Stormy J. Chamberlain, Ph.D.
Affiliations: | 2003 | University of Florida, Gainesville, Gainesville, FL, United States |
Area:
Genetics, PathologyGoogle:
"Stormy Chamberlain"Parents
Sign in to add mentor| James Resnick | grad student | 2003 | UF Gainesville | |
| (Elucidation of imprinting mechanisms and phenotypes in Prader -Willi syndrome mice.) | ||||
Children
Sign in to add trainee| Alexandra M Goetjen | grad student | 2014-2016 | University of Connecticut Health Center (Neurotree) |
| Peter A. Perrino | post-doc | 2021-2022 | University of Connecticut Health Center (Neurotree) |
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Publications
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| Perez Y, Velmeshev D, Wang L, et al. (2023) Single cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism. Biorxiv : the Preprint Server For Biology |
| Gilmore RB, Gorka D, Stoddard CE, et al. (2023) Generation of isogenic models of Angelman syndrome and Prader-Willi syndrome in CRISPR/Cas9-engineered human embryonic stem cells. Biorxiv : the Preprint Server For Biology |
| Elamin M, Dumarchey A, Stoddard C, et al. (2023) The role of UBE3A in the autism and epilepsy-related Dup15q syndrome using patient-derived, CRISPR-corrected neurons. Stem Cell Reports |
| Fink JJ, Schreiner JD, Bloom JE, et al. (2021) Hyperexcitable Phenotypes in Induced Pluripotent Stem Cell-Derived Neurons From Patients With 15q11-q13 Duplication Syndrome, a Genetic Form of Autism. Biological Psychiatry |
| Perrino PA, Chamberlain SJ, Eigsti IM, et al. (2020) Communication-related assessments in an Angelman syndrome mouse model. Brain and Behavior. e01937 |
| Langouët M, Gorka D, Orniacki C, et al. (2020) Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics |
| Chung MS, Langouët M, Chamberlain SJ, et al. (2020) Prader-Willi syndrome: reflections on seminal studies and future therapies. Open Biology. 10: 200195 |
| Sirois CL, Bloom JE, Fink JJ, et al. (2020) Abundance and localization of human UBE3A protein isoforms. Human Molecular Genetics |
| Keute M, Miller MT, Krishnan ML, et al. (2020) Angelman syndrome genotypes manifest varying degrees of clinical severity and developmental impairment. Molecular Psychiatry |
| Germain ND, Levine ES, Chamberlain SJ. (2020) IPSC Models of Chromosome 15Q Imprinting Disorders: From Disease Modeling to Therapeutic Strategies. Advances in Neurobiology. 25: 55-77 |