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[Sample] SQI gallery contest

News: June 05, 2020

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[Sample] Inaugural Collaborative Research Catalyst Award

News: June 02, 2020

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Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome. American journal of medical genetics. Part A, 179(9), 1783–1790.

Publication: Journal Article

“Expanding Phenotype With Severe Midline Brain Anomalies and Missense Variant Supports a Causal Role for FOXA2 in 20p11.2 Deletion Syndrome. American Journal of Medical Genetics. Part A, 179(9), 1783–1790.”. 2019. American Journal of Medical Genetics.

Nihan Semerci Gunay

Person: Research Associate

Tabatha de Oliveira Silva

Person: PhD Student

Bachelor of Biomedicine and specialist in Clinical Analysis by University of Minas Gerais in Brazil, 2017. Master of Science in Morphofunctional Biology by the University of Sao Paulo in Brazil, 2020. PhD student at Life Sistems Program of the Department of Anatomy of the Institute of Biomedical...

Maria Gomez

Person: NCMA, CRA-USF Advanced

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Yiwen Zha, MEd

Person: Lab Manager

Ms. Yiwen Zha is a Social and Behavioral Researcher in the Department of Emergency Medicine in the Division of Social Medicine at the Morsani College of Medicine, University of South Florida. She is passionate about using research and data analysis to inform policy decisions and drive change...