Arjen Henkes

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 9 publications

Correction: P-cadherin mutations are associated with high basal Wnt activity and stemness in canine mammary tumor cell lines.

Correction: P-cadherin mutations are associated with high basal Wnt activity and stemness in canine mammary tumor cell lines.

Journal: Oncotarget

Published: February 22, 2020

Genetic Spectrum of ABCA4-Associated Retinal Degeneration in Poland.

Genetic Spectrum of ABCA4-Associated Retinal Degeneration in Poland.

Journal: Genes

Published: October 22, 2019

P-cadherin mutations are associated with high basal Wnt activity and stemness in canine mammary tumor cell lines.

P-cadherin mutations are associated with high basal Wnt activity and stemness in canine mammary tumor cell lines.

Journal: Oncotarget

Published: October 18, 2018

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis.

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: September 15, 2015

Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration.

Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration.

Journal: PloS one

Published: September 06, 2015

Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer.

Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer.

Journal: Scientific reports

Published: June 14, 2015

Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds.

Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds.

Journal: PloS one

Published: August 29, 2014

Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosa.

Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosa.

Journal: Ophthalmology

Published: April 22, 2013

Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations.

Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations.

Journal: Human mutation

Published: March 29, 2013

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Last Updated: 09/26/2026