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Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility.
- Published in:
- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.858238
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- Article
Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 4, p. 715, doi. 10.1002/ajmg.a.36847
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- Article
Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years Old.
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- Brain Sciences (2076-3425), 2020, v. 10, n. 10, p. 741, doi. 10.3390/brainsci10100741
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- Article
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-59922-3
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- Article
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.
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- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 5, p. 2459, doi. 10.1111/jcmm.16161
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- Article
ELMOD3‐SH2D6 gene fusion as a possible co‐star actor in autism spectrum disorder scenario.
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- Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 2, p. 2064, doi. 10.1111/jcmm.14733
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- Article
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies.
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- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 3, p. 475, doi. 10.1002/acn3.722
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- Article
A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.
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- Journal of Headache & Pain, 2016, v. 17, n. 1, p. 1, doi. 10.1186/s10194-016-0705-y
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- Article
O015. Evaluation of the genetic polymorphism of the α3 (CHRNA3) and α5 (CHRNA5) nicotinic receptor subunits, in patients with cluster headache.
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- Journal of Headache & Pain, 2015, v. 16, p. 1, doi. 10.1186/1129-2377-16-S1-A88
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- Article
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.953762
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- Article
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.
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- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00411-1
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- Article