Maria M van Genderen

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Venues

Genes

NPJ genomic medicine

The Journal of physiology

Molecular genetics & genomic medicine

University Medical Center Utrecht

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University Medical Center Utrecht Jul 01 2017

Netherlands

Professor of ophthalmology :: ophthalmology

Bartiméus in Zeist Feb 01 1992

Netherlands

professor of ophthalmology :: diagnostic centre for complex visual disorders

Publications

Cansu de Muijnck, Jacoline B Ten Brink, Hugoline G de Haan, Richard J T Rodenburg, Nicole I Wolf, Arthur A Bergen, Camiel J F Boon, Maria M van Genderen
Mutations in NSUN3 , a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy. Genes 15 (5) (2024)
Cansu de Muijnck, Jacoline B Ten Brink, Hugoline G de Haan, Richard J T Rodenburg, Nicole I Wolf, Arthur A Bergen, Camiel J F Boon, Maria M van Genderen
Mutations in NSUN3 , a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy. Genes 15 (5) (2024)
Lonneke Haer-Wigman, Amber den Ouden, Ronny Derks, Maria M van Genderen, Dorien Lugtenberg, Joke Verheij, Raymon Vijzelaar, Helger G Yntema, Lisenka E L M Vissers, Kornelia Neveling
Reply to: Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjects. NPJ genomic medicine 9 (1) (2024)
Lonneke Haer-Wigman, Amber den Ouden, Ronny Derks, Maria M van Genderen, Dorien Lugtenberg, Joke Verheij, Raymon Vijzelaar, Helger G Yntema, Lisenka E L M Vissers, Kornelia Neveling
Reply to: Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjects. NPJ genomic medicine 9 (1) (2024)
Cansu de Muijnck, Jacoline B Ten Brink, Hugoline G de Haan, Richard J T Rodenburg, Nicole I Wolf, Arthur A Bergen, Camiel J F Boon, Maria M van Genderen
Mutations in NSUN3 , a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy. Genes 15 (5) (2024)
Cansu de Muijnck, Jacoline B Ten Brink, Hugoline G de Haan, Richard J T Rodenburg, Nicole I Wolf, Arthur A Bergen, Camiel J F Boon, Maria M van Genderen
Mutations in NSUN3 , a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy. Genes 15 (5) (2024)
Jessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, Mary J van Schooneveld, Jan Wijnholds, Maria M van Genderen, Nicoline E Schalij-Delfos, Caroline C W Klaver, Magda A Meester-Smoor, L Ingeborgh van den Born, Carel B Hoyng, Alberta A H J Thiadens, Arthur A Bergen, Ruth M A van Nispen, Camiel J F Boon
Quality of life in patients with CRB1-associated retinal dystrophies: A longitudinal study. Acta ophthalmologica (2023)
Maria M van Genderen
In childhood, a different electrode placement improves the recording of pattern reversal visual evoked potentials. The Journal of physiology (2023)
Maria M van Genderen
In childhood, a different electrode placement improves the recording of pattern reversal visual evoked potentials. The Journal of physiology (2023)
Lonneke Haer-Wigman, Amber den Ouden, Maria M van Genderen, Hester Y Kroes, Joke Verheij, Dzenita Smailhodzic, Attje S Hoekstra, Raymon Vijzelaar, Jan Blom, Ronny Derks, Menno Tjon-Pon-Fong, Helger G Yntema, Marcel R Nelen, Lisenka E L M Vissers, Dorien Lugtenberg, Kornelia Neveling
Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPA. NPJ genomic medicine 7 (1) (2022)
Florine Pilon, Heleen Veen, Sabina Kef, Maria M van Genderen
The impact of an eye drop booklet on distress in children when receiving eye drops. Strabismus 28 (2) (2020)
Sanne K Verbakel, Zeinab Fadaie, B Jeroen Klevering, Maria M van Genderen, Ilse Feenstra, Frans P M Cremers, Carel B Hoyng, Susanne Roosing
The identification of a RNA splice variant in TULP1 in two siblings with early-onset photoreceptor dystrophy. Molecular genetics & genomic medicine 7 (6) (2019)

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Publication Activity (10 Years)

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Maria M van Genderen