Willemijn M. Lindhout-Wissink

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 10 publications

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

Journal: Molecular psychiatry
Published: September 02, 2018

B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies.

B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies.

Journal: Genome medicine
Published: July 16, 2017

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

Journal: Molecular psychiatry
Published: November 16, 2015

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Journal: American journal of human genetics
Published: June 04, 2015

Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems.

Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems.

Journal: American journal of human genetics
Published: November 12, 2014

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

Journal: Molecular psychiatry
Published: August 04, 2014

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.

Journal: Journal of medical genetics
Published: May 09, 2014

Update on Kleefstra Syndrome.

Update on Kleefstra Syndrome.

Journal: Molecular syndromology
Published: June 07, 2012

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.

Journal: American journal of human genetics
Published: February 27, 2012

Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability.

Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability.

Journal: Journal of medical genetics
Published: October 18, 2011
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Last Updated: 09/26/2026