Svetlana Lagercrantz-Bajalica
Stockholm, AB, Sweden
Last Updated: 09/26/2026
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Found 25 publications
Surgical Outcomes After Risk-Reducing Mastectomy Among BRCA1 and BRCA2 Carriers.
Journal: JAMA network open
Published: April 03, 2026
Surveillance adherence and clinical findings in children with confirmed or familial TP53 variants: the Swedish multicenter constitutional TP53 study (SWEP53).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 14, 2025
Optimising rare tumour risk syndromes care: clinical insights and the PREVENTABLE socioeconomic framework.
Journal: European journal of human genetics : EJHG
Published: June 23, 2025
The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation.
Journal: Genome medicine
Published: May 31, 2025
Characterisation of heritable TP53-related cancer syndrome in Sweden-a nationwide study of genotype-phenotype correlations in 90 families.
Journal: European journal of human genetics : EJHG
Published: February 28, 2024
Investigation of Genetic Alterations Associated With Interval Breast Cancer.
Journal: JAMA oncology
Published: January 25, 2024
Public attitudes challenge clinical practice on genetic risk disclosure in favour of healthcare-provided direct dissemination to relatives.
Journal: European journal of human genetics : EJHG
Published: June 29, 2023
Prediction of breast cancer risk for sisters of women attending screening.
Journal: Journal of the National Cancer Institute
Published: January 09, 2023
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Journal: The Lancet. Oncology
Published: July 17, 2022
Last Updated: 09/26/2026