Table S1. Compiled list of all pathogenic variants. Table contains all pathogenic variants in the current report, previously published, and from the ClinVar database. (XLSX 18 kb)

NIAID Data Ecosystem50

Additional file 2: Table S9. of Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development

神经发育障碍遗传学

精神疾病通路分析

Pathway-based dissection of additive genetic variance in SDQ-ADHD and SCDC scores according to 50 molecular signatures database hallmark gene set collections. (XLSX 20 kb)

Figshare2017-04-04 更新30

Additional file 3 of Chd8 haploinsufficiency impairs early brain development and protein homeostasis later in life

神经发育障碍遗传学

基因表达谱分析

Additional file 3: Supplementary Data File 3. The full lists of genes in each cluster.

Figshare2020-10-05 更新50

whole exome sequencing of one patient with epilepsy and development delay

癫痫基因组学

发育异常基因诊断

clinical testing for patients with epilepsy and development delay. A trio-whole exome sequencing revealed a novel homozygous frameshift variant in CNTN2 (c.2873_c.2874delCT, p.Thr958Thrfs) . SNP mutat

NIAID Data Ecosystem40

Array-CGH in a boy with an occurrence of neurodevelopmental disorders and epilepsy

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