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Fan Zhang

Person: Assistant Professor, University of Colorado

I am a Computational Biologist and my research interests lie in the application of statistics and machine learning methods to study rheumatoid arthritis (RA) and other rheumatic diseases. My long-term goal is to integrate and interpret large-scale multi-omics immunogenomics data to discover...

Gosia Trynka

Person: Group Leader at the Sanger Institute and Experimental Science Director at Open Targets, Wellcome Trust Sanger Center, Cambridge, UK

Tobias Lenz

Person: Professor for Evolutionary Immunogenomics at the University of Hamburg

Jennie Pouget

Person: Psychiatric Resident, University of Toronto, Toronto, Canada

Nikola Teslovich

Person: MD Student, Stanford University School of Medicine, Palo Alto, CA

Summer Internship

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*****NOTE: THIS PROGRAM IS CLOSED***** This official BIDMC High School Summer Research Program allows the students to experience scientific research and gain generic skills. All students receive a stipend during this Program. You can read about this program here. Take a look at our past students'...

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Publication: Journal Article

Verhoeven, Virginie, Pirro Hysi, Robert Wojciechowski, Qiao Fan, Jeremy Guggenheim, René Höhn, Stuart Macgregor, et al. 2013. “Genome-Wide Meta-Analyses of Multiancestry Cohorts Identify Multiple New Susceptibility Loci for Refractive Error and Myopia”. Nat Genet 45 (3): 314-8.

Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy

Publication: Journal Article

Riazuddin, Amer, David Parker, Elyse McGlumphy, Edwin Oh, Benjamin Iliff, Thore Schmedt, Ula Jurkunas, Robert Schleif, Nicholas Katsanis, and John Gottsch. 2012. “Mutations in LOXHD1, a Recessive-Deafness Locus, Cause Dominant Late-Onset Fuchs Corneal Dystrophy”. Am J Hum Genet 90 (3): 533-9.

A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability

Publication: Journal Article

Louttit, Megan, Laura Kopplin, Robert Igo, Jeremy Fondran, Angela Tagliaferri, David Bardenstein, Anthony Aldave, et al. 2012. “A Multicenter Study to Map Genes for Fuchs Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability”. Cornea 31 (1): 26-35.

Molecular bases of corneal endothelial dystrophies

Publication: Journal Article

Schmedt, Thore, Mariana Mazzini Silva, Alireza Ziaei, and Ula Jurkunas. 2012. “Molecular Bases of Corneal Endothelial Dystrophies”. Exp Eye Res 95 (1): 24-34.