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  5. How Does Link.springer.com Make Money
  6. Keywords
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We are analyzing https://link.springer.com/article/10.1007/s11060-021-03874-9.

Title:
The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications | Journal of Neuro-Oncology
Description:
Introduction Meningiomas are generally considered “benign,” however, these tumors can demonstrate variability in behavior and a surprising aggressiveness with elevated rates of recurrence. The advancement of next-generation molecular technologies have led to the understanding of the genomic and epigenomic landscape of meningiomas and more recent correlations with clinical characteristics and behavior. Methods Based on a thorough review of recent peer-reviewed publications (PubMed) and edited texts, we provide a molecular overview of meningiomas with a focus on relevant clinical implications. Results The identification of specific somatic driver mutations has led to the classification of several major genomic subgroups, which account for more than 80% of sporadic meningiomas, and can be distinguished using noninvasive clinical variables to help guide management decisions. Other somatic genomic modifications, including non-coding alterations and copy number variations, have also been correlated with tumor characteristics. Furthermore, epigenomic modifications in meningiomas have recently been described, with DNA methylation being the most widely studied and potentially most clinically relevant. Based on these molecular insights, several clinical trials are currently underway in an effort to establish effective medical therapeutic options for meningioma. Conclusion As we enhance our multiomic understanding of meningiomas, our ability to care for patients with these tumors will continue to improve. Further biological insights will lead to additional progress in precision medicine for meningiomas.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Business & Finance

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We can't figure out the monetization strategy.

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. Link.springer.com might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

meningiomas, pubmed, article, google, scholar, mutations, cas, meningioma, tumors, genomic, grade, nct, recurrence, central, clinical, tumor, atypical, molecular, somatic, methylation, dna, loss, sporadic, recurrent, oncol, higher, pathway, cancer, risk, increased, cell, expression, chromosome, neuropathol, analysis, youngblood, classification, brain, aggressive, gene, found, including, ersonomay, moliterno, behavior, based, traf, hkme, acta, demonstrate,

Topics {✒️}

linc00702/mir-4652–3p/zeb1 axis promotes activating wnt/beta-catenin pathway murat günel & jennifer moliterno cyclin-dependent kinase inhibitors full size image central nervous system pi3k/akt pathway represent recent peer-reviewed publications cyclin-dependent kinase article download pdf epigenetically silenced hif-3α4 unsupervised clustering differentiated meningiomas patient-centered treatment protocols copy number variations unlike nf2-mutated meningiomas hif-3α4 impairs angiogenesis major genomic subgroups identify molecular signatures dna methylation-based classification hypoxia-inducible factor recurrence-free survival wnt signaling pathway high-grade rhabdoid meningiomas grade ii/iii lesions shankar gm progression free survival targeting chromosomal abnormalities neuro-oncology article swi/snf related de novo formation progressive/higher-grade meningiomas privacy choices/manage cookies atypical nf2-mutant meningiomas grade ii–iii meningiomas demonstrate low risk ferreira mj jr full access key transcription factor effective therapeutic options dna methylation profiling swi/snf complex lateral skull base world health organization clark ve messenger rna abundance predicts worse outcomes important signaling pathway meningioma genomics deepens somatic genomic modifications related subjects

Questions {❓}

  • Shen L, Lin D, Cheng L, Tu S, Wu H, Xu W, Pan Y, Wang X, Zhang J, Shao A (2020) Is DNA methylation a ray of sunshine in predicting meningioma prognosis?

Schema {🗺️}

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         headline:The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications
         description:Meningiomas are generally considered “benign,” however, these tumors can demonstrate variability in behavior and a surprising aggressiveness with elevated rates of recurrence. The advancement of next-generation molecular technologies have led to the understanding of the genomic and epigenomic landscape of meningiomas and more recent correlations with clinical characteristics and behavior. Based on a thorough review of recent peer-reviewed publications (PubMed) and edited texts, we provide a molecular overview of meningiomas with a focus on relevant clinical implications. The identification of specific somatic driver mutations has led to the classification of several major genomic subgroups, which account for more than 80% of sporadic meningiomas, and can be distinguished using noninvasive clinical variables to help guide management decisions. Other somatic genomic modifications, including non-coding alterations and copy number variations, have also been correlated with tumor characteristics. Furthermore, epigenomic modifications in meningiomas have recently been described, with DNA methylation being the most widely studied and potentially most clinically relevant. Based on these molecular insights, several clinical trials are currently underway in an effort to establish effective medical therapeutic options for meningioma. As we enhance our multiomic understanding of meningiomas, our ability to care for patients with these tumors will continue to improve. Further biological insights will lead to additional progress in precision medicine for meningiomas.
         datePublished:2021-11-30T00:00:00Z
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      headline:The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications
      description:Meningiomas are generally considered “benign,” however, these tumors can demonstrate variability in behavior and a surprising aggressiveness with elevated rates of recurrence. The advancement of next-generation molecular technologies have led to the understanding of the genomic and epigenomic landscape of meningiomas and more recent correlations with clinical characteristics and behavior. Based on a thorough review of recent peer-reviewed publications (PubMed) and edited texts, we provide a molecular overview of meningiomas with a focus on relevant clinical implications. The identification of specific somatic driver mutations has led to the classification of several major genomic subgroups, which account for more than 80% of sporadic meningiomas, and can be distinguished using noninvasive clinical variables to help guide management decisions. Other somatic genomic modifications, including non-coding alterations and copy number variations, have also been correlated with tumor characteristics. Furthermore, epigenomic modifications in meningiomas have recently been described, with DNA methylation being the most widely studied and potentially most clinically relevant. Based on these molecular insights, several clinical trials are currently underway in an effort to establish effective medical therapeutic options for meningioma. As we enhance our multiomic understanding of meningiomas, our ability to care for patients with these tumors will continue to improve. Further biological insights will lead to additional progress in precision medicine for meningiomas.
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               type:PostalAddress
            type:Organization
      name:Murat Günel
      affiliation:
            name:Yale School of Medicine
            address:
               name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
               type:PostalAddress
            type:Organization
            name:Smilow Cancer Hospital
            address:
               name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
               type:PostalAddress
            type:Organization
      name:Jennifer Moliterno
      url:http://orcid.org/0000-0002-6413-5874
      affiliation:
            name:Yale School of Medicine
            address:
               name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
               type:PostalAddress
            type:Organization
            name:Smilow Cancer Hospital
            address:
               name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
      name:Department of Neurological Surgery, Northwestern University, Chicago, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA
      name:Department of Neurosurgery, Yale School of Medicine, New Haven, USA
      name:The Chenevert Family Brain Tumor Center, Smilow Cancer Hospital, New Haven, USA

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