenges and opportunities

scientific article published on 23 October 2015

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

scientific article published on 12 May 2014

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

scientific article (publication date: June 2011)

Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features

scientific article published on 06 September 2016

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Observation-centered approach to ASD assessment in Tanzania

scientific article published in October 2014

Paternal sperm DNA mosaicism and recurrence risk of autism in families

scientific article published on 01 January 2020

Postictal psychosis: presymptomatic risk factors and the need for further investigation of genetics and pharmacotherapy

scientific article

Predictors of Inpatient Psychiatric Hospitalization for Children and Adolescents with Autism Spectrum Disorder

scientific article published on 23 May 2017

Quantifying the effects of rare variants in pedigrees: how far does the apple fall from the tree?

scientific article published in February 2015

Reconciling past changes in Earth's rotation with 20th century global sea-level rise: Resolving Munk's enigma

scientific article

Risk assessment models in genetics clinic for array comparative genomic hybridization: Clinical information can be used to predict the likelihood of an abnormal result in patients

scientific article

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

scientific article (publication date: 3 October 2013)

Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairment

scientific article published on 20 September 2008

Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex.

scientific article published in June 2018

Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice

scientific article

Temporal order of bipolar cell genesis in the neural retina

scientific article

The COMT Val108/158Met polymorphism and medial temporal lobe volumetry in patients with schizophrenia and healthy adults

scientific article

The Role of Mitochondrial Glutamate Metabolism in Cognitive Development and Disease

scientific article published in January 2018

The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder

scientific article published on 28 October 2013

The autism inpatient collection: methods and preliminary sample description

scientific article

The impact of copy number deletions on general cognitive ability and ventricle size in patients with schizophrenia and healthy control subjects

scientific article published on 11 December 2012

The interface of genetics and clinical psychiatry. Introduction

scientific article published in March 2006

Two phases of rod photoreceptor differentiation during rat retinal development

article

Uncovering a Role for SK2 in Angelman Syndrome

scientific article published in July 2015

Using whole-exome sequencing to identify inherited causes of autism

scientific article

Vertebrate photoreceptor cell development and disease ⬇️

scientific article published on September 1, 1998

rax, Hes1, and notch1 promote the formation of Müller glia by postnatal retinal progenitor cells

scientific journal article

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