Assistant Professor of Psychiatry, Massachusetts General Hospital
Psychiatry
Dr. Eric M. Morrow, MD
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Doctor Eric M. Morrow, MD works in the field of Psychiatry. He graduated from Harvard Medical School. Harvard Medical School is a top medical college. Harvard Medical School has a rank of 1 in research and a 12 in primary care Eric Morrow is also a published doctor. He has 43 publication published. The most recent publication is: NeuroD regulates multiple functions in the developing neural retina in rodent.
Publications
- Graph Metrics of Structural Brain Networks in Individuals with Schizophrenia and Healthy Controls: Group Differences, Relationships with Intelligence, and Genetics.
- Female Autism Phenotypes Investigated at Different Levels of Language and Developmental Abilities.
- Modeling developmental neuropsychiatric disorders with iPSC technology: challenges and opportunities.
- A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
- Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein.
- Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome.
- Genetic influences on cognitive endophenotypes in schizophrenia.
- Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2.
- Christianson Syndrome Protein NHE6 Modulates TrkB Endosomal Signaling Required for Neuronal Circuit Development.
- Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism.
- Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait.
- Distribution of disease-associated copy number variants across distinct disorders of cognitive development.
- An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma.
- Genes for endosomal NHE6 and NHE9 are misregulated in autism brains.
- The impact of copy number deletions on general cognitive ability and ventricle size in patients with schizophrenia and healthy control subjects.
- Using Whole-Exome Sequencing to Identify Inherited Causes of Autism.
- Further clinical and molecular delineation of the 15q24 microdeletion syndrome.
- A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene.
- Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing.
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism.
- Genetics in autism diagnosis: adding molecular subtypes to neurobehavioral diagnoses.
- The COMT Val108/158Met polymorphism and medial temporal lobe volumetry in patients with schizophrenia and healthy adults.
- Genomic copy number variation in disorders of cognitive development.
- Autism and brain development.
- Identifying autism loci and genes by tracing recent shared ancestry.
- BKca channel in autism and mental retardation.
- The interface of genetics and clinical psychiatry. Introduction.
- The autism inpatient collection: methods and preliminary sample description.
- Inaugural Christianson Syndrome Association conference: families meeting for the first time.
- Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy.
- Vertebrate photoreceptor cell development and disease.
- Misexpression of basic helix-loop-helix genes in the murine cerebral cortex affects cell fate choices and neuronal survival.
- Two phases of rod photoreceptor differentiation during rat retinal development.
- rax, Hes1, and notch1 promote the formation of Müller glia by postnatal retinal progenitor cells.
- Retinopathy and attenuated circadian entrainment in Crx-deficient mice.
- NeuroD regulates multiple functions in the developing neural retina in rodent.
- Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.
- Postictal psychosis: presymptomatic risk factors and the need for further investigation of genetics and pharmacotherapy.
- Temporal order of bipolar cell genesis in the neural retina.
- Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairment.
- Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice.
- Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
Schools
Harvard Medical School
Doctors Specialties
- Psychiatry
Accepted Insurances
Education
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Massachusetts General Hospital -
Harvard Medical School
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