Hans Ehrencrona

Medicon Village
Lund, M 22381, Sweden

Last Updated: 09/26/2026

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Found 69 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

Surgical Outcomes After Risk-Reducing Mastectomy Among BRCA1 and BRCA2 Carriers.

Surgical Outcomes After Risk-Reducing Mastectomy Among BRCA1 and BRCA2 Carriers.

Journal: JAMA network open

Published: April 03, 2026

Updated ENIGMA recommendations for reporting germline variants in cancer susceptibility genes and their translation into twenty languages.

Updated ENIGMA recommendations for reporting germline variants in cancer susceptibility genes and their translation into twenty languages.

Journal: Journal of medical genetics

Published: January 13, 2026

Implementing electronic informed consent in rare disease genomics.

Implementing electronic informed consent in rare disease genomics.

Journal: Scientific reports

Published: October 20, 2025

Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.

Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.

Journal: European journal of human genetics : EJHG

Published: October 14, 2025

Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.

Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.

Journal: Nature communications

Published: September 09, 2025

Flexible and rapid validation of structural variation using adaptive sampling.

Flexible and rapid validation of structural variation using adaptive sampling.

Journal: European journal of human genetics : EJHG

Published: August 06, 2025

Diagnostic Yield and Genetic Variation in 85 Swedish Patients with Mild to Profound Hearing Loss Analyzed by Whole Genome Sequencing.

Diagnostic Yield and Genetic Variation in 85 Swedish Patients with Mild to Profound Hearing Loss Analyzed by Whole Genome Sequencing.

Journal: Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale

Published: July 21, 2025

Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare.

Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare.

Journal: Nature medicine

Published: April 04, 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

Whole genome sequencing in early onset advanced heart failure.

Whole genome sequencing in early onset advanced heart failure.

Journal: Scientific reports

Published: October 04, 2024

Genetic counselling legislation and practice in cancer in EU Member States.

Genetic counselling legislation and practice in cancer in EU Member States.

Journal: European journal of public health

Published: June 21, 2024

Showing 1-12 of 69

Last Updated: 09/26/2026