Found: 52
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Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
- Published in:
- Human Genetics, 2015, v. 134, n. 2, p. 191, doi. 10.1007/s00439-014-1513-6
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- Publication type:
- Article
Recurrence quantification analysis to characterize cyclical components of environmental elemental exposures during fetal and postnatal development.
- Published in:
- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0187049
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- Publication type:
- Article
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder.
- Published in:
- Human Genetics, 2024, v. 143, n. 2, p. 169, doi. 10.1007/s00439-023-02636-z
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- Publication type:
- Article
Presynaptic dysfunction in CASK-related neurodevelopmental disorders.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-00994-0
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- Publication type:
- Article
Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs.
- Published in:
- FASEB Journal, 2016, v. 30, n. 10, p. 3578, doi. 10.1096/fj.201500124RR
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- Publication type:
- Article
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.
- Published in:
- FASEB Journal, 2008, v. 22, n. 8, p. 3001, doi. 10.1096/fj.07-104455
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- Publication type:
- Article
Preferential looking to eyes versus mouth in early infancy: heritability and link to concurrent and later development.
- Published in:
- Journal of Child Psychology, 2023, v. 64, n. 2, p. 311, doi. 10.1111/jcpp.13724
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- Publication type:
- Article
Pupil size and pupillary light reflex in early infancy: heritability and link to genetic liability to schizophrenia.
- Published in:
- Journal of Child Psychology, 2022, v. 63, n. 9, p. 1068, doi. 10.1111/jcpp.13564
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- Publication type:
- Article
Hypogonadotrophic hypogonadism, delayed puberty and risk for neurodevelopmental disorders.
- Published in:
- Journal of Neuroendocrinology, 2019, v. 31, n. 11, p. N.PAG, doi. 10.1111/jne.12803
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- Publication type:
- Article
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34112-z
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- Publication type:
- Article
2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study.
- Published in:
- Journal of Autism & Developmental Disorders, 2018, v. 48, n. 9, p. 3244, doi. 10.1007/s10803-018-3588-8
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- Publication type:
- Article
In search of environmental risk factors for obsessive-compulsive disorder: study protocol for the OCDTWIN project.
- Published in:
- BMC Psychiatry, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12888-023-04897-4
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- Publication type:
- Article
Examining neurodevelopmental problems in 15q11.2 (BP1‐BP2) copy number variation carriers at ages 9/12 and 18 in a Swedish twin sample.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 8, p. 1, doi. 10.1002/mgg3.2191
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- Publication type:
- Article
Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1002/mgg3.1013
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- Publication type:
- Article
Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-46396-1
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- Publication type:
- Article
Access, utilization, and awareness for clinical genetic testing in autism spectrum disorder in Sweden: A survey study.
- Published in:
- Autism: The International Journal of Research & Practice, 2022, v. 26, n. 7, p. 1795, doi. 10.1177/13623613211066130
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- Publication type:
- Article
Quo Vadis clinical genomics of ASD?
- Published in:
- 2016
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- Publication type:
- Editorial
Long-term social skills group training for children and adolescents with autism spectrum disorder: a randomized controlled trial.
- Published in:
- European Child & Adolescent Psychiatry, 2019, v. 28, n. 2, p. 189, doi. 10.1007/s00787-018-1161-9
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- Publication type:
- Article
The Babytwins Study Sweden (BATSS): A Multi-Method Infant Twin Study of Genetic and Environmental Factors Influencing Infant Brain and Behavioral Development.
- Published in:
- 2021
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- Publication type:
- journal article
Determining Zygosity in Infant Twins - Revisiting the Questionnaire Approach.
- Published in:
- 2021
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- Publication type:
- journal article
Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.
- Published in:
- 2018
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- Publication type:
- journal article
The Roots of Autism and ADHD Twin Study in Sweden (RATSS)
- Published in:
- 2014
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- Publication type:
- Journal Article
The Roots of Autism and ADHD Twin Study in Sweden (RATSS).
- Published in:
- Twin Research & Human Genetics, 2014, v. 17, n. 3, p. 164, doi. 10.1017/thg.2014.12
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- Publication type:
- Article
Minor physical anomalies in neurodevelopmental disorders: a twin study.
- Published in:
- Child & Adolescent Psychiatry & Mental Health, 2017, v. 11, p. 1, doi. 10.1186/s13034-017-0195-y
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- Publication type:
- Article
Screening autism-associated environmental factors in differentiating human neural progenitors with fractional factorial design-based transcriptomics.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-37488-0
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- Publication type:
- Article
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 10, p. 2752, doi. 10.1093/hmg/ddt669
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- Publication type:
- Article
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2802, doi. 10.1093/hmg/ddp215
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- Publication type:
- Article
Fetal and postnatal metal dysregulation in autism.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 15493, doi. 10.1038/ncomms15493
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- Publication type:
- Article
Rare variants in the outcome of social skills group training for autism.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2022, v. 15, n. 3, p. 434, doi. 10.1002/aur.2666
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- Publication type:
- Article
Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons.
- Published in:
- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0020580
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- Publication type:
- Article
The Association Between Somatic Health, Autism Spectrum Disorder, and Autistic Traits.
- Published in:
- Behavior Genetics, 2020, v. 50, n. 4, p. 233, doi. 10.1007/s10519-019-09986-3
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- Publication type:
- Article
SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 134, doi. 10.1007/s10519-010-9431-4
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- Publication type:
- Article
Infants' sense of approximate numerosity: Heritability and link to other concurrent traits.
- Published in:
- Developmental Science, 2023, v. 26, n. 4, p. 1, doi. 10.1111/desc.13347
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- Publication type:
- Article
A Novel Way to Measure and Predict Development: A Heuristic Approach to Facilitate the Early Detection of Neurodevelopmental Disorders.
- Published in:
- Current Neurology & Neuroscience Reports, 2017, v. 17, n. 5, p. 1, doi. 10.1007/s11910-017-0748-8
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- Publication type:
- Article
Whole-genome sequencing of quartet families with autism spectrum disorder.
- Published in:
- Nature Medicine, 2015, v. 21, n. 2, p. 185, doi. 10.1038/nm.3792
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- Publication type:
- Article
Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes.
- Published in:
- BMC Genomics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12864-018-4810-y
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- Publication type:
- Article
Dynamical properties of elemental metabolism distinguish attention deficit hyperactivity disorder from autism spectrum disorder.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41398-019-0567-6
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- Publication type:
- Article
Copy number variation and neuropsychiatric problems in females and males in the general population.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 6, p. 341, doi. 10.1002/ajmg.b.32685
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- Publication type:
- Article
Rare de novo deletion of metabotropic glutamate receptor 7 ( GRM7) gene in a patient with autism spectrum disorder.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 4, p. 258, doi. 10.1002/ajmg.b.32306
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- Publication type:
- Article
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder.
- Published in:
- Nature Genetics, 2014, v. 46, n. 7, p. 742, doi. 10.1038/ng.2980
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- Publication type:
- Article
The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder.
- Published in:
- NPJ Genomic Medicine, 2020, v. 5, n. 1, p. N.PAG, doi. 10.1038/s41525-020-00152-x
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- Publication type:
- Article
EU-AIMS Longitudinal European Autism Project (LEAP): the autism twin cohort.
- Published in:
- 2018
- By:
- Publication type:
- Letter
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
- Published in:
- JAMA: Journal of the American Medical Association, 2015, v. 314, n. 9, p. 895, doi. 10.1001/jama.2015.10078
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- Publication type:
- Article
Urine metabolomic profiles of autism and autistic traits–A twin study.
- Published in:
- PLoS ONE, 2024, v. 19, n. 9, p. 1, doi. 10.1371/journal.pone.0308224
- By:
- Publication type:
- Article
Circular RNAs arising from synaptic host genes during human neuronal differentiation are modulated by SFPQ RNA-binding protein.
- Published in:
- BMC Biology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12915-023-01627-w
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- Publication type:
- Article
Machine Learning Prediction of Autism Spectrum Disorder From a Minimal Set of Medical and Background Information.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 8, p. e2429229, doi. 10.1001/jamanetworkopen.2024.29229
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- Publication type:
- Article
Actionable and incidental neuroradiological findings in twins with neurodevelopmental disorders.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-79959-8
- By:
- Publication type:
- Article
Clinical versus automated assessments of morphological variants in twins with and without neurodevelopmental disorders.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 5, p. 1177, doi. 10.1002/ajmg.a.61545
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- Publication type:
- Article
De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1381, doi. 10.1002/ajmg.a.37050
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- Publication type:
- Article
High resolution genomic analyses of a clinically defined autism spectrum disorder cohort.
- Published in:
- International Journal of Developmental Neuroscience, 2015, v. 47, p. 76, doi. 10.1016/j.ijdevneu.2015.04.208
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- Publication type:
- Article