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Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
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- PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007535
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- Article
Potential Role of L-Carnitine in Autism Spectrum Disorder.
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- Journal of Clinical Medicine, 2021, v. 10, n. 6, p. 1202, doi. 10.3390/jcm10061202
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- Article
The Role of Inflammatory Proteins in Anti-Glucocorticoid Therapy for Treatment-Resistant Depression.
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- Journal of Clinical Medicine, 2021, v. 10, n. 4, p. 784, doi. 10.3390/jcm10040784
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- Article
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses.
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- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1851, doi. 10.3390/jcm9061851
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- Article
Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 8, p. 485, doi. 10.1002/ajmg.b.32879
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Cover Image, Volume 186B, Number 8, December 2021.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 8, p. 1, doi. 10.1002/ajmg.b.32803
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- Article
Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores.
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- Genes, Brain & Behavior, 2020, v. 19, n. 8, p. 1, doi. 10.1111/gbb.12694
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- Article
Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057241
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- Article
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
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- Journal of Psychiatry & Neuroscience, 2021, v. 46, n. 2, p. E247, doi. 10.1503/jpn.200083
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- Article
Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
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- Journal of Psychiatry & Neuroscience, 2019, v. 44, n. 5, p. 350, doi. 10.1503/jpn.180184
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- Article
Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02079-6
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- Article
Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.
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- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1694, doi. 10.1038/ejhg.2015.37
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- Article
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
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- European Journal of Human Genetics, 2009, v. 17, n. 10, p. 1347, doi. 10.1038/ejhg.2009.47
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- Article
MET and autism susceptibility: family and case–control studies.
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- European Journal of Human Genetics, 2009, v. 17, n. 6, p. 749, doi. 10.1038/ejhg.2008.215
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- Article
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 123, doi. 10.1038/sj.ejhg.5201444
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- Article
An examination of multiple classes of rare variants in extended families with bipolar disorder.
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- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0113-y
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- Article
De Novo Gene Variants and Familial Bipolar Disorder.
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- JAMA Network Open, 2020, v. 3, n. 5, p. e203382, doi. 10.1001/jamanetworkopen.2020.3382
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- Article
Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 gene.
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- Journal of Inherited Metabolic Disease, 2010, v. 33, n. 6, p. 795, doi. 10.1007/s10545-010-9196-1
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- Article
Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer.
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- International Journal of Cancer, 2020, v. 146, n. 6, p. 1568, doi. 10.1002/ijc.32683
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- Article
Alternative splicing in the dyslexia-associated gene KIAA0319.
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- Mammalian Genome, 2007, v. 18, n. 9, p. 627, doi. 10.1007/s00335-007-9051-3
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The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
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- Human Molecular Genetics, 2008, v. 17, n. 6, p. 859, doi. 10.1093/hmg/ddm358
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Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.
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- Movement Disorders, 2011, v. 26, n. 8, p. 1558, doi. 10.1002/mds.23564
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Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation.
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- Movement Disorders, 2010, v. 25, n. 8, p. 1086, doi. 10.1002/mds.23002
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- Article