Willemsen M”的用户个人学术档案

Michel AAP Willemsen

- 在 radboudumc.nl 的电子邮件经过验证 - 被引用次数:14881

Martijn C. Willemsen

- 在 tue.nl 的电子邮件经过验证 - 被引用次数:5110

Explaining the user experience of recommender systems

BP Knijnenburg, MC Willemsen, Z Gantner… - User modeling and user …, 2012 - Springer
Research on recommender systems typically focuses on the accuracy of prediction algorithms.
Because accuracy only partially constitutes the user experience of a recommender system…

Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability

…, P de Vries, BBA de Vries, MH Willemsen… - Nature …, 2016 - nature.com
To identify candidate genes for intellectual disability, we performed a meta-analysis on
2,637 de novo mutations, identified from the exomes of 2,104 patient–parent trios. Statistical …

Predicting expatriate job performance for selection purposes: A quantitative review

ST Mol, MP Born, ME Willemsen… - Journal of Cross …, 2005 - journals.sagepub.com
This article meta-analytically reviews empirical studies on the prediction of expatriate job
performance. Using 30 primary studies (total N = 4,046), it was found that predictive validities of …

[HTML][HTML] Diagnostic exome sequencing in persons with severe intellectual disability

J De Ligt, MH Willemsen, BWM Van Bon… - … England Journal of …, 2012 - Mass Medical Soc
Background The causes of intellectual disability remain largely unknown because of
extensive clinical and genetic heterogeneity. Methods We evaluated patients with intellectual …

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis

MA Willemsen, MM Verbeek, EJ Kamsteeg… - Brain, 2010 - academic.oup.com
Tyrosine hydroxylase deficiency is an autosomal recessive disorder resulting from cerebral
catecholamine deficiency. Tyrosine hydroxylase deficiency has been reported in fewer than …

Genome sequencing identifies major causes of severe intellectual disability

…, M Van De Vorst, BWM Van Bon, MH Willemsen… - Nature, 2014 - nature.com
Severe intellectual disability (ID) occurs in 0.5% of newborns and is thought to be largely
genetic in origin 1 , 2 . The extensive genetic heterogeneity of this disorder requires a genome-…

Prospective assessment of falls in Parkinson's disease

…, YAM Grimbergen, M Cramer, M Willemsen… - Journal of …, 2001 - Springer
We studied prospectively the epidemiology, clinical impact and prediction of falls in 59
moderately affected patients with Parkinson's disease (PD) (mean UPDRS motor score 31.5; …

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

…, D Webb, B Weschke, H Scheffer, MA Willemsen - Brain, 2010 - academic.oup.com
Glucose transporter-1 deficiency syndrome is caused by mutations in the SLC2A1 gene in
the majority of patients and results in impaired glucose transport into the brain. From 2004–…

Mutations in antiquitin in individuals with pyridoxine-dependent seizures

…, P Baxter, M Baumgartner, MAAP Willemsen… - Nature medicine, 2006 - nature.com
m/z of −97 precursor-ion scanning mode. (j) Analysis of mixture at time 0 showing presence
… PLP(m/z, −246.4). (k) Analysis of mixture after 24 h showing the presence of complex A (m/z…

Understanding the factors that promote employability orientation: the impact of employability culture, career satisfaction, and role breadth self‐efficacy

…, K Van Dam, M Willemsen - … of occupational and …, 2009 - Wiley Online Library
This study among 702 Dutch employees working in the health care and welfare sector
examined individual and organizational factors that are related to workers' employability …