The Danish Cancer Registry

By Marianne L. Gjerstorff. Scandinavian Journal of Public Health, 2011

1,339 citations recorded by the source corpus.

Subfields: Health Information Management, Oncology, Radiology, Nuclear Medicine and Imaging

View Paper: https://www.semanticscholar.org/paper/e61ff3b01b139420fe2b2682dc39412c3cfd8b05

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Health Information Management

1. S. Schmidt
2. M. Schmidt
3. H. Sørensen
4. Jakob Sandegaard
5. V. Ehrenstein
6. Lars Pedersen

In Oncology

1. S. Schmidt
2. H. Sørensen
3. M. Schmidt
4. Lars Pedersen
5. Jakob Sandegaard
6. V. Ehrenstein

In Radiology, Nuclear Medicine and Imaging

1. S. Schmidt
2. M. Schmidt
3. H. Sørensen
4. Jakob Sandegaard
5. V. Ehrenstein
6. Lars Pedersen

Citations in the corpus

• The Danish National Patient Registry: a review of content, data quality, and research potential (2015, methodology): “The registry also collects data for other health registries, including the Danish Psychiatric Central Research Register since 1995,(31) the Register of Legally Induced Abortions since 1995,(32) the Medical Birth Registry since 1997,(33) and the Danish Cancer Registry since 2004.(34) Updates DNPR dat”
• The Danish health care system and epidemiological research: from health care contacts to database records (2019, background): “Specific causes of death have been recorded in the Danish Registry of Causes of Deaths since 1943.(22) Suicide and suicide attempts are recorded separately in the Danish Registry of Suicide (since 1970)(22) and Registry for Suicide Attempts (since 1989).”
• Introduction to Danish (nationwide) registers on health and social issues: Structure, access, legislation, and archiving (2011, background): “For example, information on causes of death has been collected since 1875 in Denmark [1], information on compulsory schooling and continuing education are available for cohorts born after 1945 [2], information on twins are available for cohorts born after 1870 [3], and cancer incidence has been regi”