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Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.
Published in:
Movement Disorders Clinical Practice, 2023, v. 10, n. 1, p. 17, doi. 10.1002/mdc3.13577
By:
- von Scheibler, Emma N. M. M.;
- van Eeghen, Agnies M.;
- de Koning, Tom J.;
- Kuijf, Mark L.;
- Zinkstok, Janneke R.;
- Müller, Annelieke R.;
- van Amelsvoort, Thérèse A. M. J.;
- Boot, Erik
Publication type:
Article
Vitamin D status in children with a psychiatric diagnosis, autism spectrum disorders, or internalizing disorders.
Published in:
Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.958556
By:
- Muskens, Jet;
- Klip, Helen;
- Zinkstok, Janneke R.;
- van Dongen-Boomsma, Martine;
- Staal, Wouter G.
Publication type:
Article
Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 2, p. 1, doi. 10.1002/ajmg.b.32956
By:
- Korteling, Dorinde;
- Musch, Jiska L. I.;
- Zinkstok, Janneke R.;
- Boot, Erik
Publication type:
Article
Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome.
Published in:
Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01859-4
By:
- Korteling, Dorinde;
- Boks, Marco P.;
- Fiksinski, Ania M.;
- van Hoek, Ilja N.;
- Vorstman, Jacob A. S.;
- Verhoeven-Duif, Nanda M.;
- Jans, Judith J. M.;
- Zinkstok, Janneke R.
Publication type:
Article
COMT Val<sup>158</sup>met genotype and striatal D<sub>2/3</sub> receptor binding in adults with 22q11 deletion syndrome.
Published in:
Synapse, 2011, v. 65, n. 9, p. 967, doi. 10.1002/syn.20932
By:
- Boot, Erik;
- Booij, Jan;
- Zinkstok, Janneke R.;
- Baas, Frank;
- Swillen, Ann;
- Owen, Michael J.;
- Murphy, Declan G.;
- Murphy, Kieran C.;
- Linszen, Don H.;
- Van Amelsvoort, Thérèse A.
Publication type:
Article
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Published in:
Human Molecular Genetics, 2019, v. 28, n. 22, p. 3724, doi. 10.1093/hmg/ddz166
By:
- Vervoort, Lisanne;
- Demaerel, Wolfram;
- Rengifo, Laura Y;
- Odrzywolski, Adrian;
- Vergaelen, Elfi;
- Hestand, Matthew S;
- Breckpot, Jeroen;
- Devriendt, Koen;
- Swillen, Ann;
- McDonald-McGinn, Donna M;
- Fiksinski, Ania M;
- Zinkstok, Janneke R;
- Morrow, Bernice E;
- Heung, Tracy;
- Vorstman, Jacob A S;
- Bassett, Anne S;
- Chow, Eva W C;
- Shashi, Vandana;
- Brain, International 22q11.2;
- Consortium, Behavior
Publication type:
Article
Intellectual and Behavioral Phenotypes of Smith–Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant.
Published in:
Genes, 2023, v. 14, n. 8, p. 1514, doi. 10.3390/genes14081514
By:
- Linders, Cathelijne C.;
- van Eeghen, Agnies M.;
- Zinkstok, Janneke R.;
- van den Boogaard, Marie-José;
- Boot, Erik
Publication type:
Article

Found: 7

Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.

Vitamin D status in children with a psychiatric diagnosis, autism spectrum disorders, or internalizing disorders.

Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review.

Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome.

COMT Val<sup>158</sup>met genotype and striatal D<sub>2/3</sub> receptor binding in adults with 22q11 deletion syndrome.

Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.

Intellectual and Behavioral Phenotypes of Smith–Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant.