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Journal Article
PLoS ONE, ISSN 1932-6203, 12/2012, Volume 7, Issue 12, p. e51638
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 09/2019, Volume 9, Issue 1, pp. 1 - 7
Increasing evidence suggests that epigenetic mechanisms play a role in the etiology of autism spectrum disorder (ASD). To date, several studies have attempted... 
METHYLATION | PPP2R2C | EXPRESSION | MULTIDISCIPLINARY SCIENCES | Autism | Learning algorithms | Etiology | Peripheral blood | DNA methylation | Biomarkers | Epigenetics | Deoxyribonucleic acid--DNA
Journal Article
Journal of Child Psychology and Psychiatry, ISSN 0021-9630, 05/2019, Volume 60, Issue 5, pp. 585 - 598
Background Williams syndrome (WS) is a neurodevelopmental disorder that has been attributed to heterozygous deletions in chromosome 7q11.23 and exhibits a... 
autism spectrum disorder | genetics | Williams syndrome | DE-NOVO | AUTISM | BCL11A | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | PSYCHOLOGY | DELETION | DYSREGULATION | GENE-EXPRESSION | GENOME-WIDE | BRAIN | MICRORNA | BLOOD | Genetic research | Genetic aspects | Diagnosis | Risk factors | Williams' syndrome | Phenotypes | Genes | Cognitive-Behavioural factors | Network analysis | Variability | Speech | Genetic factors | Transport | Speech disorders | Chromosomes | Blood
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 13473 - 13
Journal Article
JOURNAL OF HUMAN GENETICS, ISSN 1434-5161, 05/2019, Volume 64, Issue 5, pp. 445 - 458
Seckel syndrome (SS) is a rare spectrum of congenital severe microcephaly and dwarfism. One SS-causative gene is Ataxia Telangiectasia and Rad3-Related Protein... 
NEURAL PROGENITORS | MANIPULATION | PROTEIN | PHOSPHORYLATION | CILIUM | DNA-DAMAGE | GENETICS & HEREDITY | STRESS | EXPRESSION
Journal Article
Human Mutation, ISSN 1059-7794, 08/2016, Volume 37, Issue 8, pp. 737 - 744
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 09/2018, Volume 9, p. 368
Williams-Beuren syndrome (WBS) is a multisystemic neurodevelopmental disorder caused by a hemizygous deletion on chromosome 7q11.23. Though at present there is... 
Williams-beuren syndrome | Gene expression | Non-hodgkin lymphoma | 7q11.23 | Burkitt lymphoma | williams-beuren syndrome | GENETICS & HEREDITY | NON-HODGKIN-LYMPHOMA | MALIGNANCIES | burkitt lymphoma | LEUKEMIA | CHILD | gene expression | non-hodgkin lymphoma | Research | Carcinogenesis | Risk factors | Williams syndrome | Burkitt's lymphoma | williams–beuren syndrome
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 10/2019, Volume 29, pp. S242 - S243
Journal Article
Clinical Genetics, ISSN 0009-9163, 08/2017, Volume 92, Issue 2, pp. 180 - 187
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 09/2017, Volume 114, Issue 38, p. 10268
Down syndrome (DS) caused by trisomy of chromosome 21 is the most common genetic cause of intellectual disability. Although the prenatal diagnosis of DS has... 
Brain | Therapy | Phosphorylation | Animal models | Trisomy | Intellectual disabilities | Stem cell transplantation | Cognition | Neurogenesis | Allografts | Functional anatomy | Down's syndrome | Rodents | Neurospheres | Chromosomes | Tyrosine | Neurons | Cortex | Oral administration | Down syndrome | Embryos | Studies | Pregnancy | Offspring | Prenatal diagnosis | Stem cells | Chromosome 21 | Neural stem cells | Aberration | Structure-function relationships
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 09/2017, Volume 114, Issue 38, pp. 10268 - 10273
Journal Article