Connection

Henning Bundgaard to Genetic Predisposition to Disease

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This is a "connection" page, showing publications Henning Bundgaard has written about Genetic Predisposition to Disease.
Henning Bundgaard
Connection Strength
0.125
Genetic Predisposition to Disease
  1. Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts. Eur J Hum Genet. 2019 09; 27(9):1427-1435.
    View in: PubMed
    Score: 0.067
  2. Prevalence and Progression of Late Gadolinium Enhancement in Children and Adolescents With Hypertrophic Cardiomyopathy. Circulation. 2018 08 21; 138(8):782-792.
    View in: PubMed
    Score: 0.016
  3. Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome. Nat Commun. 2017 11 22; 8(1):1696.
    View in: PubMed
    Score: 0.015
  4. The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease. Scand J Clin Lab Invest. 2017 Dec; 77(8):617-621.
    View in: PubMed
    Score: 0.015
  5. Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population. PLoS One. 2013; 8(8):e71904.
    View in: PubMed
    Score: 0.011
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.