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Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

artículo científico publicado en 2011

Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations

artículo científico publicado en 2010

DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders

artículo científico publicado en 2011

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

scientific journal article

Exome sequencing and genetic testing for MODY.

artículo científico publicado en 2012

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

artículo científico publicado en 2009

Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis

scientific journal article

Shared genetic background between children and adults with attention deficit/hyperactivity disorder

scientific article published on 12 April 2020

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