Advanced search

Authors whose works are in public domain in at least one jurisdiction

List of works by Angelien J G A M Heister

1-8 of 8 results

View this query on the Wikidata Query Service
Common genetic variants influence human subcortical brain structures

scientific article
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.

scientific article
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.

scientific article
Response to methylphenidate in adults with ADHD is associated with a polymorphism in SLC6A3 (DAT1).

scientific article published in March 2008
An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD.

scientific article published in April 2008
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation

scientific article
Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family

scientific article
Meta-analysis of the DRD5 VNTR in persistent ADHD.

scientific article published on 29 July 2016

Paulina is supported by:

About Paulina

Help