Kees E P van Roozendaal
Overview
Explore the profile of Kees E P van Roozendaal including associated specialties, affiliations and a list of published articles.
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9
Citations
674
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Recent Articles
1.
Frints S, Ozanturk A, Rodriguez Criado G, Grasshoff U, de Hoon B, Field M, et al.
Mol Psychiatry
. 2018 May;
24(11):1748-1768.
PMID: 29728705
RLIM, also known as RNF12, is an X-linked E3 ubiquitin ligase acting as a negative regulator of LIM-domain containing transcription factors and participates in X-chromosome inactivation (XCI) in mice. We...
2.
Bojesen S, Pooley K, Johnatty S, Beesley J, Michailidou K, Tyrer J, et al.
Nat Genet
. 2013 Mar;
45(4):371-84, 384e1-2.
PMID: 23535731
TERT-locus SNPs and leukocyte telomere measures are reportedly associated with risks of multiple cancers. Using the Illumina custom genotyping array iCOGs, we analyzed ∼480 SNPs at the TERT locus in...
3.
Halbach N, Smeets E, van den Braak N, van Roozendaal K, Blok R, Schrander-Stumpel C, et al.
Am J Med Genet A
. 2011 Dec;
158A(2):340-50.
PMID: 22190343
Rett syndrome (RTT; OMIM 312750) is an X-linked dominant neurodevelopmental disorder leading to cognitive and motor impairment, epilepsy, and autonomic dysfunction in females. Since the discovery that RTT is caused...
4.
Brandao R, van Roozendaal K, Tserpelis D, Caanen B, Gomez Garcia E, Blok M
Breast Cancer Res Treat
. 2011 Nov;
131(2):723-5.
PMID: 22113256
No abstract available.
5.
Sinnema M, Boer H, Collin P, Maaskant M, van Roozendaal K, Schrander-Stumpel C, et al.
Res Dev Disabil
. 2011 Apr;
32(5):1729-35.
PMID: 21454045
Previous studies have suggested an association between PWS and comorbid psychiatric illness. Data on prevalence rates of psychopathology is still scarce. This paper describes a large-scale, systematic study investigating the...
6.
Gaudet M, Kirchhoff T, Green T, Vijai J, Korn J, Guiducci C, et al.
PLoS Genet
. 2010 Nov;
6(10):e1001183.
PMID: 21060860
The considerable uncertainty regarding cancer risks associated with inherited mutations of BRCA2 is due to unknown factors. To investigate whether common genetic variants modify penetrance for BRCA2 mutation carriers, we...
7.
Sinnema M, van Roozendaal K, Maaskant M, Smeets H, Engelen J, Jonker-Houben N, et al.
Eur J Hum Genet
. 2010 May;
18(9):993-8.
PMID: 20461108
The Prader-Willi syndrome (PWS) is a genetic disorder caused by the absent expression of the paternal copy of maternally imprinted genes in chromosome region 15q11-13. The frequencies of different subtypes...
8.
Looijenga L, Stoop H, de Leeuw H, de Gouveia Brazao C, Gillis A, van Roozendaal K, et al.
Cancer Res
. 2003 May;
63(9):2244-50.
PMID: 12727846
Human germ cell tumors (GCTs) may have variable histology and clinical behavior, depending on factors such as sex of the patient, age at clinical diagnosis, and anatomical site of the...
9.
Moog U, Smeets E, van Roozendaal K, Schoenmakers S, Herbergs J, Schoonbrood-Lenssen A, et al.
Eur J Paediatr Neurol
. 2003 Mar;
7(1):5-12.
PMID: 12615169
Mutations in the MECP2 (methyl-CpG-binding protein 2) gene are known to cause Rett syndrome, a well-known and clinically defined neurodevelopmental disorder. Rett syndrome occurs almost exclusively in females and for...