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akaturk Academic measurement

OpenAlex topic

Connexins and lens biology

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 1,119 works 15 author topics

Works

1,119 works

  1. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.5%

    No abstract yet.

  2. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.5%

    No abstract yet.

  3. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.5%

    No abstract yet.

  4. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.5%

    No abstract yet.

  5. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.5%

    No abstract yet.

  6. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.7%

    No abstract yet.

  7. YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.0%

    The study aim was to determine the risk of cataract among radiologic technologists with respect to occupational and nonoccupational exposures to ionizing radiation and to personal characteristics. A prospective cohort of 35,705 cataract-free US radiologic technologists aged 24-44 years was followed for nearly 20 years…

  8. YÖKSİS SJR Q3 JCR Q2 OpenAlex top 10% OpenAlex 98.8%

    Diabetes mellitus (DM) is a chronic systemic disease that has increases in prevalence over time. DM can affect all ocular structures, with cataract being the most common ocular complication. Cataract is the leading cause of blindness worldwide. Due to several mechanisms, there is an increased incidence of cataract for…

  9. OpenAlex top 10% OpenAlex 97.0%

    No abstract yet.

  10. OpenAlex top 10% OpenAlex 93.5%

    No abstract yet.

  11. YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 98.5%

    Of the many palmoplantar keratoderma (PPK) conditions, only Papillon-Lefèvre syndrome (PLS) and Haim-Munk syndrome (HMS) are associated with premature periodontal destruction. Although both PLS and HMS share the cardinal features of PPK and severe periodontitis, a number of additional findings are reported in HMS incl…

  12. YÖKSİS JCR Q2 OpenAlex top 10% OpenAlex 97.2%

    More than 50 Percent of prelingual hearing loss is genetic in origin, and of these up to 93 Percent are monogenic autosomal recessive traits. Some forms of genetic deafness can be recognized by their associated syndromic features, but in most cases, hearing loss is the only finding and is referred to as nonsyndromic d…

Academicians

15 academicians