Merel W. Boogaard
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 13 publications
Primary Ovarian Failure in Addition to Classical Clinical Features of Coats Plus Syndrome in a Female Carrying 2 Truncating Variants of CTC1.
Journal: Hormone research in paediatrics
Published: June 07, 2021
Generation of 5 induced pluripotent stem cell lines, LUMCi007-A and B and LUMCi008-A, B and C, from 2 patients with Huntington disease.
Journal: Stem cell research
Published: May 13, 2019
Repeat variations in polyglutamine disease-associated genes and cognitive function in old age.
Journal: Neurobiology of aging
Published: April 30, 2019
Prevalence of Carriers of Intermediate and Pathological Polyglutamine Disease-Associated Alleles Among Large Population-Based Cohorts.
Journal: JAMA neurology
Published: April 02, 2019
Bioenergetics in fibroblasts of patients with Huntington disease are associated with age at onset.
Journal: Neurology. Genetics
Published: May 04, 2018
Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease.
Journal: Neurobiology of aging
Published: March 27, 2018
Generation of 3 spinocerebellar ataxia type 1 (SCA1) patient-derived induced pluripotent stem cell lines LUMCi002-A, B, and C and 2 unaffected sibling control induced pluripotent stem cell lines LUMCi003-A and B.
Journal: Stem cell research
Published: February 02, 2018
Repeat length variations in polyglutamine disease-associated genes affect body mass index.
Journal: International journal of obesity (2005)
Published: November 27, 2017
Age of onset in Huntington's disease is influenced by CAG repeat variations in other polyglutamine disease-associated genes.
Journal: Brain : a journal of neurology
Published: May 27, 2017
Huntingtin gene repeat size variations affect risk of lifetime depression.
Journal: Translational psychiatry
Published: May 01, 2017
Large normal-range TBP and ATXN7 CAG repeat lengths are associated with increased lifetime risk of depression.
Journal: Translational psychiatry
Published: April 11, 2017
Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.
Journal: Human mutation
Published: April 25, 2013
Last Updated: 09/26/2026