Neena B. Haider

Massachusetts Eye and Ear Infirmary — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

26h-index2.8kcitations75works10.02yr avg
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Research Topics

Retinal Development and Disorders(44), Retinal Diseases and Treatments(23), Retinoids in leukemia and cellular processes(17), Photochromic and Fluorescence Chemistry(12), Genetic and Kidney Cyst Diseases(7)

Publications75 total

Correction: Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa
Gene Therapy·2024· 1 citedOpen Access
Evaluating therapeutic potential of NR2E3 doses in the rd7 mouse model of retinal degeneration
Scientific Reports·2024· 3 citedOpen Access
Retinoic acid related orphan receptor α is a genetic modifier that rescues retinal degeneration in a mouse model of Stargardt disease and Dry AMD
Gene Therapy·2024· 8 citedOpen Access
Seeing the Future: A Review of Ocular Therapy
Bioengineering·2024· 18 citedOpen Access
Preclinical dose response study shows NR2E3 can attenuate retinal degeneration in the retinitis pigmentosa mouse model RhoP23H+/−
Gene Therapy·2024· 10 citedOpen Access
Alzheimer’s Disease: Models and Molecular Mechanisms Informing Disease and Treatments
Bioengineering·2024· 20 citedOpen Access
Patterns of gene expression and allele-specific expression vary among macular tissues and clinical stages of Age-related Macular Degeneration
2022· 2 citedOpen Access
Microbiota, Microbiome, and Retinal Diseases
International Ophthalmology Clinics·2022· 1 cited
Interspecies Correlations between Human and Mouse NR2E3-Associated Recessive Disease
Journal of Clinical Medicine·2021· 14 citedOpen Access
Comparison between human NR2E3-related disease and murine retinal characteristics identifies interspecies imaging correlates of key histological findings in rd7 mice
Investigative Ophthalmology & Visual Science·2020Open Access
Preclinical efficacy of AAV5-Nr2e3 in the mouse model of Nr2e3 mutation associated inherited retinal degeneration
Investigative Ophthalmology & Visual Science·2020· 1 citedOpen Access
Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa
Gene Therapy·2020· 62 citedOpen Access
HTRA1 gene interaction network informs Age-Related Macular Degeneration (AMD) risk
2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder
Genetics in Medicine·2019· 62 citedOpen Access
Animal Models of Diabetic Retinopathy
Current Diabetes Reports·2017· 215 citedOpen Access
Corrigendum to “The Nuclear Hormone Receptor Nr2c1 (Tr2) is a critical regulator of early retina cell pattering” [Dev. Biol. 16 (2017) 30797-7]
Developmental Biology·2017· 2 cited
Master Modifier Nr2e3 Rescues Disease and Promotes Retina Homeostasis in Multiple Models of RP
Investigative Ophthalmology & Visual Science·2017· 3 citedOpen Access
The nuclear hormone receptor gene Nr2c1 (Tr2) is a critical regulator of early retina cell patterning
Developmental Biology·2017· 13 citedOpen Access
Multimodal Regulation Orchestrates Normal and Complex Disease States in the Retina
Scientific Reports·2017· 21 citedOpen Access
Identifying Signature Profiles of Transcription Factors in Human and Mouse Models of Retinal Disease
Investigative Ophthalmology & Visual Science·2016Open Access
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Frequent Co-authors

Margaret M. DeAngelis(17), Yang Yuan(10), Val C. Sheffield(9), Andrew J. Sachs(9), Ana María Olivares(8), Arne Nystuen(8), Margaux A. Morrison(7), Edwin M. Stone(6), Rivka Carmi(5), Nissa Mollema(5), Austin S. Jelcick(5), Joan W. Miller(5), Lindsay A. Farrer(5), Ivana K. Kim(5), Pascal Escher(5), Shannon M. McNamee(5), Monica Akula(5), Samuel G. Jacobson(4), Charles Searby(4), Maria Kotoula(4)