Nel Tijmes

The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease

Alessandra Maugeri, Marc A. van Driel, Dorien J.R. van de Pol et al. · The American Journal of Human Genetics · 1999 · 259 citations · Full text

Mendelian Disorder, Genetic Disorder, Abcr Gene +10

Retinal arterial changes correlate with cerebral small-vessel disease

Vincent I.H. Kwa, J.J. van der Sande, J. Stam et al. · Neurology · 2002 · 221 citations

Prevalence of Symptomatic Intracranial Aneurysm and Ischaemic Stroke in Pseudoxanthoma Elasticum

JanS.P. vandenBerg, Raoul C. M. Hennekam, J.R.M. Cruysberg et al. · Cerebrovascular Diseases · 2000 · 112 citations

Changes in causes of low vision between 1988 and 2009 in a Dutch population of children

Nienke Boonstra, Hans Limburg, Nel Tijmes et al. · Acta Ophthalmologica · 2011 · 87 citations · Full text

A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome

Jacqueline J.M. Assink, Nel Tijmes, Jacoline B. ten Brink et al. · The American Journal of Human Genetics · 1997 · 67 citations · Full text

Ophthalmology, Cytogenetics, X Chromosome +6