Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Noa Sadigurschi"'
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
IntroductionThe implications of folate deficiency in neuropsychiatric disorders were demonstrated in numerous studies. Genetic deficiency in a key folate metabolism enzyme, MTHFR, is an example of the interaction between genetic and environmental ris
Externí odkaz:
https://doaj.org/article/f16d7cdf9ed54f3881fa447c5c85791b
Autor:
Rotem Tal-Ben Ishay, Apurba Shil, Shirley Solomon, Noa Sadigurschi, Hadeel Abu-Kaf, Gal Meiri, Hagit Flusser, Analya Michaelovski, Ilan Dinstein, Hava Golan, Nadav Davidovitch, Idan Menashe
Publikováno v:
Genes, Vol 13, Iss 36, p 36 (2022)
Genes; Volume 13; Issue 1; Pages: 36
Genes
Genes; Volume 13; Issue 1; Pages: 36
Genes
Whole-exome sequencing (WES) is an effective approach to identify the susceptibility of genetic variants of autism spectrum disorder (ASD). The Israel Ministry of Health supports WES as an adjunct tool for ASD diagnosis, despite its unclear diagnosti
Autor:
Noa, Sadigurschi, Hava M, Golan
Publikováno v:
Genes, brain, and behavior. 18(1)
Individuals with autism constitute a variable population whose members are spread along the autism spectrum. Subpopulations within that spectrum exhibit other conditions, such as anxiety, intellectual disabilities, hyperactivity and epilepsy, with di
Autor:
Hava Golan, Noa Sadigurschi
Publikováno v:
Genes, Brain and Behavior. :e12547
Individuals with autism constitute a variable population whose members are spread along the autism spectrum. Subpopulations within that spectrum exhibit other conditions, such as anxiety, intellectual disabilities, hyperactivity and epilepsy, with di