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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s00439-013-1358-4.

Title:
The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine | Human Genetics
Description:
The Human Gene Mutation Database (HGMD®) is a comprehensive collection of germline mutations in nuclear genes that underlie, or are associated with, human inherited disease. By June 2013, the database contained over 141,000 different lesions detected in over 5,700 different genes, with new mutation entries currently accumulating at a rate exceeding 10,000 per annum. HGMD was originally established in 1996 for the scientific study of mutational mechanisms in human genes. However, it has since acquired a much broader utility as a central unified disease-oriented mutation repository utilized by human molecular geneticists, genome scientists, molecular biologists, clinicians and genetic counsellors as well as by those specializing in biopharmaceuticals, bioinformatics and personalized genomics. The public version of HGMD ( http://www.hgmd.org ) is freely available to registered users from academic institutions/non-profit organizations whilst the subscription version (HGMD Professional) is available to academic, clinical and commercial users under license via BIOBASE GmbH.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Technology & Computing

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.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

hgmd, pubmed, article, mutation, data, google, scholar, human, cas, mutations, central, variants, disease, gene, cooper, variant, genome, database, project, users, professional, functional, information, clinical, sequencing, additional, genomes, search, genes, stenson, nature, dbsnp, hum, including, molecular, variation, kim, analysis, access, genetic, literature, frequency, consortium, wang, genet, inherited, version, databases, include, evidence,

Topics {✒️}

central unified repository article download pdf variant call format locus-specific mutation databases human phenotype ontology ca/dgv/app/home cell type-dependent manner unresolved missense/nonsense mutations human protein-coding genes combined micro-insertions/micro-deletions user-defined sequence motifs apparently disease-causing mutations genome/population screening studies natural language processing missense/nonsense mutations reported human genetic disease human inherited disease human gene mutation human genome sequencing single characterized gene gene ontology medical genetics coding region micro-lesions microrna binding sites uk/resources/software/gff/ original reporting article keywords found privacy choices/manage cookies download hgmd data human genome variation irish human genome disease-causing mutation rhesus macaque genome medical research excellent curatorial work post-translational modifications inherited mutation data genome screening projects general feature format batch search mode allowing free access record disease-causing pubmed id population-scale sequencing personalized genomic medicine gene names/aliases database issue gorilla genome sequence latent protein deficiencies silent protein deficiencies

Questions {❓}

  • ), it may be flagged with a question mark (DM?
  • The DM classification may, however, also appear with a question mark (DM?
  • The recent introduction of the DM?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine
         description:The Human Gene Mutation Database (HGMD®) is a comprehensive collection of germline mutations in nuclear genes that underlie, or are associated with, human inherited disease. By June 2013, the database contained over 141,000 different lesions detected in over 5,700 different genes, with new mutation entries currently accumulating at a rate exceeding 10,000 per annum. HGMD was originally established in 1996 for the scientific study of mutational mechanisms in human genes. However, it has since acquired a much broader utility as a central unified disease-oriented mutation repository utilized by human molecular geneticists, genome scientists, molecular biologists, clinicians and genetic counsellors as well as by those specializing in biopharmaceuticals, bioinformatics and personalized genomics. The public version of HGMD ( http://www.hgmd.org ) is freely available to registered users from academic institutions/non-profit organizations whilst the subscription version (HGMD Professional) is available to academic, clinical and commercial users under license via BIOBASE GmbH.
         datePublished:2013-09-28T00:00:00Z
         dateModified:2013-09-28T00:00:00Z
         pageStart:1
         pageEnd:9
         sameAs:https://doi.org/10.1007/s00439-013-1358-4
         keywords:
            Unify Medical Language System
            Mutation Data
            Human Gene Mutation Database
            Human Phenotype Ontology
            Variant Call Format
            Human Genetics
            Molecular Medicine
            Gene Function
            Metabolic Diseases
         image:
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         isPartOf:
            name:Human Genetics
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         author:
               name:Peter D. Stenson
               affiliation:
                     name:Cardiff University
                     address:
                        name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                        type:PostalAddress
                     type:Organization
               email:[email protected]
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               affiliation:
                     name:Cardiff University
                     address:
                        name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                        type:PostalAddress
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               name:Edward V. Ball
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                     address:
                        name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Katy Shaw
               affiliation:
                     name:Cardiff University
                     address:
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                        type:PostalAddress
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               name:Andrew D. Phillips
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                        type:PostalAddress
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                     address:
                        name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                        type:PostalAddress
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ScholarlyArticle:
      headline:The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine
      description:The Human Gene Mutation Database (HGMD®) is a comprehensive collection of germline mutations in nuclear genes that underlie, or are associated with, human inherited disease. By June 2013, the database contained over 141,000 different lesions detected in over 5,700 different genes, with new mutation entries currently accumulating at a rate exceeding 10,000 per annum. HGMD was originally established in 1996 for the scientific study of mutational mechanisms in human genes. However, it has since acquired a much broader utility as a central unified disease-oriented mutation repository utilized by human molecular geneticists, genome scientists, molecular biologists, clinicians and genetic counsellors as well as by those specializing in biopharmaceuticals, bioinformatics and personalized genomics. The public version of HGMD ( http://www.hgmd.org ) is freely available to registered users from academic institutions/non-profit organizations whilst the subscription version (HGMD Professional) is available to academic, clinical and commercial users under license via BIOBASE GmbH.
      datePublished:2013-09-28T00:00:00Z
      dateModified:2013-09-28T00:00:00Z
      pageStart:1
      pageEnd:9
      sameAs:https://doi.org/10.1007/s00439-013-1358-4
      keywords:
         Unify Medical Language System
         Mutation Data
         Human Gene Mutation Database
         Human Phenotype Ontology
         Variant Call Format
         Human Genetics
         Molecular Medicine
         Gene Function
         Metabolic Diseases
      image:
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      isPartOf:
         name:Human Genetics
         issn:
            1432-1203
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         volumeNumber:133
         type:
            Periodical
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      publisher:
         name:Springer Berlin Heidelberg
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Peter D. Stenson
            affiliation:
                  name:Cardiff University
                  address:
                     name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Matthew Mort
            affiliation:
                  name:Cardiff University
                  address:
                     name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Edward V. Ball
            affiliation:
                  name:Cardiff University
                  address:
                     name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Katy Shaw
            affiliation:
                  name:Cardiff University
                  address:
                     name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                     type:PostalAddress
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            name:Andrew D. Phillips
            affiliation:
                  name:Cardiff University
                  address:
                     name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                     type:PostalAddress
                  type:Organization
            type:Person
            name:David N. Cooper
            affiliation:
                  name:Cardiff University
                  address:
                     name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
                     type:PostalAddress
                  type:Organization
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      name:Springer Berlin Heidelberg
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         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
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      name:Cardiff University
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         name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
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         name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
         type:PostalAddress
      name:Cardiff University
      address:
         name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
         type:PostalAddress
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         name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
         type:PostalAddress
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      address:
         name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
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         name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
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Person:
      name:Peter D. Stenson
      affiliation:
            name:Cardiff University
            address:
               name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Matthew Mort
      affiliation:
            name:Cardiff University
            address:
               name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      name:Edward V. Ball
      affiliation:
            name:Cardiff University
            address:
               name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      name:Katy Shaw
      affiliation:
            name:Cardiff University
            address:
               name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      name:Andrew D. Phillips
      affiliation:
            name:Cardiff University
            address:
               name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      name:David N. Cooper
      affiliation:
            name:Cardiff University
            address:
               name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
      name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
      name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
      name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
      name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK
      name:Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK

External Links {🔗}(204)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

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CDN Services {📦}

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4.7s.