Christopher William

ORCID: 0000-0001-8933-1639
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About
Contact & Profiles
Research Areas
  • Alzheimer's disease research and treatments
  • Glioma Diagnosis and Treatment
  • Neuroscience and Neuropharmacology Research
  • Epilepsy research and treatment
  • Mitochondrial Function and Pathology
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Neonatal and fetal brain pathology
  • Acute Ischemic Stroke Management
  • Brain Metastases and Treatment
  • Cancer Genomics and Diagnostics
  • Neuroblastoma Research and Treatments
  • Intracerebral and Subarachnoid Hemorrhage Research
  • Neuroscience of respiration and sleep
  • Retinal Development and Disorders
  • Neurogenesis and neuroplasticity mechanisms
  • Developmental Biology and Gene Regulation
  • Epigenetics and DNA Methylation
  • Pituitary Gland Disorders and Treatments
  • Dementia and Cognitive Impairment Research
  • Neurosurgical Procedures and Complications
  • Spinal Hematomas and Complications
  • Axon Guidance and Neuronal Signaling
  • Autopsy Techniques and Outcomes
  • Chromatin Remodeling and Cancer
  • CNS Lymphoma Diagnosis and Treatment

New York University
2017-2024

University of California, San Diego
2024

Cornell University
2024

NYU Langone Health
2016-2023

National University of Malaysia
2023

Nationwide Children's Hospital
2019

Neurological Surgery
2019

Central University of Ecuador
2018

Massachusetts General Hospital
2011-2016

Harvard University
2010-2016

The molecular mechanism involved in the process of antigen-driven somatic hypermutation Ig genes is unknown, but it commonly believed that this restricted to loci. B cell lymphomas display multiple mutations clustering 5′-regulatory region BCL-6, a proto-oncogene encoding for POZ/Zinc finger transcriptional repressor expressed germinal center (GC) cells and required GC formation. To determine whether BCL-6 represent tumor-associated phenomenon or reflect physiologic mechanism, we screened...

10.1073/pnas.95.20.11816 article EN Proceedings of the National Academy of Sciences 1998-09-29

Soluble β-amyloid (Aβ) oligomers impair synaptic plasticity and cause loss associated with Alzheimer's disease (AD). We report that murine PirB (paired immunoglobulin-like receptor B) its human ortholog LilrB2 (leukocyte B2), present in brain, are receptors for Aβ oligomers, nanomolar affinity. The first two extracellular immunoglobulin (Ig) domains of mediate this interaction, leading to enhanced cofilin signaling, also seen AD brains. In mice, the deleterious effect on hippocampal...

10.1126/science.1242077 article EN Science 2013-09-19

Several imaging modalities are suitable for in vivo molecular neuroimaging, but the blood–brain barrier (BBB) limits their utility by preventing brain delivery of most targeted probes. We prepared biodegradable nanocarrier systems made up poly(n-butyl cyanoacrylate) dextran polymers coated with polysorbate 80 (PBCA nanoparticles) to deliver BBB-impermeable probes into neuroimaging. demonstrate that PBCA nanoparticles allow targeting contrast agents and staining reagents electron microscopy,...

10.1073/pnas.1111405108 article EN Proceedings of the National Academy of Sciences 2011-11-07

In early stages of Alzheimer's disease (AD), neurofibrillary tangles (NFT) are largely restricted to the entorhinal cortex and medial temporal lobe. At later stages, when clinical symptoms generally occur, NFT involve widespread limbic association cortices. this point in disease, amyloid plaques also abundantly distributed cortex. This observation from human neuropathological studies led us pose two alternative hypotheses: that is permissive for spread lobe, or these co-occurring but not...

10.1186/s40478-015-0199-x article EN cc-by Acta Neuropathologica Communications 2015-03-23

Sonic hedgehog signaling controls the differentiation of motor neurons in ventral neural tube, but intervening steps are poorly understood. A differential screen a cDNA library derived from single Shh-induced neuron has identified novel homeobox gene MNR2, expressed by progenitors and transiently postmitotic neurons. The ectopic expression MNR2 cells initiates program somatic characterized homeodomain proteins, neurotransmitter phenotype, axonal trajectory. Our results suggest that...

10.1016/s0092-8674(00)81783-3 article EN cc-by-nc-nd Cell 1998-10-01

Anti-amyloid-b immunization leads to amyloid clearance in patients with Alzheimer's disease, but the effect of vaccination on amyloid-b-induced neuronal pathology has not been quantitatively examined.The objectives this study were address effects anti-amyloid-b active neurite trajectories and pathological hallmarks disease human hippocampus.Hippocampal sections from five enrolled AN1792 Phase 2a trial compared those 13 non-immunized Braak-stage age-matched eight non-demented...

10.1093/brain/awq056 article EN Brain 2010-03-31

Neurofibrillary tangles are a feature of Alzheimer disease and other tauopathies, although they generally believed to be markers neuronal pathology, there is little evidence evaluating whether directly impact function. To investigate the response cells in hippocampal circuits complex behavioral stimuli, we used an environmental enrichment paradigm induce expression immediate-early gene, Arc, rTg4510 mouse model tauopathy. These mice reversibly overexpress P301L tau exhibit substantial...

10.1097/nen.0b013e318220a658 article EN Journal of Neuropathology & Experimental Neurology 2011-06-10

Abstract Background Central nervous system (CNS) cancer is the 10th leading cause of cancer-associated deaths for adults, but in pediatric patients and young adults. The variety complexity histologic subtypes can lead to diagnostic errors. DNA methylation an epigenetic modification that provides a tumor type-specific signature be used diagnosis. Methods We performed prospective study using analysis as primary method 1921 brain tumors. All tumors received pathology diagnosis profiling by...

10.1093/noajnl/vdad076 article EN cc-by-nc Neuro-Oncology Advances 2023-01-01

In the developing spinal cord, motor neurons acquire columnar subtype identities that can be recognized by distinct profiles of homeodomain transcription factor expression. The mechanisms direct differentiation neuron from an apparently uniform group progenitors remain poorly defined. chick embryo,the Mnx class protein MNR2 is expressed selectively progenitors, and has been implicated in specification fate. We show here expression persists postmitotic populate median column (MMC), whereas...

10.1242/dev.00358 article EN Development 2003-03-05

To identify predictors of early lobar intracerebral hemorrhage (ICH) recurrence, defined as a new ICH within 6 months the index event, in patients with cerebral amyloid angiopathy (CAA).Participants were consecutive survivors (age ≥55 years) spontaneous symptomatic probable or possible CAA-related according to Boston criteria, drawn from an ongoing single-center cohort study. Neuroimaging markers ascertained CT MRI included focal (≤3 sulci) disseminated (>3 cortical superficial siderosis...

10.1212/wnl.0000000000003281 article EN Neurology 2016-10-01

Amyloid-β (Aβ)-induced changes in synaptic function experimental models of Alzheimer9s disease (AD) suggest that Aβ generation and accumulation may affect fundamental mechanisms plasticity. To test this hypothesis, we examined the effect APP overexpression on a well characterized, <i>in vivo</i>, developmental model systems-level plasticity, ocular dominance Following monocular visual deprivation during critical period, mice express mutant alleles amyloid precursor protein (APPswe)...

10.1523/jneurosci.5369-11.2012 article EN Journal of Neuroscience 2012-06-06

To identify in vivo MRI markers that might correlate with cerebral microinfarcts (CMIs) on autopsy patients amyloid angiopathy (CAA).We included neuropathologic evidence of CAA and available antemortem brain MRI. Clinical characteristics CAA-related small vessel disease were recorded, including white matter hyperintensities, microbleeds, cortical superficial siderosis, centrum semiovale perivascular spaces. In addition, the presence intracerebral hemorrhage was assessed. Evaluation number...

10.1212/wnl.0000000000003184 article EN Neurology 2016-09-10

Abstract Background Isocitrate dehydrogenase (IDH) mutant astrocytoma grading, until recently, has been entirely based on morphology. The 5th edition of the Central Nervous System World Health Organization (WHO) introduces CDKN2A/B homozygous deletion as a biomarker grade 4. We sought to investigate prognostic impact DNA methylation-derived molecular biomarkers for IDH astrocytoma. Methods analyzed 98 astrocytomas diagnosed at NYU Langone between 2014 and 2022. reviewed methylation subclass,...

10.1093/neuonc/noae009 article EN Neuro-Oncology 2024-01-19

Optical imaging using multiphoton microscopy and whole body near infrared has become a routine part of biomedical research. However, optical methods rely on the availability either small molecule reporters or genetically encoded fluorescent proteins, which are challenging time consuming to develop. While directly labeled antibodies can also be used as agents, species specific, typically not tagged with multiple without interfering target binding, bioactive, almost always eliciting biological...

10.1371/journal.pone.0089901 article EN cc-by PLoS ONE 2014-02-26

Abstract Context X-linked acrogigantism (X-LAG), a condition of infant-onset marked by elevated GH, IGF-1, and prolactin (PRL), is extremely rare. Thirty-three cases, including three kindreds, have been reported. These patients pituitary adenomas that are thought to be mixed lactotrophs somatotrophs. Case Description The patient’s mother, diagnosed with at 21 months, underwent tumor excision 24 months. For more than 30 years, stable PRL, IGF-1 concentrations serial imaging studies indicated...

10.1210/jc.2019-00817 article EN The Journal of Clinical Endocrinology & Metabolism 2019-06-05

Abstract ROS1 is a transmembrane receptor tyrosine kinase proto-oncogene that has been shown to have rearrangements with several genes in glioblastoma and other neoplasms, including intrachromosomal fusion GOPC due microdeletions at 6q22.1. events are important findings these tumors, as they potentially targetable alterations newer inhibitors; however, whether tumors represent distinct entity remains unknown. In this report, we identify 3 cases of unusual pediatric glioma GOPC-ROS1 fusion....

10.1093/jnen/nlz093 article EN Journal of Neuropathology & Experimental Neurology 2019-09-16

Abstract Sudden unexplained death in childhood (SUDC) is of a child over 1 year age that after review clinical history, circumstances death, and complete autopsy with ancillary testing. Multiple etiologies may cause SUDC. SUDC sudden unexpected epilepsy (SUDEP) share pathological features, suggesting some similarities mechanism possible abnormalities hippocampus cortex. To identify molecular signaling pathways, we performed label-free quantitative mass spectrometry on microdissected frontal...

10.1007/s00401-022-02414-7 article EN cc-by Acta Neuropathologica 2022-03-25

Sudden unexplained death in childhood (SUDC) affects children >1-year-old whose cause of remains following comprehensive case investigation and is often associated with hippocampal abnormalities. We prospectively performed systematic neuropathologic 20 SUDC cases, including (i) autopsy data ancillary testing, molecular studies, (ii) ex vivo 3T MRI extensive histologic brain samples, (iii) blinded neuropathology review by 2 board-certified neuropathologists. There were 12 girls 8 boys; median...

10.1093/jnen/nlz136 article EN Journal of Neuropathology & Experimental Neurology 2020-01-29

Abnormal cerebral vasculature can be a manifestation of vascular malformation or neoplastic process. We report the case patient with angiography-negative subarachnoid hemorrhage (SAH) who re-presented 3 years later large intraparenchymal hemorrhage. Although imaging following was suggestive arteriovenous malformation, ultimately found to have an extensive glioblastoma associated abnormal tumor vasculature. The emphasizes need for magnetic resonance investigate SAH in suspicious cases rule...

10.3389/fneur.2013.00144 article EN cc-by Frontiers in Neurology 2013-01-01
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