Valerie A. Arboleda, Ph.D.
Affiliations: | 2012 | Human Genetics 0994 | University of California, Los Angeles, Los Angeles, CA |
Area:
Genetics, Human DevelopmentGoogle:
"Valerie Arboleda"Mean distance: 21373.2
Parents
Sign in to add mentor| Eric Vilain | grad student | 2012 | UCLA | |
| (Molecular Mechanisms in Male Sex Determination.) | ||||
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Publications
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| Singh M, Spendlove S, Wei A, et al. (2023) mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior cluster. Biorxiv : the Preprint Server For Biology |
| Nava AA, Arboleda VA. (2023) The omics era: a nexus of untapped potential for Mendelian chromatinopathies. Human Genetics |
| Arboleda VA, Xian RR. (2019) An Overview of DNA Analytical Methods. Methods in Molecular Biology (Clifton, N.J.). 1897: 385-402 |
| Freund MK, Burch KS, Shi H, et al. (2018) Phenotype-Specific Enrichment of Mendelian Disorder Genes near GWAS Regions across 62 Complex Traits. American Journal of Human Genetics. 103: 535-552 |
| Kennedy J, Goudie D, Blair E, et al. (2018) KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Datkhaeva I, Arboleda VA, Senaratne TN, et al. (2018) Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis. American Journal of Medical Genetics. Part A |
| Barseghyan H, Symon A, Zadikyan M, et al. (2018) Identification of novel candidate genes for 46,XY disorders of sex development (DSD) using a C57BL/6J-Y POS mouse model. Biology of Sex Differences. 9: 8 |
| Bramble MS, Roach L, Lipson A, et al. (2016) Sex-Specific Effects of Testosterone on the Sexually Dimorphic Transcriptome and Epigenome of Embryonic Neural Stem/Progenitor Cells. Scientific Reports. 6: 36916 |
| Bramble MS, Goldstein EH, Lipson A, et al. (2016) A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing. Human Reproduction (Oxford, England) |
| Borges KS, Arboleda VA, Vilain E. (2015) Mutations in the PCNA-binding site of CDKN1C inhibit cell proliferation by impairing the entry into S phase. Cell Division. 10: 2 |