Maureen Neitz Selected Research

Messenger RNA (mRNA)

1/2022	Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia.
1/2021	Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders.

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Maureen Neitz Research Topics

Disease

11	Color Vision Defects (Color Blindness) 03/2022 - 05/2006
6	Myopia 01/2022 - 02/2013
5	Vision Disorders (Hemeralopia) 01/2021 - 05/2008
5	Cone Dystrophy 12/2019 - 05/2007
3	Aniridia 11/2020 - 01/2018
3	Blue cone monochromatism 05/2017 - 12/2012
3	Bornholm Eye Disease 05/2017 - 02/2013
2	Retinitis Pigmentosa (Pigmentary Retinopathy) 03/2022 - 12/2009
2	Ganglion Cysts (Ganglion) 12/2012 - 05/2012
1	Infections 03/2022
1	Rubella (German Measles) 03/2022
1	Retinal Diseases 03/2022
1	Blindness (Hysterical Blindness) 01/2022
1	Refractive Errors (Refractive Error) 01/2019
1	congenital stationary Night blindness 12/2012
1	Oguchi disease 12/2012
1	Ocular Albinism 10/2007

Drug/Important Bio-Agent (IBA)

11	Cone OpsinsIBA 01/2022 - 05/2006
8	OpsinsIBA 01/2019 - 05/2008
7	Retinaldehyde (Retinal)IBA 03/2022 - 05/2007
2	Messenger RNA (mRNA)IBA 01/2022 - 01/2021
2	Amino Acids FDA Link 05/2017 - 05/2006
2	Rhodopsin (Visual Purple)IBA 01/2014 - 12/2009
1	Alanine (L-Alanine)FDA Link 01/2019
1	melanopsinIBA 05/2012
1	Cysteine (L-Cysteine)FDA Link 12/2009
1	Arginine (L-Arginine)FDA Link 12/2009
1	G-Protein-Coupled Receptors (Receptors, G Protein Coupled)IBA 10/2007

Therapy/Procedure

1	Lenses 01/2022
1	Eyeglasses (Spectacles) 01/2022
1	Therapeutics 05/2017