Lovisa Lovmar

Goeteborg, O, Sweden

Last Updated: 09/26/2026

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Found 18 publications

Genomic Medicine Sweden: Advancing precision medicine at the national level.

Genomic Medicine Sweden: Advancing precision medicine at the national level.

Journal: Journal of internal medicine

Published: July 07, 2026

Extracting homogenous data from heterogenous diseases: RaraSwed, the Swedish national rare disease quality registry.

Extracting homogenous data from heterogenous diseases: RaraSwed, the Swedish national rare disease quality registry.

Journal: BMC global and public health

Published: December 27, 2025

Implementing electronic informed consent in rare disease genomics.

Implementing electronic informed consent in rare disease genomics.

Journal: Scientific reports

Published: October 20, 2025

Health-related quality of life and visual function in retinoblastoma survivors with ocular prostheses: a cross-sectional study.

Health-related quality of life and visual function in retinoblastoma survivors with ocular prostheses: a cross-sectional study.

Journal: Scientific reports

Published: July 14, 2025

Survival outcomes in hormone receptor-negative breast cancer among BRCA carriers versus noncarriers in western Sweden.

Survival outcomes in hormone receptor-negative breast cancer among BRCA carriers versus noncarriers in western Sweden.

Journal: Acta oncologica (Stockholm, Sweden)

Published: March 11, 2025

Direct letters to relatives at risk of hereditary cancer-a randomised trial on healthcare-assisted versus family-mediated risk disclosure.

Direct letters to relatives at risk of hereditary cancer-a randomised trial on healthcare-assisted versus family-mediated risk disclosure.

Journal: European journal of human genetics : EJHG

Published: February 24, 2025

A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities.

A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities.

Journal: Genome research

Published: April 25, 2024

The value of genome-wide analysis in craniosynostosis.

The value of genome-wide analysis in craniosynostosis.

Journal: Frontiers in genetics

Published: October 16, 2023

Building a precision medicine infrastructure at a national level: The Swedish experience.

Building a precision medicine infrastructure at a national level: The Swedish experience.

Journal: Cambridge prisms. Precision medicine

Published: October 12, 2022

Implementing precision medicine in a regionally organized healthcare system in Sweden.

Implementing precision medicine in a regionally organized healthcare system in Sweden.

Journal: Nature medicine

Published: September 19, 2022

The outcome of targeted NGS screening in patients with syndromic forms of sagittal and pansynostosis - IL11RA is an emerging core-gene for pansynostosis.

The outcome of targeted NGS screening in patients with syndromic forms of sagittal and pansynostosis - IL11RA is an emerging core-gene for pansynostosis.

Journal: European journal of medical genetics

Published: October 29, 2021

The utility of whole genome sequencing in rare disease diagnostics

The utility of whole genome sequencing in rare disease diagnostics

Journal: Lakartidningen

Published: May 11, 2021

Showing 1-12 of 18

Last Updated: 09/26/2026