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DOI . ORG {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
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  14. CDN Services

We began analyzing https://link.springer.com/article/10.1007/s10519-020-09991-x, but it redirected us to https://link.springer.com/article/10.1007/s10519-020-09991-x. The analysis below is for the second page.

Title[redir]:
Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders | Behavior Genetics
Description:
The genetic architecture of neurodevelopmental disorders is largely polygenic, non-specific, and pleiotropic. This complex genetic architecture makes the search for specific etiological mechanisms that contribute to neurodevelopmental risk more challenging. Monogenic disorders provide an opportunity to focus in on how well-articulated signaling pathways contribute to risk for neurodevelopmental outcomes. This paper will focus on neurofibromatosis type 1 (NF1), a rare monogenic disorder that is associated with varied neurodevelopmental outcomes. Specifically, this paper will provide a brief overview of NF1 and its phenotypic associations with autism spectrum disorder, attention-deficit/hyperactivity disorder, and specific learning disorders, describe how variation within the NF1 gene increases risk for neurodevelopmental disorders via altered Ras signaling, and provide future directions for NF1 research to help elucidate the genetic architecture of neurodevelopmental disorders in the general population.

Matching Content Categories {📚}

  • Education
  • Business & Finance
  • Non-Profit & Charity

Content Management System {📝}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of doi.org audience?

🏙️ Massive Traffic: 50M - 100M visitors per month


Based on our best estimate, this website will receive around 98,426,998 visitors per month in the current month.

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How Does Doi.org Make Money? {💸}

We're unsure how the site profits.

Not every website is profit-driven; some are created to spread information or serve as an online presence. Websites can be made for many reasons. This could be one of them. Doi.org might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

pubmed, google, scholar, neurofibromatosis, type, central, disorders, autism, genet, children, disorder, spectrum, genetic, med, neurol, child, gutmann, nat, neurodevelopmental, brain, psychiatry, learning, article, cognitive, study, neurosci, gene, mol, human, research, architecture, acosta, adhd, silva, hum, function, signaling, neuropsychol, rev, dev, risk, nature, expression, res, north, deficits, ras, attentiondeficithyperactivity, access, clinical,

Topics {✒️}

gov/research/key-initiatives/ras/ras-central/blog/2015/ras-pathway-v2 dsm-iv attention-deficit/hyperactivity disorder ras pathway v2 month download article/chapter protein-protein interaction networks large-scale genomics unveils neuronal nf1/ras regulation dopamine-related locomotor signature pi3k-akt-mtor pathway akt-mtor pathway rescued gaba/glutamate neuron differentiation attention-deficit/hyperactivity disorder attention deficit/hyperactivity disorder register-based family study autistic subject-derived neurons excitation/inhibition imbalance hypothesis international neurofibromatosis web-based altered ras signaling register-based cohort study mtor-related genes associates randomized placebo-controlled study van der sluis developmental brain disorders cyclic amp phenotype privacy choices/manage cookies biological pathway abnormalities american psychiatric association full article pdf attention-deficit disorder real-world behavior erk/mapk signaling cutting le early communicative behavior related subjects human induced-neuronal o'malley kl decreased glial gaba structural brain abnormalities velez van meerbeke attention system dysfunction shared genetics malignant tumour cells swedish nationwide cohort multiple drug treatments dysregulated gene expressions dopamine-based learning cntnap2-deficient mice community twin study autism spectrum disorder acosta mt

Questions {❓}

  • Posthuma D, Polderman TJ (2013) What have we learned from recent twin studies about the etiology of neurodevelopmental disorders?

Schema {🗺️}

WebPage:
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         headline:Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders
         description:The genetic architecture of neurodevelopmental disorders is largely polygenic, non-specific, and pleiotropic. This complex genetic architecture makes the search for specific etiological mechanisms that contribute to neurodevelopmental risk more challenging. Monogenic disorders provide an opportunity to focus in on how well-articulated signaling pathways contribute to risk for neurodevelopmental outcomes. This paper will focus on neurofibromatosis type 1 (NF1), a rare monogenic disorder that is associated with varied neurodevelopmental outcomes. Specifically, this paper will provide a brief overview of NF1 and its phenotypic associations with autism spectrum disorder, attention-deficit/hyperactivity disorder, and specific learning disorders, describe how variation within the NF1 gene increases risk for neurodevelopmental disorders via altered Ras signaling, and provide future directions for NF1 research to help elucidate the genetic architecture of neurodevelopmental disorders in the general population.
         datePublished:2020-02-05T00:00:00Z
         dateModified:2020-02-05T00:00:00Z
         pageStart:191
         pageEnd:202
         sameAs:https://doi.org/10.1007/s10519-020-09991-x
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            Neurodevelopmental disorders
            Neurofibromatosis type 1
            Clinical Psychology
            Health Psychology
            Public Health
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      headline:Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders
      description:The genetic architecture of neurodevelopmental disorders is largely polygenic, non-specific, and pleiotropic. This complex genetic architecture makes the search for specific etiological mechanisms that contribute to neurodevelopmental risk more challenging. Monogenic disorders provide an opportunity to focus in on how well-articulated signaling pathways contribute to risk for neurodevelopmental outcomes. This paper will focus on neurofibromatosis type 1 (NF1), a rare monogenic disorder that is associated with varied neurodevelopmental outcomes. Specifically, this paper will provide a brief overview of NF1 and its phenotypic associations with autism spectrum disorder, attention-deficit/hyperactivity disorder, and specific learning disorders, describe how variation within the NF1 gene increases risk for neurodevelopmental disorders via altered Ras signaling, and provide future directions for NF1 research to help elucidate the genetic architecture of neurodevelopmental disorders in the general population.
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         Neurodevelopmental disorders
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               type:PostalAddress
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      affiliation:
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External Links {🔗}(398)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

Emails and Hosting {✉️}

Mail Servers:

  • mx.zoho.eu
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Name Servers:

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CDN Services {📦}

  • Crossref

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