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scopus: 35590798800

Verkerk, J.H.M.

(Annemieke Verkerk)


expression patient analysis study chromosome 10-1 level protein genet sample family netherland figure allele mutation number genetic disease table expression levels rotterdam syndrome pathway inactivation x inactivation linkage region result x chromosome development deletion photoreceptor disorder individual donor department genomic placenta 10-4 citation purposes page number center interindividual variation interindividual array microarray control patient 1 erasmu myopia retina snca gene rpe-specific cohort 10-3 association percentile variation macular group error genbank factor klf 1 genome-wide nature ingenuity pigment gene expression tissue choroid methylation brain receptor locus pigment epithelium rearrangement variant retardation rs 811563




10 Most Recent Publications

A new strategy to identify and annotate human RPE-specific gene expression (Article)
Booij, J.C. Brink, J.B. ten Swagemakers, S.M.A. Verkerk, J.H.M. Essing, A.H.W. Spek, P.J. van der Bergen, A.A.B
2010-09-14
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14 (Letter To Editor)
Solouki, A.M. Verhoeven, V.J.M. Czudowska, M.A. Kuijpers, R.W.A.M. Amin, N. Struchalin, M.V. Aulchenko, Y.S. Rij, G. van Riemslag, F.C.C. Young, T.L. Mackey, D.A. Spector, T.D. Duijn, C.M. van Gorgels, T.G.M.F. Willemse-Assink, J.J.M. Isaacs, A.J. Kramer, R. Swagemakers, S.M.A. Bergen, A.A.B Oosterhout, A.A.L.J. van Oostra, B.A. Rivadeneira Ramirez, F. Uitterlinden, A.G. Verkerk, J.H.M. Hofman, A. Jong, P.T.V.M. de Hammond, C.J. Vingerling, J.R. Klaver, C.C.W. Ikram, M.K. Hysi, P.G. Despriet, D.D.G. Koolwijk, L.M.E. van Ho, L. Ramdas, W.D.
2010-09-01
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14 (Letter To Editor)
Solouki, A.M. Verhoeven, V.J.M. Czudowska, M.A. Kuijpers, R.W.A.M. Amin, N. Struchalin, M.V. Aulchenko, Y.S. Rij, G. van Riemslag, F.C.C. Young, T.L. Mackey, D.A. Spector, T.D. Duijn, C.M. van Gorgels, T.G.M.F. Willemse-Assink, J.J.M. Isaacs, A.J. Kramer, R. Swagemakers, S.M.A. Bergen, A.A.B Oosterhout, A.A.L.J. van Oostra, B.A. Rivadeneira Ramirez, F. Uitterlinden, A.G. Verkerk, J.H.M. Hofman, A. Jong, P.T.V.M. de Hammond, C.J. Vingerling, J.R. Klaver, C.C.W. Ikram, M.K. Hysi, P.G. Despriet, D.D.G. Koolwijk, L.M.E. van Ho, L. Ramdas, W.D.
2010-09-01
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin (Article)
Borg, J. Papadopoulos, P. Cassar, W. Galdies, R. IJcken, W.F.J. van Özgür, Z. Gillemans, N. Hou, J. Bugeja, M. Grosveld, F.G. Lindern, M.M. von Felice, A.E. Georgitsi, M. Patrinos, G.P. Philipsen, S. Gutiérrez, L. Grech, G. Fanis, P. Phylactides, M. Verkerk, J.H.M. Spek, P.J. van der Scerri, C.A.
2010-08-01
Allelic imbalance of expression and epigenetic regulation within the alpha-synuclein wild-type and p.Ala53Thr alleles in Parkinson disease (Article)
Voutsinas, G.E. Stavrou, E.F. Athanassiadou, A. Karousos, G. Dasoula, A. Papachatzopoulou, A. Syrrou, M. Verkerk, J.H.M. Spek, P.J. van der Patrinos, G.P. Stöger, R.
2010-06-01
Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalus (Article)
Verkerk, J.H.M. Schot, R. Wit, M.C.Y. de Wafelman, L.S. Garavelli, L. Dobyns, W.B. Spek, P.J. van der Klein, J.E.M.M. de Mancini, G.M.S. Waterschoot, L. van Douben, H. Poddighe, P. Leguin, M. Vries, L.S. de Terhal, P. Hahnemann, J.M.D. Coo, I.F.M. de
2010-06-01
Periventricular nodular heterotopia and distal limb deficiency: A recurrent association (Article)
Wit, M.C.Y. de Coo, I.F.M. de Schot, R. Hoogeboom, A.J.M. Leguin, M. Verkerk, J.H.M. Mancini, G.M.S.
2010-04-01
Genome-wide linkage analysis in a Dutch multigenerational family with attention deficit hyperactivity disorder (Article)
Vegt, M. Bertoli Avella, A.M. Hengeveld, M.W. Oostra, B.A. Tulen, J.H.M. Graaf, B.M. de Verkerk, J.H.M. Vervoort, J. Twigt, C.M. Maat-Kievit, A.A. Tuijl, H.R. van Lijn, M. van der
2010-02-01
Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: Case report (Article)
Vree, P.J.P. de Simon, M.E.H. Dooren, M.F. van Stoevelaar, G.H.T. Hilkmann, J.T.W. Rongen, M.A. Huijbregts, G.C.M. Verkerk, J.H.M. Poddighe, P.
2009-08-27
Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy (Article)
Verkerk, J.H.M. Schot, R. Hirst, J. Wessels, M.W. Catsman-Berrevoets, C.E. Verheijen, F.W. Graaff, E. de Coo, I.F.M. de Kros, J.M. Willemsen, R. Willems, P.J. Spek, P.J. van der Dumee, B. Mancini, G.M.S. Schellekens, K. Swagemakers, S.M.A. Bertoli Avella, A.M. Leguin, M. Dudink, J. Govaert, P. Zwol, A.L. van
2009-07-10