Rosario Fernández‐Godino

Author

Massachusetts Eye and Ear Infirmary ORCID

Also Known As

Rosario Fernandez-Godino, Rosario Fernandez‐Godino, Rosario Fernández Godino, Rosario Fernández-Godino, Rosario Fernández‐Godino

Publications

652

Citations

H-Index

Concepts

All Affiliations

Massachusetts Eye and Ear Infirmary Harvard University Genomics (United Kingdom)

About

Rosario Fernández‐Godino is an author at Massachusetts Eye and Ear Infirmary specializing in medicine, cell biology, and cellular physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	210
2	Cell Biology	4	4	210
3	Cellular Physiology	3	3	195
4	Immunology	1	1	14
5	Cell Development	1	1	15

Rosario Fernández‐Godino

Publications

538

Citations

H-Index

Page 1

	Year	Citations
Isolation, culture and characterization of primary mouse RPE cells Rosario Fernández‐Godino, Donita Garland, Eric A. Pierce Nature Protocols Cell CultureCell ProliferationMedicineCell BiologyCellular Physiology	2016	109
A local complement response by RPE causes early-stage macular degeneration Rosario Fernández‐Godino, Donita Garland, Eric A. Pierce Human Molecular Genetics	2015	76
Changes in extracellular matrix cause RPE cells to make basal deposits and activate the alternative complement pathway Rosario Fernández‐Godino, Kinga M. Bujakowska, Eric A. Pierce Human Molecular Genetics Cell ProliferationCellular PhysiologyTissue DevelopmentCell RegulationCell Interaction	2017	72
Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations Kinga M. Bujakowska, Rosario Fernández‐Godino, Emily Place, Genetics in Medicine	2016	62
C3a triggers formation of sub-retinal pigment epithelium deposits via the ubiquitin proteasome pathway Rosario Fernández‐Godino, Eric A. Pierce Scientific Reports	2018	58
Mouse genetics and proteomic analyses demonstrate a critical role for complement in a model of DHRD/ML, an inherited macular degeneration Donita Garland, Rosario Fernández‐Godino, Inderjeet Kaur, Human Molecular Genetics	2013	55
AAV-Mediated Gene Augmentation Therapy Restores Critical Functions in Mutant PRPF31+/− iPSC-Derived RPE Cells Elizabeth M. Brydon, Revital Bronstein, Adriana Buskin, Molecular Therapy — Methods & Clinical Development	2019	47
Complement factor B is critical for sub-RPE deposit accumulation in a model of Doyne honeycomb retinal dystrophy with features of age-related macular degeneration Maura Crowley, Donita Garland, Holger Sellner, Human Molecular Genetics	2022	16
Characterization of lincRNA expression in the human retinal pigment epithelium and differentiated induced pluripotent stem cells Elizabeth D. Au, Rosario Fernández‐Godino, Tadeusz J. Kaczynksi, PLoS ONE GeneticsCell SpecializationLincrna ExpressionEpigeneticsRetina	2017	15
Alterations in Extracellular Matrix/Bruch’s Membrane Can Cause the Activation of the Alternative Complement Pathway via Tick-Over Rosario Fernández‐Godino Advances in experimental medicine and biology Complement SystemExtracellular Matrix/bruch ’Signal TransductionCell SignalingImmune Regulation	2018	14

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