Inga Bjornevoll
Trondheim, Norway
Last Updated: 09/26/2026
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Found 10 publications
Diagnostic uncertainties, ethical tensions, and accounts of role responsibilities in genetic counseling communication.
Journal: Journal of genetic counseling
Published: August 02, 2019
The recognition of the profession of Genetic Counsellors in Europe.
Journal: European journal of human genetics : EJHG
Published: July 05, 2018
Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility.
Journal: Journal of medical genetics
Published: August 07, 2017
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
Journal: Clinical genetics
Published: December 16, 2016
The perceived impact of the European registration system for genetic counsellors and nurses.
Journal: European journal of human genetics : EJHG
Published: December 09, 2016
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing.
Journal: European journal of human genetics : EJHG
Published: November 21, 2016
Development of a registration system for genetic counsellors and nurses in health-care services in Europe.
Journal: European journal of human genetics : EJHG
Published: July 24, 2015
A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine.
Journal: Familial cancer
Published: April 11, 2015
The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry.
Journal: Hereditary cancer in clinical practice
Published: January 30, 2014
De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype.
Journal: Neurology
Published: August 16, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026