Associate Professor, UCSF
Neurology
Dr. Elliott H. Sherr, MD
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Elliott Sherr works in the field of Neurology. He graduated from Columbia University College of Physicians & Surgeons. Columbia University College of Physicians & Surgeons is a top medical college. Columbia University College of Physicians & Surgeons is ranked 8 in research and 52 in primary care medicine He has 1 awards "Regional Top Doctor". Elliott H. Sherr is a published doctor as well. He has 64 publications published. The latest was: Mapping of unconventional myosins in mouse and human.
Publications
- Neuroimaging in Aicardi-Goutières syndrome: Biomarkers for a progressive encephalopathy.
- Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication.
- Epileptic encephalopathies: new genes and new pathways.
- Opposing brain differences in 16p11.2 deletion and duplication carriers.
- De novo ANKRD11 and KDM1A gene mutations in a male with features of KBG syndrome and Kabuki syndrome.
- Aberrant white matter microstructure in children with 16p11.2 deletions.
- Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5.
- Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.
- Resting State Networks and the Functional Connectome of the Human Brain in Agenesis of the Corpus Callosum.
- Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption.
- Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.
- Test-Retest Reliability of Computational Network Measurements Derived from the Structural Connectome of the Human Brain.
- The structural connectome of the human brain in agenesis of the corpus callosum.
- Autism Traits in Individuals with Agenesis of the Corpus Callosum.
- Children With Autism Show Reduced Somatosensory Response: An MEG Study.
- The role of corpus callosum development in functional connectivity and cognitive processing.
- VAX1 mutation associated with microphthalmia, corpus callosum agenesis and orofacial clefting-the first description of a VAX1 phenotype in humans.
- Laterality of brain and ocular lesions in aicardi syndrome.
- Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.
- Identification of genomic loci contributing to agenesis of the corpus callosum.
- Diffusion tensor imaging of Aicardi syndrome.
- Microstructural correlations of white matter tracts in the human brain.
- Agenesis of the corpus callosum in California 1983-2003: a population-based study.
- The importance of metabolic testing in the evaluation of intellectual disability.
- Dilated perivascular spaces: an informative radiologic finding in Sanfilippo syndrome type A.
- Agenesis of the corpus callosum, optic coloboma, intractable seizures, craniofacial and skeletal dysmorphisms: an autosomal recessive disorder similar to Temtamy syndr...
- Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.
- NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.
- Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations.
- The ARX story (Epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes.
- T1 hyperintensity in the pulvinar: key imaging feature for diagnosis of Fabry disease.
- Identification of a monogenic locus (jams1) causing juvenile audiogenic seizures in mice.
- Quantitative Trait Loci for Interhemispheric Commissure Development and Social Behaviors in the BTBR T(+) tf/J Mouse Model of Autism.
- GFAP mutations, age at onset, and clinical subtypes in Alexander disease.
- Expanding CEP290 mutational spectrum in ciliopathies.
- Marinesco-Sjögren syndrome in a male with mild dysmorphism.
- Case report: Y;6 translocation with deletion of 6p.
- Retinoic acid induces the differentiation of B cell hybridomas from patients with common variable immunodeficiency.
- Binding the low affinity Fc epsilon R on B cells suppresses ongoing human IgE synthesis.
- So what? Does the test lead to improved health outcomes?
- Clinical Reasoning: An encephalopathic 3-day-old infant.
- Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families.
- Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neu...
- Diffusion abnormalities and reduced volume of the ventral cingulum bundle in agenesis of the corpus callosum: a 3T imaging study.
- Variability of homotopic and heterotopic callosal connectivity in partial agenesis of the corpus callosum: a 3T diffusion tensor imaging and Q-ball tractography study.
- Agenesis of the corpus callosum: an MR imaging analysis of associated abnormalities in the fetus.
- ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal.
- Human natural killer (NK) cells produce a late-acting B-cell differentiation activity.
- Functional and phenotypic characterization of human B lymphocyte subsets isolated by unit gravity sedimentation.
- IgE-enhancing activity directly and selectively affects activated B cells: evidence for a human IgE differentiation factor.
- A mechanism for the suppression of ongoing IgE synthesis.
- Failure of B cells in common variable immunodeficiency to transit from proliferation to differentiation is associated with altered B cell surface-molecule display.
- Mapping of unconventional myosins in mouse and human.
- Mammalian myosin I alpha, I beta, and I gamma: new widely expressed genes of the myosin I family.
- Periventricular heterotopia associated with chromosome 5p anomalies.
- Mutation analysis of the FRAS1 gene demonstrates new mutations in a propositus with Fraser syndrome.
- Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies.
- Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.
- CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related Disorders.
- Hematopoietic stem cell transplantation for the treatment of childhood cerebral X-linked adrenoleukodystrophy.
- Dual-mode modulation of smad signaling by smad-interacting protein sip1 is required for myelination in the central nervous system.
- Targeted ''next-generation'' sequencing in anophthalmia and microphthalmia patients confirms SOX2, OTX2 and FOXE3 mutations.
- Relationship between M100 Auditory Evoked Response and Auditory Radiation Microstructure in 16p11.2 Deletion and Duplication Carriers.
Schools
Columbia University College of Physicians And Surgeons
Stanford University
Conditions Treated
- Ataxia
- Convulsions
- Dystonia
- Epilepsy
- View All
Doctors Specialties
- Pediatric Neurology
- Neurology
Accepted Insurances
Awards
- Regional Top Doctor
Education
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UCSF -
Columbia University College of Physicians & Surgeons
Hospital
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UCSF Medical Center
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