Daniel Navarro-Gomez

Author

Massachusetts Eye and Ear Infirmary

Also Known As

D. Navarro-Gomez, D. Navarro‐Gómez, Daniel Navarro-Gomez

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Massachusetts Eye and Ear Infirmary Harvard University Massachusetts General Hospital Children's Hospital of Los Angeles Children's Hospital of Philadelphia

About

Daniel Navarro-Gomez is an author at Massachusetts Eye and Ear Infirmary specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	564
2	Engineering	1	1	51
3	Immunology	1	1	205
4	Molecular Biology	1	1	51
5	Molecular Genetics	1	1	32

Daniel Navarro-Gomez

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing Mark Consugar, Daniel Navarro-Gomez, Emily Place, Genetics in Medicine Inherited Eye DiseasesGenetic TestingGenetic DisorderExome SequencingGenetics	2014	252
Individualized, heterologous chimpanzee adenovirus and self-amplifying mRNA neoantigen vaccine for advanced metastatic solid tumors: phase 1 trial interim results Christine D. Palmer, Amy Rappaport, Matthew J. Davis, Nature Medicine VaccinationVaccine DevelopmentMedicineImmunologyVirology	2022	205
Allele-Specific CRISPR-Cas9 Genome Editing of the Single-Base P23H Mutation for Rhodopsin-Associated Dominant Retinitis Pigmentosa Pingjuan Li, Benjamin P. Kleinstiver, Mihoko Leon, The CRISPR Journal	2018	117
Copy-number variation contributes 9% of pathogenicity in the inherited retinal degenerations Erin Zampaglione, Benyam Kinde, Emily Place, Genetics in Medicine	2020	108
Phy-Mer: a novel alignment-free and reference-independent mitochondrial haplogroup classifier Daniel Navarro-Gomez, Jeremy Leipzig, Marie T. Lott, Bioinformatics	2014	69
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
MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease Maria Angela Diroma, Michael Gonzalez, Daniel Navarro-Gomez, Human Mutation Bioinformatics Web ResourceEngineeringGeneticsGenetic EpidemiologyDatabases	2016	51
The Genetic Basis of Pericentral Retinitis Pigmentosa—A Form of Mild Retinitis Pigmentosa Jason Comander, Carol Weigel-DiFranco, Matthew Maher, Genes	2017	45
Contribution of noncoding pathogenic variants to RPGRIP1-mediated inherited retinal degeneration Farzad Jamshidi, Emily Place, Sudeep Mehrotra, Genetics in Medicine Ocular DiseaseRetinaOphthalmologyGenetic DisorderGenetics	2018	32
Expanding the phenotypic spectrum in RDH12-associated retinal disease Hilary Scott, Emily Place, Kevin Ferenchak, Molecular Case Studies	2020	29

Page 1