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“Out in Academia” Panel

Events: Tuesday, Apr 28, 2020, 12:30pm -Tuesday, Apr 28, 2020, 02:00pm

Debating whether to be out during graduate school? Curious about how to navigate your academic or industry job search as an LGBTQ+ scientist? Have questions about how to be a better ally for LGBTQ colleagues and students? Hear from a panel of faculty members and industry professionals about their...

Lit Libations - Q+ POC Bookclub

Events: Saturday, Feb 29, 2020, 12:30pm

Lit Libations is a space for us to discuss notable literature (fiction and non-fiction) and how the narratives apply to our own lives and experiences. Reading the book selection is not a requirement to attend. We are focused on igniting thought-provoking conversations that foster community and...

Zampaglione, Erin, Benyam Kinde, Emily Place, Daniel Navarro-Gomez, Matthew Maher, Farzad Jamshidi, Sherwin Nassiri, et al. 2020. “Copy-Number Variation Contributes 9% of Pathogenicity in the Inherited Retinal Degenerations”. Genet Med 22 (6): 1079-87.

MULTIMODAL IMAGING IN ACUTE RETINAL NECROSIS PRESENTING WITH MACULAR INVOLVEMENT

Publication: Journal Article

Wang, Jay, Yifan Lu, Lucia Sobrin, and Deeba Husain. 2022. “MULTIMODAL IMAGING IN ACUTE RETINAL NECROSIS PRESENTING WITH MACULAR INVOLVEMENT”. Retin Cases Brief Rep 16 (3): 347-50.

Expanding the phenotypic spectrum in RDH12-associated retinal disease

Publication: Journal Article

Scott, Hilary, Emily Place, Kevin Ferenchak, Erin Zampaglione, Naomi Wagner, Katherine Chao, Stephanie DiTroia, et al. 2020. “Expanding the Phenotypic Spectrum in RDH12-Associated Retinal Disease”. Cold Spring Harb Mol Case Stud 6 (1).

A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families

Publication: Journal Article

Bronstein, Revital, Elizabeth Capowski, Sudeep Mehrotra, Alex Jansen, Daniel Navarro-Gomez, Mathew Maher, Emily Place, et al. 2020. “A Combined RNA-Seq and Whole Genome Sequencing Approach for Identification of Non-Coding Pathogenic Variants in Single Families”. Hum Mol Genet 29 (6): 967-79.

Targeting Neurovascular Interaction in Retinal Disorders

Publication: Journal Article

Fu, Zhongjie, Ye Sun, Bertan Cakir, Yohei Tomita, Shuo Huang, Zhongxiao Wang, Chi-Hsiu Liu, et al. 2020. “Targeting Neurovascular Interaction in Retinal Disorders”. Int J Mol Sci 21 (4).

Detection of retinal microvascular changes in von Hippel-Lindau disease using optical coherence tomography angiography

Publication: Journal Article

Lu, Yifan, Jay Wang, Rebecca Zeng, Tatsuo Nagata, Raviv Katz, Shizuo Mukai, and John Miller. 2020. “Detection of Retinal Microvascular Changes in Von Hippel-Lindau Disease Using Optical Coherence Tomography Angiography”. PLoS One 15 (2): e0229213.

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“Out in Academia” Panel

Lit Libations - Q+ POC Bookclub

Just Beginning - 5 Decades of Diversity at HMS

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Copy-number variation contributes 9% of pathogenicity in the inherited retinal degenerations

MULTIMODAL IMAGING IN ACUTE RETINAL NECROSIS PRESENTING WITH MACULAR INVOLVEMENT

Expanding the phenotypic spectrum in RDH12-associated retinal disease

A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families

Targeting Neurovascular Interaction in Retinal Disorders

Detection of retinal microvascular changes in von Hippel-Lindau disease using optical coherence tomography angiography