Researcher profile · Semantic Scholar

S. van Soest

h-index: 16
Works: 35
Citations: 2,914

Most-cited papers

Prolonged fluid shear stress induces a distinct set of endothelial cell genes, most specifically lung Krüppel-like factor (KLF2).
R. Dekker, S. van Soest, R. Fontijn, Sonia Salamanca +4 more
2002Blood745 citations Open access
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Mutations in ABCC6 cause pseudoxanthoma elasticum
A. Bergen, A. Plomp, E. Schuurman, S. Terry +8 more
2000Nature Genetics592 citations
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Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
A. den Hollander, J. T. ten Brink, Yvette J. M. de Kok, S. van Soest +14 more
1999Nature Genetics478 citations
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Retinitis pigmentosa: defined from a molecular point of view.
S. van Soest, A. Westerveld, P. D. de Jong, E. M. Bleeker-wagemakers +1 more
1999Survey of ophthalmology270 citations
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Pseudoxanthoma elasticum: a clinical, histopathological, and molecular update.
Xiao-Feng Hu, A. Plomp, S. van Soest, J. Wijnholds +2 more
2003Survey of ophthalmology163 citations
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Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.
S. van Soest, L. I. van den Born, A. Gal, G. Farrar +5 more
1994Genomics140 citations
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A locus for autosomal recessive pseudoxanthoma elasticum, with penetrance of vascular symptoms in carriers, maps to chromosome 16p13.1.
S. van Soest, J. Swart, N. Tijmes, L. Sandkuijl +2 more
1997Genome Research83 citations Open access
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Comparison of human retinal pigment epithelium gene expression in macula and periphery highlights potential topographic differences in Bruch's membrane.
S. van Soest, G. D. de Wit, Anke H. W. Essing, J. T. ten Brink +3 more
2007Molecular Vision77 citations
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Comprehensive analysis of the candidate genes CCL2, CCR2, and TLR4 in age-related macular degeneration.
D. Despriet, A. Bergen, J. Merriam, J. Zernant +8 more
2008Investigative Ophthalmology and Visual Science63 citations Open access
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Functional annotation of the human retinal pigment epithelium transcriptome
J. Booij, S. van Soest, Sigrid M. A. Swagemakers, Anke H. W. Essing +4 more
2009BMC Genomics61 citations Open access
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Global gene expression profiling of ischemic preconditioning in the rat retina
W. Kamphuis, F. Dijk, S. van Soest, A. Bergen
2007Molecular Vision48 citations
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Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epithelium.
L. I. van den Born, S. van Soest, M. J. van Schooneveld, Frans C. C. Riemslag +2 more
1994American journal of ophthalmology-glaucoma45 citations
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In patients with pseudoxanthoma elasticum a thicker and more elastic carotid artery is associated with elastin fragmentation and proteoglycans accumulation.
L. Kornet, A. Bergen, A. Hoeks, J. Cleutjens +4 more
2004Ultrasound in Medicine and Biology43 citations
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Analysis of the frequent R1141X mutation in the ABCC6 gene in pseudoxanthoma elasticum.
Xiao-Feng Hu, R. Peek, A. Plomp, Jacoline ten ten Brink +5 more
2003Investigative Ophthalmology and Visual Science41 citations
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Integrated genetic and physical map of the 1q31→q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes
S. van Soest, M. van Rossem, J. Heckenlively, L. I. van den Born +6 more
1999Cytogenetic and Genome Research41 citations
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Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC).
S. van Soest, S. T. Nijenhuis, L. I. van den Born, E. Bleeker-wagemakers +4 more
1996Cytogenetics and Cell Genetics16 citations
Semantic Scholar
Current technologies in gene expression profiling: applications to cardiovascular research
S. van Soest, A. Horrevoets, N. Beauchamp, H. Pannekoek
20006 citations
Semantic Scholar
Mutations in a human homolog of Drosphila crumbs cause retinitis pigmentosa with preserved para-arteriolar retinal pigment apthelium (RP12)
A. den Hollander, J. T. ten Brink, Y. deKok, S. van Soest +14 more
19992 citations
Semantic Scholar
Prolonged fluid shear stress induces a distinct set of endothelial cell genes, most specifically lung Krüppel-like factor (KLF2)
Hans Pannekoek, A. Horrevoets, R. Dekker, S. van Soest +4 more
20021 citations
Semantic Scholar
Gene Expression and Lipofuscin Accumulation in an in vitro Model for Age- Related Macular Degeneration
D. Baas, S. van Soest, T. Gorgels, P. D. de Jong +2 more
20070 citations
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Microarray Analysis of Laser Dissected Photoreceptor and RPE Cells as a Tool to Select Novel Positional Candidate Retinal Disease Genes
J. Booij, S. van Soest, N. Yeremenko, J. F. Brinkmann +4 more
20070 citations
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Photoreceptor Gene Expression Alterations in Aging and Early Stage of Age Related Macular Degeneration
N. Yeremenko, S. van Soest, G. D. de Wit, Anke H. W. Essing +3 more
20060 citations
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Topographical Variation in Expression of Extracellular Matrix and Growth Factor Genes in Human RPE Cells
S. van Soest, G. D. de Wit, Anke H. W. Essing, E. Groot +3 more
20060 citations
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Microarray Analysis of Gene Expression Profiles in the Rat Retina After Ischemia–Reperfusion
W. Kamphuis, F. Dijk, S. van Soest, A. Bergen
20050 citations
Semantic Scholar
Whole retinal transcriptome analysis of early stages of AMD
S. van Soest, G. D. de Wit, E. Groot, C. Mooy +3 more
20040 citations
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Analysis of the frequent R1141 X mutation in the ABCC6 gene in Pseudoxanthoma Elasticum (PXE)
Xiao-Feng Hu, R. Peek, A. Plomp, J. T. ten Brink +5 more
20030 citations
Semantic Scholar
Genome-Wide Screen for Age-Related Maculopathy in an Isolated Population
M. Voorendt, J. Assink, L. Sandkuijl, J. T. ten Brink +4 more
20020 citations
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Genome-Wide Gene-Expression Profiling in Human Retinal Pigment Epithelium/Choroid and Retina Using In-Situ Oligonucleotide Microarrays
S. van Soest, M. Voorendt, G. D. de Wit, P. D. de Jong +1 more
20020 citations
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In vitro- in vivo gene expression analysis in atherosclerosis
A. Horrevoets, R. Dekker, R. Fontijn, S. van Soest +1 more
20020 citations
Semantic Scholar
Molecular analysis of Pseudoxanthoma Elasticum: spectrum of ABCC6 gene mutations in the Netherlands
Xiao-Feng Hu, A. Plomp, J. T. ten Brink, J. Wijnholds +6 more
20020 citations
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Towards the identification of the autosomal recessive RP12 gene
S. van Soest
19980 citations
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Genetics in ophthalmology.
A. Bergen, K. Devriendt, L. Messiaen, G. Mortier +3 more
1998Bulletin de la Societe belge d'ophtalmologie0 citations
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Are X-linked congenital stationary night blindness and X-linked retinitis pigmentosa genetically allelic?
A. Bergen, J. T. ten Brink, F. Riemslag, S. van Soest +4 more
19960 citations
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P 376 Phenotypical and genotypical classification of autosomal recessive RP
L. I. van den Born, S. van Soest, F. Riemslag, A. Bergen +2 more
19950 citations Open access
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3233 Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome IQ; exclusion of the phosducin gene
S. van Soest, S. T. Nijenhuis, L. I. van den Born, E. Bleeker-wagemakers +3 more
19950 citations Open access
Semantic Scholar

L. I. van den Born

×8

A. Bergen×8

A. Plomp×5

G. D. de Wit×5

Anke H. W. Essing×5

W. Kamphuis×5

A. Westerveld×4

E. Bleeker-wagemakers×4