Janine LaSalle

University of California, Davis, Davis, CA 
"Janine LaSalle"
Mean distance: 10686.6 (cluster 32)


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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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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
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