Zobrazeno 1 - 10
of 19
pro vyhledávání: '"ASD genes"'
Publikováno v:
Frontiers in Bioinformatics, Vol 4 (2024)
Autism spectrum disorder (ASD) is a highly heritable complex disease that affects 1% of the population, yet its underlying molecular mechanisms are largely unknown. Here we study the problem of predicting causal genes for ASD by combining genome-scal
Externí odkaz:
https://doaj.org/article/67ed22f0018a422cb108584b2f8445f3
Autor:
Maria Jesus Herrero, Dmitry Velmeshev, David Hernandez-Pineda, Saarthak Sethi, Shawn Sorrells, Payal Banerjee, Catherine Sullivan, Abha R. Gupta, Arnold R. Kriegstein, Joshua G. Corbin
Publikováno v:
Molecular Autism, Vol 11, Iss 1, Pp 1-14 (2020)
Abstract Background Studies of individuals with autism spectrum disorder (ASD) have revealed a strong multigenic basis with the identification of hundreds of ASD susceptibility genes. ASD is characterized by social deficits and a range of other pheno
Externí odkaz:
https://doaj.org/article/4156d40f162a400b9104025a043197f0
Akademický článek
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Autor:
Arnold R. Kriegstein, Maria Jesus Herrero, Catherine Sullivan, David Hernandez-Pineda, Shawn F. Sorrells, Payal Banerjee, Saarthak Sethi, Dmitry Velmeshev, Abha R. Gupta, Joshua G. Corbin
Publikováno v:
Molecular Autism, Vol 11, Iss 1, Pp 1-14 (2020)
Molecular Autism
Molecular autism, vol 11, iss 1
Molecular Autism
Molecular autism, vol 11, iss 1
Background Studies of individuals with autism spectrum disorder (ASD) have revealed a strong multigenic basis with the identification of hundreds of ASD susceptibility genes. ASD is characterized by social deficits and a range of other phenotypes, im
Autor:
Courchesne, Eric, Pramparo, Tiziano, Gazestani, Vahid H., Lombardo, Michael V., Pierce, Karen, Lewis, Nathan E.
Publikováno v:
Molecular Psychiatry
Molecular psychiatry
Molecular psychiatry, vol 24, iss 1
Molecular psychiatry
Molecular psychiatry, vol 24, iss 1
Autism spectrum disorder (ASD) has captured the attention of scientists, clinicians and the lay public because of its uncertain origins and striking clinical symptoms. A spectrum of candidate etiologies including evidence of genetic variants, present
Identifying disease genes from a vast amount of genetic data is one of the most challenging tasks in the post-genomic era. Also, complex diseases present highly heterogeneous genotype, which difficult biological marker identification. Machine learnin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2016::615447a09dcfc339ad7112ae1925a98d
https://hdl.handle.net/10400.18/5930
https://hdl.handle.net/10400.18/5930
Akademický článek
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Publikováno v:
International Journal of Molecular Sciences; Volume 17; Issue 5; Pages: 673
International Journal of Molecular Sciences, Vol 17, Iss 5, p 673 (2016)
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 17, Iss 5, p 673 (2016)
International Journal of Molecular Sciences
Mammalian chromosomes are comprised of complex chromatin architecture with the specific assembly and configuration of each chromosome influencing gene expression and function in yet undefined ways by varying degrees of heterochromatinization that res
Publikováno v:
International Journal of Molecular Sciences
Volume 16
Issue 3
Pages 6464-6495
International Journal of Molecular Sciences, Vol 16, Iss 3, Pp 6464-6495 (2015)
Volume 16
Issue 3
Pages 6464-6495
International Journal of Molecular Sciences, Vol 16, Iss 3, Pp 6464-6495 (2015)
Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased d
Akademický článek
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