Nickesha C Anderson
Biographic Data
| ID | 7953907 |
|---|---|
| NAME | Nickesha C Anderson |
| GIVEN NAMES | Nickesha C |
| FAMILY NAME | Anderson |
| SIGNATURE | ANDERSON N C |
| AFFILIATIONS | Harvard University |
| ORCID | 0000-0003-4168-0703 |
| VERIFIED | Yes |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2022 |
| H-INDEX | 0 |
P13.11 Deletion Variants Associated With Neuropsychiatric Disorders Cause Morphological and Synaptic Changes in Induced Pluripotent Stem Cell-Derived Neurons
16p13.11 copy number variants (CNVs) have been associated with autism, schizophrenia, psychosis, intellectual disability, and epilepsy. The majority of 16p13.11 deletions or duplications occur within three well-defined intervals, and despite growing knowledge of the functions of individual genes within these intervals, the molecular mechanisms that underlie commonly observed clinical phenotypes remain largely unknown. Patient-derived, induced plu…
No prominent works on this page.
P13.11 Deletion Variants Associated With Neuropsychiatric Disorders Cause Morphological and Synaptic Changes in Induced Pluripotent Stem Cell-Derived Neurons
16p13.11 copy number variants (CNVs) have been associated with autism, schizophrenia, psychosis, intellectual disability, and epilepsy. The majority of 16p13.11 deletions or duplications occur within three well-defined intervals, and despite growing knowledge of the functions of individual genes within these intervals, the molecular mechanisms that underlie commonly observed clinical phenotypes remain largely unknown. Patient-derived, induced plu…
Biology (1 work) · Congenital heart defects research (1 work) · Copy-number variation (1 work) · Embryonic stem cell (1 work) · Gene (1 work) · Gene expression (1 work) · Genetics (1 work) · Genetics and Neurodevelopmental Disorders (1 work) · Genome (1 work) · Genomic variations and chromosomal abnormalities (1 work)