Associated Papers
Shared and divergent mental health characteristics of ADNP-, CHD8- and DYRK1A-related neurodevelopmental conditions.
Neuhaus E et al.
Journal of Neurodevelopmental Disorders, 2024
38622540 (PubMed )
Supplement: 11689_2024_9532_MOESM1_ESM.xlsx › Sheet1
Characterizing executive functioning and associated behaviors in individuals with dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) syndrome.
Rea HM et al.
Frontiers in Neuroscience, 2024
39840013 (PubMed )
Supplement: Table_1.XLSX › Sheet1
Characterization of phenotypic range in DYRK1A haploinsufficiency syndrome using standardized behavioral measures.
Fenster R et al.
American Journal of Medical Genetics. Part A, 2022
Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly.
Rump P et al.
Bmc Medical Genomics, 2016
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