Here's how LINK.SPRINGER.COM makes money* and how much!

*Please read our disclaimer before using our estimates.
Loading...

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/s001090050122.

Title:
Are Canadian Inuit at increased genetic risk for coronary heart disease? | Journal of Molecular Medicine
Description:
 The Keewatin Inuit of the Northwest Territories of Canada have a very low age-adjusted mortality rate from coronary heart disease. We hypothesized that this apparent protection from disease has a genetic basis. We determined the prevalence of the disease-associated alleles of five candidate genes for atherosclerosis-related phenotypes. Surprisingly, four of the five alleles studied, namely AGT T235, FABP2 T54, PON R192 and APOE E4, were significantly more frequent in a sample of 175 Keewatin Inuit than among a representative control sample of whites living in the region. The high frequencies of these disease-associated alleles suggests either that they have no relationship with disease susceptibility in the Inuit, or that some unmeasured genetic and/or environmental factors mitigate disease susceptibility that is associated with these alleles. This highlights the difficulty in extrapolating findings from one population to another. Also, very modest genotype-phenotype associations were observed between APOE genotype (P=0.016) and plasma low-density lipoprotein cholesterol concentration and between FABP2 genotype and plasma 2-h postprandial glucose concentration (P=0.048). The relationship between APOE alleles and plasma low-density lipoprotein cholesterol was the same as has been previously reported in many study samples. However, the relationship between FABP2 alleles and plasma 2-h postprandial glucose concentrations was the opposite to that reported in other studies. This suggests that differences in environment, such as the type of fatty acid consumed, interacts with functional differences in gene products involved in candidate metabolic pathways to produce phenotypic differences.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {šŸ“š}

  • Science
  • Health & Fitness
  • Education

Content Management System {šŸ“}

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 {šŸ“ˆ}

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 5,000,016 visitors per month in the current month.

check SE Ranking
check Ahrefs
check Similarweb
check Ubersuggest
check Semrush

How Does Link.springer.com Make Money? {šŸ’ø}

We find it hard to spot revenue streams.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {šŸ”}

article, research, genetic, disease, alleles, privacy, cookies, content, journal, inuit, coronary, access, information, publish, search, medicine, risk, canada, apoe, genotype, plasma, association, toronto, health, data, log, heart, hegele, young, connelly, fabp, relationship, differences, gene, products, discover, biochemistry, university, sciences, springer, optional, analysis, personal, parties, protection, policy, find, track, molecular, canadian,

Topics {āœ’ļø}

fatty acid consumed modest genotype-phenotype associations month download article/chapter increased genetic risk community health sciences gene products involved privacy choices/manage cookies dna research laboratory postprandial glucose concentration full article pdf related subjects study samples original article published genetic basis unmeasured genetic atherosclerosis-related phenotypes coronary heart disease coronary artery disease european economic area scope submit manuscript postprandial glucose concentrations hakka postmenopausal women ontario m5b 1w8 check access instant access conditions privacy policy candidate metabolic pathways gene polymorphism accepting optional cookies molecular medicine aims representative control sample produce phenotypic differences journal finder publish main content log association apoe genotype fabp2 genotype article journal article hegele disease susceptibility article log risk factors privacy policy personal data usage analysis april 1997 volumeĀ 75 books a article cite optional cookies information

Questions {ā“}

  • Are Canadian Inuit at increased genetic risk for coronary heart disease?
  • Are Canadian Inuit at increased genetic risk for coronary heart disease?

Schema {šŸ—ŗļø}

WebPage:
      mainEntity:
         headline:Are Canadian Inuit at increased genetic risk for coronary heart disease?
         description: The Keewatin Inuit of the Northwest Territories of Canada have a very low age-adjusted mortality rate from coronary heart disease. We hypothesized that this apparent protection from disease has a genetic basis. We determined the prevalence of the disease-associated alleles of five candidate genes for atherosclerosis-related phenotypes. Surprisingly, four of the five alleles studied, namely AGT T235, FABP2 T54, PON R192 and APOE E4, were significantly more frequent in a sample of 175 Keewatin Inuit than among a representative control sample of whites living in the region. The high frequencies of these disease-associated alleles suggests either that they have no relationship with disease susceptibility in the Inuit, or that some unmeasured genetic and/or environmental factors mitigate disease susceptibility that is associated with these alleles. This highlights the difficulty in extrapolating findings from one population to another. Also, very modest genotype-phenotype associations were observed between APOE genotype (P=0.016) and plasma low-density lipoprotein cholesterol concentration and between FABP2 genotype and plasma 2-h postprandial glucose concentration (P=0.048). The relationship between APOE alleles and plasma low-density lipoprotein cholesterol was the same as has been previously reported in many study samples. However, the relationship between FABP2 alleles and plasma 2-h postprandial glucose concentrations was the opposite to that reported in other studies. This suggests that differences in environment, such as the type of fatty acid consumed, interacts with functional differences in gene products involved in candidate metabolic pathways to produce phenotypic differences.
         datePublished:
         dateModified:
         pageStart:364
         pageEnd:370
         sameAs:https://doi.org/10.1007/s001090050122
         keywords:
            Key words Angiotensin-converting enzyme
            Angiotensinogen
            Apolipoproteins
            Fatty acid binding protein
            Paraoxonase
            Genetic predisposition
            Molecular Medicine
            Human Genetics
            Internal Medicine
         image:
         isPartOf:
            name:Journal of Molecular Medicine
            issn:
               1432-1440
               0946-2716
            volumeNumber:75
            type:
               Periodical
               PublicationVolume
         publisher:
            name:Springer-Verlag
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:R. A. Hegele
               affiliation:
                     name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
                     address:
                        name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:T. Kue Young
               affiliation:
                     name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada
                     address:
                        name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada, , CA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Philip W. Connelly
               affiliation:
                     name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
                     address:
                        name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
                        type:PostalAddress
                     type:Organization
               type:Person
         isAccessibleForFree:
         hasPart:
            isAccessibleForFree:
            cssSelector:.main-content
            type:WebPageElement
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Are Canadian Inuit at increased genetic risk for coronary heart disease?
      description: The Keewatin Inuit of the Northwest Territories of Canada have a very low age-adjusted mortality rate from coronary heart disease. We hypothesized that this apparent protection from disease has a genetic basis. We determined the prevalence of the disease-associated alleles of five candidate genes for atherosclerosis-related phenotypes. Surprisingly, four of the five alleles studied, namely AGT T235, FABP2 T54, PON R192 and APOE E4, were significantly more frequent in a sample of 175 Keewatin Inuit than among a representative control sample of whites living in the region. The high frequencies of these disease-associated alleles suggests either that they have no relationship with disease susceptibility in the Inuit, or that some unmeasured genetic and/or environmental factors mitigate disease susceptibility that is associated with these alleles. This highlights the difficulty in extrapolating findings from one population to another. Also, very modest genotype-phenotype associations were observed between APOE genotype (P=0.016) and plasma low-density lipoprotein cholesterol concentration and between FABP2 genotype and plasma 2-h postprandial glucose concentration (P=0.048). The relationship between APOE alleles and plasma low-density lipoprotein cholesterol was the same as has been previously reported in many study samples. However, the relationship between FABP2 alleles and plasma 2-h postprandial glucose concentrations was the opposite to that reported in other studies. This suggests that differences in environment, such as the type of fatty acid consumed, interacts with functional differences in gene products involved in candidate metabolic pathways to produce phenotypic differences.
      datePublished:
      dateModified:
      pageStart:364
      pageEnd:370
      sameAs:https://doi.org/10.1007/s001090050122
      keywords:
         Key words Angiotensin-converting enzyme
         Angiotensinogen
         Apolipoproteins
         Fatty acid binding protein
         Paraoxonase
         Genetic predisposition
         Molecular Medicine
         Human Genetics
         Internal Medicine
      image:
      isPartOf:
         name:Journal of Molecular Medicine
         issn:
            1432-1440
            0946-2716
         volumeNumber:75
         type:
            Periodical
            PublicationVolume
      publisher:
         name:Springer-Verlag
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:R. A. Hegele
            affiliation:
                  name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
                  address:
                     name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:T. Kue Young
            affiliation:
                  name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada
                  address:
                     name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada, , CA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Philip W. Connelly
            affiliation:
                  name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
                  address:
                     name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
                     type:PostalAddress
                  type:Organization
            type:Person
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
["Periodical","PublicationVolume"]:
      name:Journal of Molecular Medicine
      issn:
         1432-1440
         0946-2716
      volumeNumber:75
Organization:
      name:Springer-Verlag
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
      address:
         name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
         type:PostalAddress
      name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada
      address:
         name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada, , CA
         type:PostalAddress
      name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
      address:
         name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:R. A. Hegele
      affiliation:
            name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
            address:
               name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
               type:PostalAddress
            type:Organization
      name:T. Kue Young
      affiliation:
            name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada
            address:
               name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada, , CA
               type:PostalAddress
            type:Organization
      name:Philip W. Connelly
      affiliation:
            name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada
            address:
               name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Departments of Medicine and Clinical Biochemistry, University of Toronto; DNA Research Laboratory, St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
      name:Northern Health Research Unit, Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada, , CA
      name:Departments of Medicine, Clinical Biochemistry and Biochemistry, University of Toronto; St. Michael’s Hospital Health Sciences Research Centre, 30 Bond Street, Toronto, Ontario M5B 1W8, Canada, , CA
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {šŸ”—}(29)

Analytics and Tracking {šŸ“Š}

  • Google Tag Manager

Libraries {šŸ“š}

  • Clipboard.js
  • Prism.js

CDN Services {šŸ“¦}

  • Crossref

4.91s.