Mary van Schooneveld

Author

Also Known As

F.D. Verbraak, M van Schooneveld, M. Schooneveld, M. Van Schooneveld, M. van Schooneveld, Mary J. van Schooneveld, Mary Van Schooneveld, Mary van Schooneveld, Ralph Florijn

Publications

558

Citations

H-Index

Concepts

All Affiliations

Combined Ophthalmic Research Rotterdam University Medical Center Utrecht Utrecht University Erasmus University Rotterdam Wilhelmina Children's Hospital

About

Mary van Schooneveld is an author at Combined Ophthalmic Research Rotterdam specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	126
2	Social Sciences	2	2	41
3	Neurology	2	2	41
4	Neuroscience	2	2	41
5	Molecular Genetics	1	1	40

Mary van Schooneveld

Publications

479

Citations

H-Index

Page 1

	Year	Citations
MYELINATION AS AN EXPRESSION OF THE FUNCTIONAL MATURITY OF THE BRAIN Marjo S. van der Knaap, Jaap Valk, C. J. G. Bakker, Developmental Medicine & Child Neurology	1991	134
<i>COL4A1</i> mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage Linda S. de Vries, Corine Koopman, Floris Groenendaal, Annals of Neurology	2009	120
The effect of intracranial pressure on myelination and the relationship with neurodevelopment in infantile hydrocephalus Patrick W. Hanlo, R J H M. Gooskens, Mary van Schooneveld, Developmental Medicine & Child Neurology	1997	73
Two different genes for X-linked retinitis pigmentosa Brunhilde Wirth, Michael J. Denton, Jia-De Chen, Genomics Genetic DisorderGeneticsGene CharacterizationMolecular GeneticsGene Expression	1988	40
Simultaneous Mutation Detection in 90 Retinal Disease Genes in Multiple Patients Using a Custom-designed 300-kb Retinal Resequencing Chip Judith C. Booij, Arne Bakker, Jamilia Kulumbetova, Ophthalmology Ocular DiseaseRetinaOphthalmologyGenetic DisorderMultiple Patients	2010	32
Chronic Central Serous Chorioretinopathy Associated with Serous Retinal Detachment in a Series of Asian Patients Paradee Kunavisarut, Kessara Pathanapitoon, Mary van Schooneveld, Ocular Immunology and Inflammation	2009	26
Visual evoked potentials in Prader-Willi syndrome Patricia Apkarian, Henk Spekreijse, Eveline van Swaay, Documenta Ophthalmologica NeurophysiologyNeurological DisorderPrader-willi SyndromeNeurologyNeuroscience	1989	23
Detection of Optic Pathway Misrouting in the Human Albino Neonate Patricia Apkarian, P. Eckhardt, Mary van Schooneveld Neuropediatrics Ocular DiseaseGeneticsOptogeneticsOptic NerveSocial Sciences	1991	18
A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1) Maria Teresa Bassi, Arthur A. Bergen, Martin C. Wapenaar, Human Molecular Genetics Netherlands SearchOcular DiseaseGermany SearchOphthalmologyOculoplastics	1994	13

Page 1