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Hire Dr. Erika Y.

United States

Profile Summary

My main interest is to understand how ubiquitous signaling pathways regulate development. The fine tuning of globally expressed proteins that coordinates tissue development is dependent on time, space and context. In my PhD I focused in the FGF signaling as a regulator of proper skull and bone development. During my postdoc at Stanford, I studied the opposite effects of canonical and non-canonical Wnt signaling in face development. Now my current postdoc at UCSF, is centered in the role o Ras/MAPK pathway in the brain development.

Subject Matter Expertise

• ☆ Molecular Biology
• ☆ Cell Signaling Pathways
• ☆ Stem Cell Research

Services

• Writing
• Consulting
• Product Development

Work Experience

Postdoctoral fellow

University of California San Francisco

October 2012 - Present

Postdoctoral fellow

Stanford University

October 2011 - October 2012

Education

Postdoctoral fellow (Psychiatry)

University of California San Francisco

October 2012 - Present

Postdoctoral Fellow (Surgery)

Stanford University

October 2011 - October 2012

PhD (Genetics)

Universidade de São Paulo

August 2006 - August 2011

BA

Universidade de São Paulo

February 2002 - August 2006

BSc

Universidade de São Paulo

February 2002 - December 2005

Certifications

• Certification details not provided.

Publications

JOURNAL ARTICLE

E Yeh, D Q Dao, Z Y Wu, S M Kandalam, F M Camacho, C Tom, W Zhang, R Krencik, K A Rauen, E M Ullian, et al. (2017). Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment . Molecular Psychiatry.

Erika Yeh, Ileena Mitra, Jonathan Flint, Alinoë Lavillaureix, Michela Traglia, Kathryn Tsang, Carrie E. Bearden, Katherine A. Rauen, Lauren A. Weiss (2017). Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders . PLOS Genetics.

Erika Yeh, Lauren A. Weiss (2016). If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism . Molecular and Cellular Probes.

(2016). Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome . Journal of Neuroscience.

Yeh, E., Fanganiello, R.D., Sunaga, D.Y., Zhou, X., Holmes, G., Rocha, K.M., Alonso, N., Matushita, H., Wang, Y., Jabs, E.W., et al.(2013). Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome . PLoS ONE. 8. (4).

Yeh, E., Atique, R., Ishiy, F.A.A., Fanganiello, R.D., Alonso, N., Matushita, H., da Rocha, K.M., Passos-Bueno, M.R.(2012). FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells Than in Fibroblasts . Stem Cell Reviews and Reports. 8. (3). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 685-695.

Medio, M., Yeh, E., Popelut, A., Babajko, S., Berdal, A., Helms, J.A.(2012). Wnt/β-catenin signaling and Ms×1 promote outgrowth of the maxillary prominences . Frontiers in Physiology. 3 SEP.

Bishop, J.R., Passos-Bueno, M.R., Fong, L., Stanford, K.I., Gonzales, J.C., Yeh, E., Young, S.G., Bensadoun, A., Witztum, J.L., Esko, J.D., et al.(2010). Deletion of the basement membrane heparan sulfate proteoglycan type XVIII collagen causes hypertriglyceridemia in mice and humans . PLoS ONE. 5. (11).

Yeh, E., Kimura, L., Errera, F.I.V., Angeli, C.B., Mingroni-Netto, R.C., Silva, M.E.R., Canani, L.H.S., Passos-Bueno, M.R.(2008). Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry . Brazilian Journal of Medical and Biological Research. 41. (6). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 468-472.

Fanganiello, R.D., Sertié, A.L., Reis, E.M., Yeh, E., Oliveira, N.A.J., Bueno, D.F., Kerkis, I., Alonso, N., Cavalheiro, S., Matsushita, H., et al.(2007). Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells . Molecular Medicine. 13. (7-8). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 422-442.

Errera, F.I.V., Canani, L.H., Silva, M.E.R., Yeh, E., Takahashi, W., Santos, K.G., Souto, K.E.P., Tschiedel, B., Roisenberg, I., Gross, J.L., et al.(2007). Functional vascular endothelial growth factor -634G>C SNP is associated with proliferative diabetic retinopathy: A case-control study in a Brazilian population of European ancestry . Diabetes Care. 30. (2). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 275-279.

Errera, F.I.V., Silva, M.E.R., Yeh, E., Maranduba, C.M.C., Folco, B., Takahashi, W., Pereira, A.C., Krieger, J.E., Passos-Bueno, M.R.(2006). Effect of polymorphisms of the MTHFR and APOE genes on susceptibility to diabetes and severity of diabetic retinopathy in Brazilian patients . Brazilian Journal of Medical and Biological Research. 39. (7). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 883-888.

BOOK

Passos-Bueno, M.R., Sertié, A.L., Jehee, F.S., Fanganiello, R., Yeh, E.(2008). Genetics of craniosynostosis: Genes, syndromes, mutations and genotype-phenotype correlations . Frontiers of Oral Biology. 12. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 107-143.

DISSERTATION THESIS

Erika Yeh Estudo da contribuição molecular e celular do periósteo na craniossinostose da síndrome de Apert . Universidade de Sao Paulo Sistema Integrado de Bibliotecas - {SIBiUSP}