Janine LaSalle
Affiliations: | University of California, Davis, Davis, CA |
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"Janine LaSalle"Mean distance: 10686.6 (cluster 32)
Children
Sign in to add trainee| Daniel Braunschweig | research assistant | UC Davis | |
| Rodney Samaco | research assistant | UC Davis | |
| Thomas Simcox | research assistant | UC Davis | |
| Amber Hogart | grad student | UC Davis | |
| Raman Nagarajan | grad student | UC Davis | |
| Sailaja Peddada | grad student | UC Davis | |
| Karen Thatcher | grad student | UC Davis | |
| Karen N. Leung | grad student | 2010 | UC Davis |
| Rima Woods | grad student | 2012 | UC Davis |
| Atefeh Mousavi Nik | grad student | 2014 | UC Davis |
| Damina Balmer | research scientist | UC Davis |
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Publications
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| LaSalle JM. (2023) Epigenomic signatures reveal mechanistic clues and predictive markers for autism spectrum disorder. Molecular Psychiatry |
| Maggio AG, Shu HT, Laufer BI, et al. (2022) Elevated exposures to persistent endocrine disrupting compounds impact the sperm methylome in regions associated with autism spectrum disorder. Frontiers in Genetics. 13: 929471 |
| Williams LA, LaSalle JM. (2022) Future Prospects for Epigenetics in Autism Spectrum Disorder. Molecular Diagnosis & Therapy |
| LaSalle JM. (2022) X Chromosome Inactivation Timing is Not e: Implications for Autism Spectrum Disorders. Frontiers in Genetics. 13: 864848 |
| Mouat JS, LaSalle JM. (2022) The Promise of DNA Methylation in Understanding Multigenerational Factors in Autism Spectrum Disorders. Frontiers in Genetics. 13: 831221 |
| Laufer BI, Neier K, Valenzuela AE, et al. (2022) Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure. Cell Reports. 38: 110442 |
| Zhu Y, Gomez JA, Laufer BI, et al. (2022) Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism. Genome Biology. 23: 46 |
| Sarode GV, Neier K, Shibata NM, et al. (2021) Wilson disease: intersecting DNA methylation and histone acetylation regulation of gene expression in a mouse model of hepatic copper accumulation. Cellular and Molecular Gastroenterology and Hepatology |
| Laufer BI, Gomez JA, Jianu JM, et al. (2021) Stable DNMT3L overexpression in SH-SY5Y neurons recreates a facet of the genome-wide Down syndrome DNA methylation signature. Epigenetics & Chromatin. 14: 13 |
| Mendiola AJP, LaSalle JM. (2021) Epigenetics in Prader-Willi Syndrome. Frontiers in Genetics. 12: 624581 |