Holly Cukier
Affiliations: | University of Miami, Coral Gables, FL |
Google:
"Holly Cukier"Mean distance: 16.34 (cluster 11) | S | N | B | C | P |
Cross-listing: BCM Tree
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Cukier HN, Duarte CL, Laverde-Paz MJ, et al. (2023) An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons. Neurobiology of Aging. 131: 182-195 |
| Cukier HN, Duarte CL, Laverde-Paz MJ, et al. (2023) An Alzheimer's disease risk variant in modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons. Biorxiv : the Preprint Server For Biology |
| Cukier HN, Kim H, Griswold AJ, et al. (2022) Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions. Npj Parkinson's Disease. 8: 84 |
| Cukier HN, Griswold AJ, Hofmann NK, et al. (2020) Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2. Autism Research : Official Journal of the International Society For Autism Research |
| DeRosa BA, El Hokayem J, Artimovich E, et al. (2018) Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons. Scientific Reports. 8: 8423 |
| Kozol RA, Cukier HN, Zou B, et al. (2015) Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis. Human Molecular Genetics. 24: 4006-23 |
| Cukier HN, Dueker ND, Slifer SH, et al. (2014) Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders. Molecular Autism. 5: 1 |
| Cukier HN, Lee JM, Ma D, et al. (2012) The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1. Autism Research : Official Journal of the International Society For Autism Research. 5: 385-97 |
| Griswold AJ, Ma D, Cukier HN, et al. (2012) Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human Molecular Genetics. 21: 3513-23 |
| Cukier HN, Salyakina D, Blankstein SF, et al. (2011) Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 493-501 |