Nel Tijmes
Visio(NL)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Photoreceptor and optogenetics research, Dermatological and Skeletal Disorders, Mitochondrial Function and Pathology
Most-Cited Works
- → 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(1999)260 cited
- → Retinal arterial changes correlate with cerebral small-vessel disease(2002)222 cited
- → Prevalence of Symptomatic Intracranial Aneurysm and Ischaemic Stroke in Pseudoxanthoma Elasticum(2000)112 cited
- → Changes in causes of low vision between 1988 and 2009 in a Dutch population of children(2011)88 cited
- → A Locus for Autosomal Recessive Pseudoxanthoma Elasticum, with Penetrance of Vascular Symptoms in Carriers, Maps to Chromosome 16p13.1(1997)78 cited
- → A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome(1997)67 cited
- → Paucity of signs in X linked ocular albinism with a 700 kb deletion spanning the OA1 gene(1998)15 cited
- → On the many faces of Leber hereditary optic neuropathy(1997)12 cited
- → Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.(1996)11 cited
- → Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region(1995)10 cited